Next Article in Journal / Special Issue
Charge Exchange in Low-Energy H, D + C4+ Collisions with Full Account of Electron Translation
Previous Article in Journal / Special Issue
Studies of Electron Capture by Multiply Charged Ions from Molecules using Translational Energy Spectroscopy
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Rate Coefficient Determination in Charge Transfer Reactions

1
Laboratoire de Spectrométrie Ionique et Moléculaire, UMR 5579, CNRS et Université Lyon I, 43 Bd. du 11 Novembre 1918, 69622 Villeurbanne Cedex, France
2
Laboratoire de Chimie Théorique, Université de Paris Sud (Orsay), France and Département de Chimie, Université de Liège, Institut de Chimie B6, Sart-Tilman, B-4000, Liège 1, Belgium
3
Laboratoire de Chimie Physique Moléculaire, CP 160/09 Université Libre de Bruxelles, 50 Av. F. Roosevelt, B-1050 Bruxelles, Belgium
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2002, 3(3), 176-189; https://doi.org/10.3390/i3030176
Submission received: 18 December 2001 / Accepted: 17 January 2002 / Published: 28 March 2002
(This article belongs to the Special Issue Charge Transfer in Ionic and Molecular Systems)

Abstract

:
The development of experimental ion-trap techniques provides the opportunity to compare directly theoretical rate coefficients to experimental data in the low-temperature regime. In the present work, we consider the ion-atom collisional systems, N2+, O2+, Si3+ and Si4+ on a He target, in order to examine the present status of the agreement between theory and experiment.

I. Introduction

Charge transfer processes involving low-energy multiply charged ions in collision with atomic or molecular targets are determinant in laboratory and astrophysical plasmas. In such processes, an electron is generally captured in an excited state of the ion, followed by line emission. Line intensities provide important information on the electron temperature, density and spatial distributions in the emitting region of the plasma. In some cases, however, the electron may be captured directly in a ground state of the ion, whereupon ionization may occur rapidly via the inverse charge transfer process [1,2]. A precise understanding of charge transfer processes is thus essential for the determination of the ion abundances and ionization balance of the plasmas.
From a theoretical point of view, the description of very low-velocity processes requires a complete quantum mechanical treatment of the dynamics of both electrons and nuclei. The first approach extensively used is the resolution of the stationary close-coupling equations [3]. We have analyzed recently the efficiency of a time-dependent wave packet method [4,5,6] which provides a clear and physical insight into the dynamics of the processes and may be particularly interesting for polyatomic systems since it allows the possibility of developing a fully quantal mechanical treatment for some degrees of freedom, the other ones being treated classically. In this method, a wave packet initially located in the entrance channel is propagated on the coupled electronic potential energy curves ; the collision matrix elements are then extracted by Hankel transform of the time signal obtained from a wave packet stored in the asymptotic region. The main features of this approach are summarised in section II.
The development of modern facilities such as crossed- or merged-beam techniques [7,8], and more recently ion-trap experiments [9] lead to possible experimental investigations in the very low collision energy range. Experiments using laser-induced-plasma ion sources and ion storage [9] provide for the first time a direct determination of rate coefficients at low temperatures, of the order of 103 to 104 K. Since ions are produced by laser ablation from a solid target, no source gas is required ; this avoids the potential source of systematic error due to reactions between the ions and the source gas. The ions are then stored in a cylindrical radiofrequency ion trap and the mass selectivity of the ion trap allows for the storage of a specific ion group with no other concomitant ions present. Laser ablation produces the ions in a variety of excited states, but they rapidly cascade to their ground state and low-lying metastable states through allowed transitions and collisional deexcitations with plasma electrons.
Such experimental techniques provide the possibility to compare directly theoretically determined rate coefficients at low-temperature to experimental data. The O2+/O3+ [9,10,11], N2+ [12,13], and Si3+/Si4+ [14,15] ions colliding with gaseous targets of He, H2, N2, and CO and, more recently, He+ [16] and H3+ [17] ions colliding with molecular targets of N2, CO and CH4 have been investigated experimentally. From the theoretical point of view, ion/atom collisions involving O2+, N2+, Si3+ and Si4+ on He have been extensively studied. The comparison with the experimental results appears to be quite different from one ion to another, showing good agreement in some cases, but very large discrepancies in others. The purpose of this review is to investigate the collisional systems, O2+ + He [3,18,19,20], N2+ + He [20,21], Si3+ + He [1,2,23,24,28] and Si4+ + He [5,6,23,24,25,26,27,28,29] in order to exhibit the difficulties encountered both in the theoretical and experimental approaches. The systems O2+ /He, N2+ /He, Si3+ /He are treated by the close coupling formalism. The wave packet method is applied to the Si4+ /He case.

