S, Fe dual doped and precisely regulated CoP porous nanoneedle arrays for efficient hydrogen evolution at 3 A cm−2

Transition metal phosphides (TMPs) have been proved as promising catalysts for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). However, CoP has a strong hydrogen adsorption energy, resulting in a slow Heyrovsky step in the HER. Herein, the solid phase FeS is ionized into S and Fe ions and doped into cobalt precursor during the hydrothermal process based on the precipitation dissolution equilibrium principle, and the doping strategy precisely regulated the atomic ratio of metal/P. The optimized S, [email protected] one-dimensional porous nanoneedles structure exhibit excellent HER performance, which only required 82.3 mV and 200.1 mV to achieve 100 mA cm-2 and 3 A cm-2 together with high currents stability for 100 h. It also has better OER performance, with 260 mV reaching 100 mA cm-2. Further simulated industrial test for S, [email protected] in alkaline anion-exchange membrane (AEM) cells show that only 1.75 V is required to attain 500 mA cm-2. Density functional theory (DFT) calculations confirmed that the dual-doping further modulates the electronic structure of CoP, reduces the Gibbs free energy for hydrogen adsorption. This work provides the possibility to further improve the catalytic activity of cobalt phosphide and apply it to industrial applications.