Yttrium Tantalum Oxynitride Multiphases as Photoanodes for Water Oxidation
arXiv:1911.06550 · doi:10.1021/acs.jpcc.9b05590
Abstract
Perovskite yttrium tantalum oxynitride is theoretically proposed as a promising semiconductor for solar water splitting because of the predicted bandgap and energy positions of band edges. In experiment, however, we show here that depending on processing parameters, yttrium tantalum oxynitrides exist in multiphases, including the desired perovskite YTaON2, defect fluorite YTa(O,N,o)4, and N-doped YTaO4. These multiphases have bandgaps ranging between 2.13 and 2.31 eV, all responsive to visible light. The N-doped YTaO4, perovskite main phase, and fluorite main phase derived from crystalline fergusonite oxide precursors exhibit interesting photoelectrochemical performances for water oxidation, while the defect fluorite derived from low crystallized scheelite-type oxide precursors show negligible activity. Preliminarily measurements show that loading IrOx cocatalyst on N-doped YTaO4 significantly improves its photoelectrochemical performance encouraging further studies to optimize this new material for solar fuel production.
References in corpus (4)
- LaTiOxNy thin film model systems for photocatalytic water splitting: physicochemical evolution of the solid-liquid interface and the role of the crystallographic orientation
- Oxynitride Thin Films versus Particle-Based Photoanodes: a Comparative Study for Photoelectrochemical Solar Water Splitting
- Improved Photoelectrochemical Water Splitting of CaNbO2N Photoanodes by Co-Pi Photodeposition and Surface Passivation
- Determination of conduction and valence band electronic structure of LaTiOxNy thin film