Methanol steam reforming (MSR) is a promising technology for in situ hydrogen production, while the mechanistic role of zinc in the widely used Cu/ZnO/Al2O3 catalyst remains ambiguous. Electronic metal-support interactions (EMSIs) are generally applied for modulating active sites in such heterogeneous catalysts, offering opportunities to optimize energy conversion processes. Here, we revealed that a dynamic EMSI between Cu and ZnO enhances catalytic performance by constructing ZnOx/Cu interfaces, facilitating bidirectional electron transfer between ZnOx and Cu. The electron transfer from ZnOx to Cu mitigates overoxidation of Cu0 to Cu+ during water activation, thereby improving water activation efficiency, while the electron transfer back to ZnOx accelerates the reduction of Cu+ back to Cu0, promoting dehydrogenation of reactive formate at the ZnOx/Cu interface, the rate-determining step at low temperatures. Thus, we establish a dual role for the EMSI-induced ZnOx/Cu interface in stabilizing active intermediates and facilitating redox cycling. These findings provide insights into the precise regulation of catalytic active sites via EMSI engineering, offering guidance for high-efficiency catalysts design for sustainable energy conversion.
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