High frequency dynamics in liquids and supercritical fluids: A comparative inelastic x-ray scattering study

被引:28
|
作者
Bencivenga, F. [1 ]
Cunsolo, A. [2 ]
Krisch, M. [3 ]
Monaco, G. [3 ]
Ruocco, G. [4 ,5 ]
Sette, F. [3 ]
机构
[1] Sincrotrone Trieste, I-34012 Trieste, Italy
[2] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[3] European Synchrotron Radiat Facil, F-38043 Grenoble, France
[4] Univ Roma La Sapienza, Dipartimento Fis, I-00185 Rome, Italy
[5] Univ Roma La Sapienza, CRS SOFT INFM CNR, I-00185 Rome, Italy
来源
JOURNAL OF CHEMICAL PHYSICS | 2009年 / 130卷 / 06期
关键词
acoustic wave propagation; ammonia; liquid structure; liquid-liquid transformations; neon; nitrogen; vibrational modes; water; X-ray scattering; SUPERCOOLED WATER; STRUCTURAL RELAXATION; DENSITY-FLUCTUATIONS; BRILLOUIN-SCATTERING; ENERGY RESOLUTION; GLASS; NITROGEN; NEON; SPECTROSCOPY; TERPHENYL;
D O I
10.1063/1.3073039
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
The microscopic dynamics of four prototype systems (water, ammonia, nitrogen, and neon) across the critical temperature has been investigated by means of high-resolution inelastic x-ray scattering. The experimental line shape has been described using a model based on the memory function formalism. Two main relaxations, the thermal and the structural one, were observed in all the investigated systems. We found that the microscopic mechanism driving the structural relaxation clearly changes, being mainly governed by intermolecular bond rearrangements below the critical temperature and by binary collisions above it. Moreover, we observed that the relative weight of the thermal relaxation systematically increases on approaching the critical temperature, thus allowing for the observation of a transition from an adiabatic to an isothermal regime of sound propagation. Finally, we found the presence of an additional instantaneous relaxation, likely related to the coupling between collective vibrational modes and intramolecular degrees of freedom.
引用
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页数:15
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