Anharmonic Coupling of Stretching Vibrations in Ice: A Periodic VSCF and VCI Description

被引:17
作者
Schireman, Raymond G. [1 ]
Maul, Jefferson [2 ]
Erba, Alessandro [2 ]
Ruggiero, Michael T. [1 ]
机构
[1] Univ Vermont, Dept Chem, Burlington, VT 05405 USA
[2] Univ Torino, Dipartimento Chim, I-10125 Turin, Italy
基金
美国国家科学基金会;
关键词
MOLECULAR-ORBITAL METHODS; AB-INITIO; TERAHERTZ SPECTROSCOPY; CRYSTALS; FREQUENCIES; SPECTRUM; IH;
D O I
10.1021/acs.jctc.2c00217
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The anharmonicity of O-H stretching vibrations of water ice is characterized by use of a periodic implementation of the vibrational self-consistent field (VSCF) and vibrational configuration interaction (VCI) methods, which take phonon-phonon couplings explicitly into account through numerical evaluation of high-order terms of the nuclear potential. The low-temperature, proton-ordered phase of water ice (namely, ice XI) is investigated. The net effect of a coupled anharmonic treatment of stretching modes is not just a rigid blue-shift of the respective harmonic spectral frequencies but rather a complex change of their relative spectral positions, which cannot be captured by simple scaling strategies based on harmonic calculations. The adopted techniques allow for a hierarchical treatment of anharmonic terms of the nuclear potential, which is key to an effective identification of leading factors. We show that the anharmonic independent-mode approximation.only describing the "intrinsic anharmonicity" of the O-H stretches.is unable to capture the correct physics, and that couplings among O-H stretches must be described. Inspection of harmonic normal coordinates allows identification of specific features of the O-H stretching motions which most likely enable strong mode-mode couplings. Finally, by coupling O-H stretches to all other possible modes of ice XI (THz collective vibrations, molecular librations, bendings), we identify specific types of motion which significantly affect O-H stretching states: in particular, molecular librations are found to affect the stretching states more than molecular bendings.
引用
收藏
页码:4428 / 4437
页数:10
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