Coupled-cluster studies of the electronic excitation spectra of silanes

被引:15
|
作者
Lehtonen, Olli
Sundholm, Dage
机构
[1] Helsinki Univ Technol, Dept Engn Phys & Math, FIN-02015 Helsinki, Finland
[2] Univ Helsinki, Dept Chem, FIN-00014 Helsinki, Finland
来源
JOURNAL OF CHEMICAL PHYSICS | 2006年 / 125卷 / 14期
基金
芬兰科学院;
关键词
D O I
10.1063/1.2354496
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 electronic excitation spectra of unsubstituted linear silanes (n-SimH2m+2, m=1-6), cyclopentasilane (c-Si5H10), and neopentasilane (neo-Si5H12) have been studied at the coupled-cluster approximate singles and doubles (CC2) level using Dunning's quadruple-zeta basis sets augmented with diffuse functions (aug-cc-pVQZ). Comparisons with measured ultraviolet spectra for Si2H6 and n-Si3H8 show that CC2 calculations using these basis sets yield excitation energies in good agreement with experiment. The calculated excitation thresholds for Si2H6 and n-Si3H8 of 7.61 and 6.68 eV are only 0.05 eV larger than the gas-phase values of 7.56 and 6.63 eV, respectively. For n-Si4H10, n-Si5H12, and neo-Si5H12, the calculated excitation thresholds of 6.51, 6.14, and 6.87 eV for the lowest dipole-allowed transitions are about 0.4 eV larger than the corresponding liquid-phase data of 6.05, 5.77, and 6.53 eV; the discrepancy can mainly be attributed to solvent effects. The obtained excitation thresholds for n-Si6H14 is 5.85 eV, whereas no experimental data are available for its optical gap. Calculations using the Karlsruhe triple-zeta valence basis sets augmented with single and double sets of polarization functions show that very large basis sets augmented with diffuse functions are needed for obtaining accurate excitation energies. The optical gaps for silanes obtained using the triple-zeta polarization basis sets were found to be 0.4 and 0.2 eV larger than those obtained using Dunning's quadruple-zeta basis sets. Excitation thresholds calculated at density functional theory levels using generalized gradient approximation are 0.7-1.0 eV smaller than the experimental values and by employing hybrid functionals they are 0.3-0.4 eV below the experimental thresholds. By adding the present basis-set correction and environmental effects to the previously calculated CC2 value for the excitation threshold of the Si29H36 silicon nanocluster, the extrapolated absorption threshold is 4.0 eV as compared to the recently reported experimental value of 3.7 eV. (c) 2006 American Institute of Physics.
引用
收藏
页数:9
相关论文
共 50 条
  • [31] EOMXCC: A new coupled-cluster method for electronic excited states
    Piecuch, P
    Bartlett, RJ
    ADVANCES IN QUANTUM CHEMISTRY, VOL 34, 1999, 34 : 295 - 380
  • [32] The coupled-cluster description of electronic structure: perspectives for bioinorganic chemistry
    Harvey, Jeremy N.
    JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2011, 16 (06): : 831 - 839
  • [33] A MICROSCOPIC COUPLED-CLUSTER TREATMENT OF ELECTRONIC CORRELATIONS IN HUBBARD MODELS
    BISHOP, RF
    XIAN, Y
    ZENG, C
    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 1995, 55 (02) : 181 - 186
  • [34] COUPLED-CLUSTER APPROACH IN ELECTRONIC-STRUCTURE THEORY OF MOLECULES
    KVASNICKA, V
    LAURINC, V
    BISKUPIC, S
    PHYSICS REPORTS-REVIEW SECTION OF PHYSICS LETTERS, 1982, 90 (03): : 159 - 202
  • [35] The coupled-cluster revolution
    Bartlett, Rodney J.
    MOLECULAR PHYSICS, 2010, 108 (21-23) : 2905 - 2920
  • [36] COUPLED-CLUSTER APPROACH IN THE ELECTRONIC-STRUCTURE THEORY OF MOLECULES
    KVASNICKA, V
    LAURINC, V
    BISKUPIC, S
    HARING, M
    ADVANCES IN CHEMICAL PHYSICS, 1983, 52 : 181 - 261
  • [37] The coupled-cluster description of electronic structure: perspectives for bioinorganic chemistry
    Jeremy N. Harvey
    JBIC Journal of Biological Inorganic Chemistry, 2011, 16 : 831 - 839
  • [38] A Multireference Coupled-Cluster Study of Electronic Excitations in Furan and Pyrrole
    Li, Xiangzhu
    Paldus, Josef
    JOURNAL OF PHYSICAL CHEMISTRY A, 2010, 114 (33): : 8591 - 8600
  • [39] MULTIREFERENCE COUPLED-CLUSTER METHOD FOR ELECTRONIC-STRUCTURE OF MOLECULES
    OLIPHANT, N
    ADAMOWICZ, L
    INTERNATIONAL REVIEWS IN PHYSICAL CHEMISTRY, 1993, 12 (02) : 339 - 362
  • [40] THE COUPLED-CLUSTER METHOD
    BISHOP, RF
    KUMMEL, HG
    PHYSICS TODAY, 1987, 40 (03) : 52 - 60