Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Electrochemical nitrogen reduction reaction (NRR) over nonprecious‐metal and single‐atom catalysts has received increasing attention as a sustainable strategy to synthesize ammonia. However, the atomic‐scale regulation of such active sites for NRR catalysis remains challenging because of the large distance between them, which significantly weakens their cooperation. Herein, the utilization of regular surface cavities with unique microenvironment on graphitic carbon nitride as “subnano reactors” to precisely confine multiple Fe and Cu atoms for NRR electrocatalysis is reported. The synergy of Fe and Cu atoms in such confined subnano space provides significantly enhanced NRR performance, with nearly doubles ammonia yield and 54%‐increased Faradic efficiency up to 34%, comparing with the single‐metal counterparts. First principle simulation reveals this synergistic effect originates from the unique Fe–Cu coordination, which effectively modifies the N2 absorption, improves electron transfer, and offers extra redox couples for NRR. This work thus provides new strategies of manipulating catalysts active centers at the sub‐nanometer scale.
The utilization of regular surface cavities with a unique microenvironment on graphitic carbon nitride as “subnano reactors” can precisely confine multiple Fe and Cu atoms for nitrogen reduction reaction (NRR) electrocatalysis. The synergy of the Fe and Cu atoms in such confined subnano space provides significantly enhanced NRR performance, in terms of much increased ammonia yield and faradic efficiency.