摘要
Structure modulation of transition metal phosphides at the atomic scale can significantly modify their catalytic properties. Herein, stacking faults abundant Ni 2 P/Co 2 P electrocatalysts with outstanding bifunctional oxygen evolution and hydrogen evolution property have been prepared. The stacking faults are formed by slow dissolution of Ni substrate by Mo 6+ and further redeposition of Ni 2+ during the growth of Co(OH)F crystals. Unprecedentedly, the distinct mechanistic etching-redeposition pathway dictated by the stacking faults, heterostructures and crystal lattice deformation leads to lattice expansion of Co 2 P and enables preferred reactants adsorption. Electrolysis cell employing Ni 2 P/Co 2 P electrocatalysts as a bifunctional catalyst for both the cathode and the anode delivers a current density of 10 mA cm −2 at a cell voltage of 1.57 V, which is comparable to the integrated Pt/C and IrO 2 counterparts. The exceptional electrocatalytic performance of Co 2 P/Ni 2 P-x%Mo indicates the redeposition mechanism a new methodology to modulate the structure and surface reactivity of electrocatalysts.
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