Related Experiment Video
Updated: Jan 10, 2026

Synthesis and Performance Evaluations of ZnCoS/ZnCdS with Twin Crystal Structure for Multifunctional Redox Photocatalysis in Energy Applications
Published on: July 25, 2025
Rh,Sb-codoped SrTiO3 cubic nanoparticles encapsulated by ZnIn2S4 nanosheets for efficient visible-light-driven
Junzhe Jiang1,2, Yiquan Zhan1,2, Bingxue Li1
1Jiangxi Province Key Laboratory of Functional Crystalline Materials Chemistry, School of Chemistry and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, Jiangxi Province, China. lys90s@126.com.
None:
Strontium titanate (SrTiO3) is a typical kind of titanate photocatalyst for solar-driven hydrogen production, but its sunlight absorption is confined to the ultraviolet region. Indium zinc sulfide (ZnIn2S4) materials can respond to visible light, yet suffer from the rapid recombination of photogenerated charge carriers. In this study, a Rh,Sb-codoped SrTiO3@ZnIn2S4 heterojunction photocatalyst was synthesized by encapsulating the surface of Rh,Sb-SrTiO3 cubic nanoparticles with ZnIn2S4 nanosheets. Rh and Sb ions were applied to regulate the band structure of SrTiO3, making it responsive to visible light. Constructing a heterojunction could promote the separation of photogenerated charge carriers for SrTiO3 and ZnIn2S4. The characterization results of ultraviolet-visible, X-ray photoelectron spectroscopy, and electrochemical analyses demonstrated that the difference in the work function between Rh,Sb-SrTiO3 and ZnIn2S4 formed an interfacial electric field. It facilitated the separation and migration of photogenerated charge carriers, thereby enhancing the photocatalytic hydrogen evolution activity. The visible-light-driven hydrogen evolution activity of ZnIn2S4 was unaffected by pure SrTiO3, but significantly enhanced by Rh,Sb-SrTiO3. The optimal Rh,Sb-SrTiO3@ZnIn2S4 photocatalyst provided a hydrogen evolution rate of about 107.63 μmol h-1 under visible light (λ ≥ 420 nm), which was 4.6 times that of pristine ZnIn2S4.

