Towards a microscopic description of the free-energy landscape of water

被引:16
|
作者
Prada-Gracia, Diego [1 ]
Shevchuk, Roman [1 ]
Hamm, Peter [2 ]
Rao, Francesco [1 ]
机构
[1] Freiburg Inst Adv Studies, Sch Soft Matter Res, Freiburg, Germany
[2] Univ Zurich, Inst Phys Chem, CH-8057 Zurich, Switzerland
来源
JOURNAL OF CHEMICAL PHYSICS | 2012年 / 137卷 / 14期
基金
瑞士国家科学基金会;
关键词
compressibility; free energy; hydrogen bonds; liquid structure; molecular dynamics method; solvation; water; LIQUID WATER; POTENTIAL FUNCTIONS; SUPERCOOLED WATER; DYNAMICS; TRANSITION; PATHWAYS; FUNNELS; SURFACES; CLUSTERS; NETWORK;
D O I
10.1063/1.4755746
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
Free-energy landscape theory is often used to describe complex molecular systems. Here, a microscopic description of water structure and dynamics based on configuration-space-networks and molecular dynamics simulations of the TIP4P/2005 model is applied to investigate the free-energy landscape of water. The latter is built on top of a large set of water microstates describing the kinetic stability of local hydrogen-bond arrangements up to the second solvation shell. In temperature space, the landscape displays three different regimes. At around ambient conditions, the free-energy surface is characterized by many short-lived basins of attraction which are structurally well-defined (inhomogeneous regime). At lower temperatures instead, the liquid rapidly becomes homogeneous. In this regime, the free energy is funneled-like, with fully coordinated water arrangements at the bottom of the funnel. Finally, a third regime develops below the temperature of maximal compressibility (Widom line) where the funnel becomes steeper with few interconversions between microstates other than the fully coordinated ones. Our results present a way to manage the complexity of water structure and dynamics, connecting microscopic properties to its ensemble behavior. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4755746]
引用
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页数:7
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