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Article Dans Une Revue Journal of Chemical Physics Année : 2022

Beyond single-crystal surfaces: The GAL21 water/metal force field

Résumé

Solvent effects are notoriously difficult to describe for metallic nanoparticles (NPs). Here, we introduce GAL21 which is the first pairwise additive force field that is specifically designed to modulate the near chemisorption energy of water as a function of the coordination numbers of the metallic atoms. We find a quadratic dependence to be most suitable for capturing the dependence of the adsorption energy of water on the generalized coordination number (GCN) of the metal atoms. GAL21 has been fitted against DFT adsorption energies for Cu, Ag, Au, Ni, Pd, Pt, and Co on 500 configurations and validated on about 3000 configurations for each metal, constructed on five surfaces with GCNs varying from 2.5 to 11.25. Depending on the metals, the root mean square deviation is found between 0.7 kcal mol −1 (Au) to 1.6 kcal mol −1 (Ni). Using GAL21, as implemented in the open-source code CP2K, we then evaluate the solvation energy of Au 55 and Pt 55 NPs in water using thermodynamic integration. The solvation free energy is found to be larger for Pt than for Au and systematically larger than 200 kcal mol −1 , demonstrating the large impact of solvent on the surface energetics of NPs. Still, given that the amorphous NPs are both, the most stable and the most solvated ones, we do not predict a change in the preferred morphology between the gas-phase and in water. Finally, based on a linear regression on three sizes of NPs (from 38 to 147), the solvation energy for Au and Pt surface atoms is found to be −5.2 and −9.9 kcal mol −1 , respectively.
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Dates et versions

hal-04177926 , version 1 (06-08-2023)

Identifiants

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Paul Clabaut, Matthieu Beisert, Carine Michel, Stephan N. Steinmann. Beyond single-crystal surfaces: The GAL21 water/metal force field. Journal of Chemical Physics, 2022, 157 (19), pp.194705. ⟨10.1063/5.0130368⟩. ⟨hal-04177926⟩
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