@article { ISI:000381384300030,
	title = {Effect of total and pair configurational entropy in determining dynamics of supercooled liquids over a range of densities},
	journal = {Journal of Chemical Physics},
	volume = {145},
	number = {3},
	year = {2016},
	month = {JUL},
	pages = {Article Number: 034502},
	publisher = {AMER INST PHYSICS},
	address = {1305 WALT WHITMAN RD, STE 300, MELVILLE, NY 11747-4501 USA},
	abstract = {<p>In this paper, we present a study of supercooled liquids interacting with the Lennard Jones potential and the corresponding purely repulsive (Weeks-Chandler-Andersen) potential, over a range of densities and temperatures, in order to understand the origin of their different dynamics in spite of their structures being similar. Using the configurational entropy as the thermodynamic marker via the Adam Gibbs relation, we show that the difference in the dynamics of these two systems at low temperatures can be explained from thermodynamics. At higher densities both the thermodynamical and dynamical difference between these model systems decrease, which is quantitatively demonstrated in this paper by calculating different parameters. The study also reveals the origin of the difference in pair entropy despite the similarity in the structure. Although the maximum difference in structure is obtained in the partial radial distribution function of the B type of particles, the rdf of AA pairs and AB pairs gives rise to the differences in the entropy and dynamics. This work supports the observation made in an earlier study [A. Banerjee et al., Phys. Rev. Lett. 113, 225701 (2014)] and shows that they are generic in nature, independent of density. Published by AIP Publishing.</p>},
	issn = {0021-9606},
	doi = {10.1063/1.4958627},
	author = {Banerjee, Atreyee and Nandi, Manoj Kumar and Sastry, Srikanth and Bhattacharyya, Sarika Maitra}
}
@article {47100,
	title = {Effective structure of a system with continuous polydispersity},
	journal = {Journal of Chemical Physics},
	volume = {154},
	year = {2021},
	month = {JAN },
	pages = {034503},
	type = {Article},
	abstract = {<p>In a system of N particles, with continuous size polydispersity, there exists an N(N - 1) number of partial structure factors, making it analytically less tractable. A common practice is to treat the system as an effective one component system, which is known to exhibit an artificial softening of the structure. The aim of this study is to describe the system in terms of M pseudospecies such that we can avoid this artificial softening but, at the same time, have a value of M \&lt;\&lt; N. We use potential energy and pair excess entropy to estimate an optimum number of species, M-0. We then define the maximum width of polydispersity, Delta sigma (0), that can be treated as a monodisperse system. We show that M-0 depends on the degree and type of polydispersity and also on the nature of the interaction potential, whereas Delta sigma (0) weakly depends on the type of polydispersity but shows a stronger dependence on the type of interaction potential. Systems with a softer interaction potential have a higher tolerance with respect to polydispersity. Interestingly, M-0 is independent of system size, making this study more relevant for bigger systems. Our study reveals that even 1\% polydispersity cannot be treated as an effective monodisperse system. Thus, while studying the role of polydispersity by using the structure of an effective one component system, care must be taken in decoupling the role of polydispersity from that of the artificial softening of the structure.</p>
},
	issn = {0021-9606},
	doi = {10.1063/5.0038812},
	author = {Patel, Palak and Nandi, Manoj Kumar and Nandi, Ujjwal Kumar and Bhattacharyya, Sarika Maitra}
}
