An efficient cerium dioxide incorporated nickel cobalt phosphide complex as electrocatalyst for All-pH hydrogen evolution reaction and overall water splitting.

J Colloid Interface Sci

School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 100049, PR China; Binzhou Institute of Technology, Binzhou 256606, PR China; National Engineering Laboratory for VOCs Pollution Control Material & Technology Research Center for Environment Material and Pollution Control Technology, University of Chinese Academy of Sciences, Beijing 100049, PR China. Electronic address:

Published: January 2024

Transition metal phosphides (TMPs) have been considered as potential electrocatalysts with adjustable valence states, metal characteristics, and phase diversity. However, it is necessary but remains a major challenge to obtain efficient and durable TMPs catalysts, which can realize efficiently for not only all-pH hydrogen evolution reaction (HER), but also oxygen evolution reaction (OER). Hence, cerium dioxide incorporated nickel cobalt phosphide growth on nickel foam (CeO/NiCoP) is fabricated by hydrothermal and phosphating reaction. CeO/NiCoP shows excellent activity for all-pH HER (overpotentials of 48, 58 and 72 mV in alkaline, neutral and acidic solution at the current density of 10 mA cm), and has a small OER overpotential (231 mV @ 10 mA cm). Moreover, the voltage of overall water splitting in alkaline solution and simulated seawater electrolyte is only 1.46 and 1.41 V (10 mA cm), respectively, coupled with outstanding operational stability and corrosion resistance. Further mechanism research shows that CeO/NiCoP possesses rich heterointerfaces, which serves more exposed active sites and possesses a promising superhydrophilic and superaerophobic surface. Density functional theory calculations manifest that CeO/NiCoP has appropriate energy for intermediates of reactions. This work provides a deep insight into the CeO/NiCoP catalyst for high-performance water/seawater electrolysis.

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http://dx.doi.org/10.1016/j.jcis.2023.09.144DOI Listing

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