Related Experiment Video
Updated: May 13, 2025

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
An efficient improvement for photocatalytic hydrogen peroxide production: Sulfur vacancies in CaIn2S4
Yue Mao1, Jian Zhang2, Yingji Zhao3
1Department of Materials and Environmental Engineering, Chizhou University, Chizhou 247000 PR China; School of Energy and Environment, Department of Materials Science and Engineering, Centre for Functional Photonics (CFP), City University of Hong Kong, Kowloon Tong, Hong Kong, China; New Energy Technology Engineering Lab of Jiangsu Province. College of Science. Nanjing University of Posts & Telecommunications (NUPT), Nanjing 210023, PR China; Department of Materials Process Engineering, Graduate School of Engineering, Nagoya University, Nagoya 464-8603, Japan.
Abstract:
Visible-light-driven hydrogen peroxide (H2O2) synthesis is a sustainable and economically viable strategy for green production. However, most metal sulfide semiconductors exhibit insufficient band potentials, limiting selectivity and quantum yield. Here, we introduce sulfur vacancies into CaIn2S4 to modify its band structure, enhancing the conduction band's reduction capability and shifting oxygen reduction from a single direct 2e- pathway to a dual-pathway mechanism. This adjustment improves electron utilization efficiency. Theoretical calculations reveal that sulfur vacancies act as electron traps, promoting charge separation and suppressing recombination. Structural and electronic characterizations confirm these effects, and as a result, sulfur-vacancy-rich CaIn2S4 (CaIS SV) achieves a photocatalytic H2O2 production rate 9-fold than that of pristine CaIn2S4.
More Related Videos
Related Concept Videos
Catalysis
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation

