The electrochemical CO2 reduction reaction (CO2 RR) in aqueous solution inevitably competes with the hydrogen evolution reaction (HER), which results in a difficult separation of the complex products. In this study, a Fe/N/C catalyst derived from Fe(SCN)3 (labelled SMFeSCN) revealed a high CO Faradaic efficiency (FE) of 99 % at a moderate overpotential of 0.44 V. CO2 RR and HER competed with each other for active sites on Fe/N/C. The high FE for CO production originated from the high content of micropores on the catalyst, which could suppress the side reactions by increasing CO2 uptake. More importantly, excellent tolerance towards metal-ion impurities was demonstrated in Fe/N/C, which was primarily owing to the high specific surface area with scattered active sites. Thus, the Fe/N/C catalyst showed good activity for CO2 RR without influencing the electrolyte purity, thus raising the possibility of its practical application.
Keywords: CO2 reduction; Fe/N/C; electrochemistry; micropores; selectivity.
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