Growth and Characterization of Second and Third Order Acentric Studies of L -Phenylalanine L -Phenylalaninium Malonate Single Crystal

: A single crystal of L -phenylalanine L -phenylalanininum malonate (LPPMA) was synthesized by slow evaporation and was subjected to nonlinear optical examination and physio-chemical characterization. Studies on single X-ray diffraction conﬁrm the arrangement of monoclinic space group P21 which is a vital criterion for the NLO phenomenon. The assessment of functional groups and diverse vibration modes responsible for the characteristics of the material was performed with an FTIR analysis. The UV-visible spectral examination found the wavelength of UV-cutoff at 233 nm and various optical parameters were evaluated. The mechanical strength and different criteria associated with it were assessed. The electric ﬁeld response of the material was examined in terms of the dielectric constant, dielectric loss, ac conductivity and activation energy. The spectra of emission were detailed. The efﬁcacy of second harmonic generation was studied. The parameters of nonlinearity were investigated to analyse the third-order acentric optical response in the LPPMA by Z-scan procedure.


Introduction
Materials exhibiting second (SHG), third (THG) and higher harmonic generation occupy a versatile position in the area of optical data storage with information processing. The photo-electric interface occurs in the process of nonlinear SHG, and finds promising potential in the domain of storage of data with high intensity and spectroscopy [1]. The significance of the basic types with their orientations inside the material plays a substantial part in finding or understanding the physical and chemical features of the organic

Experimental
Synthesis of LPPMA L-phenylalanine L-phenylalaninium malonate (LPPMA) was produced using slow solvent solution growth (evaporation), SSEST with deionized water, which was harvested from the starting compound L-phenylalanine (LOBA, 99%), and malonic acid (LOBA, 99%) in stoichiometric molar (2:1). The estimated quantity of materials was systematically dissolved in water. The mixture was stirred continuously using a magnetic stirrer for 6 h to ensure complete miscibility. The well saturated and filtered solution was transferred into a 250 ml beaker, covered with filter paper containing tiny pin-holes and set aside at room temperature. Colorless transparent crystals were observed in 25 days and harvested ( Figure 1). significance of the basic types with their orientations inside the material plays a substan tial part in finding or understanding the physical and chemical features of the organ molecules in a material. For a material to possess nonlinear optical characteristics, molec ular dipoles align in a noncentric fashion, which is indispensable for materials with a SHG property [2]. A greater number of organic compounds materialize in the space grou of Centro symmetry and do not have a nonlinear optical feature. To remedy this, variou molecular engineering approaches such as steric-hindrance, chirality, etc., have been pro posed [2]. The main aspect of amino acids in the nonlinear optical domain mainly solid fies in noncentrosymmetric space groups. In the organic category, α-amino acids hav distinct characteristics [3]. Crystals grown from amino acids possess fascinating feature suitable for NLO devices, because of their zwitterionic nature which initiates the hydro gen bonding network [4]. Among nonlinear optical materials, organic materials act as midway between compounds of the organic category with covalent bonds and inorgan compounds with mostly ionic bonds [5]. The production of organic acentric crystals ex poses the poor stability of their physico-chemical features and their lower mechanica strength. Amino acid-based crystals, with their outstanding electro-optic and NLO prop erties, show abundant response in photonic applications [6,7]. Currently, organic mole cules with third-order nonlinearity are essential for widespread applications in 3D optica memory and optical communication with information processing at high speeds [8]. Re latedly, L-phenylalanine-based complex materials [9][10][11][12][13] prove to be more prospectiv materials for NLO applications. Reasonably, some authors have shown interest in work ing with malonic acid-based crystals and report it as an effective NLO material [14-16 suitable for optical applications. Furthermore, the structure and certain studies of LPPMA were reported by Alagar and Prakash [17,18]. Here, we studied the growth and characte ization of LPPMA samples using the slow evaporation process. LPPMA crystals wer characterized using various instrumentation systems to check their suitability for devic fabrications.

Synthesis of LPPMA
L-phenylalanine L-phenylalaninium malonate (LPPMA) was produced using slow solvent solution growth (evaporation), SSEST with deionized water, which was harveste from the starting compound L-phenylalanine (LOBA, 99%), and malonic acid (LOBA 99%) in stoichiometric molar (2:1). The estimated quantity of materials was systematicall dissolved in water. The mixture was stirred continuously using a magnetic stirrer for 6 to ensure complete miscibility. The well saturated and filtered solution was transferre into a 250 ml beaker, covered with filter paper containing tiny pin-holes and set aside a room temperature. Colorless transparent crystals were observed in 25 days and harveste ( Figure 1).

