Nature of Molecular Rotation in Supercooled Glycerol under Nanoconfinement

被引:11
作者
Levchenko, Andrey A. [2 ,3 ]
Jain, Pragati [1 ]
Trofymluk, Olga [2 ,3 ]
Yu, Ping [1 ]
Navrotsky, Alexandra [1 ,2 ,3 ]
Sen, Sabyasachi [1 ]
机构
[1] Univ Calif Davis, Dept Chem Engn & Mat Sci, Davis, CA 95616 USA
[2] Univ Calif Davis, Peter A Rock Thermochem Lab, Davis, CA 95616 USA
[3] Univ Calif Davis, NEAT ORU, Davis, CA 95616 USA
基金
美国国家科学基金会;
关键词
GLASS-TRANSITION; LENGTH SCALE; DYNAMICS; RELAXATION; POLYMERS; CONFINEMENT; LIQUIDS; NMR;
D O I
10.1021/jp911821p
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
The dynamics of glass-forming liquids under nanoconfinement is key to understanding a variety of phenomena in nature and modern technology. We report a C-13 NMR spectroscopic Study that directly demonstrates that a-relaxation in bulk glycerol involves an isotropic rotational jump of the constituent molecules. The activation energy of this motion is similar to 78 kJ mol(-1) in the bulk, which abruptly changes to a low value of similar to 27.5 kJ mol(-1), characteristic of beta-processes, upon confinement of glycerol into similar to 2 nm pores in mesoporous Silica. This observation implies that the molecular dynamics associated with Structural relaxation near glass transition are inherently different in supercooled glycerol in the bulk and under extreme nanoconfinement.
引用
收藏
页码:3070 / 3074
页数:5
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