Infrared and Raman Studies of Charge Ordering in Organic Conductors, BEDT-TTF Salts with Quarter-Filled Bands

Abstract

This paper reviews charge ordering in the organic conductors, β″-(BEDT-TTF)(TCNQ), θ-(BEDT-TTF)₂X, and α-(BEDT-TTF)₂X. Here, BEDT-TTF and TCNQ represent bis(ethylenedithio)tetrathiafulvalene and 7,7,8,8-tetracyanoquinodimethane, respectively. These compounds, all of which have a quarter-filled band, were evaluated using infrared and Raman spectroscopy in addition to optical conductivity measurements. It was found that β″-(BEDT-TTF)(TCNQ) changes continuously from a uniform metal to a charge-ordered metal with increasing temperature. Although charge disproportionation was clearly observed, long-range charge order is not realized. Among six θ-type salts, four compounds with a narrow band show the metal-insulator transition. However, they maintain a large amplitude of charge order (Δρ~0.6) in both metallic and insulating phases. In the X = CsZn(SCN)₄ salt with intermediate bandwidth, the amplitude of charge order is very small (Δρ < 0.07) over the whole temperature range. However, fluctuation of charge order is indicated in the Raman spectrum and optical conductivity. No indication of the fluctuation of charge order is found in the wide band X = I₃ salt. In α-(BEDT-TTF)₂I₃ the amplitude of charge order changes discontinuously from small amplitude at high temperature to large amplitude (Δρ_max~0.6) at low temperature. The long-range charge-ordered state shows ferroelectric polarization with fast optical response. The fluctuation of multiple stripes occurs in the high-temperature metallic phase. Among α-(BEDT-TTF)₂MHg(SCN)₄ (X = NH₄, K, Rb, Tl), the fluctuation of charge order is indicated only in the X = NH₄ salt. α′-(BEDT-TTF)₂IBr₂ shows successive phase transitions to the ferroelectric state keeping a large amplitude of charge order (Δρ_max~0.8) over the whole temperature range. It was found that the amplitude and fluctuation of charge order in these compounds is enhanced as the kinetic energy (bandwidth) decreases.

1. Introduction

Vibrational spectroscopy is a powerful tool to detect the valence of molecules in organic charge-transfer salts. Among the normal modes of molecular vibrations, several vibrational modes change their eigenfrequencies depending on the valence of the molecule in question. These vibrational modes are called charge-sensitive modes. For example, the C=C stretching mode is utilized as a probe for detecting the valence. As the chemical bond is usually much stronger than intermolecular interactions, the vibrational frequency and symmetry of a free molecule is approximately preserved in the solid state except in the case where a strong vibronic interaction occurs between a vibrational mode and a low-energy electronic state (electron molecular vibration coupling). A vibrational mode that strongly interacts with the electronic state is called structure-sensitive mode. Knowledge of the normal mode of a free molecule is essential, because a deviation from this mode in the solid state tells us which interaction is occurring. In this sense, reliable assignments of vibrational bands in the solid state are the most critical and indispensable. The charge-sensitive mode was applied for the first time to the distribution of charges in the unit cell of Cs₂TCNQ₃, where TCNQ represents 7,7,8,8-tetracyanoquinodimethane, wherein the infrared-active external ring C=C stretching modes (ν₄) of TCNQ⁰ and TCNQ⁻ were separately observed [1]. A detailed normal mode analysis of TCNQ⁰ and TCNQ⁻ was reported by Bozio et al. [2]. Matsuzaki et al., extended the application to the TCNQ salt with fractional charge [3]. Subsequently, vibrational spectroscopy was applied to mixed-valence compounds of TCNQ [4], where one of the CN stretching modes of TCNQ was utilized as the probe.

The existence of Wigner-type charge order (CO) in organic conductors had been argued based on the finding of 4k_F modulation in quasi-one-dimensional tetrathiafulvalene-7,7,8,8-tetracyanoquinodimethane (TTF-TCNQ) [5,6,7,8] because the wavelength of the 4k_F modulation corresponds to the distance between localized electrons (holes) which are arranged with equal distance. However, the 4k_F modulation found in TTF-TCNQ was related to the 4k_F Peierls instability with on-site Coulomb repulsion. Since the amplitude of the charge density wave (CDW) is small, the charge-sensitive mode shows almost no linewidth broadening. The long-range CO of the Wigner-type was reported for quasi-one-dimensional (DI-DCNQI)₂Ag, where DI-DCNQI corresponds to 2,5-diiodo-dicyanoquinodiimine, by Hiraki and Kanoda using ¹³C-NMR [9]. They showed that the amplitude of CO (Δρ = 0.5) is much larger than that of an incommensurate CDW. At about the same time, Seo theoretically predicted the CO ground state for (TMTTF)₂X (X = Br, SCN), where TMTTF corresponds to tetramethyltetrathiafulvalene, and (DI-DCNQI)₂Ag using mean-field theory [10]. Later, Chow reported a similar charge order for (TMTTF)₂X (X = PF₆, AsF₆) using ¹³C-NMR [11]. In the case of a two-dimensional organic compound, Moldenhauer et al., reported that localization of charge occurs in one of the stacks of α-(BEDT-TTF)₂I₃ (BEDT-TTF corresponds to bis(ethylenedithio) tetrathiafulvalene) [12]. After the theoretical prediction of the CO ground state for α-(BEDT-TTF)₂I₃ by Kino and Fukuyama [13], CO in two-dimensional organic compounds was suggested in α-(BEDT-TTF)₂I₃ [14], and more clearly shown in θ-(BEDT-TTF)₂RbZn(SCN)₄ [15]. Stimulated by the experimental findings of CO, theoretical studies were conducted on the role of intersite Coulomb interaction in CO [16,17,18], lattice distortion accompanied by CO [19,20,21], the relationship between CO fluctuation and superconductivity (SC) [22], and quantum criticality at the edge of CO [23]. Subsequently, several experimental and theoretical studies have been conducted [24,25,26,27]. Some of these will be introduced from Section 3 on, in relation to the experimental results. Charge ordering continues to attract experimental and theoretical interest and attention. Some compounds in the CO state are regarded as unconventional ferroelectrics [28]. However, the ferroelectric properties have not been well investigated so far due to experimental difficulties. SC paring mediated by CO fluctuation was proposed by Merino and McKenzie [22]. Spectroscopic studies which may support the theoretical prediction for the SC mechanism have been reported [29,30,31,32,33,34]. It was also predicted that spin fluctuation mediates the SC pairing in a CO system [35]. Recently, it was pointed out that interaction with anions plays an essential role in the CO phase transition [36,37]. These subjects will be further investigated in future.

Along with NMR and x-ray diffraction, vibrational spectroscopy is a powerful tool to investigate the CO state, since the amplitude of CO is large. Raman spectroscopy was first applied to the charge ordering phase transition of θ-(BDT-TTP)₂Cu(NCS)₂, for which the spectral features drastically changed [38,39]. Although the charge-sensitive mode is expected to show a simple splitting in a CO state, the Raman spectrum showed complicated splitting due to the additional splitting of the structure-sensitive mode. The fluctuation of charge order was obviously detected in the metallic phase. These characteristics were for the most part commonly observed in the compounds discussed here. In this paper, the author reviews infrared, Raman, and optical conductivity measurements of BEDT-TTF salts, which, apart from β″-(BEDT-TTF)(TCNQ), have a herringbone arrangement. This latter compound is included in this paper, because its unique behavior is necessary for understanding the metallic phase of θ- and α-type BEDT-TTF salts.

The paper is organized as follows. Section 2 briefly describes the relation between the site charge and band structure, fluctuation of charge order and time correlation function, charge- and structure-sensitive modes of BEDT-TTF, electron-molecular vibration coupling, and the line shape when the site charge fluctuates. Section 3 describes charge disproportionation in β″-(BEDT-TTF) (TCNQ), wherein a continuous change of the electronic state is discussed combined with optical conductivity. Section 4 describes the charge-ordering phase transition θ-type BEDT-TTF salts; first, how the charge- and structure-sensitive modes split in the CO state; second, the metallic state with large CO amplitude is discussed; third, the metallic state with small CO amplitude is discussed. Section 5 introduces a spectroscopic investigation of α-type BEDT-TTF. Here, the splitting of charge- and structure-sensitive modes in CO phase and ferroelectric properties are described first. Next, the splitting of the charge-sensitive mode and fluctuation of CO in the metallic phase are discussed. Third, the non-uniform site charge distribution in the metallic phase under ambient pressure and hydrostatic pressure is compared with band calculations. Fourth, the optical conductivity is reviewed along with the collective CO excitation Finally, the successive ferroelectric transition of α′-(BEDT-TTF)₂IBr₂ is briefly described. The final section 6 presents the kinetic energy, which is associated with the bandwidth, of these compounds, and summarizes their electronic states correlated with kinetic energy.

2. Detection and Analysis of Charge Order

2.1. Site Charge and Fluctuation

In solid organic charge-transfer salts, valence electrons are delocalized depending upon the magnitude of the overlap integral. Therefore, the valence of the molecule becomes a non-integer value, when the number of valence electrons does not equal the number of molecules. The fractional valence or fractional charge at the jth site (site charge) in the unit cell, ρ_j, is given by the following equation:

(1)

where is the Bloch function of the mth band, n_M is the number of molecules in a unit cell, n_j is the number operator at the jth site, and f(ε) is the Fermi distribution function for a hole. The site charge is the integrated valence electron at each site below a Fermi level. Therefore, the site-charge distribution is sometimes non-uniform even in a metal, if the site in a unit cell is crystallographically non-equivalent. If the amplitude of charge order Δρ is small, a small portion of the valence electrons near the Fermi level contribute to the charge disproportionation, while in the case of large Δρ, most valence electrons participate in the charge disproportionation as the band structure entirely changes

When the site charge dynamically fluctuates as ρ(t), the correlation time τ is defined by the following equation,

(2)

where Δρ(t′) = ρ(t′) − < ρ(t′) ≥ ρ(t′) − 1/2 in the case of quarter filling, <Δρ(t′)Δρ(t′ + t)> is the time correlation function of ρ, and Δ² =< Δρ(t′)Δρ(t′)> is the amplitude (variance) of fluctuation. As explained in the preceding paragraph, only the valence electrons near the Fermi level fluctuate, when the fluctuation amplitude is small. The charge fluctuation in a quarter-filled-band system was theoretically discussed in refs. [40,41] using the charge correlation function C(q,ω). If the system has CO instability, the charge correlation function has a strong peak at q₀ and ω₀~0. The wave vector q₀ specifies a charge-order pattern such as checkerboard or stripe. The peak frequency ω₀ is the energy of the excited state which contributes to produce a CO wave in a uniform metal, and it may be related to the amplitude of CO fluctuation. The peak height and width are respectively associated with correlation length and correlation time. The time correlation function of the specified q₀ is the Fourier transform of C(q₀,ω).

2.2. Charge-Sensitive Mode of BEDT-TTF

A normal mode analysis of BEDT-TTF⁰ and BEDT-TTF¹⁺ was reported by Kozlov et al. [42,43]. The normal modes most sensitive to the charge (valence) of the BEDT-TTF molecule are the in-phase (ν₂, Raman active) and out-of-phase (ν₂₇ infrared active) stretching modes of the ring C=C bonds, and the stretching mode of the C=C bond bridging two five member rings (ν₃, Raman active). Kozlov et al., analyzed the normal mode assuming the D_2h symmetry, and their mode numbering is different from the subsequent numbering using more exact D₂ symmetry [44]. In this paper, Kozlov’s numbering shown in Figure 1 will be used to avoid complication. In the solid state, site symmetry is usually lower than D_2h or D₂. However, the crystal field in organic conductors is much weaker than the covalent energy within a molecule. Therefore, the symmetry of the free molecule is approximately preserved in a crystal.

Figure 1. C=C stretching modes of BEDT-TTF. The ν₂ and ν₂₇ modes are charge-sensitive, while the ν₃ mode depends upon the network of transfer integrals, and thus it is structure-sensitive.

Figure 1. C=C stretching modes of BEDT-TTF. The ν₂ and ν₂₇ modes are charge-sensitive, while the ν₃ mode depends upon the network of transfer integrals, and thus it is structure-sensitive.

An attempt to examine the linear relationship between the frequency and fractional charge of BEDT-TTF was made by Wang et al., for the Raman-active ν₂ and ν₃ modes [45]. However, the frequency data were scattered about the linear relationship. In addition, they did not consider the effect of electron-molecular vibration interaction, which will be discussed in the next subsection. The linear relationship for the infrared-active ν₂₇ was first utilized by Moldenhauer et al., for estimating the iconicity of BEDT-TTF [12]. However, this relationship is given based on the incorrect assignment of BEDT-TTF⁺ [46]. Subsequently, the relationship was not examined for long time, because this mode is usually hidden in a huge electronic absorption band when it is measured on the conducting plane or powdered samples. Recently, Yamamoto et al., have examined the assignment of Kozlov et al., and they reassigned ν₂, ν₃, and ν₂₇ of BEDT-TTF⁺ with the aid of ¹³C and deuterium substituted compounds [46]. First they examined ν₂₇ employing the polarization perpendicular to the conducting layer on the side face of single crystals. They found that the frequency of BEDT-TTF⁰ deviated from the linear relation, because it has a non-planar structure. They calculated the frequency of ν₂ and ν₂₇ assuming D₂ symmetry employing a DFT method, and found that the frequency of the flat structure BEDT-TTF⁰ satisfies the linear relationship. They presented an empirical relationship for the infrared active ν₂₇ mode, ν₂₇(ρ) = 1398 + 140(1 − ρ). Next they examined the Raman-active ν₂ and ν₃ modes. The ν₃ mode is more strongly perturbed by the electron-molecular vibration (EMV) interaction than the effect of charge. As we will explain in the next section, the highest-frequency ν₃ mode does not shift, even if the charge disproportionation occurs, whereas the ν₂ mode at charge-rich site (ν_2R) shifts toward lower frequency. Consequently, the line ν_2R(ρ) crosses the line ν₃(ρ), at ρ~0.9 (see Figure 2). As the result of the interaction between ν_2R and ν₃, the frequency of ν_2R deviates from the linear relationship. They presented the linear relationship for the infrared-active ν₂ as ν₂(ρ) = 1447 + 120(1 − ρ), which is available only in the range of 0 < ρ < 0.8. The ρ dependence of the frequency is ascribed to the ρ dependent force constant F(ρ). That is, the linear relationship requires (dF/dρ)_ρ=0 = (dF/dρ)_ρ=1 [47]. However, the frequency of BEDT-TTF^0.5+ deviates significantly from the linear relationship toward the low-frequency side, which means that |(dF/dρ)_ρ=0| > |(dF/dρ)_ρ=1| (See Figure 7 of ref. [46]). Other nonlinear relationship at ρ~0.5 will be discussed in Section 5.3.1.

Figure 2. (a) Frequency of the vibronic modes plotted against the site charge of charge-rich site (ρ_P + ρ_R = 1). The transfer integral is t = 0.2 eV, EMV coupling constants for ν₂ and ν₃ are g₂ = 0.02 eV and g₃ = 0.1 eV, respectively. The dashed line shows the site-charge dependence when g₂ = g₃ = 0, assuming a linear relationship against site charge ρ. The frequencies at ρ = 0 and 1 are ν₂(0) = 1567 cm⁻¹, ν₂(1) = 1447 cm⁻¹, ν₃(0) = 1520 cm⁻¹, and ν₃(1) = 1410 cm⁻¹; (b) Contribution of the intermolecular excitation to the Raman tensor of the vibronic modes, which are plotted against the site charge of the charge-rich site; (c) Oscillator strength of the vibronic modes plotted against the site charge of the charge-rich site.

Figure 2. (a) Frequency of the vibronic modes plotted against the site charge of charge-rich site (ρ_P + ρ_R = 1). The transfer integral is t = 0.2 eV, EMV coupling constants for ν₂ and ν₃ are g₂ = 0.02 eV and g₃ = 0.1 eV, respectively. The dashed line shows the site-charge dependence when g₂ = g₃ = 0, assuming a linear relationship against site charge ρ. The frequencies at ρ = 0 and 1 are ν₂(0) = 1567 cm⁻¹, ν₂(1) = 1447 cm⁻¹, ν₃(0) = 1520 cm⁻¹, and ν₃(1) = 1410 cm⁻¹; (b) Contribution of the intermolecular excitation to the Raman tensor of the vibronic modes, which are plotted against the site charge of the charge-rich site; (c) Oscillator strength of the vibronic modes plotted against the site charge of the charge-rich site.

