期刊
JOURNAL OF CHEMICAL PHYSICS
卷 135, 期 7, 页码 -出版社
AMER INST PHYSICS
DOI: 10.1063/1.3624571
关键词
electron correlations; hydrogen bonds; hydrogen neutral molecules; molecular configurations; molecular electronic states; Rydberg states
资金
- NRF [WCU:R32-2008-000-10180-0]
- Zhejiang National Science Foundation (NSF) [Y6100101]
- National Research Foundation of Korea [R32-2011-000-10180-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
We demonstrate and advocate the use of observable quantities derived from the two-electron reduced density matrix - pair densities, conditional densities, and exchange-correlation holes - as signatures of the type of electron correlation in a chemical bond. The prototype cases of the lowest (1)Sigma(+)(u) and (1)Sigma(+)(g) states of H-2, which exhibit large variation in types of bonding, ranging from strongly ionic to covalent, are discussed. Both the excited (1)Sigma(+)(g) and (1)Sigma(+)(u) states have been interpreted as essentially consisting of (natural) orbital configurations with an inner electron in a contracted 1s sigma(g) orbital and an outer electron in a diffuse (united atom type, Rydberg) orbital. We show that nevertheless totally different correlation behavior is encountered in various states when comparing them at a common internuclear distance. Also when following one state along the internuclear distance coordinate, strong variation in correlation behavior is observed, as expected. Switches between ionic to covalent character of a state occur till very large distances (40 bohrs for states approaching the 1s3l asymptotic limit, and 282 bohrs for states approaching the 1s4l limit). (C) 2011 American Institute of Physics. [doi:10.1063/1.3624571]
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