A supported Ni2 dual-atoms site hollow urchin-like carbon catalyst for synergistic CO2 electroreduction.

By adjusting the synthesis variation of hollow urchin-like Ni-NC(HU)-x catalyst, the content of pyridinic-N was adjusted, and the dual-atoms site was formed. Ni-NC(HU)-50 showed the best catalytic performance with FE CO of 97.2% at −0.9 V vs. RHE and sustains above 95% within 50 h. [Display omitted] Dual-atoms catalysts (DACs), while inheriting the advantages of maximum atom utilization ratio and excellent selectivity of single-atom catalysts (SACs), can better enhance the catalytic activity through the synergy of adjacent atoms. Therefore, DACs are considered to be very potential catalysts for CO 2 to CO conversion. Its catalytic activity is greatly influenced by the coordination environment and morphology. Here, hollow urchin-like Ni N C catalysts (Ni-NC(HU)-x, x = 100, 50, 25, 0) were synthesized using urchin-like nickel particles as template. By adjusting the amount of additional nitrogen source, the percentage content of pyridinic-N was adjusted as well as further affecting the coordination environment. Among them, Ni-NC(HU)-50, which had the highest content of pyridinic-N, formed a dual-atoms coordination structure and had the best catalytic performance that the CO Faradaic efficiency (FE CO) reached 97.2 % at −0.9 V vs. reversible hydrogen electrode (RHE) and sustained above 95 % within 50 h. In-situ attenuated total reflectance surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) and density functional theory (DFT) calculations showed that Ni-NC(HU)-50 exhibited the best performance of CO 2 reduction reaction (CO 2 RR) by lowering the *COOH formation free energy barrier and its favorable dual desorption mechanism of *CO L and *CO B. [ABSTRACT FROM AUTHOR]