II. Wave packet dynamics

The convention = 1 is adopted throughout. The theoretical model used to solve the time-dependent Schrödinger equation
i [ R ψ ( r , R , t ) ] / t = H ^ [ R ψ ( r , R , t ) ] ,
where Ĥ is the total transformed Hamiltonian (Ĥ =RHR-1) which has been described in detail by Vaeck et al. [4]. In summary, the wave function corresponding to the entry channel i is given by the superposition :
ψ i K ( r , R , t ) = 1 / R α Λ χ α Λ K ( R , t ) φ α Λ ( r ; R ) Y Λ K ( θ , φ ) ,
where K is the total angular momentum with Λ its projection on the internuclear axis. The nuclear wave functions are the product of an angular part, YKΛ, and a radial part which contains the entire time dependence, χKαΛ. The electronic wavefunctions φαΛ can be expressed either in the adiabatic (φαΛ=aαΛ) or in the diabatic (φαΛ=dαΛ) representation. The unitary matrix F transforming the adiabatic representation in the diabatic one is obtained by solving the equation :
R F + P F = 0 ,
where the matrix P contains the radial coupling matrix elements.
The corresponding time-dependent functions, χKαΛ(R,t)=AKαΛ(R,t) or χKαΛ(R,t)=DKαΛ(R,t) are solutions of the coupled equations :
i χ α Λ K ( R , t ) t = β Λ ' H α Λ , β Λ ' K χ β Λ ' K ( R , t ) .
When Coriolis coupling is neglected, the HK matrix is written, respectively
H K = T R I + E a + K ( K + 1 ) 2 Λ 2 2 μ R 2 I 1 2 μ [ Q + 2 P R ]
in the adiabatic representation or
H K = T R I + H d + K ( K + 1 ) 2 Λ 2 2 μ R 2 I
in the diabatic one. TR is the nuclear kinetic operator, TR=-1/2μ·∂2/∂R2. Ea is the diagonal matrix of the adiabatic energies, and Hd is the matrix of the electronic Hamiltonian in the diabatic basis set. The radial coupling P matrix elements, Pαβ=<aα∂/∂R∕aβ> have been calculated using a numerical differentiation method. The double derivative matrix elements Qαβ have been computed from the following relationship [30,31] :
Q α β = a α | 2 R 2 | a β = R a α | R | a β + k a α | R | a k a k | R | a β ,
The radial wavefunction for the initial state (α=i) at time t=0 is given by a Gaussian wave packet centered initially in R0 with a width σR at half maximum, and a mean relative kinetic energy ε0 corresponding to the wave number k0=(2με0)½ :
χα=i(R,t=0) = 1/(πσR2)¼ exp(-ik0R) exp(-½[R-R0/σR]2).
In any method based on wave packets, the extraction of energy resolved functions requires the computation of the amplitude of the initial wave packet on the stationary states
η α ( E )   =   Ψ αE + | χ α 0
χ α 0 is located in the asymptotic region so that only its limit is used
Ψ α E K ( R , r )   R   μ 2 π k α [ h K ( k α R ) ϕ α K  -  β S β α K ( E ) h K + ( k α R ) ϕ α K   ]
where h ± ( k α R ) are the Hankel-Riccatti outgoing/incomtextng wave functions corresponding to the long range potential K ( K + 1 ) / 2 μ R 2 and k α = 2 μ ( E E α ) . When χ α 0 does not contain any outgoing momentum, one has
η α ( E )   =   μ 2 π k α   0 h K ( k α R )  g α ( R )  dR
where gα(R) is a Gaussian function in the entrance channel.
Different strategies are possible in order to obtain the collision matrix elements. They have been compared in [6]
(i) Thespectralprojectionmethod. The S β α K ( E ) elements are extracted from the functions
ψ α E + ( R , r )   =   i 2 π G + ( E )   χ α 0 ( R , r )
where G + ( E )   =   ( E - H ^ + i 0 ) - 1 is the resolvant. The general relation is
S β α K ( E )   =   i 2 π   χ β |   G + ( E )   | χ α 0 η β * (E)  η α ( E )
When the probe nuclear wave packet in the asymptotical region χ β is chosen to be the delta function g β ( R ) = δ ( R R ) , one gets
S β α K ( E )   = - 2 π k β μ  h K - ( k β R )   Φ β α ( R , E ) / η α ( E )
where
Φ β α ( R , E ) = ϕ β K | ψ α E + r , Ω
The resolvant in (1) can be comptuted by time independent or time dependent methods. In the first case, G + ( E ) is expanded on the Chebyshev polynomtextals by using the Mandelshtam and Taylor modified recursion [32]
G + ( E )   χ α 0 = n = 0 a n ( E )  T n ( H ^ scale )   χ α 0
where H ^ scale is the scaled Hamtextltonian mapping the spectrum in the range [-1, 1] [33]. In the second case, G + ( E ) is expressed as the Fourier transform of the evolution operator
G + ( E )   χ α 0   =   - i 0 exp ( - i H ^ t ) χ α 0 exp ( iEt ) dt
The wave packets are then propagated on the coupled electronic potentials using the split-operator technique [34] in the diabatic representation and the more cpu time consumtextng Chebyshev scheme in the adiabatic basis set. The difference comes from the structure of the HK matrix in the two representations. The Chebyshev method only requires the computation of the ĤΨ and is thus able to account for any kind of differential operators.
(ii) The flux method. Within this approach, the square modulus of the S β α K ( E ) elements are related to the average value of the flux operator evaluated in the asymptotical region at R = Rc
Ψ α E + |   P ^ β K F ^ P ^ β K   | Ψ α E + =   1 2 π |   S β α K ( E ) | 2
where   P ^ β K is the projector on the electronic state and
F ^   =   - i 2 μ   ( R  δ ( R - R c ) + δ ( R - R c ) R )
By adding a complex absorbing potential H ^   H ^ - i W ^ in the asymptotical range, Jäckle and Meyer have derived the following expression [35]
| S β α K ( E )   | 2    =    2 π   η α ( E ) 2 ℜe  0  f β ( τ ) exp ( - iEτ )
where
f β ( τ )   =   0 χ α ( τ + t ) |   P ^ β K W ^ P ^ β K   | χ α ( t )    dt
After extracting the S β α K ( E ) elements, the final expression of the state selective charge exchange cross section is given by :
σ β , i ( E ) = π ( 2 L i + 1 ) k i 2 ( E ) K Λ Λ ' ( 2 K + 1 ) × | i ( S β Λ ' , i Λ K ( E ) δ β , i δ Λ , Λ ' ) | 2 ,
where (2Li+1) is the degeneracy of the initial state.
The rate coefficients, k(T) are then calculated by averaging the cross sections over a Maxwellian velocity distribution at temperature T.
k ( T ) = ( 2 k B T ) 3 / 2 ( 1 π μ ) 1 / 2 0 E E σ ( E ) exp ( E / k B T ) d E

