Highly Correlated Hydride Ion Tracer Diffusion in SrTiO3- x H x Oxyhydrides

Journal of the American Chemical Society
Xin LiuReidar Haugsrud

Abstract

Mixed oxide hydride anion systems constitute a novel class of materials exhibiting intriguing properties such as solid-state hydride ion conduction and fast anion exchange. In this contribution we derive the kinetics of hydride ion transport in a mixed oxide-hydride system, SrTiO3- xH x, through isotope exchange and depth profiling. Density functional theory (DFT) calculations indicate that migration of H- to neighboring vacant oxygen lattice sites is fast, but that long-range transport is impeded by slow reorganization of the oxygen sublattice. From measured hydride tracer-diffusion coefficients and the correlation factors derived from DFT, we are able to derive the hydrogen self-diffusion coefficients in SrTiO3- xH x. More generally, the explicit description of hydride ion transport in SrTiO3- xH x through combination of experimental and computational methods reported in this work can be applied to explore anion diffusion in other mixed anion systems.

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Citations

Nov 27, 2019·Angewandte Chemie·Lun Jin, Michael A Hayward
Jun 1, 2021·Chemistry of Materials : a Publication of the American Chemical Society·Rasmus LavénMaths Karlsson
Dec 4, 2021·Scientific Reports·L L RusevichA Dejneka

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