Stability of Hydride Anions in Reduced Ceria Studied by Density Functional Theory

TL;DR

This study uses density functional theory to investigate the stability and behavior of hydride anions on reduced CeO2 (111) surfaces, revealing their preferred locations and temperature-dependent transfer mechanisms.

Contribution

It provides new insights into the stability and positioning of hydride anions on reduced ceria surfaces, which was previously unclear.

Findings

Hydride stabilizes on metallic Ce3+ surfaces with outmost O vacancies.

Hydride prefers to locate between three Ce3+ ions when vacancies are deeper.

Hydride transfers to the surface and forms hydroxyl groups as temperature increases.

Abstract

Recently, the hydrogen adsorption and diffusion on the CeO2 (111) surface have been a vividly discussed topic because of its outstanding catalytic activity and selectivity in hydrogenation reactions. However, for the strongly reduced CeO2 (111) surface, the structure as well as the stability of hydride anions are still unclear. By virtue of density functional theory (DFT) calculations, we show that in the strongly reduced CeO2 (111) surface, the hydride can be stabilized on the largely metallic surface consisting of Ce3+ when O vacancies are mainly in the outmost layers. For the surface with O vacancies in deeper layers, the hydride locates in the center of three Ce3+ ions. However, the hydridic phase is not the most stable state thermodynamically. With the increase of the temperature, the hydride will transfer from the vacancies to the surface and form hydroxyl group on the outmost layer.