X-ray Diffraction (Single Crystal)
The result of the XRD showed that LPPMA crystallizes in a monoclinic arrangement. The lattice parameters revealed in the SXRD investigation are provided in Table 1, which shows the agreement between our results and those reported in the literature [18].

FTIR Vibrational Analyses
The data regarding the structure of a material are evident from this spectroscopic analysis. The absorption of IR radiation leads to diverse peaks in a particle, showing stretching and bending vibration as represented in Figure 2. A strong broad absorption in the range of 3300-2300 cm −1 agrees with the NH 3 + of the amino group [18]. The strong edge at 3081 cm −1 is C-H stretching. Overtone combination appears in the absorption region at 2090 cm −1 . The peaks at 1302, 1359 cm −1 exhibit CH 2 wagging and CH 2 deformation [19,20]. The wavenumber positioned at 1210 cm −1 is C-CH in a sharp bending vibration. C-C and C-N stretching are identifiable in wavenumbers 1140, 1183 cm −1 [18]. The vibration of C-H out of plane (bending) initiates peaks at 953 and 914 cm −1 . The wavenumber at 701 cm −1 exhibits the presence of a benzene ring. Thus, peaks which appear at 853 cm −1 , 748 cm −1 establish C-H (out of) plane deformation [17].

X-ray Diffraction (Single Crystal)
The result of the XRD showed that LPPMA crystallizes in a monoclinic arrangement. The lattice parameters revealed in the SXRD investigation are provided in Table 1, which shows the agreement between our results and those reported in the literature [18].

FTIR Vibrational Analyses
The data regarding the structure of a material are evident from this spectroscopic analysis. The absorption of IR radiation leads to diverse peaks in a particle, showing stretching and bending vibration as represented in Figure 2. A strong broad absorption in the range of 3300-2300 cm −1 agrees with the NH3 + of the amino group [18]. The strong edge at 3081 cm −1 is C-H stretching. Overtone combination appears in the absorption region at 2090 cm −1 . The peaks at 1302, 1359 cm −1 exhibit CH2 wagging and CH2 deformation [19,20]. The wavenumber positioned at 1210 cm −1 is C-CH in a sharp bending vibration. C-C and C-N stretching are identifiable in wavenumbers 1140, 1183 cm −1 [18]. The vibration of C-H out of plane (bending) initiates peaks at 953 and 914 cm −1 . The wavenumber at 701 cm −1 exhibits the presence of a benzene ring. Thus, peaks which appear at 853 cm −1 , 748 cm −1 establish C-H (out of) plane deformation [17].

Optical Studies
The optical spectrum of LPPMA was established in the 200-700 nm wavelength range. From the UV-visible spectrum (Figure 3a), it is clear that ultraviolet absorption includes electronic transitions from an unexcited state to an excited one [21]. The lower cutoff wavelength of LPPMA at 233 nm with extremely good transparency proves its applicability in second and third harmonic generation. The absorption coefficient (α) was assessed utilizing the following Formula cludes electronic transitions from an unexcited state to an excited one [21]. The lower cutoff wavelength of LPPMA at 233 nm with extremely good transparency proves its applicability in second and third harmonic generation. The absorption coefficient (α) was assessed utilizing the following Formula 2.3026 log(1 / T) d  (1) Here, d represents material thickness. The absorption coefficient represented as (α) was evaluated using Tauc's concept: where A symbolizes the constant and Eg, h and v represent the energy gap, the value of the Planck constant (6.63 × 10 −34 Jsec), and frequency of photons. The energy gap Eg of LPPMA was estimated using Tauc's plot ( Figure 3b) and its value is 5.58 eV. Thus, the organic LPPMA crystal with an enhanced optical band gap is a potential aspirant in the field of nonlinear optics.

Optical Constants Calculation
The optical nature of a material is very important in determining its usefulness in NLO application devices. The diverse optical constants were evaluated utilizing the subsequent formulae [21]. Extinction coefficient (K) can be estimated by Reflectance (R) and linear refractive index (n0) are assessed using [4] Here, d represents material thickness. The absorption coefficient represented as (α) was evaluated using Tauc's concept: where A symbolizes the constant and E g , h and v represent the energy gap, the value of the Planck constant (6.63 × 10 −34 Jsec), and frequency of photons. The energy gap E g of LPPMA was estimated using Tauc's plot ( Figure 3b) and its value is 5.58 eV. Thus, the organic LPPMA crystal with an enhanced optical band gap is a potential aspirant in the field of nonlinear optics.