III. The N2+/He system

The experimental study of the electron-capture from the ground state of helium atoms by N2+(2p) 2Po ions has received recently a lot of attention [36,37,38]. Four reaction channels and two entry channels are involved in the transfer mechanism :
Ijms 03 00176 i001
The potential energy curves have been determined by Lafyatis et al. [22] using state-averaged multiconfiguration self-consistent-field (MCSCF) calculations with Slater-type function basis sets.
Fig. 1a,b. Adiabatic potential energy curves for respectively the 2Σ+ + and 2Π states of N2+ + He [22].1 : 2Π state dissociating in N+(2p2) 3P + He+(1s) ; 2 : 2Σ and 2Π states dissociating in N+(2p2) 1D + He+(1s) ; 3 : entry channel N2+(2p) 2Po + He ; 4 : 2Σ state dissociating in N+(2p2) 1S + He+(1s).
Fig. 1a,b. Adiabatic potential energy curves for respectively the 2Σ+ + and 2Π states of N2+ + He [22].1 : 2Π state dissociating in N+(2p2) 3P + He+(1s) ; 2 : 2Σ and 2Π states dissociating in N+(2p2) 1D + He+(1s) ; 3 : entry channel N2+(2p) 2Po + He ; 4 : 2Σ state dissociating in N+(2p2) 1S + He+(1s).
Ijms 03 00176 g001
The results displayed in Fig. 1a,b show clearly a very sharp avoided crossing in the 2Σ and 2Π symmetry between the entry channel and the N+(2p2) 1D + He+(1s) level around R=9 a.u. A smoother one is also observed in the 2Π manifold with the N+(2p2) 3P + He+(1s) channel around R=6 a.u. The 2Σ+, N+(2p2) 1S + He+(1s) level crosses the entry channel at very large interatomic distances, around 30 a.u. Therefore its influence on the charge transfer process is negligible.
The charge transfer cross sections have been evaluated using the close-coupling formalism [21] and the rate coefficient may be compared to the recent multichannel Landau-Zener calculations of Wang et al. [20] and to the recent ion-trap experimental result of Fang and Kwong [12]. These results are presented in Fig. 2. They show clearly that the two exit channels N+(2p2) 1D and N+(2p2) 3P provide important contributions to the total rate coefficient, N+(2p2) 3P being the dominant channel at higher temperatures. The experimental temperature of the ions Ti determined from the mean energy of the ions in the trap may be quite different in the presence of neutral atoms of helium produced at room temperature. Fang and Kwong proposed to introduce an equivalent temperature Tequiv obtained from the mean relative velocity between the ion at temperature Ti and the neutral atom at temperature Tn [12]. Both temperatures have been displayed on Fig. 2, and differ by about a power of ten, 2900K for Tequiv and 2.1 104K for Ti. The close-coupling result [21] appears to be in good agreement with the ion-trap experimental data of Fang and Kwong [12] when the Tequiv is considered. On the other hand, the multichannel Landau-Zener approach [20] underestimates by more than an order of magnitude the close-coupling calculation.
Fig. 2. Rate coefficients as a function of temperature for N2+ + He. Comparison of close-coupling calculations [21] (full curves) and multichannel Landau-Zener approach [20] (dotted-broken curve) with ion-trap experiment at Ti and Tequiv [12].
Fig. 2. Rate coefficients as a function of temperature for N2+ + He. Comparison of close-coupling calculations [21] (full curves) and multichannel Landau-Zener approach [20] (dotted-broken curve) with ion-trap experiment at Ti and Tequiv [12].
Ijms 03 00176 g002

IV. The O2+/He system

The capture of one electron by the ground state O2+ 3P ion from He also involves four reaction channels, corresponding to the 3Π and 3Σ- molecular symmetry of the entry channels:
Ijms 03 00176 i002
where the labels B, C, D correspond to the peaks in the translational energy spectrum of McLaughlin et al. [39]. The potential energy curves determined by ab-initio calculations using the CIPSI algorithm with Gaussian basis sets [40] are displayed in Fig. 3a,b. Similar results have been obtained by Kimura et al. [18] with MRD-CI (multireference single- and double-excitation configuration interaction) calculations with a large basis set. The potential energy curves show a sharp avoided crossing around 5.5 a.u. between the 3Π, O+(2p3) 2Po + He+(1s) level and the 3Π entry channel, and a smoother one at about 4.5 a.u. between the 3Π, O+(2p3) 2Po + He+(1s) and O+(2p3) 2Do + He+(1s) exit channels. An avoided crossing between the 3Σ-, O+(2p3) 2Do + He+(1s) level and the 3Σ- entry channel is also observed at about 4.5 a.u.
Fig. 3a,b. Adiabatic potential energy curves for respectively the 3Σ- and 3Π states of O2+ + He [40].(labels defined in the text)
Fig. 3a,b. Adiabatic potential energy curves for respectively the 3Σ- and 3Π states of O2+ + He [40].(labels defined in the text)
Ijms 03 00176 g003
A quantum mechanical close-coupling calculation [3] of the cross sections and the rate coefficients may be compared to a similar calculation of Kimura et al. [18] and to the experimental data of Kwong et al. [9,10]. These data can also be compared to the previous calculation of Butler et al. [19] and the recent multichannel Landau-Zener calculations of Wang et al [20]. The results are displayed in Fig. 4. As far as the close-coupling calculations are concerned, the results of Gargaud et al [3] are in quite good agreement with the extensive calculation of Kimura et al. [18] for the O2+3P ground state ion. Nevertheless, these results appear to provide rate coefficients largely overestimated with regard to the previous calculation of Butler et al. [19] and the multichannel Landau-Zener approach [20], similarly to the case of the N2+ + He collisional system. The close coupling results appear to be two orders of magnitude higher than the ion-trap experiment of Fang and Kwong [10], considering either Ti (2.0 104K) or Tequiv (4200 K). These results obtained from very accurate molecular calculations are about a factor two larger than the previous experimental value performed using drift tube techniques [41] which lies one order of magnitude above the results of Fang and Kwong. However, the rate coefficients calculated by Kimura et al. [18] for the O2+(2p2) 1D excited entry channel appear to be of the same order of magnitude than the ion-trap result. A fraction of metastable ions in the beam could be a possible source of discrepancy between theoretical approaches and experimental data. Effectively, in the ion-trap experiment, ions produced by laser ablation can be in a variety of excited electronic states immediately after their production, but as measurements are performed 0.4 s after the ions have been produced and trapped, all the stored ions are expected to be in their ground-state [10] and the presence of excited states seems unlikely.
Fig. 4. Rate coefficients as a function of temperature for O2+ + He. Comparison of close-coupling calculations, Gargaud et al. [3] (full curve) ; Kimura et al. [18] (broken curves) ; Butler et al. [19] (dotted curve) and multichannel Landau-Zener approach, Wang et al. [20] (dotted-broken curve) with ion trap experiment at Ti and Tequiv [9,10] and drift tube technique experiments (J) [41].
Fig. 4. Rate coefficients as a function of temperature for O2+ + He. Comparison of close-coupling calculations, Gargaud et al. [3] (full curve) ; Kimura et al. [18] (broken curves) ; Butler et al. [19] (dotted curve) and multichannel Landau-Zener approach, Wang et al. [20] (dotted-broken curve) with ion trap experiment at Ti and Tequiv [9,10] and drift tube technique experiments (J) [41].
Ijms 03 00176 g004

