Activation of Transition Metal (Fe, Co and Ni)‐Oxide Nanoclusters by Nitrogen Defects in Carbon Nanotube for Selective CO2 Reduction Reaction

The electrochemical carbon dioxide reduction reaction (CO 2 RR), which can produce value‐added chemical feedstocks, is a proton‐coupled‐electron process with sluggish kinetics. Thus, highly efficient, cheap catalysts are urgently required. Transition metal oxides such as CoO x , FeO x , and NiO x are low‐cost, low toxicity, and abundant materials for a wide range of electrochemical reactions, but are almost inert for CO 2 RR. Here, we report for the first time that nitrogen doped carbon nanotubes (N‐CNT) have a surprising activation effect on the activity and selectivity of transition metal‐oxide (MO x where M = Fe, Ni, and Co) nanoclusters for CO 2 RR. MO x supported on N‐CNT, MO x /N‐CNT, achieves a CO yield of 2.6–2.8 mmol cm −2 min −1 at an overpotential of −0.55 V, which is two orders of magnitude higher than MO x supported on acid treated CNTs (MO x /O‐CNT) and four times higher than pristine N‐CNT. The faraday efficiency for electrochemical CO 2 ‐to‐CO conversion is as high as 90.3% at overpotential of 0.44 V. Both in‐situ XAS measurements and DFT calculations disclose that MO x nanoclusters can be hydrated in CO 2 saturated KHCO 3 , and the N defects of N‐CNT effectively stabilize these metal hydroxyl species under carbon dioxide reduction reaction conditions, which can split the water molecules and provide local protons to inhibit the poisoning of active sites under carbon dioxide reduction reaction conditions.