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We revisit the controversy, discussed recently by Goldstein in this journal[J. Chem. Phys. 128,154510 (2008)], whether the residual entropy is real or fictional. It is shown that the residual entropy loss conjecture (ELC) at the glass transition, which results in a discontinuous entropy violates many fundamental principles of classical thermodynamics, and also contradicts some experimental facts. Assuming, as is common in the field, that glasses are in internal equilibrium, we show that the continuity of enthalpy and volume at the glass transition require the continuity of the Gibbs free energy and the entropy, which contradicts ELC. It is then argued that ELC is founded on an incorrect understanding of what it means for a glass to be kinetically trapped in a basin and of the concept of probability and entropy. Once this misunderstanding is corrected in our approach by the proper identification of entropy as the ensemble entropy, which is in accordance with the principle of reproducibility (see Sect. II), it follows immediately that the residual entropy does not disappear in a kinetically frozen glassy state and all the violations of thermodynamics disappear. We show that the temporal definition of entropy over finite times does not make sense for glasses as it is not unique. There is no loss of ergodicity and causality, contrary to some recent claims.
A glass is a non-equilibrium thermodynamic state whose physical properties depend on time. Glass formation from the melt, as well as the inverse process of liquid structural recovery from the glass are non-equilibrium processes. A positive amount of
We compare the macroscopic and the local plastic behavior of a model amorphous solid based on two radically different numerical descriptions. On the one hand, we simulate glass samples by atomistic simulations. On the other, we implement a mesoscale
A Potts model and the Replica Exchange Wang-Landau algorithm are used to construct an energy landscape for a crystalline solid containing surfaces and grain boundaries. The energy landscape is applied to an equation of motion from the steepest-entrop
Entropy is a fundamental thermodynamic quantity that is a measure of the accessible microstates available to a system, with the stability of a system determined by the magnitude of the total entropy of the system. This is valid across truly mind bogg
We analyze the nature of the structural order established in liquid TIP4P water in the framework provided by the multi-particle correlation expansion of the statistical entropy. Different regimes are mapped onto the phase diagram of the model upon re