2.3. Electron-Molecular Vibration (EMV) Coupling in BEDT-TTF

The EMV interaction was first studied to interpret the strong infrared signal in the reflectivity polarized along the stacking axis in K-TCNQ [48]. Rice et al., reported a symmetric dimer model and presented a comprehensive explanation for the EMV interaction [49]. According to the dimer model, the a_g mode of each molecule splits into in-phase and out-of-phase modes depending upon the magnitude of the coupling constant and transfer integral. The EMV interaction works only for the out-of-phase mode, and the coupling constant is estimated from the frequency difference between the Raman-active in-phase mode and the infrared-active out-of-phase mode. The EMV effect on the Raman-active mode was first pointed out by Girlando et al., in TTF-CA [50].

Based on the formulation by Painelli and Girlando [51], Yamamoto and Yakushi extended this idea to a disproportionate (asymmetric) dimer with average charge ρ = 0.5, in which each site has a non-equivalent charge like (BEDT-TTF)^ρ+(BEDT-TTF)^(1-ρ)+ [52]. Figure 2 shows the numerical calculation of the frequency and intensity of vibronic modes plotted as a function of the site charge of the charge-rich site (ρ > 0.5). In this calculation, the transfer integral between two molecules is taken as t = 0.2 eV, and the coupling constants of ν₂ and ν₃ mode are taken as g₂ = 0.02 eV and g₃ = 0.1 eV. ν_2P and ν_2R, denote the ν₂ mode of the charge-poor and charge-rich site (molecule), respectively, and ν_3A, and ν_3B denote the ν₃ mode for the in-phase and out-of-phase oscillation, respectively. The coupling constant in BEDT-TTF is estimated in refs. [43,53]. The coupling constants of ν₂ and ν₃ were respectively estimated to be g₂ = 0.043 and g₃ = 0.071 eV from an analysis of the infrared spectrum of the isolated dimer (BEDT-TTF)₂²⁺ [53]. The parameters estimated from the infrared spectra were very scattered (g₂ ~ 0.007–0.039 eV and g₃ = 0.007–0.081 eV) depending upon the compounds [54]. A more recent estimation gives g₃ = 0.076 eV from the analysis of the infrared spectrum of κ-(BEDT-TTF)₂Cu[N(CN)₂]-Br_0.85Cl_0.15 [55]. Using the same data, Girlando interpreted this as g₂ = 0.075 eV [56]. The estimation of the coupling constants of ν₂ and ν₃ from the infrared spectrum seems to be unfixed still now. The coupling constants used for the model calculation (Figure 2) are qualitatively consistent with ref. [55] and with the interpretation of the Raman spectra of various compounds appearing in this paper.

As shown in Figure 2a, the weakly coupled modes, ν_2P and ν_2R, approximately conform to a linear relationship. However, the strongly coupled modes, ν_3A and ν_3B, deviate remarkably from the linear relation, although the frequency of ν₃ of the free molecule follows a linear relationship as shown by the dashed lines in Figure 2a [56]. The ν_3A and ν_3B modes are respectively the in-phase and out-of-phase vibrations at ρ = 0.5. The noteworthy point here is that the ν_3A mode that is Raman-active keeps the frequency corresponding to ρ = 0.5 in the range of 0.2 < ρ < 0.8. This is because the in-phase vibrations at two sites are not perturbed by the EMV interaction [49]. Actually, the frequencies of ν₃ of the 2:1 salts are nearly equal to those of the 3:2 salts in the work by Wang et al. [45] although they claim a linear relationship for ν₃ in their paper. Near ρ~0.8, mixing between ν_2R and ν_3A occurs, and the assignment becomes meaningless. This situation is sometimes seen in the charge-ordered state (See Section 4.1, Section 5.1, and Section 5.3.3). This result means that Raman spectroscopy cannot determine the fractional charge when the molecular vibrations strongly interact with each other through the EMV mechanism. Fortunately, in the case of BEDT-TTF, the ν₂ mode is available to determine the fractional charge, because the EMV coupling is weak enough. However, this mode is available only in the range of 0 < ρ < 0.8. In this sense, the infrared-active mode, for example, ν₂₇ of BEDT-TTF is the best probe to determine the site charge in a charge-ordered system. From the viewpoint of experimental technique, it is extremely difficult to observe ν₂₇ in the conducting plane, because the phonon mode is screened by the strong electronic absorption band. Usually the crystal face parallel to a conducting plane is most developed. Therefore, the best way to detect ν₂₇ is to measure the reflectivity on the thin side face of the crystal with the polarization perpendicular to the conducting plane.

In the infrared spectrum, we can observe only the out-of-phase mode ν_3B, which shows a large downshift due to the large EMV coupling constant, as shown in Figure 2c. As the out-of-phase mode dynamically modulates the orbital energy of the highest occupied molecular orbital (HOMO) of BEDT-TTF in the dimer, it transfers charge back and forth inducing an oscillating dipole along the direction connecting the centers of the molecules [49]. Accordingly, the out-of-phase ν₃ mode is usually found very strongly in the optical conductivity of the conducting plane (See Section 4 and Section 5). The downshift of this mode is sensitive to the transfer integrals between BEDT-TTF molecules (see ref. [54] for example). Yamamoto et al., discussed the relation between the downshift of ν_3B and transfer integrals comparing the ν₃ modes among several θ-type of BEDT-TTF salts. [57] Utilizing this property, the symmetry can be determined, for example, by the presence of a glide plane (See Section 4.1) and breaking of inversion symmetry (See Section 5.1). The Raman intensity of the same vibronic mode ν_3B is calculated to be strong in the disproportionate dimer (See Figure 2b). In this model, only the intermolecular excitation is considered for the calculation of the Raman tensor in the off-resonance condition. Actually, intramolecular excitations contribute more to the Raman tensor, and the resonance effect is sometimes quite large in the charge-transfer salts of BEDT-TTF. This calculation shows the additional contribution of the intermolecular excitation to the Raman tensor. As shown in Figure 2b, the contribution of this intermolecular excitation is largest in the vibronic ν₃ mode that has a large EMV coupling constant. Actually, the vibronic ν₃ mode is frequently found in the Raman spectrum of charge-ordered system (See Section 4 and Section 5).

2.4. The Line Shape of Charge-Sensitive Mode

The frequency of the charge-sensitive mode strongly depends upon the site charge, for example, Δω/Δρ ≈ 140 cm⁻¹/e or Δω/Δρ ≈ −140 cm⁻¹/h for the ν₂₇ mode. Let us consider a system in which the unit cell involves two sites (molecules) and one hole. If every site is equivalent, then every site has a uniform site charge (hole) ρ = 0.5. When the system undergoes a charge-ordering transition, the site charge is disproportioned into ρ_R and ρ_P. Therefore, the charge-sensitive mode splits into two vibrational bands from a single band. If the site charge fluctuates around ρ = 1/2, the frequency also fluctuates around ν(ρ), and the linewidth is broadened depending on the fluctuation rate. This relation is illustrated in Figure 3.

Figure 3. Linear relationship between the site charge and frequency of ν₂₇ [46]. The schematic sketch of the spectrum shows that the charge-sensitive mode of uniform site charge (green) is split into two (blue) by charge disproportionation, and the linewidth is broadened by the fluctuation of the site charge.

Figure 3. Linear relationship between the site charge and frequency of ν₂₇ [46]. The schematic sketch of the spectrum shows that the charge-sensitive mode of uniform site charge (green) is split into two (blue) by charge disproportionation, and the linewidth is broadened by the fluctuation of the site charge.

Figure 4. (a) Two-states-jump model calculated by Equation (3) with ω_1/2 = 0, Г/Δ = 0.04, a_R = 10, and a_P = 0.3; (b) Gaussian model calculated using Equation (4). τ and Δ are the correlation time and amplitude of fluctuation, respectively.

Figure 4. (a) Two-states-jump model calculated by Equation (3) with ω_1/2 = 0, Г/Δ = 0.04, a_R = 10, and a_P = 0.3; (b) Gaussian model calculated using Equation (4). τ and Δ are the correlation time and amplitude of fluctuation, respectively.

The fluctuation of the site charge is characterized by its amplitude (or variance ) and correlation time , where Δρ = ρ(t) − 1/2 is the time-dependent site-charge variation from the average site charge 1/2. This charge fluctuation modulates the frequencies of ν₂₇ and ν₂ with an amplitude Δ_f and correlation time τ. When the site charge fluctuates stochastically between two values such as ρ_R and ρ_P and thus the frequency fluctuates between ω_R and ω_P with a transition rate γ, then the line shape of the charge-sensitive mode is described by the following equation [58].

(3)

here ω_1/2 is the frequency for ρ = 1/2, Δ = (ω_P − ω_R)/2, Г is the natural width in the solid state, and a_R and a_P are parameters proportional to the transition dipole moment or Raman tensor of the charge-sensitive mode at charge-rich and charge-poor sites, respectively. In this case, the correlation time is equal to the staying time at a site which is given by τ = 1/γ. When τΔ << 1 or τΔ >> 1, the lineshape approaches a Lorentzian.

When the site charge fluctuates stochastically as a Gaussian process, the correlation function has an exponential decay as, , where Δ_c is the amplitude of the fluctuation and γ is the decay rate. In this case, the modulation of the site charge is transformed to a modulation of the frequency of the charge-sensitive mode, and the line shape of the charge-sensitive mode is given by the following equation [59,60],

(4)

where Δ is the amplitude (variance) of the modulation frequency of the charge-sensitive mode. In this case the correlation time is equal to the inverse of the decay rate, τ = 1/γ. When τΔ >> 1 and τΔ << 1, the lineshape approaches a Gaussian and a Lorentzian, respectively. Figure 4 shows the spectral line shape of these two cases plotted as a function of ωΔ for various τΔ with ω_1/2 = 0. In both cases, the line shape is determined by the parameter τΔ. When both τ and Δ vary with temperature, it is difficult to determine them from an analysis of the line shape.

3. β″-(BEDT-TTF)(TCNQ)

3.1. Crystal Structure and Superlattice

β″-(BEDT-TTF)(TCNQ) has a segregated stack structure, in which BEDT-TTF and TCNQ are regularly stacked along the c axis. The degree of the charge transfer of (BEDT-TTF)^+ρ(TCNQ)^−ρ is estimated to be ρ = 0.5 from the frequency shift of ν₂₁, ν₃₄, and ν₄ of TCNQ [61]. Therefore, this compound is regarded as a quarter-filled system. BEDT-TTF has the largest transfer integral along the side-by-side direction (a axis) and TCNQ has the largest transfer integral along the stacking direction [62]. The hopping interaction between BEDT-TTF and TCNQ along the b axis is negligibly small. These theoretical predictions are qualitatively supported by the anisotropic optical conductivity [61]. Very weak superlattice spots are reported in ref. [61]. The observation of vibronic bands of TCNQ only in the E||c optical conductivity suggests that TCNQ is dimerized whereas BEDT-TTF is not. Based on these spectroscopic results and assuming the space group , the proposed model of this superstructure is shown in Figure 5. TCNQ is connected by a center of symmetry (4k_F modulation) and BEDT-TTF is located on the center of symmetry. Therefore, the two TCNQs in the unit cell are crystallographically equivalent, whereas the two BEDT-TTFs are non-equivalent. These superlattice spots disappear at around 170 K. However, the vibronic bands of TCNQ still remain after the superlattice spots vanish. This result implies that the short-range ordered 4k_F modulation remains in the TCNQ stack or another superlattice forms. According to the X-ray diffraction study by Nogami, a new superlattice spot for 2a × 2c was found below 170 K. [63]. In any case, the valence electron in the TCNQ stack is localized within the dimer, and the valence electron in the pseudo-one-dimensional BEDT-TTF band is responsible for the charge carriers.

β″-(BEDT-TTF)(TCNQ) is metal-like down to 1.8 K with three anomalies at ~170 K, ~80 K, and ~20 K [62,64]. The magneto-resistance below 20 K was extensively studied by Yasuzuka et al. They found five distinct small Fermi surfaces through the Shubnikov-de-Haas oscillations [65,66,67]. A quasi-one-dimensional periodic orbit resonance was found through the magneto-optical measurement [68,69]. The magneto-resistance and magneto-optical experiments demonstrate the existence of the Fermi surface below 20 K, which implies that the ground state is a Fermi liquid metal. On the other hand, charge disproportionation with an amplitude of Δρ~0.6 was reported at room temperature based on the observation of the splitting of charge-sensitive ν₂₇ mode of BEDT-TTF [70]. Such a large amplitude at high-temperature indicates a localized nature, so suggesting a phase change between the high- and low-temperature regions.

Figure 5. Arrangement of molecules in β″-(BEDT-TTF)(TCNQ). Average lattice (dotted line; crystal axes are a, b, and c), superlattice above 170 K (solid line; crystal axes are a′, b′, and c′), and superlattice 2a × 2c below 170 K (dash dot line; crystal axes are a″, b″, and c″). Arrangement in (a) BEDT-TTF (ET) and TCNQ; (b) BEDT-TTF; and (c) TCNQ.

Figure 5. Arrangement of molecules in β″-(BEDT-TTF)(TCNQ). Average lattice (dotted line; crystal axes are a, b, and c), superlattice above 170 K (solid line; crystal axes are a′, b′, and c′), and superlattice 2a × 2c below 170 K (dash dot line; crystal axes are a″, b″, and c″). Arrangement in (a) BEDT-TTF (ET) and TCNQ; (b) BEDT-TTF; and (c) TCNQ.

3.2. Crossover from Uniform Metal to Charge-Ordered Metal

Uruichi et al., have discussed the infrared, Raman, and optical conductivity of β″-(BEDT-TTF) (TCNQ) [61]. Figure 6 shows the infrared-active ν₂₇ mode and Raman active ν₂ mode of BEDT-TTF along with the electrical resistivity. Both charge-sensitive modes, ν₂₇ and ν₂, appear as a single band at ρ~0.5 below 100 K. Upon increasing the temperature, they split into high-frequency and low-frequency modes. This splitting is comparable with ν₂₇ and ν₂ in the CO state of θ-(BEDT-TTF)₂RbZn [71,72]. This splitting clearly shows the charge disproportionation from uniform site charge with Δρ~0 to two different site charges with an amplitude of Δρ~0.6. Above 150 K, these two sites appear to correspond to the two non-equivalent sites in the superlattice (center and corner sites in Figure 5b). However, the intensity of the superlattice reflection is extremely weak compared with Bragg reflections. This observation means that the two independent sites are approximately equivalent. Therefore, this charge disproportionation seems not to be long-range ordered, and probably the short-range ordered site charges are dynamically fluctuating. The correlation time was estimated to be τ > ~ 0.3 ps at room temperature assuming a two-states-jump model [61]. This will be further discussed below along with the optical conductivity. On the other hand, the charge-sensitive modes ν₂₁, ν₃₄, and ν₄ of TCNQ show no change. This observation is consistent with the speculation that the valence electrons of TCNQ are localized within the TCNQ dimer over the whole temperature range.

Figure 7 shows the optical conductivity polarized along the a axis, which is the direction of the maximum transfer integral between BEDT-TTF. The temperature dependence is peculiar in that the spectral weight shifts to the low-frequency region on decreasing temperature. At the same time the resistivity also decreases. This characteristic spectral change seems to be interpreted by the theoretical model of Merino et al. [40]. They computed the optical conductivity for a quarter-filled square lattice with various V/t values under the condition of U/t = 20, where U, V, ant t are the on-site Coulomb energy, intersite Coulomb energy, and intersite hopping energy, respectively. When V/t exceeds the critical value (V/t)_c, a CO state is more stable than a metallic state. According to their theory, the density of states in a metallic phase (V/t < (V/t)_c) is triply peaked at around the Fermi energy (See the inset of Figure 7). From a low energy, these peaks correspond to the incoherent band associated with the lower Hubbard band, quasiparticle band, and upper incoherent band. When V/t increases, the quasiparticle peak in the density of states decreases, and finally vanishes in the CO state (V/t > (V/t)_c). Consequently the optical conductivity consists of three terms, σ(ω) = σ_D(ω) + σ_IQ(ω) + σ_II(ω), where σ_D(ω) is the Drude term that peaks at ω = 0 which corresponds to the excitation within the quasiparticle band, σ_IQ(ω) is the optical transition between the incoherent bands and the quasiparticle band, and σ_II(ω) is the optical transition between the incoherent bands (transition between the neighbor sites in real space description) [73]. In the CO state, the gap is open, so that σ_D(ω) and σ_IQ(ω) vanish. When V/t decreases, the CO state is melted, and σ_D(ω) and σ_IQ(ω) gain the intensity and σ_II(ω) loses the intensity. At the same time, the peaks of σ_IQ(ω) and σ_II(ω) shift toward lower energy. The observation of σ_D(ω) is a sign of the coherent quasiparticle band and the intensity decrease and the low-energy shift of σ_IQ(ω) and σ_II(ω) corresponds to growth of the coherent band of the quasiparticle. This trend of σ_IQ(ω) and σ_II(ω) is seen in Figure 8b with decreasing temperature. The Drude term σ_D(ω) appearing below 600 cm⁻¹ has not been measured in this compound. Probably σ_D(ω) will quickly grows below 20 K, as the dc conductivity increases remarkably below 20 K as shown in Figure 7.

