The potential energy landscape (PEL) formalism is a statistical mechanical approach to describe supercooled liquids and glasses. Here, we use the PEL formalism to study the pressure-induced transformations between low-density amorphous ice (LDA) and high-density amorphous ice (HDA) using computer simulations of the TIP4P/2005 molecular model of water. We find that the properties of the PEL sampled by the system during the LDA-HDA transformation exhibit anomalous behavior. In particular, at conditions where the change in density during the LDA-HDA transformation is approximately discontinuous, reminiscent of a first-order phase transition, we find that (i) the inherent structure (IS) energy, e(IS)(V), is a concave function of the volume and (ii) the IS pressure, P-IS(V), exhibits a van der Waals-like loop. In addition, the curvature of the PEL at the IS is anomalous, a nonmonotonic function of V. In agreement with previous studies, our work suggests that conditions (i) and (ii) are necessary (but not sufficient) signatures of the PEL for the LDA-HDA transformation to be reminiscent of a first-order phase transition. We also find that one can identify two different regions of the PEL, one associated with LDA and another with HDA. Our computer simulations are performed using a wide range of compression/decompression and cooling rates. In particular, our slowest cooling rate (0.01 K/ns) is within the experimental rates employed in hyperquenching experiments to produce LDA. Interestingly, the LDA-HDA transformation pressure that we obtain at T = 80 K and at different rates extrapolates remarkably well to the corresponding experimental pressure. Published under license by AIP Publishing.

Glass polymorphism in TIP4P/2005 water: A description based on the potential energy landscape formalism / Handle, Philip H.; SCIORTINO, Francesco; Giovambattista, Nicolas. - In: THE JOURNAL OF CHEMICAL PHYSICS. - ISSN 0021-9606. - 150:24(2019). [10.1063/1.5100346]

Glass polymorphism in TIP4P/2005 water: A description based on the potential energy landscape formalism

Francesco Sciortino;
2019

Abstract

The potential energy landscape (PEL) formalism is a statistical mechanical approach to describe supercooled liquids and glasses. Here, we use the PEL formalism to study the pressure-induced transformations between low-density amorphous ice (LDA) and high-density amorphous ice (HDA) using computer simulations of the TIP4P/2005 molecular model of water. We find that the properties of the PEL sampled by the system during the LDA-HDA transformation exhibit anomalous behavior. In particular, at conditions where the change in density during the LDA-HDA transformation is approximately discontinuous, reminiscent of a first-order phase transition, we find that (i) the inherent structure (IS) energy, e(IS)(V), is a concave function of the volume and (ii) the IS pressure, P-IS(V), exhibits a van der Waals-like loop. In addition, the curvature of the PEL at the IS is anomalous, a nonmonotonic function of V. In agreement with previous studies, our work suggests that conditions (i) and (ii) are necessary (but not sufficient) signatures of the PEL for the LDA-HDA transformation to be reminiscent of a first-order phase transition. We also find that one can identify two different regions of the PEL, one associated with LDA and another with HDA. Our computer simulations are performed using a wide range of compression/decompression and cooling rates. In particular, our slowest cooling rate (0.01 K/ns) is within the experimental rates employed in hyperquenching experiments to produce LDA. Interestingly, the LDA-HDA transformation pressure that we obtain at T = 80 K and at different rates extrapolates remarkably well to the corresponding experimental pressure. Published under license by AIP Publishing.
2019
potential energy landscape; supercooled water; numerical simulation
01 Pubblicazione su rivista::01a Articolo in rivista
Glass polymorphism in TIP4P/2005 water: A description based on the potential energy landscape formalism / Handle, Philip H.; SCIORTINO, Francesco; Giovambattista, Nicolas. - In: THE JOURNAL OF CHEMICAL PHYSICS. - ISSN 0021-9606. - 150:24(2019). [10.1063/1.5100346]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1364620
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