Parmar Anshul D S, Sastry Srikanth
Jawaharlal Nehru Centre for Advanced Scientific Research , Bengaluru 560 064, India.
TIFR Centre for Interdisciplinary Sciences , Hyderabad 500 075, India.
J Phys Chem B. 2015 Aug 27;119(34):11243-52. doi: 10.1021/acs.jpcb.5b03122. Epub 2015 Jul 15.
An understanding of the origin of fragility, which the rapidity of change of viscosity and related dynamical quantities, has been sought by a variety of approaches over the years. Within the framework of the Adam-Gibbs relation, fragility is in principle related to both the temperature variation of configurational entropy and the high temperature activation energy. Many theoretical analyses have been focused on the variation of configuration entropy, although the importance of the high temperature activation energy in determining the fragility of a glass former has also been emphasized. We explore the latter aspect by considering a model liquid whose high temperature activation energy is modified by hand, through the introduction of a tunable barrier to bond breaking. We show that changes in such a barrier are able to modify the fragility measured from the temperature dependence of dynamical quantities, while a thermodynamic measure of fragility obtained from the configurational entropy remains unchanged. We discuss the implications of our results to our understanding of fragility, and outline open questions that merit further investigation.
多年来,人们通过各种方法来探寻对脆性起源的理解,脆性与粘度及相关动力学量的变化速度有关。在亚当 - 吉布斯关系的框架内,脆性原则上与构型熵的温度变化以及高温活化能都有关系。许多理论分析都集中在构型熵的变化上,尽管高温活化能在决定玻璃形成体脆性方面的重要性也得到了强调。我们通过考虑一种模型液体来探索后一个方面,该模型液体的高温活化能通过引入一个可调的键断裂势垒来手动修改。我们表明,这种势垒的变化能够改变从动力学量的温度依赖性测量得到的脆性,而从构型熵获得的脆性的热力学度量保持不变。我们讨论了我们的结果对我们理解脆性的影响,并概述了值得进一步研究的开放性问题。