Abstract
AbstractPhotocatalytic water splitting provides an economically feasible way for converting solar energy into hydrogen. Great efforts have been devoted to developing efficient photocatalysts; however, the surface catalytic reactions, especially for the sluggish oxygen evolution reaction (OER), still remain a challenge, which limits the overall photocatalytic energy efficiency. Herein, we design a Rhn cluster cocatalyst, with Rh0‐Rh3+ sites anchoring the Mo‐doped BiVO4 model photocatalytic system. The resultant photocatalyst enables a high visible‐light photocatalytic oxygen production activity of 7.11 mmol g−1 h−1 and an apparent quantum efficiency of 29.37 % at 420 nm. The turnover frequency (TOF) achieves 416.73 h−1, which is 378 times higher than that of the photocatalyst only with Rh3+ species. Operando X‐ray absorption characterization shows the OER process on the Rh0‐Rh3+ sites. The DFT calculations further illustrate a bifunctional OER mechanism over the Rh0‐Rh3+ sites, in which the oxygen intermediate attacks the Rh3+ sites with assistance of a hydrogen atom transfer to the Rh0 sites, thus breaking the scaling relationship of various oxygen intermediates.
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 callDisclaimer: 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.
