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
  • [41] Properties of coupled-cluster equations originating in excitation sub-algebras
    Kowalski, Karol
    JOURNAL OF CHEMICAL PHYSICS, 2018, 148 (09):
  • [42] Investigation of an asymmetric triple-excitation correction for coupled-cluster energies
    Crawford, TD
    Stanton, JF
    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 1998, 70 (4-5) : 601 - 611
  • [43] Triplet excitation energies in full configuration interaction and coupled-cluster theory
    Larsen, H
    Hald, K
    Olsen, J
    Jorgensen, P
    JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (07): : 3015 - 3020
  • [44] Complex ground-state and excitation energies in coupled-cluster theory
    Thomas, Simon
    Hampe, Florian
    Stopkowicz, Stella
    Gauss, Juergen
    MOLECULAR PHYSICS, 2021, 119 (21-22)
  • [45] COMPARISON OF COUPLED-CLUSTER AND BRUECKNER COUPLED-CLUSTER CALCULATIONS OF MOLECULAR-PROPERTIES
    KOBAYASHI, R
    KOCH, H
    JORGENSEN, P
    LEE, TJ
    CHEMICAL PHYSICS LETTERS, 1993, 211 (01) : 94 - 100
  • [46] ALTERNATIVE COUPLED-CLUSTER ANSATZE .2. THE UNITARY COUPLED-CLUSTER METHOD
    BARTLETT, RJ
    KUCHARSKI, SA
    NOGA, J
    CHEMICAL PHYSICS LETTERS, 1989, 155 (01) : 133 - 140
  • [47] A COUPLED-CLUSTER STUDY OF THE PHOTOELECTRON-SPECTRA OF C4(-)
    WATTS, JD
    CERNUSAK, I
    BARTLETT, RJ
    CHEMICAL PHYSICS LETTERS, 1991, 178 (2-3) : 259 - 265
  • [48] ECONOMICAL TRIPLE EXCITATION EQUATION-OF-MOTION COUPLED-CLUSTER METHODS FOR EXCITATION-ENERGIES
    WATTS, JD
    BARTLETT, RJ
    CHEMICAL PHYSICS LETTERS, 1995, 233 (1-2) : 81 - 87
  • [49] Coupled-cluster and density functional theory studies of the electronic 0-0 transitions of the DNA bases
    Ovchinnikov, Vasily A.
    Sundholm, Dage
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2014, 16 (15) : 6931 - 6941
  • [50] Coupled-cluster theory for large molecules: The natural linear scaled coupled-cluster method
    Bartlett, Rodney J.
    Flocke, Norbert
    Hughes, Thomas
    RECENT PROGRESS IN COMPUTATIONAL SCIENCES AND ENGINEERING, VOLS 7A AND 7B, 2006, 7A-B : 992 - 994