Oxygen vacancies enhanced electrocatalytic water splitting of P-FeMoO4 initiated via phosphorus doping
Transition metal oxides (TMOs) are abundant and cost-effective materials. However, poor conductivity and low intrinsic activity limit their application in electrolyzed water catalysts. Herein, we prepared P-FeMoO 4 in situ on nickel foam (P-FMO@NF) by phosphorylation-modified FeMoO 4 to optimize its electrocatalytic properties. Interestingly, phosphorus doping is accompanied by the generation of oxygen vacancies and surface phosphates . Oxygen vacancies accelerated Mo dissolution during the oxygen evolution reaction (OER), leading to the rapid reconfiguration of P-FMO@NF to FeOOH and regulating the electronic structure of P-FMO@NF. The formation of phosphates is caused by the substitution of some molybdates with phosphates, which further increases the amount of oxygen vacancies . Hence, the OER overpotential of P-FMO@NF at a current density of 10 mA cm −2 is only 206 mV, and the hydrogen evolution reaction (HER) overpotential is 154 mV. It was assembled into a water splitting cell with a voltage of just 1.59 V at 10 mA cm −2 and shows excellent stability over 50 h. These excellent electrocatalytic properties are mainly attributed to the oxygen vacancies , which improve the interfacial charge transfer properties of the catalysts. This study provides new insights into phosphorus doping and offers a new perspective on the design of electrocatalysts.
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