LIQUIDS AT INTERFACES - WHAT CAN A THEORIST CONTRIBUTE

被引:59
作者
EVANS, R
PARRY, AO
机构
[1] H.H. Wills Phys. Lab., Bristol Univ.
关键词
D O I
10.1088/0953-8984/2/S/003
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
This lecture reviews some recent theoretical and computer simulation studies of simple (atomic) fluids adsorbed at structureless substrates. Emphasis is placed on phase transitions, especially the various types of wetting transition. Critically is associated with capillary-wave-like fluctuations in a continuously growing wetting film. This is of a subtle nature, which is best understood in terms of the pairwise correlation function of the fluid. Other surface phase transitions, such as prewetting and layering, occur out of bulk coexistence. Theory suggests that for sufficiently attractive substrates a sequence of first-order transitions, corresponding to the growth of new adsorbed liquid layers, should occur as the pressure of the bulk gas increases towards saturation at temperatures not too far above the bulk triple point. The extent to which such behaviour is found in adsorption experiments is discussed. We also argue that a simple fluid confined between two parallel hard-walls can exhibit surprisingly rich phase equilibria.
引用
收藏
页码:SA15 / SA32
页数:18
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