Abstract
In this study, we report an economic and noble-metal-free photosynthetic system of Ni(dmgH)2/CdS composites (dmgH = dimethylglyoxime). This system, consisting of CdS as a photocatalyst and Ni(dmgH)2 as a co-catalyst, exhibits enhanced photoresponse, accelerated charge transfer, facilitating the separation of electrons and holes, and efficient hydrogen evolution under visible light. It was found that the catalytic efficiency of CdS was significantly influenced by the loading amount of Ni(dmgH)2. An optimum activity was achieved at 10 wt% Ni(dmgH)2, resulting a stable hydrogen generation rate of 32.744 mmol h−1 g−1. This rate is nearly 98 times higher than that of bare CdS under similar conditions, indicating that Ni(dmgH)2 can be a highly efficient noble-metal-free co-catalyst for photocatalytic hydrogen evolution with CdS. The mechanism for the hydrogen evolution of the Ni(dmgH)2/CdS composites was also proposed. This study demonstrates that the combination CdS semiconductor with small proportion of transition-metal-based co-catalyst may provide a reliable platform for a stable, earth-abundant, and low-cost system for solar-to-hydrogen conversion, paving the way for promising advancements in green energy research.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Colloids and Surfaces A: Physicochemical and Engineering Aspects
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.