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Electrochemical conversion of carbon dioxide (CO2) into high-value chemical products has become a dramatic research area because of the efficient exploitation of carbon resources and simultaneous reduction of atmospheric CO2 concentration. Herein, we report the bismuth-based catalyst in the efficient electroconversion of CO2 for the formation of formate with a maximum Faradaic efficiency of 91% and partial current density of ∼8 mA cm–2 at −0.9 V vs RHE. Experimental and theoretical results show that the bismuth–oxygen structure of bismuth oxides is beneficial for a higher adsorption of CO2 and the rate-determining route switching from the initial fast pre-equilibrium of electron transfer process to the subsequent hydrogenation step, accompanied by a lower free energy of intermediate. This work may offer valuable insights into crystal structure engineering to achieve efficient electrocatalysts for selective CO2 reduction toward generation of valuable products.
Deng et al. (2019) studied this question.