Intensification of anodic charge transfer by contaminant degradation for efficient H2 production

Abstract

Hydrogen (H₂) production from electrocatalytic water splitting is at present limited by the sluggish oxygen evolution reaction (OER). Breakthroughs in low overpotential and stable anodic reactions are urgently needed to complement the rapid advancements in H₂ production. Using nickel (Ni)-based catalysts as an example, we intensified charge transfer on a nickel phosphide (Ni₂P) anode for efficient H₂ production using substitution of contaminant degradation for the OER. Based on X-ray photoelectron spectroscopy (XPS) and in situ Raman spectroscopy, we confirmed that a decreased two-electron-transfer pathway was responsible for the superior formate oxidation, whereas the formation of the desired oxidation state of Ni^III accounted for the efficient urea degradation. Both scenarios were beneficial for accelerating charge transfer across the interface between the anode and electrolyte, thus achieving high H₂ production efficiency at low voltage. A voltage of only 1.40 V supported currents of 12.5 and 6.0 mA in urea- and formate-containing solutions, respectively, which reached 150 and 60 mA after the voltage was increased to 1.70 V, several times higher than that under basic conditions.