Optical Constants Calculation
The optical nature of a material is very important in determining its usefulness in NLO application devices. The diverse optical constants were evaluated utilizing the subsequent formulae [21]. Extinction coefficient (K) can be estimated by Reflectance (R) and linear refractive index (n 0 ) are assessed using [4] Figure 4a,b, depict that R and K fully rely on incident photon energy [21]. Figure 4c,d depicts (R) and (K) versus the absorption coefficient (α). The device internal efficacy mainly relies on this absorption coefficient (α) [21]. Figure 4e displays the dependence of linear n 0 (refractive index) versus incident energy (photon). The minimum value of n 0 highlights that LPPMA has a regular dispersion nature. The high optical transparency of LPPMA in the Ultraviolet-visible section illustrates it as a good optical behavior candidate for use in device applications.
Figure 4e describes the elevation of optical conductivity with the increase in hυ, for which a large value confirms the elevated photo-tunable feature of crystal [4]. Figure 4f concludes that the value of electrical and optical conductivity depends on the photon energy. Hence, this potential material is suitable in the ultrafast data transmission process (optical) [21].
The below relation depicts electric susceptibility (χc), The electric susceptibility χc is 0.1314 for the wavelength 390 nm (Figure 4g). The dielectric constants can be estimated using the following: εr = n0 2 − K 2 and εi = 2n0K (12) At the wavelength of 390 nm, the real (εr) and imaginary (εi) parts were estimated as 1.6235 and 6.7139 × 10 −7 . Hence, the low magnitude of the dielectric constant with a broad energy gap of the L-phenylalanine L-phenylalaninium malonate crystal suggests its fitness for optoelectronic devices.

Determination of Urbach Energy (Eu)
The dependence of α on hυ in the Urbach relation is [22], The slope is 1.0817. Figure 5 illustrates the logarithm of (α) with the incident energ of the photon (hυ). The inverse of the linear plot measures the Urbach energy (Eu), whic was evaluated as 0.9244 eV. The lower calculated value of Eu indicates less flaws i LPPMA which validates its usage in nonlinear optics.

Mechanical Stability Analysis
The hardness of the material determines its features, including its mechanic strength and its properties [23]. The mechanical stability of an optical crystal plays a ke The optical conductivity (σ op ) is, and also the electrical conductivity (σ ele ) can be evaluated using the following formula, Figure 4e describes the elevation of optical conductivity with the increase in hυ, for which a large value confirms the elevated photo-tunable feature of crystal [4]. Figure 4f concludes that the value of electrical and optical conductivity depends on the photon energy. Hence, this potential material is suitable in the ultrafast data transmission process (optical) [21].
The below relation depicts electric susceptibility (χ c ), (Or) The electric susceptibility χ c is 0.1314 for the wavelength 390 nm (Figure 4g). The dielectric constants can be estimated using the following: ε r = n 0 2 − K 2 and ε i = 2n 0 K At the wavelength of 390 nm, the real (ε r ) and imaginary (ε i ) parts were estimated as 1.6235 and 6.7139 × 10 −7 . Hence, the low magnitude of the dielectric constant with a broad energy gap of the L-phenylalanine L-phenylalaninium malonate crystal suggests its fitness for optoelectronic devices.

Determination of Urbach Energy (E u )
The dependence of α on hυ in the Urbach relation is [22], The slope is 1.0817. Figure 5 illustrates the logarithm of (α) with the incident energy of the photon (hυ). The inverse of the linear plot measures the Urbach energy (Eu), which was evaluated as 0.9244 eV. The lower calculated value of E u indicates less flaws in LPPMA which validates its usage in nonlinear optics.  energy (a,b), (ii) absorption coefficient (α) (c,d). Plot of photon energy vs. (i) refractive index (n0) (e). (ii) electrical conductivity and optical conductivity (f) (iii) Electric susceptibility (χc) (g).

Determination of Urbach Energy (Eu)
The dependence of α on hυ in the Urbach relation is [22], The slope is 1.0817. Figure 5 illustrates the logarithm of (α) with the incident energy of the photon (hυ). The inverse of the linear plot measures the Urbach energy (Eu), which was evaluated as 0.9244 eV. The lower calculated value of Eu indicates less flaws in LPPMA which validates its usage in nonlinear optics.

