Buffering the local pH via single-atomic Mn–N auxiliary sites to boost CO2 electroreduction. Issue 44 (2nd November 2022)

• Record Type: Journal Article
• Authors: Yang, Yan; Tang, Tang; Lyu, Zhen-Hua; Zheng, Li-Rong; Zhang, Qing-Hua; Fu, Jiaju; Hu, Jin-Song
• Is Part Of: Chemical science. Volume 13:Issue 44(2022)
• Page Start: 13172
• Page End: 13177
• Publication Date: 2022-11-02
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d2sc04776d
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : An effective strategy is developed to regulate the local microenvironment of single atomic Ni–N–C sites for accelerating CO2 to CO conversion. The Ni/Mn–N–C catalysts shows a CO faradaic efficiency of 96.6% due to the accelerated reaction kinetics. Abstract : Electrocatalytic CO2 reduction driven by renewable energy has become a promising approach to rebalance the carbon cycle. Atomically dispersed transition metals anchored on N-doped carbon supports (M-N-C) have been considered as the most attractive catalysts to catalyze CO2 to CO. However, the sluggish kinetics of M-N-C limits the large-scale application of this type of catalyst. Here, it is found that the introduction of single atomic Mn–N auxiliary sites could effectively buffer the locally generated OH − on the catalytic interface of the single-atomic Ni–N–C sites, thus accelerating proton-coupled electron transfer (PCET) steps to enhance the CO2 electroreduction to CO. The constructed diatomic Ni/Mn–N–C catalysts show a CO faradaic efficiency of 96.6% and partial CO current density of 13.3 mA cm −2 at −0.76 V vs. RHE, outperforming that of monometallic single-atomic Ni–N–C or Mn–N–C counterparts. The results suggest that constructing synergistic catalytic sites to regulate the surface local microenvironment might be an attractive strategy for boosting CO2 electroreduction to value-added products.