Prediction of 2D heterostructure GaSe/YGaS3 for highly efficient photocatalytic water splitting

Abstract

Photocatalytic water splitting technology stands out in the field of green hydrogen production due to its environmental friendliness and broad prospects, becoming a key force in promoting environmental sustainability and efficient energy utilization. The core of this study lies in the exploration of ultra-efficient catalysts. Based on this, we have meticulously constructed a type-II band-aligned GaSe/YGaS3 heterostructure and conducted an in-depth analysis of its photocatalytic performance through detailed firstprinciples calculations. Notably, the built-in electric field within the YGaS 3 monolayer can surpass the bandgap threshold (>1.23 eV) set by traditional photocatalytic water splitting theory, thereby significantly enhancing the utilization efficiency of solar energy. The research results indicate that, compared to individual GaSe and YGaS3 monolayers, the GaSe/YGaS3 heterostructure exhibits a significantly enhanced optical absorption coefficient. Specifically, its corrected solar-to-hydrogen efficiency has increased by 356% and 103%, respectively, reaching an impressive 34.82%. More excitingly, after applying biaxial tensile strain, this efficiency is further elevated to 36.30%. These remarkable characteristics not only highlight the immense potential and broad application prospects of the GaSe/YGaS3 heterostructure in the field of photocatalytic water splitting but also lay a solid scientific foundation and provide valuable experimental guidance for the future development of innovative, highperformance photocatalysts.

Supplementary files

Article information

Article type
Paper
Submitted
15 Sep 2025
Accepted
29 Oct 2025
First published
31 Oct 2025

Phys. Chem. Chem. Phys., 2025, Accepted Manuscript

Prediction of 2D heterostructure GaSe/YGaS3 for highly efficient photocatalytic water splitting

C. He, H. Liu, Q. Lv, B. Tan, B. Peng, H. Wang, J. Yuan and J. Wang, Phys. Chem. Chem. Phys., 2025, Accepted Manuscript , DOI: 10.1039/D5CP03551A

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