Orientational Time Correlation Functions for Vibrational Sum-Frequency Generation. 1. Acetonitrile

被引:11
|
作者
Liu, Shule [1 ]
Fourkas, John T. [1 ,2 ,3 ,4 ]
机构
[1] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[2] Univ Maryland, Inst Phys Sci & Technol, College Pk, MD 20742 USA
[3] Univ Maryland, Maryland NanoCtr, College Pk, MD 20742 USA
[4] Univ Maryland, Ctr Nanophys & Adv Mat, College Pk, MD 20742 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2013年 / 117卷 / 29期
基金
美国国家科学基金会;
关键词
2ND-HARMONIC GENERATION; RAMAN-SPECTRA; SPECTROSCOPY; SURFACE; LIQUID; INTERFACES; SIMULATIONS; MOLECULES; DYNAMICS; WATER;
D O I
10.1021/jp306296s
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
Orientational time correlation functions (TCFs) are derived for vibrational sum-frequency generation (VSFG) spectroscopy of the symmetric and asymmetric stretches of high-symmetry oscillators such as freely rotating methyl groups, acetylenic C-H groups, and cyanide groups. Molecular dynamics simulations are used to calculate these TCFs and the corresponding elements of the second-order response for acetonitrile at the liquid/vapor and liquid/silica interfaces. We find that the influence of reorientation depends significantly on both the functional group in question and the polarization conditions used. Additionally, under some circumstances, reorientation can cause the VSFG response function to grow with time, partially counteracting the effects of other dephasing mechanisms.
引用
收藏
页码:5853 / 5864
页数:12
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