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Updated: May 6, 2026

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
Published on: April 12, 2019
On the melting points of the TIP4P/2005 and TIP4P/Ice water models using particle mesh Ewald for dispersive
C Romero-Guzmán1, J Algaba1, C Vega2
1Laboratorio de Simulación Molecular y Química Computacional, CIQSO-Centro de Investigación en Química Sostenible and Departamento de Ciencias Integradas, Universidad de Huelva, 21006 Huelva, Spain.
Abstract:
The melting point of water is a fundamental thermodynamic property and a key benchmark for molecular simulations of phase behavior. Here, we estimate the melting temperature of the TIP4P/2005 and TIP4P/Ice models at ambient pressure using the direct coexistence method. We simulate systems containing up to 8640 water molecules and treat long-range interactions with the particle mesh Ewald approach for both electrostatics and dispersion [Lennard-Jones Particle-Mesh Ewald (LJ-PME)], thereby substantially reducing finite-size and cutoff-truncation artifacts. We find that, once these effects are properly accounted for, the melting point of both models increases by nearly 1 K relative to the values obtained from truncating the dispersion interactions at 8.5 Å. The resulting melting temperatures are 250.25 and 270.75 K for the TIP4P/2005 and TIP4P/Ice water models, respectively, thereby bringing the latter significantly closer to experiment. We also evaluate melting enthalpies at coexistence and find them largely insensitive to system size and the long-range treatment. Overall, these results highlight the importance of accurate long-range interactions in phase-coexistence simulations of water.
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