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• W2997409265 abstract "The Adam–Gibbs theory of glass formation posits that the growth in the activation barrier of fragile liquids on cooling emerges from a loss of configurational entropy and concomitant growth in “cooperatively rearranging regions” (CRRs). A body of literature over 2 decades has suggested that “string-like” cooperatively rearranging clusters observed in molecular simulations may be these CRRs—a scenario that would have profound implications for the understanding of the glass transition. The central element of this postulate is the report of an apparent zero-parameter relationship between the mass of string-like CRRs and the relaxation time. Here, we show, based on molecular dynamics simulations of multiple glass-forming liquids, that this finding is the result of an implicit adjustable parameter—a “replacement distance”. This parameter is equivalent to an adjustable exponent within a generalized Adam–Gibbs relation, such that it tunes the entire functional form of the relation. Moreover, we are unable to find any objective criterion, based on the radial distribution function or the cluster fractal dimension, for selecting this replacement distance across multiple systems. We conclude that the present data do not establish that string-like cooperative rearrangements, as presently defined, are predictive of segmental relaxation via an Adam–Gibbs-like physical model." @default.
• W2997409265 created "2020-01-10" @default.
• W2997409265 creator A5061564974 @default.
• W2997409265 creator A5090428395 @default.
• W2997409265 date "2019-12-30" @default.
• W2997409265 modified "2023-09-27" @default.
• W2997409265 title "Do String-like Cooperative Motions Predict Relaxation Times in Glass-Forming Liquids?" @default.
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• W2997409265 doi "https://doi.org/10.1021/acs.jpcb.9b09468" @default.
• W2997409265 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31886663" @default.
• W2997409265 hasPublicationYear "2019" @default.
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