摘要
Highly efficient and stable electrocatalysts toward hydrogen evolution reaction (HER) under large current density are essential for alkaline water splitting. Herein, an active and durable CoMoO 4 -based HER electrocatalyst is developed, with a coupling of surface phosphorization and polypyrrole (PPy) modification to accelerate water dissociation and prevent alkaline corrosion during HER process, ensuring great catalyst stability. The prepared PPy-CoMoO 4 /P@NF catalyst achieves perfect HER activity with only 242.1 mV overpotential at the industrial current density of 1000 mA·cm −2 in 1.0 M KOH as well as a low Tafel slope of 39.0 mV dec −1 . Moreover, PPy modification greatly inhibits the alkaline corrosion and the catalyst exhibits stable operation for 100 h at 1000 mA·cm −2 with a conservation rate of 98.5 %. Electrochemical tests and theoretical calculations reveal that the multiple interfaces formed by CoMoO 4 /CoP/PPy significantly reduce the energy barrier of hydrolysis and improve the interfacial adsorption of H ads . Meanwhile, the surface phosphating changes the Gibbs free energy of rate-determining step (RDS) from −0.54 to −0.29 eV, optimizing the energy barriers for hydrogen adsorption-desorption. Remarkably, an electrolyzer with PPy-CoMoO 4 /P @NF as cathode catalyst only needs a cell voltage of 1.92 V at 1000 mA cm −2 for overall water splitting. This study provides an effective way to develop highly efficient and stable HER catalysts toward industrial water splitting.
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