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Direct splitting of water under visible light irradiation with an oxide semiconductor photocatalyst

Abstract

The photocatalytic splitting of water into hydrogen and oxygen using solar energy is a potentially clean and renewable source for hydrogen fuel. The first photocatalysts suitable for water splitting1, or for activating hydrogen production from carbohydrate compounds made by plants from water and carbon dioxide2, were developed several decades ago. But these catalysts operate with ultraviolet light, which accounts for only 4% of the incoming solar energy and thus renders the overall process impractical. For this reason, considerable efforts have been invested in developing photocatalysts capable of using the less energetic but more abundant visible light3,4,5,6,7, which accounts for about 43% of the incoming solar energy. However, systems that are sufficiently stable and efficient for practical use have not yet been realized. Here we show that doping of indium-tantalum-oxide with nickel yields a series of photocatalysts, In1-xNixTaO4 (x = 0–0.2), which induces direct splitting of water into stoichiometric amounts of oxygen and hydrogen under visible light irradiation with a quantum yield of about 0.66%. Our findings suggest that the use of solar energy for photocatalytic water splitting might provide a viable source for ‘clean’ hydrogen fuel, once the catalytic efficiency of the semiconductor system has been improved by increasing its surface area and suitable modifications of the surface sites.

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Figure 1: Schematic illustration of the InTaO4 structure.
Figure 2: Photocatalytic H2 and O2 generation.
Figure 3: Optical properties of the photocatalyst.
Figure 4: Changes in crystal structure with doping.

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Acknowledgements

This work was supported in part by the COE project, Japan Ministry of Education and Science.

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Correspondence to Zhigang Zou.

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Zou, Z., Ye, J., Sayama, K. et al. Direct splitting of water under visible light irradiation with an oxide semiconductor photocatalyst. Nature 414, 625–627 (2001). https://doi.org/10.1038/414625a

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