Figure 6. Temperature dependences of the (a) ν₂₇ mode (blue); (b) ν₂ (blue) and ν₃ (green) modes; and (c) electrical resistivity of BEDT-TTF in β″-(BEDT-TTF)(TCNQ). Note that the charge-sensitive modes merge into a single band on decreasing the temperature. This figure is modified from Figures 3,4,7 in ref. [61].

Figure 6. Temperature dependences of the (a) ν₂₇ mode (blue); (b) ν₂ (blue) and ν₃ (green) modes; and (c) electrical resistivity of BEDT-TTF in β″-(BEDT-TTF)(TCNQ). Note that the charge-sensitive modes merge into a single band on decreasing the temperature. This figure is modified from Figures 3,4,7 in ref. [61].

Figure 7. Temperature dependence of the E||a optical conductivity of β″-(BEDT-TTF)(TCNQ). Circles at zero wavenumber denote the dc conductivity at several temperatures. The inset shows the schematic figure of density of states in the quarter-filled band system. See the text for the meaning of the electronic transitions, σ_D(ω), σ_IQ(ω), and σ_II(ω).

Figure 7. Temperature dependence of the E||a optical conductivity of β″-(BEDT-TTF)(TCNQ). Circles at zero wavenumber denote the dc conductivity at several temperatures. The inset shows the schematic figure of density of states in the quarter-filled band system. See the text for the meaning of the electronic transitions, σ_D(ω), σ_IQ(ω), and σ_II(ω).

Figure 8. Temperature dependences of the following quantities of β″-(BEDT-TTF)(TCNQ). (a) electrical resistivity; (b) peak frequency of electronic transition; (c) partial effective hole number; (d) peak frequency of ν₂₇, where squares and triangles are the data of independent experiment; and (e) product of correlation time and splitting width of ν₂₇. Lines are included as guide to the eye. The inset of Figure 8a shows that the resistivity below 20 K follows the relation for a Fermi liquid, ρ = ρ₀ + AT₂. Figure 8a,b are taken from Figure 7 of ref. [61].

Figure 8. Temperature dependences of the following quantities of β″-(BEDT-TTF)(TCNQ). (a) electrical resistivity; (b) peak frequency of electronic transition; (c) partial effective hole number; (d) peak frequency of ν₂₇, where squares and triangles are the data of independent experiment; and (e) product of correlation time and splitting width of ν₂₇. Lines are included as guide to the eye. The inset of Figure 8a shows that the resistivity below 20 K follows the relation for a Fermi liquid, ρ = ρ₀ + AT₂. Figure 8a,b are taken from Figure 7 of ref. [61].

According to the charge correlation function C(q, ω) near CO calculated by Merino et al., the excitation energy ω approaches zero and the correlation length diverges [40,41], when the parameters V/t approach the critical value for long-range CO. Accordingly, the amplitude of CO fluctuation Δρ increases and the correlation time τ is expected to diverge. This trend is seen in Figure 8e on increasing the temperature, where the product τΔν is estimated from the two-states-jump model as explained in Section 2.4. Therefore, together with the optical conductivity, β″-(BEDT-TTF)(TCNQ) approaches the long-range CO state with increasing temperature. Above 200 K the increase in the product τΔν levels off, and the optical conductivity appears to have a gap. If this compound attains a long range order above 200 K, the charge-rich and charge-poor molecules are fixed at crystallographically independent sites. In spite of the large amplitude of CO, the two independent sites are approximately equivalent, as described in the first paragraph of this section. This result suggests that short-range charge order fluctuates, and it is not long-range ordered above 200 K. The absence of long-range order as well as the sizable dc conductivity with dρ/dT > 0 in this temperature range, as shown in Figure 8a, suggests the existence of a finite density of states at the Fermi level as schematically drawn in the inset in Figure 7. The apparent optical gap is regarded as a pseudogap. Therefore the high-temperature state is considered to be a charge-ordered metal [74].The amplitude Δρ~0.6 and correlation time τ > ~ 0.3 ps may characterize the charge-ordered metal of this compound. The optical conductivity below 600 cm⁻¹ is necessary to clarify the finite density of state near the Fermi level.

In contrast, at low temperatures, the CO fluctuation is significantly suppressed, as τΔν is decreased by three orders of magnitude. Merino predicted a transition between a uniform metal and a charge-ordered metal [74]. As shown in Figure 8d, the spectral variation of ν₂₇ looks to be continuous at around 100 K. Therefore, this compound shows a crossover from a charge-ordered metal to a uniform metal upon lowering the temperature. Comparing with the theoretical model, it turns out that decreasing temperature corresponds to a decrease of V/t. Although the lattice contraction increases both V and t, the latter is more sensitive to an intermolecular distance. Therefore, lattice contraction is responsible for this crossover behavior. Actually, the increase in t is indicated by an increase in the partial effective number, which is defined by the following equation,

(5)

where m and e are the electron mass and electron charge respectively, N is the hole density of BEDT-TTF, ω_c1 = 600 cm⁻¹ and ω_c2 = 9000 cm⁻¹ are the cut-off frequencies, and σ(ω) are the cut-off frequencies, N^p_eff increases by about 30% from 280 K to 6 K as shown in Figure 8c, though the spectral weight below 600 cm⁻¹ is not taken into account. The role of lattice contraction on the electronic state is also supported by high pressure experiment. When a hydrostatic pressure is applied to this compound at room temperature, the Raman spectrum shows a similar variation as a decrease in the temperature. The split ν₂ modes merge at about 2 kbar [61], that is, the charge-ordered metal changes into a uniform metal due to lattice contraction. Possibly, a quasiparticle band is formed below 20 K because of the high conductivity and Fermi liquid behavior of transport properties [65,66,67,68,69]. To confirm this, the Drude response should be examined in the optical conductivity below 600 cm⁻¹. Finally, the structural change in the superlattice at ~170 K and anomalies in resistivity at ~80 K and ~20 K seem to have no influence on the optical conductivity and the line shape of the charge-sensitive mode. More extensive investigation is necessary for the understanding of this compound.

4. θ-(BEDT-TTF)₂X

The θ-type BEDT-TTF salts, θ-(BEDT-TTF)₂X, have a herringbone arrangement of BEDT-TTF, forming a two-dimensional quarter-filled system. This family includes metallic compounds and several compounds which undergo a charge-ordering (CO) phase transition. The electronic phase diagram of this family has been composed employing the dihedral angle φ between the adjacent BEDT-TTF molecules (See Figure 9), which is related to the bandwidth [74]. The dihedral angle was subsequently linked to t_c/t_p to explain the phase diagram, where t_c and t_p are the transfer integrals along the c (stacking) direction and a ± c (diagonal) directions forming a triangular lattice [75,76,77,78]. Watanabe discussed this phase diagram using t_c/t_p as follows [78]. As the dihedral angle φ decreases, the bandwidth increases [79], and the ground state is stabilized in the order of a stripe CO, frustrating CO between the stripe and the threefold lattice, and uniform metal. Accordingly, the temperature range of the highly conductive phase expands to the low-temperature region, as φ is decreased. In the small φ region, X = I₃ (φ = 100°) [80] and X=CsZn(SCN)₄ (φ = 104°) [81] salts, the high-temperature phase is metallic, with dρ/dT > 0, whereas it is non-metallic, with dρ/dT < 0 above the CO transition temperature in the large φ region. The activation energy increases with increasing φ as follows: 0.02 eV for X = RbZn(SCN)₄ (φ = 111°) [81], 0.08 eV for orthorhombic TlZn(SCN)₄ (φ = 117°) [81], 0.11 eV for monoclinic TlZn(SCN)₄ (φ = 121°) [81], and 0.17–0.19 eV for Cu₂(CN)[N(CN)₂]₂ (φ = 132°) [82]. Hereafter, θ-(BEDT-TTF)₂MM′(SCN)₄ and θ-(BEDT-TTF)₂X are abbreviated as θ-MM′ and θ-X, respectively.

Figure 9. Phase diagram of θ-(BEDT-TTF)₂X [79]. The squares and the circle represent the charge-ordering phase transition and the superconducting phase transition, respectively.

Figure 9. Phase diagram of θ-(BEDT-TTF)₂X [79]. The squares and the circle represent the charge-ordering phase transition and the superconducting phase transition, respectively.

4.1. Charge-Ordered Phase of X = RbZn(SCN)₄, TlZn(SCN)₄, Cu₂(CN)[N(CN)₂]₂

θ-RbZn undergoes the CO phase transition accompanying a structural change, and this compound has been very extensively studied. As shown in the left panel of Figure 10, Raman-active ν₂ and ν₃ modes show remarkable change in the CO transition. Yamamoto et al., analyzed the spectra comparing them with the spectra for the ¹³C-substituted compound, in which the carbon atoms in the central bridge C=C bond are substituted by ¹³C [72]. Since the ν₂ mode is mainly the C=C stretching vibration in the five-member rings and the ν₃ mode is mainly the C=C stretching vibration of the central bridge C=C bond, (See Figure 1) the isotope shift of the latter mode is expected to be significantly larger than the former. Utilizing this property, they assigned all the observed bands as shown in Figure 10. Actually, the isotope shifts of ν_3A, ν_3B, ν_3B, and ν_3A, are much larger than those of ν_2P and ν_2R, while ν₄, and ν₅ show no isotope shift [72]. It becomes clear from this assignment that the ν₂ mode splits into two and the ν₃ mode split into four [83]. As we explained in Section 2.3, the ν₂ mode splits owing to the charge difference and the ν₃ mode splits owing to the EMV mechanism. From the splitting of ν₂, the site-charge difference or amplitude of CO is estimated to be Δρ~0.6. This large amplitude is approximately consistent with the site-charge ratio ρ_P:ρ_R = 1:6 estimated from ¹³C-NMR experiment [15]. From the splitting of ν₃, it is concluded that the single conducting layer in the unit cell contains four molecules. This means that the unit cell is doubled below the CO phase transition.

As shown in the right panel of Figure 10, the four ν₃ modes are classified into two groups by the polarization of the incident and scattered light. The two ν_3A modes and two ν_3B modes, respectively, have the character of species A and B in the C₂ symmetry. This means that the four molecules in a conducting layer are classified into two groups, and in each group, two equivalent molecules are connected by a screw axis. These groups correspond to charge-rich and charge-poor molecules. Therefore, the charge-rich (charge-poor) molecules are arranged to form a horizontal stripe. This conclusion is consistent with the space group P2₁2₁2₁ which was determined by the low-temperature x-ray diffraction measurements [84]. The factor group of P2₁2₁2₁ is D₂, which is reduced to C₂ for a single conducting layer [85]. The horizontal stripe in the θ-RbZn salt is claimed by Tajima et al., through the analysis of the mid-infrared band in the optical conductivity [86]. Based on the mode of the horizontal stripe, Suzuki et al. [85] and Yamamoto et al. [57] conducted a numerical calculation of the splitting of ν₂ and ν₃. According to their analysis, the four vibronic modes are expressed by the following symmetry coordinates,

(6)

where Q_P1 and Q_P2 (Q_R1 and Q_R2) are the normal coordinates of charge-poor (charge-rich) site. The different character between ν₂ and ν₃ is ascribed to the difference in EMV coupling constants, which are small for ν₂ and large for ν₃ compared to transfer integrals. When the normal coordinate has a_g symmetry in a free molecule, Q_A1 and Q_A2 have A symmetry and Q_B1 and Q_B2 have B symmetry. In the case of ν₂ mode, a ≈ 1 and b ≈ 1, since the coupling constant is small, in other words, the interaction between charge-rich and charge-poor site is small. Therefore, both ν_2P (ν_A1, ν_B1) and ν_2R (ν_A2, ν_B2) are doubly degenerate. On the other hand, the four ν₃ modes, ν_3A (ν_A1, ν_A2) and ν_3B (ν_B1, ν_B2) are split through the strong EMV interaction.

Figure 10. (left panel) Temperature dependence of the Raman spectrum and the electrical resistivity of θ-(BEDT-TTF)₂RbZn(SCN)₄. The ν₂ and ν₃ modes are shown by blue and green colors. The inset shows the herringbone arrangement of BEDT-TTF with respect to the crystallographic axes; (right panel) Polarized Raman spectrum of θ-RbZn measured at 20 K. The four ν₃ modes (green) in the top panel are classified into two groups by polarization. The Raman spectra are modified from Figures 14,15 of ref. [24].

Figure 10. (left panel) Temperature dependence of the Raman spectrum and the electrical resistivity of θ-(BEDT-TTF)₂RbZn(SCN)₄. The ν₂ and ν₃ modes are shown by blue and green colors. The inset shows the herringbone arrangement of BEDT-TTF with respect to the crystallographic axes; (right panel) Polarized Raman spectrum of θ-RbZn measured at 20 K. The four ν₃ modes (green) in the top panel are classified into two groups by polarization. The Raman spectra are modified from Figures 14,15 of ref. [24].

Similar analyses were conducted for θ_o-TlZn [85], θ_m-TlZn [85], and θ-Cu₂(CN)[N(CN)₂]₂ [57] salts. Since θ_o-TlZn and θ-Cu₂(CN)[N(CN)₂]₂ are isostructural to θ-RbZn, the Raman spectra below T_CO are exactly the same as that of θ-RbZn as shown in Figure 11. However, θ_m-TlZn belongs to monoclinic system with space group C2. Reflecting this structural difference, the Raman spectrum and electrical resistivity shown in Figure 12 are different from those of the orthorhombic salts [85]. The spectrum at 60 K is interpreted assuming pseudo inversion symmetry in the following way. The ν₂ mode is split into the charge-rich and charge-poor sites, and two in-phase modes are observed among four ν₃ modes. Based on this interpretation a diagonal stripe is claimed to be the CO pattern [85]. A diagonal stripe is theoretically predicted to be almost degenerate with a horizontal stripe. It is theoretically considered that the lattice distortion below T_CO stabilizes the horizontal stripe in θ-RbZn [87]. If θ_m-TlZn takes a diagonal stripe, the low-temperature structure is expected to be distorted differently from θ-RbZn.

Figure 11. Temperature dependence of the Raman spectrum of θ_o-(BEDT-TTF)₂TlZn(SCN)₄ along with the electrical resistivity. The inset shows the herringbone arrangement of BEDT-TTF with respect to the crystallographic axes. The spectral change is almost exactly the same as that of θ-(BEDT-TTF)₂RbZn(SCN)₄. The Raman spectrum is modified from Figure 4 of ref. [85].

Figure 11. Temperature dependence of the Raman spectrum of θ_o-(BEDT-TTF)₂TlZn(SCN)₄ along with the electrical resistivity. The inset shows the herringbone arrangement of BEDT-TTF with respect to the crystallographic axes. The spectral change is almost exactly the same as that of θ-(BEDT-TTF)₂RbZn(SCN)₄. The Raman spectrum is modified from Figure 4 of ref. [85].

Figure 12. Temperature dependence of the Raman spectrum of θ-(BEDT-TTF)₂Cu(CN)[N(CN)₂]₂ (left) and θ_m-(BEDT-TTF)₂TlZn(SCN)₄ (middle) along with the electrical resistivity. The inset shows the herringbone arrangement of BEDT-TTF with respect to the crystallographic axes. The spectral change and resistivity are rather continuous. The left spectrum is modified from Figure 5 of ref. [57]. The right spectrum is modified from Figure 7 of ref. [85].

