拉曼光谱
分子内力
旋转-振动耦合
分子间力
分子振动
谱线
红外光谱学
化学
联轴节(管道)
分子物理学
红外线的
光谱学
分析化学(期刊)
二维红外光谱
热带
相干反斯托克斯拉曼光谱
拉曼散射
材料科学
分子
光学
物理
立体化学
有机化学
量子力学
天文
冶金
作者
Kazuki Inoue,Yair Litman,David M. Wilkins,Yuki Nagata,Masanari Okuno
标识
DOI:10.1021/acs.jpclett.3c00398
摘要
The impact of the vibrational coupling of the OH stretch mode on the spectra differs significantly between IR and Raman spectra of water. Unified understanding of the vibrational couplings is not yet achieved. By using a different class of vibrational spectroscopy, hyper-Raman (HR) spectroscopy, together with machine-learning-assisted HR spectra calculation, we examine the impact of the vibrational couplings of water through the comparison of isotopically diluted H2O and pure H2O. We found that the isotopic dilution reduces the HR bandwidths, but the impact of the vibrational coupling is smaller than in the IR and parallel-polarized Raman. Machine learning HR spectra indicate that the intermolecular coupling plays a major role in broadening the bandwidth, while the intramolecular coupling is negligibly small, which is consistent with the IR and Raman spectra. Our result clearly demonstrates a limited impact of the intramolecular vibration, independent of the selection rules of vibrational spectroscopies.
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