Journal
RSC ADVANCES
Volume 12, Issue 15, Pages 9051-9057Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ra00099g
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This paper presents the synthesis of nickel cobalt phosphide microstructure with high electrocatalytic activity and stability for hydrogen and oxygen evolution reactions in alkaline electrolyte. The introduction of cobalt and phosphorus atoms reduces the reaction barrier and improves electron transfer ability.
The development of low-cost, high-efficiency, and stable bifunctional electrocatalysts for large-scale water electrolysis is very important for the sustainable development of energy. In this paper, the nickel cobalt phosphide (CoNiP) microstructure was prepared by the in situ growth-ion exchange-phosphating method. Due to the flake structure and the synergistic effect of the bimetal, the synthesized CoNiP microstructure exhibited high electrocatalytic activity and stability for hydrogen and oxygen evolution in alkaline electrolyte. The optimized CoNiP showed low overpotential of 116 mV at 10 mA cm(-2) for hydrogen evolution reaction and 400 mV at 50 mA cm(-2) for oxygen evolution reaction in KOH solution. In addition, it exhibited long-term stability at a high constant current density of 100 mA cm(-2) for 48 hours at room temperature and for 65 hours at 80 degrees C without significant degradation. Theoretical results showed that the introduction of Co and P atoms could reduce the reaction barrier and improve the electron transfer ability. This work provides a simple and economical way for the synthesis of electrocatalytic bimetal phosphide catalysts.
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