Two-dimensional infrared-Raman spectroscopy as a probe of water's tetrahedrality

被引:9
|
作者
Begusic, Tomislav [1 ]
Blake, Geoffrey A. [1 ,2 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[2] CALTECH, Div Geol & Planetary Sci, Pasadena, CA 91125 USA
基金
瑞士国家科学基金会; 美国国家科学基金会;
关键词
LIQUID WATER; TEMPERATURE-DEPENDENCE; VIBRATIONAL SPECTROSCOPY; COMBINATION BAND; ASSOCIATION BAND; FREQUENCY; DYNAMICS; SPECTRA; INTENSITY; LIBRATION;
D O I
10.1038/s41467-023-37667-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Direct spectroscopic probes of the impact of structure on dynamical processes in liquids remain scarce. Here, the authors use molecular dynamics simulations to show that the correlation between vibrational coupling and the local tetrahedral structure of liquid water can be studied via hybrid terahertz- and infrared-Raman spectroscopy. Two-dimensional spectroscopic techniques combining terahertz (THz), infrared (IR), and visible pulses offer a wealth of information about coupling among vibrational modes in molecular liquids, thus providing a promising probe of their local structure. However, the capabilities of these spectroscopies are still largely unexplored due to experimental limitations and inherently weak nonlinear signals. Here, through a combination of equilibrium-nonequilibrium molecular dynamics (MD) and a tailored spectrum decomposition scheme, we identify a relationship between the tetrahedral order of liquid water and its two-dimensional IR-IR-Raman (IIR) spectrum. The structure-spectrum relationship can explain the temperature dependence of the spectral features corresponding to the anharmonic coupling between low-frequency intermolecular and high-frequency intramolecular vibrational modes of water. In light of these results, we propose new experiments and discuss the implications for the study of tetrahedrality of liquid water.
引用
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页数:10
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