Journal
CHEMICAL PHYSICS
Volume 440, Issue -, Pages 64-68Publisher
ELSEVIER
DOI: 10.1016/j.chemphys.2014.06.007
Keywords
Double core-hole spectroscopy; K-shell; Hartree-Fock; Density functional theory
Funding
- Cooperative Research Program of the Network Joint Research Center for Materials and Devices of MEXT
- Asahi Glass Foundation
- JSPS
- MEXT
- IMRAM research program
- Grants-in-Aid for Scientific Research [25108003] Funding Source: KAKEN
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The double ionization energies of two-site double core-hole states were calculated for several systems: C-60, dicyano molecules, and disilyl compounds. For C-60, the interatomic relaxation energy decreases from positive to negative values with increasing core-hole distances. For dicyano molecules, the interatomic relaxation energy increases monotonically from a negative value toward zero with an increase in the carbon chain length. For disilyl compounds, the energy first decreases from positive to negative and then approaches zero with an increase in the carbon chain length. The results based on density functional theory agree with those based on Hartree-Fock theory for all systems, illustrating similar tendencies and confirming the validity of using density functional theory for calculations of double core-hole states. The origin of the different behaviors in interatomic relaxation energies is also discussed. (C) 2014 Elsevier B.V. All rights reserved.
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