Youqi Zhang, Yong Zhang, Ying Qi, Haiqing Zhou, Yan Zhang, Yan Zhang, Jiayi Hu, Wenqi Ma, Fang Yu, Ligang Feng, Fang Yu
Glycerol electrooxidation emerges as an electrochemically cogent paradigm to supplant the sluggish oxygen evolution reaction in water electrolysis. However, most non-precious catalysts still suffer from large electrolytic voltage and poor stability when operating at industrially relevant current densities. Here, we develop a heterostructure catalyst by immobilizing abundant cobalt phosphide (CoP) nanoparticles on conductive cobalt nitride (Co2N0.67) support, which results in the construction of a strong built-in electric field at the heterointerface. The optimal catalyst demonstrates effective bifunctional catalytic performance, yielding an industrial-level current density of 500 mA cm−2 at low potentials of −141 mV and 1.44 V for hydrogen evolution and glycerol oxidation, respectively. When integrated into a flow cell system, this catalyst maintains good stability for 260 hours at 1 A cm−2 (1.67 V) while preserving > 85% Faradaic efficiency for formate production. Both theoretical and experimental analyses substantiate that the built-in electric field drives directional electron transfer from CoP to Co2N0.67, forming an electron-deficient region at the CoP interface that enriches OH* species, and an electron-rich region at the Co2N0.67 interface, facilitating hydrogen adsorption, thereby expediting the glycerol and H* co-adsorption process. Multiple in-situ spectroscopic characterizations verify the existence of a combined direct/indirect oxidation mechanism for glycerol electrooxidation. This discovery sets the stage for low-voltage hydrogen production by hybrid water splitting using the excess electrical power whenever and wherever available. The electrochemical oxidation of glycerol is a promising strategy for sustainable clean energy, although it still faces several challenges. Here, the authors report a catalyst that can spontaneously generate a strong built-in electric field, thereby simultaneously enhancing both hydrogen evolution and glycerol oxidation reaction processes for low-voltage hydrogen production.