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      Visible light-driven efficient overall water splitting using p-type metal-nitride nanowire arrays

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          Abstract

          Solar water splitting for hydrogen generation can be a potential source of renewable energy for the future. Here we show that efficient and stable stoichiometric dissociation of water into hydrogen and oxygen can be achieved under visible light by eradicating the potential barrier on nonpolar surfaces of indium gallium nitride nanowires through controlled p-type dopant incorporation. An apparent quantum efficiency of ∼12.3% is achieved for overall neutral (pH∼7.0) water splitting under visible light illumination (400-475 nm). Moreover, using a double-band p-type gallium nitride/indium gallium nitride nanowire heterostructure, we show a solar-to-hydrogen conversion efficiency of ∼1.8% under concentrated sunlight. The dominant effect of near-surface band structure in transforming the photocatalytic performance is elucidated. The stability and efficiency of this recyclable, wafer-level nanoscale metal-nitride photocatalyst in neutral water demonstrates their potential use for large-scale solar-fuel conversion.

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          Photocatalyst releasing hydrogen from water.

          Direct splitting of water using a particulate photocatalyst would be a good way to produce clean and recyclable hydrogen on a large scale, and in the past 30 years various photocatalysts have been found that function under visible light. Here we describe an advance in the catalysis of the overall splitting of water under visible light: the new catalyst is a solid solution of gallium and zinc nitrogen oxide, (Ga(1-x)Zn(x))(N(1-x)O(x)), modified with nanoparticles of a mixed oxide of rhodium and chromium. The mixture functions as a promising and efficient photocatalyst in promoting the evolution of hydrogen gas.
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            Artificial photosynthesis for solar water-splitting

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              Advanced nanoarchitectures for solar photocatalytic applications.

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                Author and article information

                Journal
                Nature Communications
                Nat Commun
                Springer Nature
                2041-1723
                December 2015
                April 9 2015
                : 6
                : 1
                Article
                10.1038/ncomms7797
                25854846
                6f9ceb3d-818a-4f59-b4e3-bbc1735fe4cb
                © 2015

                http://www.springer.com/tdm

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