V. The Si3+/He system

The charge transfer recombinations of Si3+ ions with atomic hydrogen and helium are critical processes in determining the ionization balance of astrophysical plasmas as they lead to the formation of the ground-state ion and therefore can induce rapid ionization via the inverse process. The theoretical treatment of the Si3++He collisional process involves the complete network of exit channels interacting with both the ground-state Si3+(3s) and the excited Si3+(3p) + He entry channels. The total manifold of following channels must be considered :
Ijms 03 00176 i003
The potential energy curves have been calculated [1] by means of ab-initio configuration interaction methods based on the CIPSI algorithm with Gaussian basis sets constructed from McLean and Chandler [42]. A non-local pseudo-potential [43] has been used to represent the core electrons of the Si atom. The results are displayed in Fig. 5a,b. From a dynamical point of view, the ground-state entry channel 2Σ+, Si3+(3s) 2S + He(1s2) 1S leads to a simple electron capture process with a pronounced avoided crossing with the 2Σ+, Si2+(3s2) 1S + He+(1s) 2S around R=6 a.u.. It interacts also with the 2Σ+, Si2+(3s3p) 3Po + He+(1s) 2S level around R=3.2 a.u. The excited Si3+(3p) entry channel shows important avoided crossings around R=7 a.u. and 5 a.u. with respectively the Si2+(3s3p) 1Po and Si2+(3s3p) 3Po channels, both in the 2Σ+ and 2Π symmetry. These potential energy curves are in satisfactory agreement with the spin-coupled valence bond calculations of Clarke and Cooper [44].
Fig. 5. Adiabatic potential energy curves for respectively the 2Σ+ + and 2Π states of Si3+ + He [1].
Fig. 5. Adiabatic potential energy curves for respectively the 2Σ+ + and 2Π states of Si3+ + He [1].
Ijms 03 00176 g005
From these molecular data, a quantum mechanical collisional treatment taking account simultaneously of all the levels involved in the process has been performed [1] and the rate coefficients are displayed in Fig. 6. They may be compared to the quantum mechanical close-coupling treatment of Stancil et al. [2] and to the previous Landau-Zener calculations of Butler and Dalgarno [24], as well as the experimental data of Fang and Kwong [14]. For the capture process by the ground-state Si3+(3s) ion, a global agreement is observed between the Landau Zener calculations and the ab-initio treatments, showing a similar shape with a decrease of the rate coefficients with decreasing temperature. These results appear to be 35% to 47% lower than the ion-trap experimental data at Tequiv = 3900 K. Nevertheless, as already pointed out in the previous section, the determination of this equivalent temperature based on the assumption of a thermodynamic equilibrium between the ion at temperature Ti = 2.9 104 K and a neutral atom at room temperature may be questioned. As Ti is about two orders of magnitude larger than the room temperature of the helium gas, it should be rather close to the real temperature of the process. Both Ti and Tequiv temperatures have been drawn on the graph and show clearly that an uncertainty on the temperature of the reactants in the trap can modify the conclusion on the agreement between theory and experiment. Furthermore, it is important to ask if the measurement of Fang and Kwong obtained using an ion trap with cylindrical symmetry can be compared with a calculation based on the use of a Maxwell-Boltzmann distribution. On the other hand, the calculated rate coefficients [1] from the excited Si3+(3p) entry channel appear to be of the same order of magnitude than experimental data points for both Ti and Tequiv. This could suggest, as already pointed out for the O2+ ions, that the presence of a fraction of excited ions in the trap could be a possible source of discrepancy between theoretical approaches and experimental results. Nevertheless, the life-time of Si3+ ions being about 1.3ns, one would expect all of the 3p states to have radiatively decayed to the ground state as ion-trap measurements are performed 0.4s after the production of the ions. Measurements at different temperatures could however be particularly interesting, since the rate coefficients for the ground state Si3+(3s) ion exhibit a very different temperature dependence than the Si3+(3p) entry channel which is almost constant with temperature.
Fig. 6. Rate coefficients as a function of temperature for Si3+ + He. Comparison of close coupling calcula-tions, Honvault et al. [1] (full curves) ; Stancil et al. [2] (broken curves) and Landau-Zener approach, Butler et al. [24] (dotted curve) with ion trap experiment at Ti and Tequiv [14].
Fig. 6. Rate coefficients as a function of temperature for Si3+ + He. Comparison of close coupling calcula-tions, Honvault et al. [1] (full curves) ; Stancil et al. [2] (broken curves) and Landau-Zener approach, Butler et al. [24] (dotted curve) with ion trap experiment at Ti and Tequiv [14].
Ijms 03 00176 g006

