As a traditional method of ammonia (NH3 ) synthesis, Haber-Bosch method expends a vast amount of energy. An alternative route for NH3 synthesis is proposed from nitrate (NO3 - )… Click to show full abstract
As a traditional method of ammonia (NH3 ) synthesis, Haber-Bosch method expends a vast amount of energy. An alternative route for NH3 synthesis is proposed from nitrate (NO3 - ) via electrocatalysis. However, the structure-activity relationship remains challenging and requires in-depth research both experimentally and theoretically. Here an N-coordinated Cu-Ni dual-single-atom catalyst anchored in N-doped carbon (Cu/Ni-NC) is reported, which has competitive activity with a maximal NH3 Faradaic efficiency of 97.28%. Detailed characterizations demonstrate that the high activity of Cu/Ni-NC mainly comes from the contribution of Cu-Ni dual active sites. That is, (1) the electron transfer (Ni → Cu) reveals the strong electron interaction of Cu-Ni dual-single-atom; (2) the strong hybridizations of Cu 3d-and Ni 3d-O 2p orbitals of NO3 - can accelerate electron transfer from Cu-Ni dual-site to NO3 - ; (3) Cu/Ni-NC can effectively decrease the rate-limiting step barriers, suppress N-N coupling for N2 O and N2 formation and hydrogen production.
               
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