偶极子
化学物理
润湿
位阻效应
化学极性
凝聚态物理
分子
固体表面
物理
分子动力学
表面电荷
相变
电荷(物理)
化学
极地的
材料科学
电荷密度
伊辛模型
单层
分子物理学
表面张力
承压水
计算化学
物理化学
立体化学
有机化学
复合材料
量子力学
天文
作者
Chunlei Wang,Bo Zhou,Yusong Tu,Manyi Duan,Peng Xiu,Jingye Li,Haiping Fang
摘要
The wetting behavior of water on the solid surfaces is fundamental to various physical, chemical and biological processes. Conventionally, the surface with charges or charge dipoles is hydrophilic, whereas the non-polar surface is hydrophobic though some exceptions were recently reported. Using molecular dynamics simulations, we show that there is a critical length of the charge dipoles on the solid surface. The solid surface still exhibited hydrophobic behavior when the dipole length was less than the critical value, indicating that the water molecules on the solid surface seemed not "feel" attractive interactions from the charge dipoles on the solid surface. Those unexpected observations result from the collective interactions between the water molecules and charge dipoles on the solid surface, where the steric exclusion effect between water molecules greatly reduces the water-dipole interactions. Remarkably, the steric exclusion effect is also important for surfaces with charge dipole lengths greater than this critical length.
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