@article { ISI:000350657700011,
	title = {Role of structure and entropy in determining differences in dynamics for glass formers with different interaction potentials},
	journal = {Physical Review Letters},
	volume = {113},
	number = {22},
	year = {2014},
	month = {NOV},
	pages = {225701},
	publisher = {AMER PHYSICAL SOC},
	address = {ONE PHYSICS ELLIPSE, COLLEGE PK, MD 20740-3844 USA},
	abstract = {<p>We present a study of two model liquids with different interaction potentials, exhibiting similar structure but significantly different dynamics at low temperatures. By evaluating the configurational entropy, we show that the differences in the dynamics of these systems can be understood in terms of their thermodynamic differences. Analyzing their structure, we demonstrate that differences in pair correlation functions between the two systems, through their contribution to the entropy, dominate the differences in their dynamics, and indeed overestimate the differences. Including the contribution of higher order structural correlations to the entropy leads to smaller estimates for the relaxation times, as well as smaller differences between the two studied systems.</p>},
	issn = {0031-9007},
	doi = {10.1103/PhysRevLett.113.225701},
	author = {Banerjee, Atreyee and Sengupta, Shiladitya and Sastry, Srikanth and Bhattacharyya, Sarika Maitra}
}
@article {44109,
	title = { Role of the pair correlation function in the dynamical transition predicted by mode coupling theory},
	journal = {Physical Review Letters},
	volume = {119},
	year = {2017},
	month = {DEC},
	type = {Article},
	abstract = {In a recent study, we have found that for a large number of systems the configurational entropy at the pair level S-c2, which is primarily determined by the pair correlation function, vanishes at the dynamical transition temperature T-c. Thus, it appears that the information of the transition temperature is embedded in the structure of the liquid. In order to investigate this, we describe the dynamics of the system at the mean field level and, using the concepts of the dynamical density functional theory, show that the dynamical transition temperature depends only on the pair correlation function. Thus, this theory is similar in spirit to the microscopic mode coupling theory (MCT). However, unlike microscopic MCT, which predicts a very high transition temperature, the present theory predicts a transition temperature that is similar to T-c. This implies that the information of the dynamical transition temperature is embedded in the pair correlation function.},
	doi = {10.1103/PhysRevLett.119.265502},
	author = {Nandi, Manoj Kumar and Banerjee, Atreyee and Dasgupta, Chandan and Bhattacharyya, Sarika Maitra}
}
