Temperature‐Dependent CO<sub>2</sub> Electroreduction over Fe‐N‐C and Ni‐N‐C Single‐Atom Catalysts
Long Lin, Haobo Li, Yi Wang, Hefei Li, Pengfei Wei, Bing Nan, Rui Si, Guoxiong Wang, Xinhe Bao
Abstract
Abstract Reaction temperature is an important parameter to tune the selectivity and activity of electrochemical CO 2 reduction reaction (CO 2 RR) due to different thermodynamics of CO 2 RR and competitive hydrogen evolution reaction (HER). In this work, temperature‐dependent CO 2 RR over Fe‐N‐C and Ni‐N‐C single‐atom catalysts are investigated from 303 to 343 K. Increasing the reaction temperature improves and decreases CO Faradaic efficiency over Fe‐N‐C and Ni‐N‐C catalysts at high overpotentials, respectively. CO current density over Fe‐N‐C catalyst increases with temperature, then gets into a plateau at 323 K, finally reaches the maximum value of 185.8 mA cm −2 at 343 K. While CO current density over Ni‐N‐C catalyst achieves the maximum value of 252.5 mA cm −2 at 323 K, and then drops significantly to 202.9 mA cm −2 at 343 K. Temperature programmed desorption results and density functional theory calculations reveal that the difference of temperature‐dependent variation on CO Faradaic efficiency and current density between Fe‐N‐C and Ni‐N‐C catalysts results from the varied adsorption strength of key reaction intermediates during CO 2 RR.