Role of Presolvation and Anharmonicity in Aqueous Phase Hydrated Proton Solvation and Transport
Author(s) -
Rajib Biswas,
YingLung Steve Tse,
Andrei Tokmakoff,
Gregory A. Voth
Publication year - 2015
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/acs.jpcb.5b09466
Subject(s) - anharmonicity , hydronium , solvation , valence bond theory , proton , chemistry , chemical physics , molecular dynamics , hydrogen bond , ab initio , molecule , computational chemistry , proton transport , thermodynamics , physics , molecular orbital , organic chemistry , quantum mechanics
Results from condensed phase ab initio molecular dynamics (AIMD) simulations suggest a proton transfer reaction is facilitated by "presolvation" in which the hydronium is transiently solvated by four water molecules, similar to the typical solvation structure of water, by accepting a weak hydrogen bond from the fourth water molecule. A new version 3.2 multistate empirical valence bond (MS-EVB 3.2) model for the hydrated excess proton incorporating this presolvation behavior is therefore developed. The classical MS-EVB simulations show similar structural properties as those of the previous model but with significantly improved diffusive behavior. The inclusion of nuclear quantum effects in the MS-EVB also provides an even better description of the proton diffusion rate. To quantify the influence of anharmonicity, a second model (aMS-EVB 3.2) is developed using the anharmonic aSPC/Fw water model, which provides similar structural properties but improved spectroscopic responses at high frequencies.
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