Structural Relaxation in Nanometer Thin Layers of Glycerol

被引:35
作者
Capponi, S. [1 ]
Napolitano, S. [1 ]
Behrnd, N. R. [2 ]
Couderc, G. [2 ]
Hulliger, J. [2 ]
Wubbenhorst, M. [1 ]
机构
[1] Katholieke Univ Leuven, Dept Phys & Astron, B-3001 Leuven, Belgium
[2] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
关键词
GLASS-TRANSITION TEMPERATURE; SUPERCOOLED GLYCEROL; ULTRATHIN FILMS; BULK BEHAVIOR; T-G; DYNAMICS; SPECTROSCOPY; DEVIATIONS; REACTIVITY; MOBILITY;
D O I
10.1021/jp108151p
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 molecular dynamics in nanometer thin films of glycerol was investigated upon thickness reduction by combining organic molecular deposition with in situ broadband dielectric spectroscopy. Changes in the cooperative dynamics with respect to bulk glycerol were observed for films of thicknesses down to 1.6 nm (corresponding to roughly three molecular layers). Systematic investigation revealed no pure size effects addressable merely to geometrical constraints. However, an increase in the glass transition temperature by 3.5 K was observed for the thinnest film, indicating the presence of a layer with reduced mobility in close proximity to the substrate. The impact of both the upper and lower interfaces has been disentangled by measurements performed during slow desorption. Moreover, proof is given for the existence of a layer with enhanced mobility in the vicinity of the free surface enslaved to the dynamics of the rest of the film.
引用
收藏
页码:16696 / 16699
页数:4
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