Abstract

The artificial Z-scheme system that mimics natural photosynthesis is encompassed of two semiconductors which generates two sets of charge carriers at different locations under solar irradiation. Researchers are trying to improve the efficacy of these systems by engineering highly stable redox couples, enhancing their light absorption capability, and discovering new cocatalysts. Herein, we report the fabrication of Au decorated LaFeO3-g-C3N4-BiFeO3 (Au/LFO-CN-BFO) catalyst as dual Z-scheme system for photocatalytic water splitting reactions. The photocatalytic performances of Au/LFO-CN-BFO, LFO-CN-BFO, LaFeO3, g-C3N4 and BiFeO3 were compared and the mechanism on the symmetric double Z-scheme Au/LFO-CN-BFO photocatalytic system was proposed. The results display that Au/LFO-CN-BFO has more superior photocatalytic performance compared to its counter parts (LaFeO3, g-C3N4 and BiFeO3), which is due to the symmetric double Z-scheme nature of photocatalyst. The as-fabricated Au/LFO-CN-BFO photocatalyst reveals high performance for photocatalytic water reduction to evolve H2 (i.e., 698.4 µmol h-1g−1) under visible light irradiation (λ ≥ 420 nm), which is far greater compared to that of its counterparts. As confirmed from various observations, the improved H2 evolution performance of the dual Z-scheme system is accredited to the improved light absorption and significantly promoted charge carrier’s separation. The design of this highly efficient dual Z-scheme composite photocatalyst would trigger the development of new artificial Z-scheme scheme systems that will solve the energy and associated environmental issues.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.