Figure 12. Temperature dependence of the Raman spectrum of θ-(BEDT-TTF)₂Cu(CN)[N(CN)₂]₂ (left) and θ_m-(BEDT-TTF)₂TlZn(SCN)₄ (middle) along with the electrical resistivity. The inset shows the herringbone arrangement of BEDT-TTF with respect to the crystallographic axes. The spectral change and resistivity are rather continuous. The left spectrum is modified from Figure 5 of ref. [57]. The right spectrum is modified from Figure 7 of ref. [85].

4.2. Metallic Phase of X = RbZn(SCN)₄, TlZn(SCN)₄, Cu₂CN[N(CN)₂]₂

The high-temperature phase of θ-RbZ is regarded as an unconventional metal. There is a finite density of states at the Fermi level, though the temperature derivative of resistivity is negative. This unusual behavior in the high-temperature phase of θ-RbZn was reported in ¹³C-NMR experiment. The linewidth shows a broadening as the temperature approaches T_CO [15]. Chiba analyzed this behavior, and reported the following results [88]. Above T_CO, fluctuation of CO arises in space (the fractional charge is distributed from +0.3 to +0.7) and in time (extremely slow on the time scale of ¹³C-NMR). This short-range ordered CO is related to the x-ray diffuse scattering at q₁ ≈ (1/4, k, 1/3), which corresponds to the short-range ordered 4a × 3c superlattice (short-range ordered threefold CO) [84]. When the sample is rapidly cooled, the phase transition is suppressed [89]. This rapid-cooling state is regarded as a frozen state of the metal, and it is in a glassy state [90]. In this frozen state, another diffuse scattering at q₂ = (0, k, 1/2) is found in addition to weak q₁ [91]. The diffuse scattering at q₂ corresponds to the short-range ordered 2c superlattice (short-range ordered stripe CO). As this metastable state relaxes, the volume fraction of the 2c superlattice decreases, whereas the 4a × 3c superlattice becomes dominant [92]. This result means that threefold CO and stripe CO are competing in the glassy state.

The Raman spectrum shows a single broad band above T_CO as shown in Figure 10. This broad band is assigned to the ν₂ mode based on the isotope shift of the ¹³C-substituted compound [93]. If the high-temperature phase is a metal, the ν₂ mode should be observed between the ν_2P and ν_2R bands. However, the broad ν₂ band above T_CO is located at the ν_2R band, and thus ν_2R is regarded as being hidden in the background. This result as well as the ¹³C-NMR data is direct evidence for the fluctuation of charge order in the metallic phase. The large splitting, Δν₂ = ν_2P − ν_2R, means a large amplitude (Δρ~0.6) of fluctuation. If the correlation time is very long on the time scale of vibrational spectroscopy as claimed by NMR [88], the line shape is regarded as the case of τΔν₂ > 1 (See Figure 4a, Δ = Δν₂/2), that is, motional narrowing does not work. Therefore, Raman spectroscopy yields a snap shot of the slow fluctuation, and thus the broad linewidth reflects spatially inhomogeneous charge distribution. Accordingly, the line shape of the ν₂ mode in the rapid-cooling state is almost exactly the same as that of the high-temperature spectrum [24,94]. The strong inhomogeneity probably comes from the short-range ordered 3a × 4c superlattice, which involves 48 sites in the unit cell. On the other hand, in the case of ¹³C-NMR, the line broadening due to the spatial inhomogenity is wiped out at higher temperature due to the motional narrowing, because the time scale of ¹³C-NMR is slower than that for vibrational spectroscopy. The line broadening comes back at low temperature due to the slower dynamics.

The optical conductivity of θ-RbZn has been reported by Wang et al., down to 50 cm⁻¹ [95]. As shown in Figure 13f,g, the optical conductivity above 200 K consists of a broad peak at around 2000 cm⁻¹ with no Drude response. Theoretically, the 3a × 4c superlattice is metallic with Fermi surfaces [76]. Nishimoto et al., calculated the optical conductivity of threefold lattice. They show that the Drude weight is significantly suppressed, and the spectral weight shifts to high-frequency excitation (See Figure 13a–e) [96]. The resultant small Drude response may be overdamped in the short-range ordered 3a × 4c superlattice, which results in the pseudogap like optical conductivity. The optical conductivity in the metallic phase exhibits strong vibronic band of ν₃ at ~1300 cm⁻¹ [72,95]. As the vibronic band is forbidden in the structure of the metallic phase, this vibronic band is activated due to the local lattice distortion by the fluctuation of threefold and stripe CO. In other words, the appearance of the vibronic band in θ-type BEDT-TTF salts indicates the fluctuation of CO in the metallic phase.

Figure 13. Reflectivity and optical conductivity of θ-(BEDT-TTF)₂RbZn(SCN)₄. and theoretical calculation of the optical conductivity of a triangular lattice. The arrows in (c), (d), and (e) denote the Drude peaks, which appear at finite energy because the open-end boundary condition is applied for a finite size cluster of L_a = 8 and L_c = 6 [96]. Figure 13a–e are taken from ref. [96], and Figure 13f,g are taken from ref. [95].

Figure 13. Reflectivity and optical conductivity of θ-(BEDT-TTF)₂RbZn(SCN)₄. and theoretical calculation of the optical conductivity of a triangular lattice. The arrows in (c), (d), and (e) denote the Drude peaks, which appear at finite energy because the open-end boundary condition is applied for a finite size cluster of L_a = 8 and L_c = 6 [96]. Figure 13a–e are taken from ref. [96], and Figure 13f,g are taken from ref. [95].

Other compounds with φ > 111° also show similar τΔν₂ » 1 spectra with a broad linewidth as shown in Figure 14b,c [97]. As the dihedral angle increases, the ν_2P mode, the counterpart of ν_2R, appears more clearly. In addition, ν₃ mode in the low-frequency region of the broad ν_2R is more enhanced above T_CO (See Figure 14b). In particular, in θ-Cu₂(CN)[N(CN)₂]₂, another broad ν₃ mode is found at ~1390 cm⁻¹ (not shown) above T_CO, when a 780 nm excitation laser is used [57]. The observation of the precursor band ν₃ means that short-range ordered horizontal and diagonal stripes grow more extensively toward T_CO. Actually, x-ray diffuse scattering is observed at q₂ = 1/2c* above T_CO = 220 K in θ-Cu₂(CN)[N(CN)₂]₂ [57]. Although no diffuse scattering has been found in θ_m-TlZn, the vibronic band of ν₃ is clearly found in the optical conductivity as shown in Figure 15a. Differently from θ-RbZn, the fluctuation of the threefold lattice is absent, whereas the short-range 2c superlattice is dominant. Watanabe explained this trend theoretically as the result of t_c/t_p [78], which decreases from positive value (~0.5) to a negative value (−0.5) according to the increase in the dihedral angle in the phase diagram of the θ-type BEDT-TTF salts [98,99]. In these two compounds, the frustration with threefold CO seems to be reduced more than in θ-RbZn and θ_o-TlZn. This may be related to the continuous transformation of the Raman and optical conductivity spectra and the resistivity of θ_m-TlZn and θ-Cu₂(CN)[N(CN)₂]₂ in contrast to θ-RbZn and θ_o-TlZn (See Figure 12, Figure 15).

Figure 14. Comparison of the Raman spectra of (a) the CO state of θ-(BEDT-TTF)₂RbZn(SCN)₄; (b) high-temperature phase of θ-(BEDT-TTF)₂Cu₂CN[N(CN)₂]₂; and the metallic phase of (c) θ_m-(BEDT-TTF)₂TlZn(SCN)₄; (d) θ-(BEDT-TTF)₂RbZn(SCN)₄; (e) θ-(BEDT-TTF)₂CsZn(SCN)₄; and (f) θ-(BEDT-TTF)₂I₃. Note that the ν₂ mode is split in (a), (b), (c), and (d), while ν₂ is merged in (e) and (f). The assignments in θ-(BEDT-TTF)₂MZn(SCN)₄ (M = Rb, Cs) in the metallic phase are conducted with the aid of ¹³C-substituted compounds [94].

Figure 14. Comparison of the Raman spectra of (a) the CO state of θ-(BEDT-TTF)₂RbZn(SCN)₄; (b) high-temperature phase of θ-(BEDT-TTF)₂Cu₂CN[N(CN)₂]₂; and the metallic phase of (c) θ_m-(BEDT-TTF)₂TlZn(SCN)₄; (d) θ-(BEDT-TTF)₂RbZn(SCN)₄; (e) θ-(BEDT-TTF)₂CsZn(SCN)₄; and (f) θ-(BEDT-TTF)₂I₃. Note that the ν₂ mode is split in (a), (b), (c), and (d), while ν₂ is merged in (e) and (f). The assignments in θ-(BEDT-TTF)₂MZn(SCN)₄ (M = Rb, Cs) in the metallic phase are conducted with the aid of ¹³C-substituted compounds [94].

Figure 15. Optical conductivity of (a) θ_m-(BEDT-TTF)₂TlZn(SCN)₄ and (b) θ_o-(BEDT-TTF)₂TlZn(SCN)₄. Note that the spectral variation is discontinuous in θ_o-(BEDT-TTF)₂TlZn(SCN)₄, whereas it is continuous in θ_m-(BEDT-TTF)₂TlZn(SCN)₄. The arrow denotes the vibronic band of ν₃.

Figure 15. Optical conductivity of (a) θ_m-(BEDT-TTF)₂TlZn(SCN)₄ and (b) θ_o-(BEDT-TTF)₂TlZn(SCN)₄. Note that the spectral variation is discontinuous in θ_o-(BEDT-TTF)₂TlZn(SCN)₄, whereas it is continuous in θ_m-(BEDT-TTF)₂TlZn(SCN)₄. The arrow denotes the vibronic band of ν₃.

4.3. θ-(BEDT-TTF)₂X (X = CsZn(SCN)₄, I₃)

The θ-CsZn salt is located at the boundary between the metallic θ-I₃ salt and the large φ salts that undergo CO transition. The x-ray diffuse rods are found at q₁ = (2/3, k, 1/3) and q₂ = (0, k, 1/2) below 120 K [100,101]. This finding implies that a short-range ordered 3a × 3c superlattice (fluctuation of threefold CO) coexists with the 2c superlattice (fluctuation of stripe CO). The 2c lattice is regarded as the fluctuation of the horizontal stripe which is found in θ-RbZn below T_CO. On lowering the temperature, the intensity of q₂ increases as the resistivity increases from about 140 K. Although the correlation length of the 2c lattice grows up on lowering the temperature, it does not attain a long-range order. Interestingly, an external current suppresses the q₂ domain at 12 K keeping the q₁ domain intact [100]. This finding is related to the nonlinear conduction [102] and the thyristor effect [103]. The ¹³C-NMR study argued the following points. (1) Remarkable charge disproportionation with extremely slow fluctuations is observed in the temperature range of 294 K–140 K; (2) The short-range CO with the amplitude of Δρ~0.4–0.6 becomes almost static in the region of 140 K–50 K; (3) The amplitude of the CO fluctuation becomes very much reduced below 30 K [104]. The dielectric permittivity study proposes a glass-like state at low-temperature which consists of conglomerate domains of short-range ordered threefold and stripe CO [105]. Several theoretical studies have been conducted to explain the coexistent and/or frustrating CO fluctuation using a triangular lattice model [76,78,96,106]. The stripes and non-stripe threefold CO are competing near an isotropic triangular lattice (V_c~V_p), forming a charge-ordered metal [78,96]. The origin of the threefold CO is the nesting of the Fermi surface, while the origin of the stripe CO is the off-site Coulomb interaction [106], or both instabilities come from the Fermi surface nesting [76]. In all cases, there is a wide metallic region due to the frustration between the stripe and threefold CO fluctuation near the isotropic triangular lattice.

Figure 16 shows the Raman spectra of θ-CsZn and θ-I₃ along with the electrical resistivity of θ-CsZn [94]. θ-(ET)₂I₃ is metallic down to low temperature and undergoes a superconducting transition at 3.6 K [107,108]. In both compounds, ν₂ appears as a single peak near the frequency of ρ = 0.5 [46] over the whole temperature range. Different from θ-I₃, a very broad vibronic mode is observed at 1200–1300 cm⁻¹ in θ-CsZn as shown in Figure 16. The Raman cross section of this vibronic mode is enhanced when charge disproportionation is enlarged as shown in Figure 2b (Section 2). This observation suggests that the correlation length of the CO fluctuation grows upon decreasing the temperature, since the intensity of the vibronic band increases. From the polarization dependence, ν_3A and ν_3B are respectively classified into A and B species in the factor group C₂ [94]. This result means that the short-range CO domain has a screw axis symmetry. Therefore, the 2c superlattice with the horizontal stripe seems to contribute to this vibronic mode [109]. This observation is consistent with x-ray diffuse scattering that shows the evolution of the short-range ordered 2c superlattice. Although threefold CO fluctuation is observed in both θ-CsZn and θ-RbZn, the features of ν₂ of θ-CsZn are very different from that of θ-RbZn. The ν₂ mode of θ-CsZn appears as a slightly broad single band at the frequency of ρ~0.5, whereas the ν₂ mode of θ-RbZn appears as a much broader band at the frequency of the charge-rich site. The infrared-active mode ν₂₇ also appears in the same way as ν₂ [94]. This result means that the product of the correlation time and splitting width is smaller than unity, τΔν₂ < 1, in θ-CsZn (See Figure 4a, Δ = Δν₂/2), whereas τΔν₂ > 1 in θ-RbZn as described in Section 4.2. Therefore, the correlation time and/or CO amplitude of θ-CsZn is much smaller than that of θ-RbZn. If the fluctuation is almost static on the time scale of vibrational spectroscopy as suggested by NMR [104], Δν₂ is dominated by spatial inhomogeneity. The linewidth is about 10 cm⁻¹ below 100 K. If we assume a static Gaussian distribution for the site charge, the amplitude is roughly estimated as Δρ < 0.08. This small amplitude is inconsistent with the argument of ¹³C-NMR [104]. However, the small amplitude is consistent with the much weaker intensity (diffuse/Bragg ~ 10⁻⁵) of the diffuse scattering in θ-CsZn [100] compared with that (diffuse/Bragg ~ 10⁻³) in θ-RbZn [91]. The small amplitude seems to be attributed mainly to the strong frustration between the threefold and stripe fluctuation. Seo demonstrated that in such a case, both peaks in the charge correlation function C(q,ω) corresponding to stripe and threefold fluctuation have higher excitation energy compared to the non-frustrate system [41]. This result implies that the amplitude of CO cannot grow when they are competing.

The optical conductivity of θ-CsZn is shown in Figure 17 [94]. Compared with the optical conductivity of θ-RbZn [95], the spectral weight of θ-CsZn is located in the low-frequency region, which is similar to the optical conductivity of β″-(ET)(TCNQ) shown in Figure 8. Since the conductivity should approach the dc conductivity shown in Figure 17, the peak which corresponds to σ_IQ is expected below 600 cm⁻¹, and the Drude response is likely to be missing. This speculation is consistent with the optical conductivity reported by Wang [110], wherein a strong peak accompanied by several vibronic bands appears below 600 cm⁻¹ without Drude response. The V/t dependence of the optical conductivity similar to β″-(ET)(TCNQ) has been theoretically calculated for a triangular lattice [96]. The dips at 1300 cm⁻¹ and 877 cm⁻¹ are the vibronic modes respectively corresponding to ν₃ and ν₇, which arise from the EMV interaction. These vibronic modes are forbidden in the average structure of θ-CsZn. The appearance of these vibronic modes also strongly indicates structural fluctuations, which probably corresponds to the 3a × 3c and 2c short-range superlattices.

Figure 16. Temperature dependence of the Raman spectra of θ-(BEDT-TTF)₂I₃ and θ-(BEDT-TTF)₂CsZn(SCN)₄ along with the electrical resistivity of θ-(BEDT-TTF)₂CsZn(SCN)₄. The inset shows the temperature dependence of the linewidth of the ν₂ mode. The Raman spectra of θ-(BEDT-TTF)₂I₃ and θ-(BEDT-TTF)₂CsZn(SCN)₄ are modified from Figure 2c of ref. [111] and Figure 3 of ref. [94], respectively.

