Frequency-dependent hyperpolarizabilities of the Ne, Ar, and Kr atoms using the approximate coupled cluster triples model CC3 -: art. no. 094303

被引:12
作者
Host, S [1 ]
Jorgensen, P
Köhn, A
Pawlowski, F
Klopper, W
Hättig, C
机构
[1] Univ Aarhus, Dept Chem, DK-8000 Aarhus, Denmark
[2] Univ Oslo, Dept Chem, N-0315 Oslo, Norway
[3] Univ Karlsruhe TH, Inst Phys Chem, Lehrstuhl Theoret Chem, D-76128 Karlsruhe, Germany
[4] Forschungszentrum Karlsruhe, Inst Nanotechnol, D-76021 Karlsruhe, Germany
关键词
D O I
10.1063/1.2008211
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The frequency-dependent electric field-induced second harmonic generation (ESHG) second hyperpolarizabilities gamma of neon, argon, and krypton are calculated using the approximate coupled cluster triples model CC3. Systematic basis set investigations are carried out to establish basis set limits, and scalar relativistic effects are accounted for by direct perturbation theory. To estimate higher-order correlation effects, full configuration-interaction results are used to benchmark the accuracy of CC3. The best theoretical estimates obtained thereby for the static second hyperpolarizabilities gamma(0) are 107.4, 1159, and 2589 a.u. for neon, argon, and krypton, respectively. These values as well as the results for the dispersion curve of the parallel component gamma(parallel to) agree well with the latest experimental values from electric field-induced second harmonic generation. In addition, the dispersion of the perpendicular component gamma(perpendicular to) and the hyperpolarizability ratios gamma(parallel to)/gamma(perpendicular to) has been studied for the first time on a consistently correlated ab initio level. The analysis of the results indicates that, in particular for neon and krypton, the presently available experimental values are flawed. (C) 2005 American Institute of Physics.
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页数:10
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共 46 条
[1]   The accurate determination of molecular equilibrium structures [J].
Bak, KL ;
Gauss, J ;
Jorgensen, P ;
Olsen, J ;
Helgaker, T ;
Stanton, JF .
JOURNAL OF CHEMICAL PHYSICS, 2001, 114 (15) :6548-6556
[2]   Accuracy of atomization energies and reaction enthalpies in standard and extrapolated electronic wave function/basis set calculations [J].
Bak, KL ;
Jorgensen, P ;
Olsen, J ;
Helgaker, T ;
Klopper, W .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (21) :9229-9242
[3]   MEASUREMENT OF HYPERPOLARIZABILITY RATIO XYYYY(-2-OMEGA-0,OMEGA,OMEGA)-XYYXX(-2-OMEGA-0,OMEGA,OMEGA) FOR INERT-GASES [J].
BIGIO, IJ ;
WARD, JF .
PHYSICAL REVIEW A, 1974, 9 (01) :35-39
[4]   GENERAL DISPERSION FORMULAS FOR ATOMIC 3RD-ORDER NON-LINEAR OPTICAL-PROPERTIES [J].
BISHOP, DM .
CHEMICAL PHYSICS LETTERS, 1988, 153 (05) :441-445
[5]   IMPROVED DYNAMIC HYPERPOLARIZABILITIES AND FIELD-GRADIENT POLARIZABILITIES FOR HELIUM [J].
BISHOP, DM ;
PIPIN, J .
JOURNAL OF CHEMICAL PHYSICS, 1989, 91 (06) :3549-3552
[6]  
Cencek W, 2001, PHYS REV LETT, V86, P5675, DOI 10.1103/PhysRevLett86.5675
[7]   THE 2ND-ORDER APPROXIMATE COUPLED-CLUSTER SINGLES AND DOUBLES MODEL CC2 [J].
CHRISTIANSEN, O ;
KOCH, H ;
JORGENSEN, P .
CHEMICAL PHYSICS LETTERS, 1995, 243 (5-6) :409-418
[8]  
Christiansen O, 1998, INT J QUANTUM CHEM, V68, P1, DOI 10.1002/(SICI)1097-461X(1998)68:1<1::AID-QUA1>3.0.CO
[9]  
2-Z
[10]   RESPONSE FUNCTIONS IN THE CC3 ITERATIVE TRIPLE EXCITATION MODEL [J].
CHRISTIANSEN, O ;
KOCH, H ;
JORGENSEN, P .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (17) :7429-7441