Cobalt phosphide-based electrocatalysts: synthesis and phase catalytic activity comparison for hydrogen evolution

Abstract

Cobalt phosphides have been used as promising electrocatalysts for catalyzing the hydrogen evolution reaction (HER) in acidic aqueous solutions. In order to further explore the influence of phase structure and support effect on the catalytic activity for HER, herein, a series of cobalt phosphide-based electrocatalysts, including Co₂P, CoP, Co₂P/CNTs, CoP/CNTs, Co₂P/NCNTs and CoP/NCNTs, were synthesized successfully via a facile thermal decomposition approach. The crystalline phase can be controlled by changing the phosphide source species. When the phosphide source was trioctylphosphine, CoP-based catalysts were obtained. However, Co₂P-based catalysts can be obtained by using triphenylphosphine as the phosphide source. Then the phase catalytic activity and stability of the as-synthesized cobalt phosphide-based catalysts for hydrogen evolution were compared. The results show that the catalytic activity followed the order CoP/NCNTs > Co₂P/NCNTs > CoP/CNTs > Co₂P/CNTs > CoP > Co₂P, which can be attributed to the different atomic ratios of Co to P, the strong interaction between cobalt phosphide and carbon species and the doping of N atoms into CNTs. Our studies indicate that the HER catalytic efficiency of transition metal phosphide catalysts can be improved significantly by adjusting active phase and carbon species structures.