Figure 16. Temperature dependence of the Raman spectra of θ-(BEDT-TTF)₂I₃ and θ-(BEDT-TTF)₂CsZn(SCN)₄ along with the electrical resistivity of θ-(BEDT-TTF)₂CsZn(SCN)₄. The inset shows the temperature dependence of the linewidth of the ν₂ mode. The Raman spectra of θ-(BEDT-TTF)₂I₃ and θ-(BEDT-TTF)₂CsZn(SCN)₄ are modified from Figure 2c of ref. [111] and Figure 3 of ref. [94], respectively.

Figure 17. Optical conductivity of θ-(BEDT-TTF)₂CsZn(SCN)₄. Blue colored circles in the bottom panel show the dc conductivity values. The arrows show the vibronic modes appearing as dips. The color of the E||c spectrum denotes the same temperature as that of the E||a spectrum.

Figure 17. Optical conductivity of θ-(BEDT-TTF)₂CsZn(SCN)₄. Blue colored circles in the bottom panel show the dc conductivity values. The arrows show the vibronic modes appearing as dips. The color of the E||c spectrum denotes the same temperature as that of the E||a spectrum.

The dihedral angle of θ-I₃ is the largest among the θ-type BEDT-TTF salts, and the fluctuation of CO is suppressed in θ-I₃ [78]. If we estimate the amplitude in the same way as for θ-CsZn, the amplitude is estimated as Δρ < 0.07. Actually the ν₂ mode appears as a single band and the vibronic band is not found in the Raman spectrum of θ-I₃ as shown in the left panel of Figure 16. Takenaka et al., reported the optical conductivity in the frequency range of 80–48000 cm⁻¹ [112]. As the bandwidth is widest among the θ-type BEDT-TTF salts, the spectral weight of the optical conductivity in θ-I₃ is located in the frequency region lower than that of θ-CsZn. As is the case of β″-(BEDT-TTF)(TCNQ), the collapse of the coherent quasiparticle state accompanying the high-frequency shift of the spectral weight is observed upon increasing the temperature. The sublattice of BEDT-TTF in θ-I₃ is described by the orthorhombic cell which is the same as the average unit cell of θ-CsZn [113]. However, a weak vibronic mode is found at ~1410 cm⁻¹ as a dip [112,114]. This vibronic band might suggest structural fluctuation perhaps associated with charge order.

5. α-(BEDT-TTF)₂I₃ and Related Compounds

Among the various known organic conductors [115,116,117,118], α-(BEDT-TTF)₂I₃ (abbreviated as α-I₃) shows rich electronic properties such as charge ordering [119], superconductivity [120], zero-gap state (ZGS) [121,122], photo-induced phase transition [123], and nonlinear optical response [124].The crystal structure of α-I₃ consists of alternating layers of the anion and donor [125]. The donor layer has a herringbone arrangement of BEDT-TTF molecules. The unit cell accommodates two holes, which are distributed in four BEDT-TTFs named A, A′, B, and C. At room temperature, A and A′ are connected by inversion symmetry, and B and C are located on the inversion center. α-I₃ exhibits a first-order metal-insulator (MI) phase transition at T_MI = 135 K [125]. Kino and Fukuyama examined the effect of on-site Coulomb interaction within the Hartree-Fock approximation, and they predicted that a charge localization with a vertical stripe is the cause of the MI transition [13,126]. Before the theoretical prediction, Moldenhauer et al., reported that the localization of electrons occurs at the B and C sites whereas the electrons at the A and A′ sites are delocalized below T_MI [12]. The ¹³C-NMR study suggested the existence of two differently charged molecules below T_MI [119,127]. Seo introduced intersite Coulomb interaction V, and he proposed that the localized charge would form a horizontal stripe [16]. These two models can be distinguished by the symmetry consideration, since the vertical stripe is compatible with the space group , whereas the horizontal stripe requires P1. Raman spectroscopy was used to examine the selection rule of the charge-sensitive mode and the symmetry reduction from to P1 below T_MI was claimed [111]. An x-ray diffraction study supported P1, and showed a horizontal stripe structure [128]. Decisive evidence for the breaking of inversion symmetry was given by the experiment of second harmonic generation (SHG) [124]. Recently, Alemany et al., pointed out that the hydrogen bond between the ethylene groups of BEDT-TTF and I₃⁻ plays an essential role in the CO transition of α-I₃ [129].

In the MI transition of α-I₃, Raman [111] and infrared [130] spectra showed drastic changes as seen in Figure 18. The assignment of these bands along with vibronic bands was conducted with the aid of ¹³C and deuterium substituted compounds. The CO and metallic phases will be discussed respectively in Section 5.1 and Section 5.2 along with the detailed assignment. Unlike θ-type BEDT-TTF salts, it has been reported for α-I₃ that the site-charge distribution is non-uniform in the metallic phase [13,111,128], although the average hole number per site is 0.5 in the case of uniform distribution. The non-uniform site charge distribution of metallic α-I₃ will be discussed along with the isostructural metallic α-(BEDT-TTF)₂NH₄(SCN)₄ in Section 5.3. One of the most attractive properties of α-I₃ is the ferroelectric properties in the CO state. In this context, another herringbone type compound α′-IBr₂ will discussed in Section 5.4.

Figure 18. (a) Temperature dependence of the Raman spectrum of α-(BEDT-TTF)₂I₃. The ν₂ and ν₃ modes are shown as blue and green, respectively. A drastic spectral change is observed below 120 K. The difference in the transition temperature comes from the laser heating effect; (b) Temperature dependence of the infrared spectrum of α-(BEDT-TTF)₂I₃, which was obtained by the Kramer-Kronig transformation of the reflectivity polarized along the c-axis (perpendicular to the conducting plane). The 6 K spectrum drawn by the dashed line is the optical conductivity of the deuterium substituted compound, α-(d₈-BEDT-TTF)₂I₃; (c) Electrical resistivity normalized by room temperature value. The optical conductivity is taken from Figure 1 of ref. [130].

Figure 18. (a) Temperature dependence of the Raman spectrum of α-(BEDT-TTF)₂I₃. The ν₂ and ν₃ modes are shown as blue and green, respectively. A drastic spectral change is observed below 120 K. The difference in the transition temperature comes from the laser heating effect; (b) Temperature dependence of the infrared spectrum of α-(BEDT-TTF)₂I₃, which was obtained by the Kramer-Kronig transformation of the reflectivity polarized along the c-axis (perpendicular to the conducting plane). The 6 K spectrum drawn by the dashed line is the optical conductivity of the deuterium substituted compound, α-(d₈-BEDT-TTF)₂I₃; (c) Electrical resistivity normalized by room temperature value. The optical conductivity is taken from Figure 1 of ref. [130].

5.1. Charge-Ordered Phase of α-(BEDT-TTF)₂I₃

Figure 19 shows infrared and Raman spectra of α-I₃, α-(d₈-BEDT-TTF)₂I₃, and α-(¹³C-BEDT-TTF)₂I₃, all in the CO state. In this spectral region, BEDT-TTF has three C=C stretching modes, ν₂, ν₃, and ν₂₇ which are shown in Figure 1, and bending modes of ethylene groups. The assignment of the Raman-active modes is the same as in ref. [111], except for the Raman bands at 1476 cm⁻¹ and 1462 cm⁻¹, which were assigned to ν₃¹ and ν_2R², respectively. These are interchanged in Table 1, as the isotope shift of ν₂ and ν₃ became closer to each other within each mode. Strictly speaking, however, this kind of assignment makes no sense, as these two modes are strongly mixed with each other. The vibronic modes in the conducting plane are assigned with the aid of isotope shift and comparison with the Raman spectrum. The very broad band, wherein the peak was different between the E||a and E||b spectra, was assigned to ν₃⁴, since the frequency of the vibronic mode depended upon the electronic excitation spectrum. The vibrational ν₂₇ mode is observable in the optical conductivity spectrum polarized along the c-axis. Some bending modes of ethylene group are overlapped in the region of the ν_27R modes (See Table 1 and Figure 19a). Therefore, the spectrum of α-(d₈-BEDT-TTF)₂I₃ is necessary for the assignment of ν_27R. The large dip at ~2690 cm⁻¹ appearing in the high-frequency region of the optical conductivity (not shown) is interpreted by Yamamoto as the Fano anti-resonance due to the vibronic overtone of ν₃ [131]. Recently, Yamamoto et al., have discussed the relationship between the vibronic overtone and optical nonlinearity and ferroelectricity [132].

Figure 19. (a) Optical conductivity polarized along the b and a directions, Raman spectra of α-(BEDT-TTF)₂I₃, and optical conductivity polarized along the c direction; (b) Optical conductivity polarized along the b and a directions and Raman spectra of α-(¹³C-BEDT-TTF)₂I₃.

Figure 19. (a) Optical conductivity polarized along the b and a directions, Raman spectra of α-(BEDT-TTF)₂I₃, and optical conductivity polarized along the c direction; (b) Optical conductivity polarized along the b and a directions and Raman spectra of α-(¹³C-BEDT-TTF)₂I₃.

Table 1. Assignment of the infrared and Raman modes of α-(BEDT-TTF)₂I₃. The Δν values show the isotope shift, Δν_j = ν_j¹²− ν_j¹³.

	Raman (20 K)			Infrared (50 K)
	α-I3	α-(13C)2I3	Δν	α-I3	α-(13C)2I3	Δν
dip (2ν33)	-	-	-	2688	2628	60
ν2P1	1536	1517	19		(1518?)	-
ν2P2	-	-	-	-	(1508?)	-
ν2R1	1483	1465	18	-	-	-
ν2R2	1476	1452	24	1477	1454	23
ν31	1462	-	-	1462	1431	31
ν32	1458	-	-	-	-	-
ν33	1349	1315	34	1346	1315	31
ν34	-	-	-	~1300 (E|| b) ~1230 (E||a)	~1300(E|| b) ~1230(E||a)	-
		1431	-	-	-	-
CH2-		1420	-	-	-	-
Bending		1414	-	-	-	-
		1402	-	-	-	-
ν27P1	-	-	-	1506 (E||c)	1505 (E||c)	-
ν27P2	-	-	-	1501 (E||c)	1500 (E||c)	-
ν27R1	-	-	-	1435 (E||c)	1432 (E||c)	-
ν27R2	-	-	-	1425 (E||c)	1423 (E||c)	-

Table 1. Assignment of the infrared and Raman modes of α-(BEDT-TTF)₂I₃. The Δν values show the isotope shift, Δν_j = ν_j¹²− ν_j¹³.

	Raman (20 K)			Infrared (50 K)
	α-I3	α-(13C)2I3	Δν	α-I3	α-(13C)2I3	Δν
dip (2ν33)	-	-	-	2688	2628	60
ν2P1	1536	1517	19		(1518?)	-
ν2P2	-	-	-	-	(1508?)	-
ν2R1	1483	1465	18	-	-	-
ν2R2	1476	1452	24	1477	1454	23
ν31	1462	-	-	1462	1431	31
ν32	1458	-	-	-	-	-
ν33	1349	1315	34	1346	1315	31
ν34	-	-	-	~1300 (E|| b) ~1230 (E||a)	~1300(E|| b) ~1230(E||a)	-
		1431	-	-	-	-
CH2-		1420	-	-	-	-
Bending		1414	-	-	-	-
		1402	-	-	-	-
ν27P1	-	-	-	1506 (E||c)	1505 (E||c)	-
ν27P2	-	-	-	1501 (E||c)	1500 (E||c)	-
ν27R1	-	-	-	1435 (E||c)	1432 (E||c)	-
ν27R2	-	-	-	1425 (E||c)	1423 (E||c)	-

If the unit cell has inversion symmetry, Raman-active band cannot be observed in an infrared spectrum and vice versa. As shown in Table 1, ν_2R², ν₃¹, and ν₃³ are found in both the Raman and infrared spectra, which violate the mutual exclusion rule. As describe above, comparison of the Raman spectrum with the infrared spectrum is a good method to judge the breaking of inversion symmetry. Based on the assignment, it becomes clear that the ν₂ and ν₂₇ modes are split into two groups, ν_2P and (ν_2R1, ν_2R2) in the Raman spectrum and (ν_27P¹, ν_27P²) and (ν_27R¹, ν_27R²) in the infrared spectrum as shown in Figure 18. Applying the linear relationship [46] to the ν₂₇ mode (50 K), the site charge distribution is estimated as (0.8, 0.7, 0.3, 0.2) [130], which are approximately equal to the values (0.85, 0.80, 0.20, 0.15) estimated by Ivek et al. [133]. The CO amplitude (Δρ_max = 0.6) is comparable to that of θ-RbZn. Kakiuchi et al., examined the breakdown of Friedel’s law by anomalous scattering effect, and they concluded a symmetry reduction from to P1 [128]. Using the space group P1, they determined the molecular geometry of each site, and provided consistent result for the site charge distribution as ρ_A = 0.82(9), ρ_B = 0.73(9), ρ_A’ = 0.29(9), ρ_C = 0.26(9) at 20 K. Recently, Alemany et al., reported the site charges as ρ_A = 0.638, ρ_B = 0.577, ρ_A′ = 0.438, ρ_C = 0.359 using a numerical atomic orbital density functional theory (DFT) approach [129]. This CO amplitude ρ_max = 0.28 is significantly smaller than the experimentally estimated value of ρ_max = 0.56–0.70. The site charge distribution has been estimated from the ¹³C-NMR shift, which consists of Knight shift and chemical shift [15,134]. The chemical shift reflects the local charges, whereas the Knight shift is proportional to the local spin susceptibility which reflects the density of states at the Fermi level [135]. Therefore, the chemical shift should be analyzed to estimate the site charges. Kawai and Kawamoto conducted a ¹³C-NMR study using a single side ¹³C-enriched molecule [135]. To avoid the effect of the Knight shift and ring current within the molecule, they applied a magnetic field nearly parallel to the long axis of the molecule in the non-magnetic state (at 60 K). They determined the chemical shift tensor of the four sites, and estimated the site charge to be ρ_R~0.74 and ρ_P~0.19. If we simply apply the relation between the chemical shift and site charge which they present, site charge distribution is estimated as ρ_A = 0.74, ρ_B = 0.76, ρ_A’ = 0.18, and ρ_C = 0.20. All of these results studied by vibrational spectroscopy, x-ray diffraction, and ¹³C-NMR approximately consistent with each other.

Yamamoto et al., found strong second harmonic generation (SHG) in the CO state, using 4 ps pulse laser with a wavelength of 1.4 µm as the fundamental light [124,136]. The evolution of the second harmonic light just below T_CO is direct evidence for the breakdown of the inversion symmetry. They determined the nonlinear electric susceptibility χ⁽²⁾_ij(2ω; ω, ω), where i and j denote the polarization of the second harmonic light and fundamental light, respectively. The relative values against BBO (β-barium borate), which is a representative crystal for nonlinear optics, are 21, 8.5, 44, 31 for the polarization aa, ab, ba, and bb. Such a strong susceptibility value suggests that the generated electric dipole in a unit cell is coherently extended over a macroscopic domain, that is, a ferroelectric domain. As in conventional ferroelectrics, the crystal is expected to form a multiple domain structure. Ferroelectric domains with opposite polarization are observed utilizing the experimental technique of SHG interferometry [137]. The domain size is found to be more than 0.2 mm × 0.2 mm, which is almost a single domain. Although polarization reversal by an external electric field has not been realized due to high conductivity and low breakdown field, this compound in the CO state is classified as an unconventional ferroelectrics called electronic ferroelectrics [138]. In conventional ferroelectrics, ionic polarization coming from displacement or ordering of ions plays a role in creating a polar domain. On the other hand, in electronic ferroelectrics, ions are replaced by electrons, and electronic polarization by charge order causes a polar domain. To show that the polar domain mainly originated from electrons, Yamamoto demonstrated fast photoresponse where the second harmonics diminish by 50% within 100 fs and recovers within several tenths of a picosecond after the irradiation of a 100 fs laser. This fast photoresponse was studied by Iwai et al., as a photoinduced insulator-to-metal phase transition. Using mid-infrared pump-probe spectroscopy, they observed the transient reflectivity change in the mid-infrared region [123,139]. The decay process depends on the intensity of the light pulse. In the case of weak excitation, one photon produces a microscopic metallic domain consisting of about 100 molecules, which decays quickly. In the case of strong excitation, on the other hand, the microscopic domains aggregate with each other forming a quasi-macroscopic metallic domain, which decays slowly. The recovery of the second harmonics corresponds to this slow decay. Recently, Kawakami et al., uncovered the early dynamic process of the photoinduced phase transition using a 12 fs laser [140].

