In this article, we report on advanced molecular dynamics simulations of the atomistic DMASnBr –water interface, which, coupled with a grand-canonical formulation of adsorbates and defects, elucidate the surface chemistry and reactivity of this novel water-stable perovskite and highlight the role of small electron bipolarons in photocatalytic hydrogen production. We find that the extremely acidic nature of the surface Br atoms does not allow for significant adsorption of protons at the interface under charge-neutral conditions. However, when electrons are accumulated on the surface, the formation of a small electron bipolaron in the form of a Sn-Sn dimer provides the required electron localization to drive adsorption of H, which is assimilated on surface Sn atoms as hydride. Finally, we estimate a favourable alignment between the bipolaron energy level and the H /H redox level, which suggests the occurrence of a feasible route for hydrogen evolution, bypassing the common reaction mechanism.

Electron bipolarons at the DMASnBr3–water interface: Effect on the photocatalytic hydrogen production

Ricciarelli D.;Mosconi E.;Malavasi L.;
2024

Abstract

In this article, we report on advanced molecular dynamics simulations of the atomistic DMASnBr –water interface, which, coupled with a grand-canonical formulation of adsorbates and defects, elucidate the surface chemistry and reactivity of this novel water-stable perovskite and highlight the role of small electron bipolarons in photocatalytic hydrogen production. We find that the extremely acidic nature of the surface Br atoms does not allow for significant adsorption of protons at the interface under charge-neutral conditions. However, when electrons are accumulated on the surface, the formation of a small electron bipolaron in the form of a Sn-Sn dimer provides the required electron localization to drive adsorption of H, which is assimilated on surface Sn atoms as hydride. Finally, we estimate a favourable alignment between the bipolaron energy level and the H /H redox level, which suggests the occurrence of a feasible route for hydrogen evolution, bypassing the common reaction mechanism.
2024
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC - Sede Secondaria Perugia
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/513539
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