Molecular Statistics (MST) Source Codes

This approach bypasses the need for thermodynamic integration, directly sampling the Helmholtz free energy, which further minimizes computational expense. To validate MST, we benchmark its performance against state-of-the-art methods, including nonequilibrium molecular dynamics (NEMD), and the local harmonic approximation (LHA), a rapid yet less precise method. The evaluation demonstrates MST’s accuracy in predicting key thermodynamic properties, such as Gibbs free energy, entropy, and heat capacity, for several transition metals, aligning closely with experimental data.

Furthermore, MST achieves these calculations within seconds, competitive with NEMD in both runtime and accuracy, underscoring its potential as an efficient alternative for high-temperature thermodynamic simulations. The MST framework thus emerges as a promising tool for materials science applications, particularly for complex systems where traditional methods become computationally prohibitive. Please cite the following article, when using the codes: Vincent Feyen, Nele Moelans, Molecular statistics: A novel computationally efficient modeling approach to simulate thermodynamic properties of solid materials up to the melting point, Computational Materials Science, Volume 248, 2025, 113558, ISSN 0927-0256, doi.org/10.1016/j.commatsci.2024.113558.

(sciencedirect.com/science/article/pii/S0927025624007791)