The shapes of cooperatively rearranging regions in glass-forming liquids

被引:246
作者
Stevenson, JD [1 ]
Schmalian, J
Wolynes, PG
机构
[1] Univ Calif San Diego, Dept Phys, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[3] Iowa State Univ, Dept Phys & Astron, Ames, IA 50011 USA
[4] Iowa State Univ, Ames Lab, Ames, IA 50011 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/nphys261
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The cooperative rearrangement of groups of many molecules has long been thought to underlie the dramatic slowing of liquid dynamics on cooling towards the glassy state. For instance, there exists experimental evidence for cooperatively rearranging regions (CRRs) on the nanometre length scale near the glass transition. The random first-order transition (RFOT) theory of glasses predicts that, near the glass-transition temperature, these regions are compact, but computer simulations and experiments on colloids suggest CRRs are string-like. Here, we present a microscopic theory within the framework of RFOT, which unites the two situations. We show that the shapes of CRRs in glassy liquids should change from being compact at low temperatures to fractal or 'stringy' as the dynamical crossover temperature from activated to collisional transport is approached from below. This theory predicts a correlation of the ratio of the dynamical crossover temperature to the laboratory glass-transition temperature, and the heat-capacity discontinuity at the glass transition. The predicted correlation quantitatively agrees with experimental results for 21 materials.
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页码:268 / 274
页数:7
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