5.2. Metallic Phase of α-(BEDT-TTF)₂I₃ and Isostructural Metallic Compounds

5.2.1. Assignment in Metallic Phase

We have shown that charge order is the origin of the splitting of the ν₂ and ν₂₇ modes. If a metallic compound involves crystallographically non-equivalent sites in the unit cell, the charge-sensitive modes split reflecting the non-equivalent sites. This splitting is also described by Equation (1). Figure 20 shows the Raman spectra of metallic α-I₃, α-(BEDT-TTF)₂NH₄Hg(SCN)₄, (abbreviated as α-NH₄Hg) and θ-I₃. The first two compounds are isostructural with each other, while the latter one takes herringbone arrangement with higher symmetry. α-NH₄Hg is metallic down to low temperature, and shows superconductivity at 1 K [141]. Similar to α-I₃, the unit cell of α-NH₄Hg involves four ET molecules (see Figure 1 of ref. [142] for the definition of A, A′, B, and C). As described in the last section, the unit of the α-type compound involves three Raman-active modes and one infrared-active mode for ν₂ and ν₃. In the case of α-I₃, one ν₂ mode is missing, whereas all of the three appear to be present in ¹³C-substitued compound as shown in Figure 20a,a′,b,b′. From the isotope shift, the three bands in Figure 20a can be safely assigned to ν₂¹, ν₂², and ν₃³. In the case of α-NH₄Hg, three ν₂ and two ν₃ modes are found and they are assigned based on the isotope shift shown in Figure 20c,c′.The remaining Raman-active ν₃ mode is missing from this Raman spectrum. Similar splitting of ν₂₇ is described in ref. [130]. The crystal of θ-I₃ belongs to the monoclinic system with space group of P2₁/c, and the unit cell contains four BEDT-TTFs. However, the arrangement of BEDT-TTF can be approximately described by the orthorhombic system with space group Pnma with the unit cell accommodating two crystallographically equivalent BEDT-TTFs [113,143]. Due to the high symmetry of the unit cell, ν₂ and ν₃ appear as a single band at ρ~0.5 as shown in Figure 20d. The frequencies of the ν₂ and ν₃ modes of these compounds are shown in Table 2.

Figure 20. Raman spectra of α-(BEDT-TTF)₂I₃ and α-(BEDT-TTF)₂NH₄Hg(SCN)₄, and the ¹³C-substitued compound, in which two carbon atoms of the central C=C bond of BEDT-TTF are substituted by ¹³C. (a) and (b) α-(BEDT-TTF)₂I₃; (a′) and (b′) α-(¹³C-BEDT-TTF)₂I₃; (c) α-(BEDT-TTF)₂NH₄Hg(SCN)₄; (c′) α-(¹³C-BEDT-TTF)₂NH₄Hg-(SCN)₄, and (d) θ-(BEDT-TTF)₂I₃.

Figure 20. Raman spectra of α-(BEDT-TTF)₂I₃ and α-(BEDT-TTF)₂NH₄Hg(SCN)₄, and the ¹³C-substitued compound, in which two carbon atoms of the central C=C bond of BEDT-TTF are substituted by ¹³C. (a) and (b) α-(BEDT-TTF)₂I₃; (a′) and (b′) α-(¹³C-BEDT-TTF)₂I₃; (c) α-(BEDT-TTF)₂NH₄Hg(SCN)₄; (c′) α-(¹³C-BEDT-TTF)₂NH₄Hg-(SCN)₄, and (d) θ-(BEDT-TTF)₂I₃.

Table 2. Assignment of the Raman modes of α-(BEDT-TTF)₂I₃, α-(BEDT-TTF)₂NH₄Hg(SCN)₄, and θ-(BEDT-TTF)₂I₃.

	α-(12C-ET)2I3	α-(13C-ET)2I3		α-(12C-ET)2 NH4Hg(SCN)4	α-(13C-ET)2 NH4Hg(SCN)4		θ-(ET)2I3
	Raman (150 K)	Raman (150 K)	Isotope shift ν12-ν13	Raman (10 K)	Raman (15 K)	Isotopeshift ν12-ν13	Raman (20 K)
ν21	1516	1496	~20	1515	1503	13
ν22	-	~1484	-	1500	1490	10	1496
ν23	1487	1470	17	1492	1479	14
ν31	1471	~1415	~56	1471	1423	48
ν32	-	-	-	~1300	~1250	~50	1469

Table 2. Assignment of the Raman modes of α-(BEDT-TTF)₂I₃, α-(BEDT-TTF)₂NH₄Hg(SCN)₄, and θ-(BEDT-TTF)₂I₃.

	α-(12C-ET)2I3	α-(13C-ET)2I3		α-(12C-ET)2 NH4Hg(SCN)4	α-(13C-ET)2 NH4Hg(SCN)4		θ-(ET)2I3
	Raman (150 K)	Raman (150 K)	Isotope shift ν12-ν13	Raman (10 K)	Raman (15 K)	Isotopeshift ν12-ν13	Raman (20 K)
ν21	1516	1496	~20	1515	1503	13
ν22	-	~1484	-	1500	1490	10	1496
ν23	1487	1470	17	1492	1479	14
ν31	1471	~1415	~56	1471	1423	48
ν32	-	-	-	~1300	~1250	~50	1469

5.2.2. Fluctuation of Charge Order in Metallic Phase

Although ν₂ and ν₂₇ of α-I₃ and α-NH₄Hg are split into three with similar split widths, the linewidth of each mode is very different. Yue et al., showed that the linewidth of metallic α-I₃ is about two to three times as large as that of α-NH₄Hg [130]. As shown in Figure 21a, the linewidth of ν₂₇ of α-I₃ is much broader than the charge-insensitive mode such as the CH₂ bending mode. As the frequencies of ν₂₇ and ν₂ strongly depend upon the site charge (140 cm⁻¹/e for ν₂₇ and 120 cm⁻¹/e for ν₂) [46], such a broad linewidth should be associated with fluctuation of the site charge. Assuming that the site charge fluctuates stochastically as a Gaussian process, Yue et al., analyzed the line shape of the somewhat isolated ν₂¹ mode, and obtained a width of Δν ~ 9−17 cm⁻¹, which corresponds to the CO amplitude of Δρ ≈ 0.08−0.14. Comparing with the theoretical curve, they estimated the parameter to be τΔν ~ 0.7–10 and the correlation time for the fluctuation to be τ⁻¹ ~ 1−25 cm⁻¹. This fluctuation rate is much faster than that of θ-RbZn, but it is sufficiently slow for the electron dynamics. This slow fluctuation rate suggests collective motion of site charge. In contrast to the θ-type BEDT-TTF salts, x-ray diffuse scattering has not been reported. Tanaka and Yonemitsu calculated the finite temperature free energy for the horizontal, vertical, and diagonal stripes, and threefold CO of α-I₃ within the framework of the mean-field approximation, using realistic parameters and taking electron-lattice coupling into account [87]. At low temperatures, these CO states and the paramagnetic metallic state are distributed within a narrow energy range. Therefore, the free energy in the metallic phase above T_MI is approximately multiply degenerate. Yue et al., speculated that the metallic state of α-I₃ above T_MI involves short-range correlation of these multiple stripes to increase entropy. This situation at finite temperature resembles the case of θ-CsZn in which stripe and threefold CO are competing. The slow fluctuation of the site charge is regarded as dynamical fluctuation of various types of CO domains. Such CO fluctuation modulates the charge density at each site and broadens the linewidth of the charge-sensitive mode, when the fluctuation rate is sufficiently slow.

Figure 21. The linewidth of ν₂₇ and ν₂³ of α-(BEDT-TTF)₂I₃. (a) Temperature dependence of the linewidth of infrared-active ν₂₇, which becomes very broad in the metallic phase; (b) Pressure dependence of the linewidth of Raman active ν₂³, which decreases on increasing pressure. These figures are modified from parts of Figures 2,4 of ref. [130].

Figure 21. The linewidth of ν₂₇ and ν₂³ of α-(BEDT-TTF)₂I₃. (a) Temperature dependence of the linewidth of infrared-active ν₂₇, which becomes very broad in the metallic phase; (b) Pressure dependence of the linewidth of Raman active ν₂³, which decreases on increasing pressure. These figures are modified from parts of Figures 2,4 of ref. [130].

As shown in Figure 21b, the linewidth of ν₂³ of α-I₃ decreases by almost half at 0.65 GPa and it becomes comparable to the linewidth of ν₂³ of α-NH₄Hg at 100 K. It is known that the application of hydrostatic pressure suppresses the long-range CO state [144]. This result implies that the paramagnetic metal is stabilized more than other stripe COs, and thus the energy difference between them is enlarged under hydrostatic pressure. Therefore, the fluctuation of stripe COs is suppressed under hydrostatic pressure, and the amplitude and correlation length may be reduced, leading to a higher fluctuation rate. This fast modulation narrows the linewidth of the charge-sensitive mode in addition to the small amplitude under hydrostatic pressure. The same speculation is applicable to stable metal α-NH₄Hg. The narrow linewidth of the charge-sensitive mode of α-NH₄Hg is consistent with this speculation.

The existence of CO fluctuation in α-NH₄Hg is indicated by the vibronic band ν₃² in the Raman spectrum (See Figure 20c,c′) as in the case of θ-CsZn. On the other hand, the vibronic band is not found in the Raman spectrum of the isostructural α-KHg, α-RbHg and α-TlHg salts. This results suggests that the fluctuation in α-NH₄Hg is largest in the group of α-MHg (M = NH₄, K, Rb, Tl). Hiejima et al., observed the infrared-active ν₂₇ modes on the side face of the crystal with the polarization perpendicular to the conducting plane [145]. In addition to the three ν₂₇ modes, they found a weak new band growing below 200 K in α-MHg (M = K, Rb, Tl). They interpreted this band as the forbidden mode among the four ν₂₇ modes, which means breaking of inversion symmetry. They speculated that fluctuation of stripe CO locally breaks the inversion symmetry as in α-I₃. If this is the case, the CO fluctuation in α-NH₄Hg is negligibly small, since the weak band is not found in α-NH₄Hg.

To reconcile these contradictory arguments, the charge density wave (CDW) should be reconsidered. Foury-Leylekian reported an incommensurate CDW for α-MHg (M = K, Rb) using x-ray diffraction [146]. The satellite reflections are already detected at high temperature (250–300 K). Recently, they pointed out the anion sublattice instability leading to deformation of the SCN tetrahedral coordination of Hg²⁺ and SCN tetragonal antiprismatic coordination of K⁺ in α-KHg [147]. They claimed that the Fermi-surface-nesting instability of the BEDT-TTF layer is coupled with the instability of the anion sublattice. This sublattice instability is common in K, Rb, and Tl. As this deformation breaks inversion symmetry, the deformation of the anion sublattice brings about the non-centrosymmetric displacement of BEDT-TTF. This mechanism seems to be more reasonable to account for the breaking of the selection rule of ν₂₇. Since this CDW is incommensurate, the ν₂₇ modes will become broad and unresolved, if the amplitude of CDW is large enough Δρ > 0.05 [148]. Actually, the ν₂₇ modes of α-NH₄Hg are more resolved than those of α-MHg (M = K, Rb, Tl) [145]. As the ν₂₇ modes of the latter compounds are barely resolved, the CDW amplitude is considered to be Δρ < 0.05. The above discussion leads to the conclusion that the fluctuation of CO is indicated only in α-NH₄Hg which shows superconductivity.

5.3. Non-Uniform Site-Charge Distribution in Metallic Phase

Non-uniform site charges in α-I₃ have been reported using Raman spectroscopy [111] and ¹³C-NMR [134] experiments. Wojciechowski et al., interpreted them simply by non-uniform (anisotropic) network of transfer integrals in the unit cell using Equation (1) [111]. Yamamoto et al., conducted a systematic study of β″-type BEDT-TTF salts [149]. They qualitatively interpreted the site-charge distribution from non-uniform (anisotropic) intersite Coulomb interaction especially along the stacking direction. Band calculation that takes Coulomb interaction into account will incorporate the effect of both anisotropic networks on some level. Moroto et al., claimed that the non-uniform site charges are a precursor of charge order [134]. Bangura et al., attributed the splitting of ν₂ in metallic β″-(BEDT-TTF)₄[(H₃O)Ga(C₂O₄)]·C₆H₅NO₂ to the signature of charge order [150]. Recently, Kaiser et al., reported the splitting of ν₂₇ in metallic β″-(BEDT-TTF)₂SF₅CH₂CF₂SO₃, and they interpreted the growth of splitting as a fluctuation of CO [31]. All of these compounds involve non-equivalent sites in the unit cell: three sites in α-I₃ and two sites in the latter two compounds. Therefore, the splitting of the charge-sensitive mode in a metallic state is not always caused by charge order. The splitting of the charge-sensitive mode in the metallic phase should be carefully interpreted, considering the splitting width, line broadening, indication of symmetry breaking, etc. In this section, site-charges in metallic phase are more precisely discussed to compare the band calculation.

5.3.1. Relation between Frequency and Site Charge Near ρ = 0.5

The relationship between the frequency of ν₂ and the valence of the molecule, ρ, was examined by Yamamoto [46]. They assumed a linear relationship in the range of 0 ≤ ρ ≤ 0.8 [151]. The ρ dependence of the frequency of ν₂ mode is ascribed to the ρ dependent force constant F(ρ). That is, the linear relationship requires (dF/dρ)_ρ=0 = (dF/dρ)_ρ=1 [152]. However, the frequency of BEDT-TTF^0.5+ significantly deviates from the linear relationship toward the low-frequency side, which implies the relation |(dF/dρ)_ρ=0| > |(dF/dρ)_ρ=1|. To estimate the site charge more reliably at ρ~0.5, the empirical equation, (ρ~0.5) is proposed, using ν₂(0) = 1570 cm⁻¹ for the calculated frequency of the flat neutral BEDT-TTF molecule, [46] ν₂(0.5) = 1494 cm⁻¹, 1494 cm⁻¹, 1495 cm⁻¹ respectively for β′-(BEDT-TTF)₂ICl₂, κ-(BEDT-TTF)₂Cu₂(CN)₃, and κ-(BEDT-TTF)₂Cu[N(CN)₂]Cl at room temperature, and ν₂(1) = 1447 cm⁻¹ for (BEDT-TTF)ClO₄ and (BEDT-TTF)AuBr₂Cl₂ at room temperature [153]. All of the compounds with ρ = 0.5 shows a frequency upshift by ~6 cm⁻¹ on cooling from room temperature to 10 K due to hardening of the crystal lattice. The frequency shift due to lattice expansion is described by the equation, , where γ is the optical Gruneisen parameter and β(T) is the coefficient of volume thermal expansion. Therefore, this temperature dependence is given by the following equation, , if β(T) is approximated by the equation, β(T) = β₀ + β₁T [154]. The examples of for the ν₂ modes of κ-Cu[N(CN)₂]Cl and β′-ICl₂ are shown in Figure 22. Although the function form of β(T) is too crude to express actual one, the frequency shift is well reproduced. If we assume that ν₂(0) and ν₂(1) also show the same temperature dependence, the quadratic expression can be corrected as

(7)

for T < 300 K. However, the temperature dependence of molecular vibration varies depending on the compound. For example, the ν₂ mode of θ-I₃ shifts less than 3 cm⁻¹ at 10 K. Therefore the estimated site charge has an ambiguity of about ±0.03.

Figure 22. Temperature dependence of the frequency of ν₂ of κ-(BEDT-TTF)₂-Cu[N(CN)₂]Cl and β′-(BEDT-TTF)₂ICl₂. The red line is the best fit equation, ω = Aexp(−BT−CT²/2), where A = ω₀, B = γβ₀, and C = γβ₁.

Figure 22. Temperature dependence of the frequency of ν₂ of κ-(BEDT-TTF)₂-Cu[N(CN)₂]Cl and β′-(BEDT-TTF)₂ICl₂. The red line is the best fit equation, ω = Aexp(−BT−CT²/2), where A = ω₀, B = γβ₀, and C = γβ₁.

