Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.
RIKEN Center for Integrative Medical Sciences, Yokohama 230-0045, Japan.
J Phys Chem B. 2021 Feb 18;125(6):1632-1639. doi: 10.1021/acs.jpcb.0c10154. Epub 2021 Jan 4.
This study investigated the broadband terahertz and low-frequency Raman spectroscopy of liquid water (HO, DO, and HO) over 2 decades of frequency to address long-standing challenges regarding the interpretation of the intermolecular stretching mode at around 5 THz. We experimentally demonstrated that the intermolecular stretching mode of liquid water obtained via terahertz spectroscopy is significantly redshifted and broadened compared with that via Raman. This result was rationalized by the enhanced dynamical collectivity probed by terahertz spectroscopy, although both have a common origin in the kinetic motion. Their temperature and isotope dependences emphasize the significance of oscillation mass in determining the intermolecular stretching lineshape, while quantum effects cannot be overlooked in both terahertz and low-frequency Raman spectra.
本研究通过宽频太赫兹和低频拉曼光谱技术,对液态水(HO、DO 和 HO)进行了长达 20 年的频率探测,旨在解决长期以来对 5THz 附近分子伸缩模式解释的挑战。我们通过实验证明,与拉曼光谱相比,通过太赫兹光谱获得的液态水的分子伸缩模式明显红移和展宽。尽管两者都源于动力学运动,但太赫兹光谱探测到的增强的动力学集体性可以解释这一结果。它们的温度和同位素依赖性强调了振动质量在确定分子伸缩线形状方面的重要性,而在太赫兹和低频拉曼光谱中都不能忽视量子效应。