化学
乙烯
催化作用
氧烷
选择性
介孔材料
法拉第效率
电极
光谱学
无机化学
电化学
物理化学
有机化学
量子力学
物理
作者
Zhouyang Yin,Jiaqi Yu,Zhenhua Xie,Shen‐Wei Yu,Liyue Zhang,Tangi Akauola,Jingguang G. Chen,Wenyu Huang,Long Qi,Sen Zhang
摘要
A hybrid catalyst with integrated single-atom Ni and nanoscale Cu catalytic components is reported to enhance the C–C coupling and ethylene (C2H4) production efficiency in the electrocatalytic CO2 reduction reaction (eCO2RR). The single-atom Ni anchored on high-surface-area ordered mesoporous carbon enables high-rate and selective conversion of CO2 to CO in a wide potential range, which complements the subsequent CO enrichment on Cu nanowires (NWs) for the C–C coupling to C2H4. In situ surface-enhanced infrared absorption spectroscopy (SEIRAS) confirms the substantially improved CO enrichment on Cu, once the incorporation of single-atom Ni occurs. Also, in situ X-ray absorption near-edge structure (XANES) demonstrates the structural stability of the hybrid catalyst during eCO2RR. By modulating hybrid compositions, the optimized catalyst shows 66% Faradaic efficiency (FE) in an alkaline flow cell with over 100 mA·cm–2 at −0.5 V versus reversible hydrogen electrode, leading to a five-order enhancement in C2H4 selectivity compared with single-component Cu NWs.
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