VI. The Si4+/He system

From a theoretical point of view, the most extensively studied system with regard to the ion-trap experiment of Kwong et al. [15], is undoubtedly the Si4+ + He collisional system [5,6,23,25,26,27,28]. This system presents a relatively simple molecular structure with three singlet electron capture channels :
Ijms 03 00176 i004
The potential energy curves and couplings have been determined with the code MOLPRO [45] using a state-average complete active space self-consistent field (CASSCF) calculation followed by a multireference configuration interaction calculation (MRCI) with Gaussian basis set augmented with extra f orbitals [46]. A pseudopotential [47] has been used to describe the core orbitals of the Si atom. The corresponding potential energy curves are displayed in Fig. 7. A sharp avoided crossing is clearly observed between the entry channel and the Si3+(3p) 2Po + He+(1s) 2S level at about R=7 a.u. and a smoother one around R=4.5 a.u. between the two Si3+ channels. These results are in good agreement with previous configuration interaction calculations using the CIPSI algorithm [25] and other ab-initio calculations, using the spin-coupled valence bond method (SCVB) [26,44] or the configuration interaction MRD-CI method [27].
Fig. 7. Adiabatic potential energy curves for the 1Σ+ (full lines) and 2Π (dotted line) of Si4++He.
Fig. 7. Adiabatic potential energy curves for the 1Σ+ (full lines) and 2Π (dotted line) of Si4++He.
Ijms 03 00176 g007
Wave packet propagation approaches [5,6] as summarized in part II has been applied in order to determine the cross sections and rate coefficients at low temperatures. The results are presented in Fig. 8 and compared to the time-independent close-coupling approaches [26,27,29]. The agreement between the theoretical calculations is good and presents a similar temperature dependence. The introduction of the Hankel-Ricatti functions [6] to replace the approximate plane wave functions [5] in extracting the S-matrix in the time-dependent approach improves the accuracy of the calculation. However, all the calculations appear to be in complete disagreement, by a two order of magnitude difference, with the experimental point of Fang and Kwong [15]. This is all the more surprising because recent cross section measurements at ion energies of 100-500 eV [28] appear to be in good agreement with theoretical calculations. Of course the problem of temperature determination still exists as shown by the Ti and Tequiv temperatures presented on the graph, but this could never explain such a discrepancy. As shown for the O2+ + He system, the existence of an excited state could eventually explain a two order difference in rate coefficients, but the first excited state, Si3+(2p53s), is definitely too high in energy to be a reasonable candidate. In conclusion, it appears clearly that all the theoretical approaches converge to the same result but cannot explain the experimental data.
Fig. 8. Rate coefficients as a function of temperature for Si4+ + He. Comparison of ion trap experiment at Ti and Tequiv [15] with calculations using time-dependent (full line : Hankel-Ricatti functions [6] ; dotted line : plane wave functions [5]) or time-independent methods (S : Stancil et al. [26] ; Opradolce et al. [29]).
Fig. 8. Rate coefficients as a function of temperature for Si4+ + He. Comparison of ion trap experiment at Ti and Tequiv [15] with calculations using time-dependent (full line : Hankel-Ricatti functions [6] ; dotted line : plane wave functions [5]) or time-independent methods (S : Stancil et al. [26] ; Opradolce et al. [29]).
Ijms 03 00176 g008

