Hydrogen Bonding Slows Down Surface Diffusion of Molecular Glasses

被引:53
作者
Chen, Yinshan [1 ]
Zhang, Wei [1 ]
Yu, Lian [1 ,2 ]
机构
[1] Univ Wisconsin, Sch Pharm, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53705 USA
基金
美国国家科学基金会;
关键词
SELF-DIFFUSION; PHYSICAL-PROPERTIES; SOLID-SURFACE; O-TERPHENYL; VISCOSITY; TRANSITION; CRYSTALLIZATION; INDOMETHACIN; DYNAMICS; LIQUID;
D O I
10.1021/acs.jpcb.6b05658
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
Surface-grating decay has been measured for three organic glasses with, extensive hydrogen bonding: sorbitol, maltitol, and maltose. For 1000 nm wavelength gratings, the decay occurs by viscous flow in the entire range of temperature studied, covering the viscosity range 10(5)-10(11) Pa s, whereas under the same conditions, the decay mechanism transitions from viscous, flow to surface diffusion for organic glasses of similar molecular sizes but with no or limited hydrogen bonding. These results indicate that extensive hydrogen bonding slows down surface diffusion in organic glasses. This effect arises because molecules can preserve hydrogen bonding even near the surface so that the, loss of nearest neighbors does not translate into a proportional decrease of the kinetic barrier for diffusion. This explanation is consistent with a strong correlation between liquid fragility and the surface enhancement of diffusion, both reporting resistance of a liquid to dynamic excitation. Slow surface diffusion is,expected to hinder any processes that rely on surface transport, for example, surface crystal growth and formation of stable glasses by vapor deposition.
引用
收藏
页码:8007 / 8015
页数:9
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