Surface Strain Effects on the Water-Graphene Interfacial and Confinement Behavior

被引:22
作者
Chialvo, Ariel A. [1 ]
Vlcek, Lukas [1 ,2 ]
Cummings, Peter T. [3 ]
机构
[1] Oak Ridge Natl Lab, Chem Sci Div, Geochem & Interfacial Sci Grp, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Joint Inst Computat Sci, Oak Ridge, TN 37831 USA
[3] Vanderbilt Univ, Dept Chem & Biomol Engn, Nashville, TN 37235 USA
关键词
MOLECULAR-DYNAMICS SIMULATION; NEUTRON-SCATTERING; THERMAL-EXPANSION; MEAN FORCE; HYDROPHOBICITY; WETTABILITY; EVAPORATION; GRAPHITE; SHELLS; C-60;
D O I
10.1021/jp501776m
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 studied via molecular dynamics the link between the strain-driven hydration free-energy changes in the association process involving finite-size graphene surfaces, the resulting water graphene interfacial tension, and the combined effect of the surface strain and confinement on the thermodynamic response functions and the dynamics of confined water. We found that an in-plane biaxial tensile strain epsilon = 10% enhances significantly not only the water graphene hydrophobicity with respect to that of the unstrained counterpart but also the confinement effect on the thermodynamic response functions and slowing down of the dynamics of water over those of the corresponding bulk counterpart. The interfacial behavior of water in contact with strained-graphene plates resembles that observed for "pp" corrugated-plate configuration, as reported earlier [Chialvo et al. J. Phys. Chem. C 2013, 117, 23875], exibiting a significant enhancement of the fluid surface hydrophobicity and response functions relative to those of the unstrained surface. In contrast, the slowing down of the dynamics of the confined water does not show any differentiation with respect to the type of surface.
引用
收藏
页码:19701 / 19711
页数:11
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