Developing efficient platinum group metal (PGM)-free catalysts for the hydrogen evolution reaction (HER) in alkaline electrolytes is crucial for anion-exchange membrane water electrolyzers (AEMWEs) to produce low-cost hydrogen. Despite the promising activity often observed in aqueous electrolytes on HER catalysts, catalytic performance in the actual AEMWE cathode environment is primarily limited by insufficient water and proton supply under desirable dry-cathode operating conditions. Herein, we develop a Re2P/MoP heterostructure catalyst that overcomes these mass-transport and interfacial limitations, enabling a high-performance PGM-free cathode in AEMWEs. Relative to the individual Re2P and MoP counterparts, the Re2P/MoP heterostructure catalyst exhibits significantly lower HER overpotentials. Electrochemical measurements and theoretical calculations suggest that coupling between Re2P and MoP can regulate the electronic structure of each component, thereby optimizing hydrogen adsorption and water dissociation kinetics and enhancing intrinsic HER activity. Moreover, the Re2P/MoP heterostructure can populate interfacial water molecules and form a connected/dynamic hydrogen-bond network near the catalyst/electrolyte interface, thereby facilitating water replenishment and proton/hydroxide transfer, which are essential for high-current-density operations even at low water content. The assembled Re2P/MoP||NiFe foam PGM-free membrane electrode assembly (MEA) delivers an industrial-level current density of 1.0 and 3.0 A cm-2 at 1.73 and 1.95 V, respectively, comparable to the PtRu/C||IrOx PGM benchmark. The PGM-free MEA can maintain stable operation at 2.0 A cm-2 for over 1000 h, making it one of the most promising MEAs for AEMWEs. This work emphasizes that catalyst/electrolyte interface engineering is critical for achieving high-performance electrochemical systems.
Liang et al. (2026) studied this question.