Configurational entropy and diffusivity of supercooled water

被引:319
作者
Scala, A
Starr, FW
La Nave, E
Sciortino, F
Stanley, HE
机构
[1] Boston Univ, Ctr Polymer Studies, Boston, MA 02215 USA
[2] Boston Univ, Ctr Computat Sci, Boston, MA 02215 USA
[3] Boston Univ, Dept Phys, Boston, MA 02215 USA
[4] Univ Roma La Sapienza, Dipartimento Fis, I-00185 Rome, Italy
[5] Univ Roma La Sapienza, Ist Nazl Fis Mat, I-00185 Rome, Italy
关键词
D O I
10.1038/35018034
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
As a liquid approaches the glass transition, its properties are dominated by local potential minima(1,2) in its energy landscape. The liquid experiences localized vibrations in the basins of attraction surrounding the minima, and rearranges via relatively infrequent inter-basin jumps(3). As a result, the liquid dynamics at low temperature are related to the system's exploration of its own configuration space. The 'thermodynamic approach' to the glass transition considers the reduction in configuration space(4-8) explored as the system cools, and predicts that the configurational entropy(5,9,10) (a measure of the number of local potential energy minima sampled by the liquid) is related to the diffusion constant. Here we report a stringent test of the thermodynamic approach for liquid water (a convenient system to study because of an anomalous pressure dependence in the diffusion constant). We calculate the configurational entropy at points spanning a large region of the temperature-density plane, using a model(11) that reproduces the dynamical anomalies of liquid water. We find that the thermodynamic approach can be used to understand the characteristic dynamic anomalies, and that the diffusive dynamics are governed by the configurational entropy. Our results indicate that the thermodynamic approach might be extended to predict the dynamical behaviour of supercooled liquids in general.
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页码:166 / 169
页数:4
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