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      Precisely engineered type II ZnO-CuS based heterostructure: A visible light driven photocatalyst for efficient mineralization of organic dyes

      , , , , , ,
      Applied Surface Science
      Elsevier BV

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          Heterogeneous photocatalyst materials for water splitting.

          This critical review shows the basis of photocatalytic water splitting and experimental points, and surveys heterogeneous photocatalyst materials for water splitting into H2 and O2, and H2 or O2 evolution from an aqueous solution containing a sacrificial reagent. Many oxides consisting of metal cations with d0 and d10 configurations, metal (oxy)sulfide and metal (oxy)nitride photocatalysts have been reported, especially during the latest decade. The fruitful photocatalyst library gives important information on factors affecting photocatalytic performances and design of new materials. Photocatalytic water splitting and H2 evolution using abundant compounds as electron donors are expected to contribute to construction of a clean and simple system for solar hydrogen production, and a solution of global energy and environmental issues in the future (361 references).
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            TiO2-assisted photocatalytic degradation of azo dyes in aqueous solution: kinetic and mechanistic investigations

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              Visible-light driven heterojunction photocatalysts for water splitting – a critical review

              We summarise current state-of-the-art efficient visible-light driven heterojunction water splitting photo(electro)catalysts and describe how theoretical modelling of electronic structures at interfaces can explain their functionality. Solar driven catalysis on semiconductors to produce clean chemical fuels, such as hydrogen, is widely considered as a promising route to mitigate environmental issues caused by the combustion of fossil fuels and to meet increasing worldwide demands for energy. The major limiting factors affecting the efficiency of solar fuel synthesis include; (i) light absorption, (ii) charge separation and transport and (iii) surface chemical reaction; therefore substantial efforts have been put into solving these problems. In particular, the loading of co-catalysts or secondary semiconductors that can act as either electron or hole acceptors for improved charge separation is a promising strategy, leading to the adaptation of a junction architecture. Research related to semiconductor junction photocatalysts has developed very rapidly and there are a few comprehensive reviews in which the strategy is discussed (A. Kudo and Y. Miseki, Chemical Society Reviews , 2009, 38, 253–278, K. Li, D. Martin, and J. Tang, Chinese Journal of Catalysis , 2011, 32, 879–890, R. Marschall, Advanced Functional Materials , 2014, 24, 2421–2440). This critical review seeks to give an overview of the concept of heterojunction construction and more importantly, the current state-of-the art for the efficient, visible-light driven junction water splitting photo(electro)catalysts reported over the past ten years. For water splitting, these include BiVO 4 , Fe 2 O 3 , Cu 2 O and C 3 N 4 , which have attracted increasing attention. Experimental observations of the proposed charge transfer mechanism across the semiconductor/semiconductor/metal junctions and the resultant activity enhancement are discussed. In parallel, recent successes in the theoretical modelling of semiconductor electronic structures at interfaces and how these explain the functionality of the junction structures is highlighted.
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                Author and article information

                Journal
                Applied Surface Science
                Applied Surface Science
                Elsevier BV
                01694332
                July 2022
                July 2022
                : 590
                : 153053
                Article
                10.1016/j.apsusc.2022.153053
                fe0ae615-cc9b-440f-befc-3d52b81000cf
                © 2022

                https://www.elsevier.com/tdm/userlicense/1.0/

                https://doi.org/10.15223/policy-017

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-012

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-004

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