Mechanical Stability Analysis
The hardness of the material determines its features, including its mechanical strength and its properties [23]. The mechanical stability of an optical crystal plays a key role in the fabrication of the device. The mechanical hardness of the LPPMA sample was

Mechanical Stability Analysis
The hardness of the material determines its features, including its mechanical strength and its properties [23]. The mechanical stability of an optical crystal plays a key role in the fabrication of the device. The mechanical hardness of the LPPMA sample was tested utilizing an MH-112 Vickers hardness tester. The application of the load is (25 g, 50 g, 100 g) on the surface of LPPMA. The Vickers hardness number H v of LPPMA was premeditated using the following expression (Table 2): The plot (Figure 6a) revealed that the elevation in H v (hardness number) with load (25 g, 50 g, 75 g) emphasizes the reverse-indentation-size effect [23]. As can be observed from Figure 6b, the hardening coefficient is 3.71. Hence, the Meyer's index magnitude (n) infers that LPPMA possesses the feature of a soft nature. The yield strength of LPPMA (Figure 6c) can be found using [24] Table 2, Here, the value of n = n + 2.
The stiffness constant C 11 is calculated using the following [25] Figure 6d): The Knoop hardness number (H k ) is determined by [24]

Determination of Dielectric Studies
The dielectric measurement provides details about the electrical response parameter of a periodic solid [26]. The dielectric constant and loss in LPPMA was performed across diverse temperature ranges using an LCR meter. This was calculated by: and ε" = ε tan δ Here, C represents the capacitance specified by micro farad, t the thickness specified in mm, ε 0 is the dielectric constant in vacuum (ε 0 = 8.854 × 10 −12 Fm −1 ) and A indicates the area of the testing material in mm 2 . Figure 7a,b shows variations of ε and ε" with log frequency and it reduces with a rise in frequency. The higher values of ε at smaller frequencies is a result of all polarization mechanisms. The lower range of (ε ) at the domain of a higher range of frequency may possibly originate with respect to the electric field applied [26]. The lower measure of ε and ε" at a high frequency range indicates the enhanced optical nature with the minimal amount of defects in LPPMA, which furthermore fulfills the requirements for use in the opto-electronic sector and in nonlinear optical devices [26]. tested utilizing an MH-112 Vickers hardness tester. The application of the load is (25 g, 50 g, 100 g) on the surface of LPPMA. The Vickers hardness number Hv of LPPMA was premeditated using the following expression (Table 2): The plot (Figure 6a) revealed that the elevation in Hv (hardness number) with load (25 g, 50 g, 75 g) emphasizes the reverse-indentation-size effect [23]. As can be observed from Figure 6b, the hardening coefficient is 3.71. Hence, the Meyer's index magnitude (n) infers that LPPMA possesses the feature of a soft nature.
The yield strength of LPPMA (Figure 6c) can be found using [24] (15) Here, the value of n′ = n + 2. The stiffness constant C11 is calculated using the following [25] (16) The Knoop hardness number (Hk) is determined by [24]

Determination of Dielectric Studies
The dielectric measurement provides details about the electrical response parameter of a periodic solid [26]. The dielectric constant and loss in LPPMA was performed across diverse temperature ranges using an LCR meter. This was calculated by: and εʺ = εʹ tan δ Here, C represents the capacitance specified by micro farad, t the thickness specified in mm, ε0 is the dielectric constant in vacuum (ε0 = 8.854 × 10 −12 Fm −1 ) and A indicates the area of the testing material in mm 2 . Figure 7a,b shows variations of ε′ and ε″ with log frequency and it reduces with a rise in frequency. The higher values of ε′ at smaller frequencies is a result of all polarization mechanisms. The lower range of (ε′) at the domain of a higher range of frequency may possibly originate with respect to the electric field applied [26]. The lower measure of ε′ and ε″ at a high frequency range indicates the enhanced optical nature with the minimal amount of defects in LPPMA, which furthermore fulfills the requirements for use in the opto-electronic sector and in nonlinear optical devices [26].
The ac conductivity σac (Ω m) −1 was evaluated using the following relation (23): The variation of conductivity with log ω at diverse temperatures is depicted in Figure  7c.

Energy of Activation
Ea (activation energy) estimated using the formula, where σac represents conductivity and kB signifies the Boltzmann constant. Figure 7d displays the relation of logarithm of ac conductivity with 1000/T which is found to be nearly linear in nature and Ea is evaluated using the following expression, Ea = −slope * 1000 * kB (22) The Ea values are 0.3733, 0.055 and 0.093 eV at the frequency of 30 KHz, 900 KHz and 5 MHz. Its lower value indicates that the LPPMA contains a lower number of defects, which is suitable for device fabrication [23].

