Correlation between macroscopic and microscopic relaxation dynamics of water: Evidence for two liquid forms

被引:5
|
作者
Vinh, Nguyen Q. [1 ,2 ,3 ]
Doan, Luan C. [1 ,2 ,3 ]
Hoang, Ngoc L. H. [1 ,2 ]
Cui, Jiarong R. R. [1 ,2 ]
Sindle, Ben [1 ,2 ]
机构
[1] Virginia Tech, Dept Phys, Blacksburg, VA 24061 USA
[2] Virginia Tech, Ctr Soft Matter & Biol Phys, Blacksburg, VA 24061 USA
[3] Virginia Tech, Dept Mech Engn, Blacksburg, VA 24061 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2023年 / 158卷 / 20期
基金
美国国家科学基金会;
关键词
STATIC DIELECTRIC-CONSTANT; GLASS-TRANSITION; ATMOSPHERIC-PRESSURE; OPTICAL-CONSTANTS; DEBYE RELAXATION; PROTEIN DYNAMICS; SPECTROSCOPY; TEMPERATURE; FREQUENCY; THZ;
D O I
10.1063/5.0142818
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
Water is vital for life, and without it, biomolecules and cells cannot maintain their structures and functions. The remarkable properties of water originate from its ability to form hydrogen-bonding networks and dynamics, which the connectivity constantly alters because of the orientation rotation of individual water molecules. Experimental investigation of the dynamics of water, however, has proven challenging due to the strong absorption of water at terahertz frequencies. In response, by employing a high-precision terahertz spectrometer, we have measured and characterized the terahertz dielectric response of water from supercooled liquid to near the boiling point to explore the motions. The response reveals dynamic relaxation processes corresponding to the collective orientation, single-molecule rotation, and structural rearrangements resulting from breaking and reforming hydrogen bonds in water. We have observed the direct relationship between the macroscopic and microscopic relaxation dynamics of water, and the results have provided evidence of two liquid forms in water with different transition temperatures and thermal activation energies. The results reported here thus provide an unprecedented opportunity to directly test microscopic computational models of water dynamics.
引用
收藏
页数:9
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