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Positively charged Pt-based cocatalysts: an orientation for achieving efficient photocatalytic water splitting

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Abstract

Considerable effort has been made to develop efficient water-splitting photocatalysts, which are generally composed of light-absorbing semiconductors and so-called cocatalysts that play a key role in accelerating the reaction kinetics of water splitting. Platinum (Pt)-based catalysts have been widely regarded as excellent cocatalysts for photocatalytic water splitting, but the relationship between their valence state and reaction activity for photocatalytic water splitting had never been summarized. This review presents positively charged Pt nanoparticles, clusters and even single atoms that can boost the reaction activity dramatically, and summarises several strategies and techniques to tailor the positive valence states of Pt-based cocatalysts such as by using oxygen atoms. By tailoring the valence states of Pt-based cocatalysts, the capacities of these cocatalysts for water splitting can be significantly enhanced. Moreover, the operando analyses that can determine the real structures of this type of cocatalyst under working conditions are also discussed. These developments suggest that positively charged Pt-based cocatalysts could determine the direction and efficiency of photocatalytic water splitting, which may provide an ideal orientation to design state-of-the-art catalysts for achieving efficient photocatalytic water splitting.

Graphical abstract: Positively charged Pt-based cocatalysts: an orientation for achieving efficient photocatalytic water splitting

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Publication details

The article was received on 24 Sep 2019, accepted on 18 Nov 2019 and first published on 22 Nov 2019


Article type: Review Article
DOI: 10.1039/C9TA10568A
J. Mater. Chem. A, 2020, Advance Article

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    Positively charged Pt-based cocatalysts: an orientation for achieving efficient photocatalytic water splitting

    J. Liu, Y. Li, X. Zhou, H. Jiang, H. G. Yang and C. Li, J. Mater. Chem. A, 2020, Advance Article , DOI: 10.1039/C9TA10568A

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