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    Complex-Mediated Synthesis of Tantalum Oxyfluoride Hierarchical Nanostructures for Highly Efficient Photocatalytic Hydrogen Evolution

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    In this work, we have, for the first time, developed a facile wet-chemical route to obtain a novel photocatalytic material of tantalum oxyfluoride hierarchical nanostructures composed of amorphous cores and single crystalline TaO<sub>2</sub>F nanorod shells (ACHNs) by regulating the one-step hydrothermal process of TaF<sub>5</sub> in a mixed solution of isopropanol (i-PrOH) and H<sub>2</sub>O. In this approach, elaborately controlling the reaction temperature and volume ratio of i-PrOH and H<sub>2</sub>O enabled TaF<sub>5</sub> to transform into intermediate coordination complex ions of [TaOF<sub>3</sub>·2F]<sup>2–</sup> and [TaF<sub>7</sub>]<sup>2–</sup>, which subsequently produced tantalum oxyfluoride ACHNs via a secondary nucleation and growth due to a stepwise change in hydrolysis rates of the two complex ions. Because of the unique chemical composition, crystal structure and micromorphology, the as-prepared tantalum oxyfluoride ACHNs show a more negative flat band potential, an accelerated charge transfer, and a remarkable surface area of 152.4 m<sup>2</sup> g<sup>–1</sup> contributing to increased surface reaction sites. As a result, they exhibit a photocatalytic activity for hydrogen production up to 1.95 mmol h<sup>–1</sup> g<sup>–1</sup> under the illumination of a simulated solar light without any assistance of co-catalysts, indicating that the as-prepared tantalum oxyfluoride ACHNs are a novel promising photocatalytic material for hydrogen production
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