Ab initio quantum dynamics with very weak van der Waals interactions: Structure and stability of small Li2(1Σg+)–(He)n clusters
Author(s) -
Enrico Bodo,
F. Sebastianelli,
F. A. Gianturco,
E. Yurtsever,
Mine Yurtsever
Publication year - 2004
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.1701834
Subject(s) - van der waals force , triatomic molecule , ab initio , chemistry , quantum , ab initio quantum chemistry methods , electronic structure , anisotropy , potential energy surface , molecular physics , atomic physics , chemical physics , physics , computational chemistry , quantum mechanics , molecule , organic chemistry
The potential energy surface (PES) for the interaction between Li2(1Sigmag+) and 4He has been computed using an accurate, post-Hartree-Fock quantum calculation for its ground electronic state. The orientational anisotropy of the forces and the interplay between repulsive and attractive effects within the PES are analyzed to extract information on the possible existence of bound states in the triatomic system. The structures of a few of the Li2(He)n small clusters are examined by comparing a classical approach with a full quantum one to generate bound configurations and to extract information on the possible spatial arrangements of the smaller clusters via à vis the location of the Li2 dopant. Some significant consequences on the Li2 behavior in larger clusters and droplets are drawn from the above findings.
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