4.7 Article

Research progress in metal sulfides for photocatalysis: From activity to stability

期刊

CHEMOSPHERE
卷 303, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.135085

关键词

Semiconductor photocatalysis; Metal sulfides; Photocorrosion; Activity; Stability

资金

  1. National Natural Science Foundation of China [51672312, 52073263]
  2. Fundamental Research Funds for the Central Universities, South-Central Minzu University [CZP22001]
  3. FCT - Fundacao para a Ciencia e a Tecnologia, I.P. [CEECINST/00102/2018]
  4. Associate Laboratory for Green Chemistry-LAQV
  5. FCT/MCTES [UIDB/50006/2020, UIDP/50006/2020]

向作者/读者索取更多资源

This review introduces the unique photocatalytic performance of metal sulfide photocatalysts in solar-to-fuel conversion and environmental purification, and discusses strategies to improve their photocatalytic activity and photostability.
Metal sulfides are a type of reduction semiconductor photocatalysts with narrow bandgap and negative conduction band potential, which make them have unique photocatalytic performance in solar-to-fuel conversion and environmental purification. However, metal sulfides also suffer from low quantum efficiency and photocorrosion. In this review, the strategies to improve the photocatalytic activity of metal sulfide photocatalysts by stimulating the charge separation and improving light-harvesting ability are introduced, including morphology control, semiconductor coupling and surface modification. In addition, the recent research progress aiming at improving their photostability is also illustrated, such as, construction of hole transfer heterojunctions and deposition of hole transfer cocatalysts. Based on the electronic band structures, the applications of metal sulfides in photocatalysis, namely, hydrogen production, degradation of organic pollutants and reduction of CO2, are summarized. Finally, the perspectives of the promising future of metal-sulfide based photocatalysts and the challenges remaining to overcome are also presented.

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