Interpretation of IR and Raman Line Shapes for H2O and D2O Ice Ih

被引:92
|
作者
Shi, L.
Gruenbaum, S. M.
Skinner, J. L. [1 ]
机构
[1] Univ Wisconsin, Inst Theoret Chem, Madison, WI 53706 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2012年 / 116卷 / 47期
基金
美国国家科学基金会;
关键词
OH-STRETCHING REGION; AMORPHOUS SOLID WATER; PARTICLE MESH EWALD; LIQUID WATER; KINDS; VIBRATIONAL-SPECTRUM; INFRARED-SPECTRA; HEXAGONAL ICE; H-BONDS; SPECTROSCOPY;
D O I
10.1021/jp3059239
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
Noticeable differences between the Vibrational (IR and Raman) spectra. of neat H2O and D2O ice Ih are observed experimentally. Here, we employ our theoretical mixed quantum/classical approach to investigate these differences. We find reasonable agreement between calculated and experimental line shapes at both high and low temperatures. From understanding the structure Of ice Ih:and its vibrational exciton Hamiltonian, we provide assignments Of the IR and Raman spectral features for both H2O and D2O ice Ih. We find that in H2O ice these are due to strong and weak: intermolecular coupling, not to intramolecular coupling. The differences between H2O and D2O ice spectra are attributed to the significantly stronger intra- molecular coupling in D2O ice. Our conclusion for both H2O and D2O ice is that the molecular symmetric and antisymmetric normal modes do not form a Useful basis for understanding OH or OD stretch spectroscopy.
引用
收藏
页码:13821 / 13830
页数:10
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