Fluorescence Analysis
The luminescence spectrum of LPPMA was measured to emphasize its emission nature and its spectra are presented in Figure 8a, using a wavelength of excitation of 233 nm. The highest peak in emission occurred at 535 nm (2.31 eV), in the visible range spectrum. The peaks at 454 nm (2.73 eV) and 511 nm (2.42 eV) were attributed to defects existing in the material. The ac conductivity σ ac (Ω m) −1 was evaluated using the following relation (23): The variation of conductivity with log ω at diverse temperatures is depicted in Figure 7c.
Energy of Activation E a (activation energy) estimated using the formula, where σ ac represents conductivity and k B signifies the Boltzmann constant. Figure 7d displays the relation of logarithm of ac conductivity with 1000/T which is found to be nearly linear in nature and E a is evaluated using the following expression, E a = −slope * 1000 * k B The E a values are 0.3733, 0.055 and 0.093 eV at the frequency of 30 KHz, 900 KHz and 5 MHz. Its lower value indicates that the LPPMA contains a lower number of defects, which is suitable for device fabrication [23].

Fluorescence Analysis
The luminescence spectrum of LPPMA was measured to emphasize its emission nature and its spectra are presented in Figure 8a, using a wavelength of excitation of 233 nm. The highest peak in emission occurred at 535 nm (2.31 eV), in the visible range spectrum. The peaks at 454 nm (2.73 eV) and 511 nm (2.42 eV) were attributed to defects existing in the material.

NLO Characterization
The proficiency of SHG was established using Kurtz' and Perry's analysis [27,28] in comparison with KH 2 PO 4 (KDP). Here, LPPMA was illuminated using a Neodymium:YAG laser (1064 nm) with a specified pulse width (10 ns). The conversion efficiency in SHG of LPPMA was 0.38 times that of KH 2 PO 4 .

Z-Scan Measurements
The third-order acentric nonlinearities likely have a nonlinear refractive index (n 2 ) nonlinear absorption coefficient (β) and III-order optical susceptibility (χ (3) ), which were assessed using the Z-scan method [29]. β and n 0 values were measured by the closed and open aperture Z-scan method.
The difference in transmittance (peak and valley) (∆T P−V ) along with on-axis phase shift |∆Φ 0 | is, Here, S and r a, denote aperture transmittance and aperture radius. The third-order nonlinear refractive index is [21], The imaginary portion (χ (3) ) is calculated by β (nonlinear absorption), which is obtained using the following formula, Reχ (3) (esu) = 10 −4 (ε 0 C 2 n o 2 n 2 ) π Imχ (3) (esu) = 10 −2 (ε 0 C 2 n 0 λβ) 4π 2 cm 2 W (28) The closed aperture plot for LPPMA is specified in Figure 9a. The peak followed by a valley in the curve (normalized transmittance) is a sign of negative non-linearity and the self-defocusing effect [29,30] which makes it a suitable candidate in the optical sensor domain [31]. The curve in open aperture is presented in Figure 9b.The magnitude of β is premeditated, which shows a positive measure that indicates the absorption processes [21]. The materials that demonstrate two photon practices are broadly applied in light-based power limiting uses [32][33][34][35]. The calculated data of Z-scan visibly specify that LPPMA displays excellent third-order acentric characteristics, which are presented in Table 3. The value of χ (3) has a higher magnitude in comparison to other NLO materials in Table 4. Thus, the excellent NLO characteristics of LPPMA prove it to be suited to optical limiting applications.

Conclusions
LPPMA were efficiently produces using a slow evaporation process with water as the solvent at a constant temperature. The lattice parameters were estimated using singlecrystal XRD. The existence of functional groups in the material was established with an

Conclusions
LPPMA were efficiently produces using a slow evaporation process with water as the solvent at a constant temperature. The lattice parameters were estimated using singlecrystal XRD. The existence of functional groups in the material was established with an FTIR analysis. The UV-visible spectrum study revealed good transmittance in the area of the visible spectrum, which indicates a cut-off wavelength at 233 nm and energy-gap value of 5.53 eV from which various optical parameters were evaluated to analyze its suitability in optical processing. LPPMA belongs to the soft material group which was identified during the hardness analysis. The dielectric studies prove the presence of a flawless material. The second harmonic generation was observed through the Kurtz Perry procedure, which revealed SHG efficiency of 0.38 times that of KDP. The third order acentric parameters were estimated and attest to its reliable usage in future photonics applications.