VII. Conclusions

This work presents a comparative study between recent theoretical approaches and ion-trap experiments which provide for the first time a direct determination of rate coefficients at low temperature. For N2+ + He, a good agreement is found between ion-trap experiments and ab-initio calculations, but for three of the collisional systems considered here (O2+, Si3+ and Si4+ on He target), the theoretical values show significant differences with ion trap experimental data, from 40% for Si3+, to one or two orders of magnitude for O2+ and Si4+. The difficulty to determine precisely the temperature of the reactants in the trap appears to be a fundamental difficulty in such experiments, associated with the assumption of a nearly thermal ion velocity distribution. A more appropriate description of the energy distribution in the ion trap must be considered. The eventual presence of excited states or impurity in the trap could also be suggested with respect to the production of the ions, but it seems unlikely considering the long waiting time before collecting data. However, despite all these possible sources of imprecision, the very large discrepancies between the experimental data of Fang and Kwong and all the theoretical predictions in the case of the Si4+ + He collisional system is still totally unaccounted for.

References

  1. Honvault, P.; Bacchus-Montabonel, M.C.; Gargaud, M.; McCarroll, R. Chem. Phys. 1998, 238, 401.
  2. Stancil, P.C.; Clarke, N.J.; Zygelman, B.; Cooper, D.L. J. Phys. B : At. Mol. Opt. Phys. 1999, 32, 1523. [CrossRef]
  3. Gargaud, M.; Bacchus-Montabonel, M.C.; McCarroll, R. J. Chem. Phys. 1993, 99, 4495.
  4. Vaeck, N.; Desouter-Lecomte, M.; Liévin, J. J. Phys. B : At. Mol. Opt. Phys. 1999, 32, 409. [CrossRef]
  5. Vaeck, N.; Bacchus-Montabonel, M.C.; Baloïtcha, E.; Desouter-Lecomte, M. Phys. Rev. 2001, A63, 042704.
  6. Baloïtcha, E.; Desouter-Lecomte, M.; Bacchus-Montabonel, M.C.; Vaeck, N. J. Chem. Phys. 2001, 114, 8741.
  7. Havener, C.C.; Huq, M.S.; Krause, H.F.; Schultz, P.A.; Phaneuf, R.A. Phys. Rev. 1989, A39, 1725.
  8. Olamba, K.; Szücs, S.; Chenu, J.P.; El Arbi, N.; Brouillard, F. J. Phys. B : At. Mol. Opt. Phys. 1996, 29, 2837. [CrossRef]
  9. Kwong, V.H.S.; Fang, Z. Phys. Rev. Lett. 1993, 71, 4127. [CrossRef]
  10. Fang, Z.; Kwong, V.H.S. Phys. Rev. 1995, A51, 1321.
  11. Gao, H.; Fang, Z.; Kwong, V.H.S. Phys. Rev. 2001, A63, 032704.
  12. Fang, Z.; Kwong, V.H.S. Astrophys. J. 1997, 474, 529.
  13. Fang, Z.; Kwong, V.H.S. Phys. Rev. 1997, A55, 440.
  14. Fang, Z.; Kwong, V.H.S. Astrophys. J. 1997, 483, 527.
  15. Fang, Z.; Kwong, V.H.S. Phys. Rev. 1999, A59, 342.
  16. Fang, Z.; Chen, D.; Kwong, V.H.S. Phys. Rev. 2000, A62, 042709.
  17. Kwong, V.H.S.; Fang, Z. Astrophys. J. 2001, 536, 954.
  18. Kimura, M.; Gu, J.P.; Hirsch, G.; Buenker, R.J. Phys. Rev. 1996, A53, 4164.
  19. Butler, S.E.; Heil, T.G.; Dalgarno, A. J. Chem. Phys. 1984, 80, 4986.
  20. Wang, J.G.; Stancil, P.C.; Kingdon, J.B.; Rakovic’, M.; Schultz, D.R.; Dalgarno, A. 2002; (to be submitted).
  21. Sun, Y.; Sadeghpour, H.R.; Kirby, K.; Dalgarno, A. Inter. Rev. Phys. Chem. 1996, 15, 53.
  22. Lafyatis, G.P.; Kirby, K.; Dalgarno, A. Phys. Rev. 1993, A48, 321.