5.3.2. Site Charge Distribution in Metallic Phase at Ambient Pressure

The second column of Table 3 shows the site charge of α-I₃ in the metallic phase estimated from the frequency of ν₂ using Equation (7). According to an x-ray diffraction study, the site charge follows the order, ρ_B > ρ_A = ρ_A′ > ρ_C, in the metallic state [128]. ρ_A = ρ_A′ shown in parentheses in Table 3 is calculated assuming this order. This assumption is consistent with the assignment that ν₂² is missing in α-I₃ (See Figure 20a,a′). These hole numbers are compared with the corresponding values estimated from the infrared-active ν₂₇ mode [130], assuming a linear relationship [155].The site charge was calculated by Wojciechowski et al., neglecting Coulomb interaction [111]. Katayama et al., examined the effect of the anion potential, and they showed that anion potential has a small influence on the site charge [156]. Kobayashi et al., calculated the temperature dependence of the site hole number within the mean-field approximation for extended Hubbard model [157]. Ishibashi et al., made Mulliken charge analyses in their ab initio calculation of the band structure of α-I₃ [158]. Recently, the site hole numbers were reported by Alemany using the DFT approach considering only the valence electrons [129]. In Table 3, their results are compared with the experimental results. The mean-field calculation overestimates the site-charge difference between the sites B and C. The simplified Coulomb energy parameters may be one of the reasons for the overestimation. In the ab initio and DFT calculations, this site-charge difference is more suppressed, and the agreement with experimental values is good taking the experimental errors into account.

Table 3. Site hole numbers of metallic α-(BEDT-TTF)₂I₃. MF denotes mean-field calculation, and DFT denotes density functional theory.

	Raman (150 K)	Infrared [130] (140 K)	X-ray [128] (150 K)	MF [157] (150 K)	ab initio [158]		DFT [129]
					(298 K)	(8 K)	(RT)
ρA = ρA′	(0.52(3))	~0.6	0.59(3)	0.52	0.53	0.54	0.521
ρB	0.60(3)	0.68	0.67(2)	0.71	0.55	0.57	0.546
ρC	0.37(3)	0.44	0.42(2)	0.25	0.40	0.37	0.382

Table 3. Site hole numbers of metallic α-(BEDT-TTF)₂I₃. MF denotes mean-field calculation, and DFT denotes density functional theory.

	Raman (150 K)	Infrared [130] (140 K)	X-ray [128] (150 K)	MF [157] (150 K)	ab initio [158]		DFT [129]
					(298 K)	(8 K)	(RT)
ρA = ρA′	(0.52(3))	~0.6	0.59(3)	0.52	0.53	0.54	0.521
ρB	0.60(3)	0.68	0.67(2)	0.71	0.55	0.57	0.546
ρC	0.37(3)	0.44	0.42(2)	0.25	0.40	0.37	0.382

In the same way, the site charges of metallic α-NH₄Hg at 10 K are estimated to be 0.57(3), 0.50(3), and 0.39(3) using the frequencies of ν₂ shown in Table 2. Although the corresponding site cannot be decided by vibrational spectroscopy, Hiejima et al., assigned the three infrared-active ν₂₇ modes with the aid of ¹³C-NMR, and they interpreted the site A to be most charge-poor [145]. Apart from the result of ¹³C-NMR, the following argument also supports the above interpretation. In Section 5.2.2. we discussed the breaking of inversion symmetry in α-MHg (M = K, Rb, Tl), based on the growth of the forbidden mode. The forbidden mode is the out-of-phase mode between ν_27A and ν_27A′ which are coupled through dipole-dipole interaction [145]. As the dipole is induced parallel to the long axis of molecule, the frequency of the out-of-phase mode is lower than that of the in-phase mode. The out-of-phase mode grows at a slightly lower frequency of the highest frequency mode among the three ν₂₇ modes, in-phase mode, ν_27B and ν_27C. This means that the highest frequency mode is the in-phase mode of ν_27A, that is, the A site is the most charge-poor. As the other sites cannot be decided, the assignment of ρ_B and ρ_C in Table 4 is interchangeable. These hole numbers are compared with the corresponding values estimated from the infrared-active ν₂₇ mode [130], assuming a linear relationship [155]. Table 4 shows the site-charge distribution of α-NH₄Hg calculated by the mean-field approximation with the transfer integrals given by Mori et al. [142] and Coulomb interaction parameters, U = 0.4, V_c = 0.17, V_p = 0.05 eV [157]. Foury-Leylekian et al., calculated the band structure of isostructural α-KHg at 104 K using a numerical atomic orbital DFT approach, and presented the site charges [147]. Their values are shown in Table 4 along with the hole numbers of isostructural compounds, α-MHg (M = K, Rb, Rl). The mean-field calculation underestimates the non-uniformity among site charges, while the first-principles calculation enhances the non-uniformity and approaches the experimental values. However, the most charge-poor site is the B site in both theoretical calculations. This result is different from the interpretation of the experimental result of the ν₂₇ mode (See Figure 1 of ref. [145]).

Table 4. Site hole numbers of α-(BEDT-TTF)₂MHg(SCN)₄ (M = NH₄, K, Rb, Tl). MF denotes mean-field calculation.

	α-NH4Hg			α-KHg		α-RbHg	α-TlHg
	Raman (10 K)	Infrared [130] (150 K)	MF (10 K)	Raman (10 K)	ab initio [147] (104 K)	Raman (10 K)	Raman (10 K)
ρA = ρA’	0.39(3)	0.40	0.51	0.42(3)	0.520	0.42(3)	0.42(3)
ρB			0.47		0.424
ρC			0.50		0.527

Table 4. Site hole numbers of α-(BEDT-TTF)₂MHg(SCN)₄ (M = NH₄, K, Rb, Tl). MF denotes mean-field calculation.

	α-NH4Hg			α-KHg		α-RbHg	α-TlHg
	Raman (10 K)	Infrared [130] (150 K)	MF (10 K)	Raman (10 K)	ab initio [147] (104 K)	Raman (10 K)	Raman (10 K)
ρA = ρA’	0.39(3)	0.40	0.51	0.42(3)	0.520	0.42(3)	0.42(3)
ρB			0.47		0.424
ρC			0.50		0.527

From the symmetry of the unit cell of θ-I₃, every site is approximately equivalent. Therefore, the site charge should be ρ = 0.5. Applying the empirical Equation (7), the site charge is calculated as ρ = 0.51(3) at 298 K (1493 cm⁻¹) and ρ = 0.54(3) (1496 cm⁻¹) at 20 K. The deviation from 0.5 at 20 K comes from the temperature dependence of the ν₂ mode that is different from that for κ-type ET salts which are used to obtain the first term of Equation (7).

5.3.3. Site-Charge Distribution under Hydrostatic Pressure

Tamura et al., showed that metallic θ-I₃ undergoes a first order phase transition showing a resistivity jump at around 0.5 GPa [159]. Tajima et al., further investigated the transport properties under hydrostatic pressure [160]. They found that the electrical resistance under 1 GPa behaves similar to that of α-I₃ at the same pressure. In addition, the Hall coefficient showed the same temperature dependence as that of α-I₃ at the same pressure. These two transport properties suggest a zero-gap state (ZGS) in θ-I₃ as well as in α-I₃ [120,121]. Recently, Miyagawa et al., investigated θ-I₃ under hydrostatic pressure using ¹³C-NMR [161]. The behavior of the spin shift and spin-lattice relaxation rate is also consistent with ZGS. They suggested a structural transformation to the α-type structure at 0.5 GPa. Figure 23a shows the pressure dependence of the Raman spectrum of ν₂ and ν₃ measured at 50 K. The Raman spectrum shows a frequency upshift under hydrostatic pressure. However, no distinct change was observed, and the spectrum is different from that of α-I₃ under hydrostatic pressure (See Figure 23a). This result suggests that high symmetry of the unit cell of θ-I₃ is preserved at least approximately up to 3.1 GPa. If this compound is in a ZGS above 0.5 GPa, there should be a contact point at the Fermi level. However, it is concluded from Figure 23a that the band structure of θ-I₃ at 0.5 GPa is quite different from that of α-I₃. The conservation of the pseudo-symmetry provides a restriction when we speculate the crystal and band structure under hydrostatic pressure.

Figure 23. (a) Pressure dependence of the Raman spectrum of θ-(BEDT-TTF)₂I₃ measured at 50 K; (b) Pressure dependence of the frequency of ν₂ in θ-(BEDT-TTF)₂I₃.

Figure 23. (a) Pressure dependence of the Raman spectrum of θ-(BEDT-TTF)₂I₃ measured at 50 K; (b) Pressure dependence of the frequency of ν₂ in θ-(BEDT-TTF)₂I₃.

When hydrostatic pressure is applied, the molecular vibration shows a frequency upshift (ω + Δω) due to hardening of the lattice. In addition to the lattice phonon mode, the frequency shift against pressure is described by Δω/ΔP = ωγκ, where γ and κ are the Gruneisen constant and compressibility, respectively. Therefore, the pressure dependent frequency is given by the equation, ω(P) = ω(1 + γκP). It is found that γκ is approximately temperature independent within an error of 10% in the temperature range from 20 K to 150 K as shown in Figure 23b. Since the hydrostatic pressure induces no structural change in this compound, the parameter was estimated to be γκ ≈ 3 × 10⁻³ GPa⁻¹ from Figure 23b.

Figure 24 shows the pressure dependence of the Raman spectrum of α-I₃ at 150 K, 100 K, and 20 K. At 150 K, the compound is metallic at ambient pressure. On increasing pressure, the Raman spectrum does not show a drastic change. At 100 K and 20 K, the compound is in a CO phase at ambient pressure. In this case, remarkable spectral changes are found to occur between 0.1 GPa and 0.45 GPa at 100 K and between 1.2 GP and 1.5 GPa at 20 K. These spectral changes correspond to the phase transition from the CO phase to the metallic phase, which is consistent with the suppression of the MI transition by hydrostatic pressure. In the metallic phase, the ν₂¹ and ν₂² modes do not show a parallel shift, rather they tend to merge on increasing the pressure. This trend is much more remarkable in the CO phase as shown in Figure 24c. Hydrostatic pressure not only hardens the lattice but also modulates the transfer integrals non-uniformly, which changes the site-charge distribution. After eliminating the lattice hardening effect assuming γκ ≈ 3 × 10⁻³ GPa⁻¹ for α-I₃, the site charge is estimated using Equation (7). The results are shown in the bottom panel of each figure. In a CO phase, the amplitude of charge order decreases on increasing pressure [162]. This trend is probably associated with the increase of transfer integrals under hydrostatic pressure.

Figure 24. Pressure dependence of the Raman spectra and site charges of α-(BEDT-TTF)₂I₃ analyzed at (a) 150 K; (b) 100 K; and (c) 20 K. Ambiguity of the hole numbers at charge-rich site is very large, because ν_2R is mixed with ν₃ in the CO state. The symbols, ▲ and ■, in parentheses show the nominal site charge calculated by Equation (7). Figure 24 is modified from Figure 5 of ref. [111].

Figure 24. Pressure dependence of the Raman spectra and site charges of α-(BEDT-TTF)₂I₃ analyzed at (a) 150 K; (b) 100 K; and (c) 20 K. Ambiguity of the hole numbers at charge-rich site is very large, because ν_2R is mixed with ν₃ in the CO state. The symbols, ▲ and ■, in parentheses show the nominal site charge calculated by Equation (7). Figure 24 is modified from Figure 5 of ref. [111].

In a metallic phase, the site charges approach uniform charge distribution as in θ-I₃ due to a non-uniform increase in transfer integrals on increasing hydrostatic pressure. This result suggests that the crystal structure of the zero-gap state of α-I₃ is slightly modulated so as to equalize sites B and C. However, there still remains a site-charge difference in ZGS. Alemany et al., reported the band calculation of α-I₃ [129] using the atomic parameters at 1.76 GPa that is determined by Kondo et al. [163]. They used the generalized gradient approximation to DFT, and found the contact point at the Fermi level. According to their calculation, the site hole numbers changes from ρ_A = ρ_A’ = 0.521, ρ_B = 0.546, ρ_C = 0.382 at ambient pressure to ρ_A = ρ_A′ = 0.576, ρ_B = 0.457, ρ_C = 0.361 at 1.76 GPa, where the most charge-rich site is interchanged between A=A′ and B sites and the maximum amplitude is enlarged from Δρ_max = 0.164 at ambient pressure to Δρ_max = 0.215. This change is opposite to the above mentioned trend shown in Figure 24a.

5.4. Optical Conductivity of α-(BEDT-TTF)₂I₃

The optical conductivity of α-I₃ has been published by several groups. Yakushi et al., reported optical conductivity from 720 cm⁻¹ to 25000 cm⁻¹ [164]. They found a drastic change in reflectivity at T_MI, and presented a calculation of the optical conductivity in the metallic phase based on a tight-binding approximation neglecting Coulomb interaction. The polarization (anisotropic) ratio of the optical weight was qualitatively reproduced. Zelezny et al., reported temperature dependent reflectivity in the range of 10–700 cm⁻¹, and transmittance in the 10–33 cm⁻¹ range [165]. They found a gap-like decrease in optical conductivity below 100 cm⁻¹ in the CO phase, and they found a lattice phonon at 31.7 cm⁻¹ in the E||b spectrum at 20 K. Dressel et al., reported optical conductivity in the range of 15–5500 cm⁻¹ along with temperature-dependent microwave conductivity (10, 12, 35, 60, and 100 GHz) [166]. They determined the optical gap to be 400 cm⁻¹, and found a strong phonon at 35 cm⁻¹ below T_MI. The similarity to the CDW system was pointed out from the experimental findings of non-linear transport, high dielectric permittivity, and 35 cm⁻¹ band, although α-I₃ is not a CDW system. More recently, Clauss et al., reported the optical conductivity in the range of 10–10000 cm⁻¹ [133,167]. They found no Drude response above T_MI, and they determined the CO gap to be 600 cm⁻¹ below T_MI. They estimated the effective transfer integrals comparing with theoretical calculation of the extended Hubbard model for a quarter-filled square lattice [40]. Figure 25 shows the reflectivity and optical conductivity of α-I₃ that is reported by Yue et al. [130]. The optical conductivity agrees well with that reported by Clauss et al. [133,167]. According to the theoretical model by Merino et al. [40], the spectral weight of the electronic excitation at ~6t (t is the transfer integral of square lattice) in the CO phase shifts to ~2t–3t with Drude response in the metallic phase. The corresponding peak shift is not clear in the E||b spectrum. As Clauss et al., pointed out, the spectral weight in the infrared region shifts to the gap region in the metallic phase. This behavior is typically found in the E||a spectrum. No Drude response was observed in the metallic phase. It is difficult to specify the cause of non-Drude behavior, because the metallic phase exists only at high temperature, at which thermal excitations collapse the quasi-particle band as described for the optical conductivity of θ-I₃ in Section 4.3, and/or they blur the small semimetallic Fermi surface. Incidentally, a well-defined Drude response is observed in α-MHg (M = NH₄, K, Rb, Tl), because these compounds are a metallic down to low temperature [29,30].

The collective excitation in the CO state has been investigated in analogy with CDW. The experimental findings of large permittivity in the range of 50–50000 Hz and nonlinear conductivity of α-I₃ in the CO phase recalled the sliding of CDW [166]. The observation of the voltage oscillation in the 7–28 kHz region suggests collective transport [168]. A recent permittivity experiment from 1 Hz to 1 MHz indicates the existence of a large dielectric relaxation mode [133,169]. Ivek et al., interpreted this low-frequency dielectric relaxation mode to be a phason-like behavior. Dressel et al., reported an attempt to find a collective CO mode in the low-frequency region, and they assigned the strong 35 cm⁻¹ band to a collective CO excitation [170]. However, the corresponding strong band is not indicated in ref. [133,167]. Yue et al., reported the transmittance of the single crystal of α-I₃.down to 28 cm⁻¹ [130]. They confirmed the 31 cm⁻¹ band which Zelezny et al., reported [165] but did not find such a strong band at 35 cm⁻¹. More extensive experimental and theoretical studies will be necessary to establish collective CO excitation.

Figure 25. Temperature dependent reflectivity and optical conductivity of α-(BEDT-TTF)₂I₃. The optical conductivities are taken from ref. [130].

Figure 25. Temperature dependent reflectivity and optical conductivity of α-(BEDT-TTF)₂I₃. The optical conductivities are taken from ref. [130].

