1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Large improvement of visible-light photocatalytic H 2-evolution based on cocatalyst-free Zn 0.5Cd 0.5S synthesized through a two-step process

      Read this article at

      ScienceOpenPublisher
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Cocatalyst-free Zn 0.5Cd 0.5S (ZnCdS-CH) is synthesized through a two-step process as a highly active and stable photocatalyst for visible-light hydrogen evolution.

          Abstract

          Final metal sulfides Zn 0.5Cd 0.5S (ZnCdS-CH) are synthesized through a coprecipitation process followed by hydrothermal treatment. The morphological, structural and optical properties have been investigated extensively viadiverse analytical techniques. The ZnCdS-CH solid solution without noble metal loading is employed in photocatalytic H 2evolution under visible light irradiation ( λ≥ 420 nm) and achieves a superior activity rate of 0.971 mmol h −1, which exceeds those of coprecipitated Zn 0.5Cd 0.5S (ZnCdS-C) samples by more than 13 times. Moreover, in the recycle test, the ZnCdS-CH photocatalyst shows a stable photocatalytic activity for H 2evolution under long-term visible-light irradiation. Characterization analyses demonstrate that the excellent photocatalytic H 2-evolution performance of the ZnCdS-CH sample arises predominantly from the two-step processing procedure of coprecipitation followed by hydrothermal treatment at 200 °C, which makes it possess a hexagonal (wurtzite) structure, good dispersity, enhanced crystallinity, an appropriate band gap, a more negative conduction band, as well as a large number of surface defect states. This finding is of great significance for designing a facile, reproducible and inexpensive method to realise the potential of Zn xCd 1−xS ternary metal sulfides in the field of H 2evolution by water splitting.

          Related collections

          Most cited references36

          • Record: found
          • Abstract: not found
          • Article: not found

          Electrochemical Photolysis of Water at a Semiconductor Electrode

            Bookmark
            • Record: found
            • Abstract: found
            • Article: found

            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.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Enhancement of photocatalytic H2 evolution on CdS by loading MoS2 as Cocatalyst under visible light irradiation.

              This communication presents our recent results that the activity of photocatalytic H2 production can be significantly enhanced when a small amount of MoS2 is loaded on CdS as cocatalyst. The MoS2/CdS catalysts show high rate of H2 evolution from photocatalytic re-forming of lactic acid under visible light irradiation. The rate of H2 evolution on CdS is increased by up to 36 times when loaded with only 0.2 wt % of MoS2, and the activity of MoS2/CdS is even higher than those of the CdS photocatalysts loaded with different noble metals, such as Pt, Ru, Rh, Pd, and Au. The junction formed between MoS2 and CdS and the excellent H2 activation property of MoS2 are supposed to be responsible for the enhanced photocatalytic activity of MoS2/CdS.
                Bookmark

                Author and article information

                Contributors
                Journal
                CSTAGD
                Catalysis Science & Technology
                Catal. Sci. Technol.
                Royal Society of Chemistry (RSC)
                2044-4753
                2044-4761
                2017
                2017
                : 7
                : 4
                : 961-967
                Affiliations
                [1 ]Division of Nanomaterials and Chemistry
                [2 ]Hefei National Laboratory for Physical Sciences at Microscale
                [3 ]Department of chemistry
                [4 ]University of Science and Technology of China
                [5 ]Hefei 230026
                Article
                10.1039/C6CY02382G
                8dd35513-9999-4e0c-9ef0-046c81ab9f5e
                © 2017
                History

                Comments

                Comment on this article