J. Mater. Sci. Technol. ›› 2025, Vol. 211: 22-29.DOI: 10.1016/j.jmst.2024.05.047

• Research Article • Previous Articles     Next Articles

An S-scheme artificial photosynthetic system with H-TiO2/g-C3N4 heterojunction coupled with MXene boosts solar H2 evolution

Depeng Menga, Xiaowen Ruanb,*, Minghua Xua, Dongxu Jiaoa, Guozhen Fanga, Yu Qiua, Yueyang Zhangb, Haiyan Zhanga, Sai Kishore Ravib,*, Xiaoqiang Cuia,*   

  1. aState Key Laboratory of Automotive Simulation and Control, School of Materials Science and Engineering, Key Laboratory of Automobile Materials of MOE, Jilin Provincial International Cooperation Key Laboratory of High-Efficiency Clean Energy Materials, Jilin University, Changchun 130012, China;
    bSchool of Energy and Environment, City University of Hong Kong, Tat Chee Avenue, Kowloon, SAR, Hong Kong, China
  • Received:2024-01-28 Revised:2024-05-04 Accepted:2024-05-11 Published:2025-03-10 Online:2024-06-14
  • Contact: * E-mail addresses: xiaoruan@cityu.edu.hk (X. Ruan), skravi@cityu.edu.hk (S.K. Ravi), xqcui@jlu.edu.cn (X. Cui).

Abstract: Solar hydrogen production via water splitting is pivotal for solar energy harnessing, addressing key challenges in energy and environmental sustainability. However, two critical issues persist with single-component photocatalysts: suboptimal carrier transport and inadequate light absorption. While heterojunction-based artificial photosynthetic systems like Z-scheme photocatalysts have been explored, their charge recombination and light harvesting efficiency are still unsatisfactory. S-scheme heterojunctions have gained attention in photocatalysis, owing to their pronounced built-in electric field and superior redox capabilities. In this study, we introduce a MXene-based S-scheme H-TiO2/g-C3N4/Ti3C2 heterojunction (TCMX), synthesized through electrostatic self-assembly. The as-prepared TCMX exhibited an excellent photocatalytic hydrogen evolution rate of 53.67 mmol g-1 h-1 surpassing the performance of commercial Rutile TiO2, H-TiO2, g-C3N4, and HTCN. The effectiveness of TCMX is largely due to the built-in electric field in the S-scheme heterojunction and the cocatalytic activity of MXene promoting rapid separation of photogenerated charges and resulting in well-separated electron and hole enriched sites. This study offers a new approach to enhance photocatalytic hydrogen evolution efficiency and paves the way for the future design of S-scheme heterojunctions.

Key words: S-scheme, MXene, Heterojunction, Hydrogen, Charge transfer