Hydrophobic Interactions and Dewetting between Plates with Hydrophobic and Hydrophilic Domains

被引:95
|
作者
Hua, Lan [1 ]
Zangi, Ronen [1 ]
Berne, B. J. [1 ]
机构
[1] Columbia Univ, Dept Chem, New York, NY 10027 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2009年 / 113卷 / 13期
基金
美国国家科学基金会;
关键词
SOLVENT-INDUCED FORCES; MOLECULAR SIMULATION; TEMPERATURE-DEPENDENCE; ANTI-COOPERATIVITY; SPATIAL DEPENDENCE; AQUEOUS UREA; LONG-RANGE; WATER; HYDRATION; COLLAPSE;
D O I
10.1021/jp8088758
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 study by molecular dynamics simulations the wetting/dewetting transition and the dependence of the free energy on the distance between plates that contain both hydrophobic and hydrophilic particles. We show that dewetting is very sensitive to the distribution of hydrophobic and hydrophilic domains. In particular, we find that plates characterized by a large domain of hydrophobic sites induce a dewetting transition and an attractive solvent-induced interaction. On the other hand, a homogeneous distribution of the hydrophobic and hydrophilic particles on the plates prevents the dewetting transition and produces a repulsive solvent-induced interaction. We also present results for a system resembling a "Janus interface" in which one plate consists of hydrophobic particles and the other consists of hydrophilic particles showing that the interplate gap remains wet until steric constraints at small separations eject the water molecules. Our results indicate that the Cassie equation, for the contact angle of a heterogeneous plate, can not be used to predict the critical distance of dewetting. These results indicate that hydrophobic interactions between nanoscale surfaces with strong large length-scale hydrophobicity can be highly cooperative and thus they argue against additivity of the hydrophobic interactions between different surface domains in these cases. These findings are pertinent to certain protein-protein interactions where additivity is commonly assumed.
引用
收藏
页码:5244 / 5253
页数:10
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