Abstract
Effective bulk phase and surface charge separation is critical for charge utilization during the photocatalytic energy conversion process. In this work, the ternary Ni2P-NiS/twinned Mn0.5Cd0.5S (T-MCS) nanohybrids were successfully constructed via combining Ni2P-NiS with T-MCS solid solution for visible light photocatalytic H2 evolution. T-MCS is composed of zinc blende Mn0.5Cd0.5S (ZB-MCS) and wurtzite Mn0.5Cd0.5S (WZ-MCS) and those two alternatively arranged crystal phases endow T-MCS with excellent bulk phase charge separation performance for the slight energy level difference between ZB-MCS and WZ-MCS. S-scheme carriers transfer route between NiS and T-MCS can accelerate the interfacial charge separation and retain the active electrons and holes, meanwhile, co-catalyst Ni2P as electron receiver and proton reduction center can further optimize the H2 evolution reaction kinetics based on the surface Schottky barrier effect. The above-formed homo-heterojunctions can establish multiple charge transfer channels in the bulk phase of T-MCS and interface of T-MCS and Ni2P-NiS. Under the synergistic effect of twinned homojunction, S-scheme heterojunction, and Schottky barrier, the ternary Ni2P-NiS/T-MCS composite manifested an H2 production rate of 122.5 mmol h–1 g–1, which was 1.33, 1.24, and 2.58 times higher than those of the NiS/T-MCS (92.4 mmol h–1 g–1), Ni2P/T-MCS (98.4 mmol h–1 g–1), and T-MCS (47.5 mmol h–1 g–1), respectively. This work demonstrates a promising strategy to develop efficient sulfides photocatalyst toward targeted solar-driven H2 evolution through homo-heterojunction engineering.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.