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Structuring molecular hydrogen around ionic dopants: Li(+) cations in small pH(2) clusters.

小型パラ水素クラスターにおけるLi⁺カチオン周囲の分子状水素の構造形成

other not specified not assessed

Abstract

This computational study examined the structural organization of para-hydrogen (pH2) molecules around a Li+ cation acting as an ionic dopant. A composite interaction model was constructed by combining an anisotropic Li+-H2 potential energy surface with a spherical H2-H2 pair potential, treating pH2 as structureless bosonic solvent molecules. Geometry optimization and minimum energy configurations were determined using a genetic algorithm, with subsequent corrections to account for quantum effects. The results revealed distinct shell structures: the innermost shell is completed by six pH2 molecules arranged in an octahedral geometry, while outer shells are governed predominantly by dispersive interactions among pH2 molecules. In larger clusters, the solvent arrangement around the ionic center becomes progressively less ordered, reflecting the diminishing influence of the ionic charge at greater distances.

Mechanism

Anisotropic electrostatic interactions between Li+ and pH2 drive octahedral first-shell formation, while dispersive pH2-pH2 forces dominate outer shells, progressively reducing structural order at larger cluster sizes.

Bibliographic

Authors
Ponzi A, Marinetti F, Gianturco FA
Journal
Phys Chem Chem Phys
Year
2009 (2009-05-28)
PMID
19440614
DOI
10.1039/b820190k

Delivery context

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

Safety notes

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

See also:

Cite as: H2 Papers — PMID 19440614. https://h2-papers.org/en/papers/19440614
Source: PubMed PMID 19440614