The prospect of CuX (X=O, S, Se) co-catalysts in photocatalysis: From engineering heterostructural integrity towards enhanced photocatalytic activities – A concise review

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Shruti Jain
  • Swati
  • Mohammed Ismael
  • Muhammad Tahir
  • Pardeep Singh
  • Pankaj Raizada
  • Bhupinder Singh
  • Van Huy Nguyen
  • Naveen Kumar

External Research Organisations

  • Maharshi Dayanand University
  • United Arab Emirates University
  • Shoolini University of Biotechnology and Management Sciences
  • Bhagat Phool Singh Mahila Vishwavidyalaya university khanpur
  • Chettinad Academy of Research and Education
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Details

Original languageEnglish
Article number112634
JournalJournal of Physics and Chemistry of Solids
Volume201
Early online date16 Feb 2025
Publication statusE-pub ahead of print - 16 Feb 2025

Abstract

Recent progress in photocatalytic degradation and hydrogen generation highlights the role of co-catalysts in the efficiency of semiconductors-based photocatalysts. Co-catalysts provide an adequate solution to boost photocatalytic performance. This review first covers the synthesis methods for CuX along with the loading method of the co-catalysts to the base catalyst. Because of cost-effectiveness, compositional flexibility, outstanding physiochemical stability, tunable crystal phase narrow band gap, non-toxicity, adjustable microstructure, etc., copper-based co-catalysts have stimulated immense attention as they can magnify photocatalytic performance. The fundamental principles of photocatalytic degradation of organic molecules and hydrogen production are highly outlined. Then, the co-catalytic activities of various Cu-based materials involving Cu oxides, Cu sulfides, and Cu selenide are thoroughly discussed when they are coupled with base semiconductor materials (metal oxides, metal sulfides, nitrides, etc.), to attain a rationally designed photocatalyst for enhancing photocatalytic reactions. This review is expected to upgrade research on efficient co-catalyst design to refine the charge carrier separation in photocatalytic systems for CO2 adsorption ability, light harvesting, and acting as reactive sites for the reduction reaction.

Keywords

    Co-photocatalyst, CuO, CuS, CuSe, Degradation, Photocatalyst

ASJC Scopus subject areas

Sustainable Development Goals

Cite this

The prospect of CuX (X=O, S, Se) co-catalysts in photocatalysis: From engineering heterostructural integrity towards enhanced photocatalytic activities – A concise review. / Jain, Shruti; Swati; Ismael, Mohammed et al.
In: Journal of Physics and Chemistry of Solids, Vol. 201, 112634, 06.2025.

Research output: Contribution to journalArticleResearchpeer review

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abstract = "Recent progress in photocatalytic degradation and hydrogen generation highlights the role of co-catalysts in the efficiency of semiconductors-based photocatalysts. Co-catalysts provide an adequate solution to boost photocatalytic performance. This review first covers the synthesis methods for CuX along with the loading method of the co-catalysts to the base catalyst. Because of cost-effectiveness, compositional flexibility, outstanding physiochemical stability, tunable crystal phase narrow band gap, non-toxicity, adjustable microstructure, etc., copper-based co-catalysts have stimulated immense attention as they can magnify photocatalytic performance. The fundamental principles of photocatalytic degradation of organic molecules and hydrogen production are highly outlined. Then, the co-catalytic activities of various Cu-based materials involving Cu oxides, Cu sulfides, and Cu selenide are thoroughly discussed when they are coupled with base semiconductor materials (metal oxides, metal sulfides, nitrides, etc.), to attain a rationally designed photocatalyst for enhancing photocatalytic reactions. This review is expected to upgrade research on efficient co-catalyst design to refine the charge carrier separation in photocatalytic systems for CO2 adsorption ability, light harvesting, and acting as reactive sites for the reduction reaction.",
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