Abstract

With the increasing urgency of clean energy, photocatalytic hydrogen production serves as a sustainable hydrogen manufacturing method to improve the increasing scarcity of fossil fuels and environmental pollution. Herein, Cd0.2Zn0.8S (CZS)-modified Metal-Organic Framework (MOF) composites Pr–NO2–TPTC/CZS were successfully prepared through the reaction of Pr3+, aromatic tetracarboxylic acid, and Cd0.2Zn0.8S nanoparticles. Pr–NO2–TPTC/CZS composite materials exhibited enhanced photolysis performance compared to pure Pr–NO2–TPTC and Cd0.2Zn0.8S materials. With the decrease of Cd0.2Zn0.8S in Pr–NO2–TPTC/CZS composites, the photocatalytic performance of the synthesized composites is constantly improved. Pr–NO2–TPTC/CZS (1:1) photocatalyst exhibited excellent hydrogen evolution performance, with a hydrogen production capacity of 6321 μmol g−1 h−1. Photoluminescence spectroscopy (PL), photocurrent-time test (I-t), and electrochemical impedance spectroscopy (EIS) confirmed that the heterojunction interface formed between Pr–NO2–TPTC and CZS promoted electron-hole separation and transfer. Electron paramagnetic resonance (EPR) indicated that CZS-modified Pr–NO2–TPTC can promote the production of ·OH and ·O2− in the system, thereby increasing the photocatalytic hydrogen production performance. This work provides an effective solution for photocatalytic hydrogen production and a potential method for solving the energy crisis and environmental pollution.

Full Text
Paper version not known

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.