Ta(3)N(5) Nanosheets Derived from TaS(2) as Efficient Photocatalysts for Water Oxidation.

The morphology and crystalline structure of semiconductor materials both play important roles in determining the photocatalytic activity of such materials. In this regard, tantalum nitride (TaN) shows promise as a visible-light-responsive photocatalyst for solar-driven water splitting. Even so, the performance of this material is limited by its bulk morphology and by high defect densities and inefficient charge transport. The present work synthesized single-crystalline TaN nanosheets having reduced defect concentrations and an increased specific surface area via the direct nitridation of two-dimensional TaS nanosheets. The TaN nanosheets had a thickness of approximately 30 nm with well-defined exposed facets and a uniform single-crystalline structure, and so led to a shorter charge-carrier diffusion length along with efficient charge separation and transport. When modified with IrO as a cocatalyst, these nanosheets provided an apparent quantum yield of 32.4% at 420 nm during photocatalytic oxygen evolution with sacrificial electron acceptors, outperforming TaN synthesized from TaO. This material was also integrated into Z-scheme photocatalyst sheets together with LaTiCuAgOS as the hydrogen evolution photocatalyst and carbon nanotubes as the electron mediator. These sheets enabled overall water splitting with stoichiometric H and O evolution in response to visible light, with a light absorption range extended to approximately 600 nm. This work underscores the critical roles of precursor selection and nanoscale morphological control in the development of photocatalysts with minimal defects and provides new insights expected to advance the field of solar-to-chemical energy conversion.