Abstract
AbstractOxygen and hydrogen evolution reactions (OER and HER) are crucial for electrochemical water splitting, which is however hindered by the high cost of noble metal catalysts. Here, we present that by designing the core‐shell distribution of Prussian blue analogues, NiFe‐P@CoFe‐P nanocubes with various shell‐thickness are obtained to unlock the synergy of metal phosphides. The NiFe‐P@CoFe‐P nanocubes display a low overpotential of 248 mV at 10 mA cm−2 and great stability that outperform commercial RuO2 catalyst towards OER. We find that the OER and HER activity of NiFe‐P@CoFe‐P are dependent on the shell thickness, suggesting both the surface and sublayers determine the catalytic performance. Moreover, we demonstrate the water splitting under alkaline condition in an H‐cell powered by commercial photovoltaics using NiFe‐P@CoFe‐P catalyst, which is a promising approach for the conversion of solar energy.
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.