Mutual information reveals multiple structural relaxation mechanisms in a model glass former

被引:51
作者
Dunleavy, Andrew J. [1 ,2 ,3 ]
Wiesner, Karoline [3 ,4 ]
Yamamoto, Ryoichi [5 ]
Royall, C. Patrick [1 ,2 ,6 ]
机构
[1] HH Wills Phys Lab, Bristol BS8 1TL, Avon, England
[2] Univ Bristol, Sch Chem, Bristol BS8 1TL, Avon, England
[3] Bristol Ctr Complex Sci, Bristol BS8 1TW, Avon, England
[4] Univ Bristol, Sch Math, Bristol BS8 1TW, Avon, England
[5] Kyoto Univ, Dept Chem Engn, Kyoto 6158510, Japan
[6] Ctr Nanosci & Quantum Informat, Bristol BS8 1FD, Avon, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
GROWING LENGTH; SUPERCOOLED LIQUIDS; DYNAMICS; HETEROGENEITY; SCALES;
D O I
10.1038/ncomms7089
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Among the key challenges to our understanding of solidification in the glass transition is that it is accompanied by little apparent change in structure. Recently, geometric motifs have been identified in glassy liquids, but a causal link between these motifs and solidification remains elusive. One 'smoking gun' for such a link would be identical scaling of structural and dynamic lengthscales on approaching the glass transition, but this is highly controversial. Here we introduce an information theoretic approach to determine correlations in displacement for particle relaxation encoded in the initial configuration of a glass-forming liquid. We uncover two populations of particles, one inclined to relax quickly, the other slowly. Each population is correlated with local density and geometric motifs. Our analysis further reveals a dynamic lengthscale similar to that associated with structural properties, which may resolve the discrepancy between structural and dynamic lengthscales.
引用
收藏
页数:8
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