4.7 Article

Fabrication of noble-metal-free CdSnanorods-carbon layer-cobalt phosphide multiple heterojunctions for efficient and robust photocatalyst hydrogen evolution under visible light irradiation

Journal

RENEWABLE ENERGY
Volume 131, Issue -, Pages 180-186

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.renene.2018.07.028

Keywords

Cadmium sulfide; Carbon layer; Photocatalytic hydrogen evolution; Non-noble metal

Funding

  1. National Science Funds for Creative Research Groups of China [51421006]
  2. Key Program of National Natural Science Foundation of China [91647206]
  3. Fundamental Research Funds for The Central Universities [2018B14514]
  4. National Science Fundation of China for Excellent Young Scholars [51422902]
  5. National Key Plan for Research and Development of China [2016YFC0502203]
  6. Natural Science Foundation of China [51679063]
  7. PAPD

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Photocatalytic water splitting has aroused great interest as a clean and renewable energy conversion process. In this study, we prepared a novel noble-metal-free multiple heterojunction photocatalyst (CdS@C-CoP) composed of CdS nanorods, conducting carbon layer and CoP nanoparticles cocatalyst for the first time. The obtained CdS@C-CoP composites exhibited excellent performance and stability under visible light irradiation when it was used as photocatalysts for hydrogen evolution. For the optimum CdS@C-CoP sample, an average hydrogen evolution rate reached up to 10089 mu mol g(-1) h(-1), nearly 6 fold as high as that of pure CdS. The enhanced photocatalytic hydrogen production rate can be ascribed to the synergistic effect between conductive carbon layer and surface cocatalyst CoP, which resulted in efficient separation of photoexcited charge carriers and abundant active sites for hydrogen reduction. This work presented a novel way to design composite photocatalyst with efficient hydrogen generation properties through combining two kinds of surface modification methods: thin carbon layer coating and surface cocatalysts loading. (C) 2018 Elsevier Ltd. All rights reserved.

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