  23. Bacchus-Montabonel, M.C. Theor. Chem. Acc. 2000, 104, 296. [CrossRef]
  24. Butler, S.E.; Dalgarno, A. Astrophys. J. 1980, 241, 838.
  25. Bacchus-Montabonel, M.C.; Ceyzeriat, P. Phys. Rev. 1998, A58, 1162.
  26. Stancil, P.C.; Zygelman, B.; Clarke, N.J.; Cooper, D.L. Phys. Rev. 1997, A55, 1064.
  27. Suzuki, R.; Watanabe, A.; Sato, H.; GU, J.G.; Hirsch, G.; Buenker, R.J.; Kimura, M.; Stancil, P.C. Phys. Rev. 2001, A63, 042717.
  28. Tawara, H.; Okuno, K.; Fehrenbach, C.W.; Verzani, C.; Stockli, M.P.; Depaola, B.D.; Richard, P.; Stancil, P.C. Phys. Rev. 2001, A63, 062701.
  29. Opradolce, L.; McCarroll, R.; Valiron, P. Astron. Astrophys. 1982, 106, 197.
  30. Parlant, G.; Yarkony, D.R. Int. J. Quantum Chem. 1992, Symp.26, 737. [CrossRef]
  31. Lengsfield, B.H., III; Yarkony, D.R. Adv. Chem. Phys. 1991, 82, 1.
  32. Mandelshtam, V.A.; Taylor, H.S. J. Phys. Chem 1995, 102, 7390, Mandelshtam, V.A. J. Phys. Chem, 2001, 105, 2764. [CrossRef]
  33. Tal-Ezer, H.; Kosloff, R. J. Chem. Phys. 1984, 81, 3967.
  34. Feit, M.D.; Fleck, J.A.; Steiger, A. J. Comput. Phys. 1982, 47, 412. [CrossRef]
  35. Jäckle, A.; Meyer, H.D. J. Chem. Phys. 1996, 105, 6778.
  36. Burns, D.; Thompson, W.R.; Greenwood, J.B.; McCullough, R.W.; Geddes, J.; Gilbody, H.B. J. Phys. B : At. Mol. Opt. Phys. 1997, 30, 4559. [CrossRef]
  37. Lee, A.R.; Wilkins, A.C.R.; Enos, C.S.; Brenton, A.G. Phys. Rev. 1993, A48, 2934.
  38. Sadilek, M.; Vancura, J.; Farnik, J.; Herman, Z. Int. J. Mass Spectrom. Ion Processes 1990, 100, 197. [CrossRef]
  39. McLaughlin, T.K.; Wilson, S.M.; McCullough, R.W.; Gilbody, H.B. J. Phys. B : At. Mol. Opt. Phys. 1990, 23, 737.
  40. Bacchus-Montabonel, M.C.; Courbin, C.; McCarroll, R. J. Phys. B : At. Mol. Opt. Phys. 1991, 24, 4409. [CrossRef]
  41. Johnsen, R.; Biondi, M.A. J. Chem. Phys. 1981, 74, 305.
  42. McLean, A.D.; Chandler, G.S. J. Chem. Phys. 1980, 72, 5639.
  43. Pelissier, M.; Komiha, N.; Daudey, J.P. J. Comput. Chem. 1988, 9, 298. [CrossRef]
  44. Clarke, N.J.; Cooper, D.L. J. Chem. Soc. Faraday Trans. 1998, 94, 3295. [CrossRef]
  45. MOLPRO (version 98.1) is a package of ab-initio programs written by Werner, H.J. and Knowles, P. with contributions from Almlöf, J.; Amos, R.D.; Deegan, M.J.O.; Elbert, S.T.; Hampel, C.; Meyer, W.; Peterson, K.; Pitzer, R.; Stone, A.J.; Taylor, P.R.; Lindh, R.
  46. Dunning, T.H. J. Chem. Phys. 1989, 90, 1007.
  47. Hay, P.J.; Wadt, W.R. J. Chem. Phys. 1985, 82, 270.

Share and Cite

MDPI and ACS Style

Bacchus-Montabonel, M.-C.; Baloïtcha, E.; Desouter-Lecomte, M.; Vaeck, N. Rate Coefficient Determination in Charge Transfer Reactions. Int. J. Mol. Sci. 2002, 3, 176-189. https://doi.org/10.3390/i3030176

AMA Style

Bacchus-Montabonel M-C, Baloïtcha E, Desouter-Lecomte M, Vaeck N. Rate Coefficient Determination in Charge Transfer Reactions. International Journal of Molecular Sciences. 2002; 3(3):176-189. https://doi.org/10.3390/i3030176

Chicago/Turabian Style

Bacchus-Montabonel, Marie-Christine, Ezinvi Baloïtcha, Michèle Desouter-Lecomte, and Nathalie Vaeck. 2002. "Rate Coefficient Determination in Charge Transfer Reactions" International Journal of Molecular Sciences 3, no. 3: 176-189. https://doi.org/10.3390/i3030176

Article Metrics

Back to TopTop