Intensifying Interfacial Reverse Hydrogen Spillover for Boosted Electrocatalytic Nitrate Reduction to Ammonia

Angew Chem Int Ed Engl. 2025 Jan 7:e202422585. doi: 10.1002/anie.202422585. Online ahead of print.

Abstract

Rational regulation of active hydrogen (*H) behavior is crucial for advancing electrocatalytic nitrate reduction reaction (NO3RR) to ammonia (NH3), yet in-depth understanding of the *H generation, transfer, and utilization remains ambiguous, and explorations for *H dynamic optimization are urgently needed. Herein we engineer a Ni3N nanosheet array intimately decorated with Cu nanoclusters (NF/Ni3N-Cu) for remarkably boosted NO3RR. From comprehensive experimental and theoretical investigations, the Ni3N moieties favors water dissociation to generate *H, and then *H can rapidly transfer to the Cu via unique reverse hydrogen spillover mediating interfacial Ni-N-Cu bridge bond, thus increasing *H coverage on the Cu site for subsequent deoxygenation/hydrogenation. More impressively, such intriguing reverse hydrogen spillover effect can be further strengthened via elegant engineering of the Ni3N/Cu heterointerface with more intimate contact. Consequently, the NF/Ni3N-Cu with Cu nanoclusters intimate anchoring presents record NH3 yield rate of 1.19 mmol h-1 cm-2 and Faradaic efficiency of 98.7% at -0.3 V vs. RHE, being on par with the state-of-the-art ones. Additionally, with NF/Ni3N-Cu as the cathode, a high-performing Zn-NO3- battery can be assembled. This contribution illuminates a novel pathway to optimize *H behavior via distinct reverse hydrogen spillover for promoted NO3RR and other hydrogenation reactions.

Keywords: Active hydrogen; Electrochemical nitrate reduction; Electronic Metal-Support Interaction; reverse hydrogen spillover; zinc-nitrate battery.