Investigation of the temperature dependence of dielectric relaxation in liquid water by THz reflection spectroscopy and molecular dynamics simulation

被引:488
作者
Ronne, C
Thrane, L
Astrand, PO
Wallqvist, A
Mikkelsen, KV
Keiding, SR
机构
[1] UNIV COPENHAGEN, HC ORSTED INST, CHEM LAB 3, DK-2100 COPENHAGEN O, DENMARK
[2] NCI, FREDERICK CANC RES & DEV CTR, SCI APPLICAT INT CORP, FREDERICK, MD 21702 USA
关键词
D O I
10.1063/1.474242
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
We report measurements of the real and imaginary part of the dielectric constant of liquid water in the far-infrared region from 0.1 to 2.0 THz in a temperature range from 271.1 to 366.7 K. The data have been obtained with the use of THz time domain reflection spectroscopy, utilizing ultrashort electromagnetic pulses generated from a photoconductive antenna driven by femtosecond laser pulses. A Debye model with an additional relaxation time is used to fit the frequency dependence of the complex dielectric constants, We obtain a fast (fs) and a Debye (ps) relaxation time for the macroscopic polarization. The corresponding time correlation functions have been calculated with molecular dynamics simulations and are compared with experimental relaxation times. The temperature dependence of the Debye relaxation time is analyzed using three models: Transition state theory, a Debye-Stoke-Einstein relation between the viscosity and the Debye time, and a model stating that its temperature dependence can be extrapolated from a singularity of liquid water at 228 K. We find an excellent agreement between experiment and the two latter models. The simulations, however, present results with too large statistical error for establishing a relation for the temperature dependence. (C) 1997 American Institute of Physics.
引用
收藏
页码:5319 / 5331
页数:13
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