5.5. α′-(BEDT-TTF)₂IBr₂

α′-(BEDT-TTF)₂IBr₂ (abbreviated as α′-IBr₂) has a layered structure similar to α-I₃, but it is not isostructural with the α-type BEDT-TTF salts [171]. Similar to α-I₃, the unit cell contains four molecules with a herringbone arrangement. Unlike α-I₃, on the other hand, the unit cell contains two crystallographically independent groups (A, A′) and (B, B′), in which A and A′ (B and B′) are connected by inversion symmetry within each group. The band structure is calculated to be semimetallic, and the bandwidth of α′-IBr₂ is the narrowest among the α-type BEDT-TTF salts [171]. Reflecting the narrow bandwidth, α′-IBr₂ is semiconducting (ρ_RT~0.3 Ωcm) with an activation energy of ~0.16 eV at around room temperature. The electrical resistivity increases steeply by an order of magnitude at around 200 K, and this compound moves into a high-resistivity state with the same activation energy [172]. The phase transition of α′-IBr₂ was investigated by means of NMR [173] and x-ray diffraction [171,174] experiments. The NMR study suggested that the thermal motion of the ethylene groups of BEDT-TTF begins to freeze gradually at around 250 K [173]. X-ray diffraction study confirmed this suggestion analyzing the temperature factors of the carbon atoms in one of the ethylene groups [171]. The ordering of the ethylene group occurs continuously from room temperature down to 70 K. Except for this ordering, no distinct structural change was reported above and below 200 K. Neither superlattice spots nor diffuse x-ray scattering has been found down to 20 K [171]. The magnetic susceptibility also shows no clear anomaly at around 200 K [172]. Inokuchi et al., reported the optical conductivity and Raman spectrum of this compound, and they suggested that the unit cell involves two non-equivalent molecules with different valence [175]. X-ray diffraction study suggested that the electron-phonon interaction is extremely weak in this system.

Yue et al., investigated the infrared and Raman spectra of α′-IBr₂, and assigned the Raman spectrum with the aid of polarization dependence and ¹³C-substituted compounds [176]. Based on the assignment, they showed clear evidence that the low-temperature high-resistivity phase is a charge-ordered state. Combined with the ν₂₇ mode, they estimated the site charge distribution to be (0.9, 0.8, 0.2, 0.1), and thus the maximum CO amplitude is very large, Δρ_max = 0.8. Although the side band of ν_27R² (indicated by an arrow in Figure 26) is assigned to CH₂ bending mode, it may be assigned to ν_27R¹ instead of another side band, because the low-frequency side band is observed in the deuterium-substituted compound. In this case, the site charge distribution and Δρ_max are estimated to be (1.0, 0.8, 0.2, 0.1) and Δρ_max = 0.9. Furthermore, they found that the inversion symmetry is broken in the CO state. If the unit cell has inversion symmetry, the ν₂ mode is classified into two Raman-active (in-phase) modes and two infrared-active (out-of-phase) modes. In the CO phase, they found four ν₂ modes in the Raman spectrum of the ¹³C-substituted α-IBr₂. They took notice of the stretching vibration of IBr₂⁻ as a marker band for the inversion symmetry. However, the splitting of this band seems not to be decisive to judge the breaking of inversion symmetry, as the frequency of this mode is comparable with the lattice phonon. Since IBr₂⁻ is not located on the center of symmetry in the unit cell, the intramolecular vibration is influenced by the non-centrosymmetric crystal field. The ν₂ or ν₃ mode is much safer as a marker band. Taking the symmetry into account, they proposed two possible arrangements, diagonal stripes along the a-b and b axes, as the CO pattern. These two stripes are probably competing and generate frustration in this compound.

Figure 26. Temperature dependences of the (a) Infrared-active ν₂₇ mode; (b) Raman-active ν₂ and ν₃ modes; and (c) electrical resistivity in α′-(BEDT-TTF)₂IBr₂. See ref. [176] for the argument of assignment. Figure 26a,c are taken from ref. [58].

Figure 26. Temperature dependences of the (a) Infrared-active ν₂₇ mode; (b) Raman-active ν₂ and ν₃ modes; and (c) electrical resistivity in α′-(BEDT-TTF)₂IBr₂. See ref. [176] for the argument of assignment. Figure 26a,c are taken from ref. [58].

Yue et al., analyzed the resistivity and magnetic susceptibility [58]. They found that the resistivity curve is approximately expressed by a single exponential curve below ~210 K, whereas it cannot be expressed by a single exponential curve above ~210 K, where the activation energy exponentially decreases against 1/T. The magnetic susceptibility is expressed by an alternating Heisenberg model down to 30 K. At around 30 K this compound abruptly loses susceptibility and becomes non-magnetic with hysteresis [177]. They pointed out that every crystal cracked when the crystal was cooled across this transition temperature. As the deuterium substituted α’-IBr₂ does not show the 30 K phase transition, the interaction with IBr₂⁻ may be associated with this magnetic phase transition. Yamamoto et al., found an onset of SHG at 160 K using an SHG microscope, and they argued for the growth of ferroelectric polarization below 160 K [136,178]. Therefore, this compound has three phase transitions at ~210 K, ~160 K, and ~30 K. This behaviour is different from that of α-I₃, in which all of these transitions occur at the same temperature (~135 K).

Figure 26 shows the infrared-active ν₂₇ mode and Raman-active ν₂ and ν₃ modes along with the electrical resistivity [58]. The charge-sensitive ν₂₇ and ν₂ modes are already split at room temperature, and the spectral change against temperature is continuous as in θ-Cu₂(CN)[N(CN)₂]₂ and θ_m-TlZn. It is therefore obvious that the line shapes of the ν₂₇ and ν₂ modes reflect the case of τΔν >> 1 over the whole temperature range. On increasing temperature, as shown in Figure 26b, the ν₃ mode is weakened toward the transition temperature at ~210 K. This spectral change suggests shortening of the coherence length ζ of the CO domain [58]. The optical conductivity has a clear gap below 200 K, whereas it has finite density of states above 210 K. The temperature dependence is continuous as for θ_m-TlZn. In the limit of ζ = 0, the individual holes, perhaps polaron, are randomly hopping at high temperature. Assuming this extreme case, Yue et al., interpreted the phase transition at 210 K as an order-disorder transition [58]. They qualitatively explained the optical conductivity change based on the order-disorder model of the atomic limit. According to this simple model, the finite density of states above 210 K is generated by the disordered configurations of localized holes, the energy of which is given by the coordination number around the hole [58,177]. The electrical and magnetic properties and spectroscopic feature closely resemble those of θ-Cu₂(CN)[N(CN)₂]₂, hence the high-temperature phase might be understood in the same way as θ-Cu₂(CN)[N(CN)₂]₂, in which the short-range CO domain grows extensively. However, strong frustration perhaps suppresses the growth of short-range order in this compound.

This simple model cannot explain the difference in temperature between the order-disorder (~210 K) and ferroelectric (~160 K) transitions. In the atomic limit, the Coulomb repulsion along two diagonal stripes is nearly the same. These nearly degenerate short-range CO domains compete with each other and generate frustration, when the coherence length of CO increases. This frustration may cause the above successive ferroelectric transition. Recently, weak superlattice spots for a × b × 2c were found in an x-ray study conducted at BL-8A beamline of the Photon Factory Facility, KEK [179]. Based on the structural modulation, an antiferroelectric state is proposed as the intermediate phase (160–210 K) before the ferroelectric transition.

Yue et al., estimated the kinetic energy from the integration of optical conductivity [177], which is 0.1, 0.3, and 0.4 eV per unit cell for α′-IBr₂, α-I₃, and α-NH₄Hg, respectively. This result indicates that the transfer integrals of α′-IBr₂ are very small compared with those of α-I₃, and α-NH₄Hg. Therefore, in the case of α′-IBr₂, the spin degree of freedom survives after the CO transition due to the small spin gap (~82 K) coming from the small exchange energy along the stripe. On the other hand, in α-I₃, the exchange energy is larger and the dimerization along the stripe is larger than that in α′-IBr₂, and furthermore, the dimerization is enhanced below the phase transition of α-I₃ [128,171]. These two factors result in a large spin gap (440 K) as reported by Sugano et al. [180]. The difference in the magnitude of spin gap is the cause of the simultaneous transition of charge order and non-magnetic state. The difference in ferroelectric transition is not clear at the moment. Possibly, the frustration plays a role in the successive transition to the ferroelectric state in α′-IBr₂.

6. Summary

The charge-ordering phase transition arises from the competition between the kinetic energy gain and the cost of on-site and nearest-neighbor inter-site Coulomb energy. In some compounds such as θ-type BEDT-TTF salts, geometrical frustration stabilizes the metallic state, and lattice distortion sometimes plays a dominant role for dissolving the frustration. Even in such a case, the transfer integral plays an essential role for the properties of the materials [78]. Transfer integrals depend considerably on the counter anions and temperature, whereas Coulomb interaction is almost insensitive to such a modification. The rough values of the kinetic energy per unit formula (=hole) are shown in Figure 27, which are estimated from the room-temperature optical conductivity [181]. The kinetic energy is a stabilization energy due to the delocalization of the valence electron over the crystal. The kinetic energy is associated with the bandwidth: the wider the bandwidth, the larger the kinetic energy. The kinetic energy including the correlation effect is experimentally estimated from the optical conductivity [182]. The kinetic energy –E_K was calculated in the same way as reported by Yue et al. [177].

The kinetic energy of β″-(BEDT-TTF)(TCNQ) is comparable with those of θ_m-TlZn and θ_o-TlZn, which undergo a metal-insulator transition while maintaining a large CO amplitude (Δρ~0.6) over the whole temperature range. In contrast to the θ-type salts, this compound continuously changes the spectral feature from a large CO amplitude (Δρ~0.6) to a small amplitude (Δρ~0) on lowering the temperature. Experimentally, the split charge-sensitive modes merge into a single mode in the low-temperature region. The transport properties below 20 K indicate Fermi-liquid behavior. It is speculated from the optical conductivity and charge-sensitive modes that the coherent state below 20 K collapses above 20 K and continuously changes into a charge-ordered metal with a pseudogap. As the hydrostatic pressure reproduces the same spectral change for the Raman-active mode, the variation of the transfer integral due to lattice contraction has a big influence on the electronic state of this compound.

Figure 27. Kinetic energy per a formula unit (■) plotted as a function of the lattice parameter ratio. In the case of the θ-type crystal, the crystal axis along the stacking direction is doubled. The inset shows the schematic molecular arrangement and crystal axes. In the compounds framed by the green rectangle, the CO amplitude is small (Δρ~0.1) over the whole temperature range. In the compounds framed by the yellow rounded rectangle, the CO amplitude is large (Δρ~0.6) over the whole temperature range. In the compound framed by the triangle, the CO amplitude changes at the phase transition, small amplitude (Δρ~0.2) at high temperature and large amplitude (Δρ_max~0.6) at low temperature. In the compound framed by the inverted triangle, the amplitude changes continuously, large amplitude at high temperature (Δρ~0.6) and small amplitude (Δρ~0) at low temperature.

Figure 27. Kinetic energy per a formula unit (■) plotted as a function of the lattice parameter ratio. In the case of the θ-type crystal, the crystal axis along the stacking direction is doubled. The inset shows the schematic molecular arrangement and crystal axes. In the compounds framed by the green rectangle, the CO amplitude is small (Δρ~0.1) over the whole temperature range. In the compounds framed by the yellow rounded rectangle, the CO amplitude is large (Δρ~0.6) over the whole temperature range. In the compound framed by the triangle, the CO amplitude changes at the phase transition, small amplitude (Δρ~0.2) at high temperature and large amplitude (Δρ_max~0.6) at low temperature. In the compound framed by the inverted triangle, the amplitude changes continuously, large amplitude at high temperature (Δρ~0.6) and small amplitude (Δρ~0) at low temperature.

The four θ-type BEDT-TTF salts, θ-RbZn, θ_o-TlZn, θ_m-TlZn, and θ-Cu₂(CN)[N(CN)₂]₂, (yellow color in Figure 27) show an MI transition. However, they maintain a large CO amplitude (Δρ~0.6) in both metallic and insulating phases. In the CO phase of the θ-type BEDT-TTF salts, the CO pattern is a horizontal stripe in θ-RbZn, θ_o-TlZn, and θ-Cu₂(CN)[N(CN)₂]₂, as concluded by the selection rule of the ν₃ modes. On the other hand, the diagonal stripe is claimed in θ_m-TlZn. In contrast to the α-type BEDT-TTF salts, the θ-type compounds except θ_m-TlZn have a non-polar space group P2₁2₁2₁ in the CO phase. Probably, the θ-type compounds except for θ_m-TlZn do not have ferroelectric polarization in the CO phase in spite of the non-centrosymmetric space group. As the CO amplitude is large even in the metallic phase, this phase is regarded as a CO metal. However, the compound can be classified into two groups, [θ-RbZn, θ_o-TlZn] and [θ_m-TlZn, θ-Cu₂(CN)[N(CN)₂]₂]. The phase transition in the former is discontinuous, whereas it is continuous in the latter. The activation energy of the resistivity in the latter is significantly larger, and the precursor ν₃ bands are found in the latter. In the metallic phase of the latter group, short-range stripe CO probably grows more extensively than in the former group.

The kinetic energy of θ-CsZn and θ-I₃ is significantly larger than the others among the θ-type BEDT-TTF salts (green color in Figure 27). The CO amplitude of these compounds is much smaller than in the others. The amplitude of the former is Δρ < 0.08, and Δρ < 0.07 in the latter. An indication of CO fluctuation is found in the Raman spectrum and optical conductivity of θ-CsZn, in which the frustration between the stripe and threefold COs is dominant. θ-I₃ has a zero-energy (Drude) peak in the optical conductivity at 4 K, while the coherent state collapses at 100 K.

The kinetic energy of α-I₃ is comparable with that of θ-RbZn. The amplitude of CO discontinuously changes from a small amplitude (at high temperature) to a large amplitude (at low temperature) at the MI transition temperature. Below the MI transition temperature, the localized charge is arranged in a horizontal stripe involving two charge-rich sites and two charge-poor sites with an amplitude of Δρ ≈ 0.4–0.6. In the CO phase, the inversion symmetry is broken, and strong SHG is found. Observation of a macroscopic polar (ferroelectric) domain is demonstrated by SHG interferometry. A fast optical response is also reported. This unconventional ferroelectricity is called electronic ferroelectricity. In the metallic phase, the broad linewidth of the charge-sensitive mode indicates fluctuation of the CO. This fluctuation is well suppressed by hydrostatic pressure.

The kinetic energy of α-NH₄Hg is significantly larger than that of α-I₃. The linewidth of the charge-sensitive mode is narrow in α-MHg (M = NH₄, K, Rb, Tl). Among these four compounds, the inversion symmetry is locally broken in α-MHg (M = K, Rb, Tl). This phenomenon is attributed to the anion-sublattice coupled incommensurate CDW. The amplitude of the CDW is estimated to be Δρ < 0.05. On the other hand, the fluctuation of CO is indicated in the Raman spectrum of α-NH₄Hg which undergoes superconducting state at 1 K.

α-I₃ in the metallic phase and α-NH₄Hg involve three non-equivalent sites in the unit cell. Reflecting the non-uniform site, the charge-sensitive mode split into three. The maximum site-charge difference is estimated to be Δρ_max~0.2 both in metallic α-I₃ and α-NH₄Hg. The most charge-poor site is the C site in α-I₃ and the A site in α-NH₄Hg. First principle calculation agrees with the experimental results for α-I₃. In α-NH₄Hg, however, there is disagreement in the most charge-poor site, between the band calculation and the interpretation of the charge-sensitive mode. The site charge distribution under hydrostatic pressure is estimated for α-I₃ and θ-I₃. In the metallic phase, the site charge distribution approaches a uniform charge distribution on increasing pressure. However, a non-uniform site charge distribution remains in the zero-gap state of α-I₃. The zero-gap state of θ-I₃ under hydrostatic pressure keeps uniform charge distribution unlike in α-I₃.

The kinetic energy of α′-IBr₂ is smallest among the compounds discussed in this paper, and probably comparable with that of θ-Cu₂(CN)[N(CN)₂]₂. The electrical and magnetic properties and spectroscopic feature closely resemble each other. The ground state is a non-magnetic CO state with large amplitude (Δρ ≈ 0.6–0.8). α′-IBr₂ shows successive transitions at ~210 K and ~160 K and magnetic transition at ~30 K. The large CO amplitude is maintained over the whole temperature range. The ordering of charge sets in at ~210 K, the ferroelectric domain begins to grow at ~160 K, and spin singlet state is formed at ~30 K accompanied by structural distortion.