Tuning C₁/C₂ Selectivity of CO₂ Electrochemical Reduction over in‐Situ Evolved CuO/SnO₂ Heterostructure

Abstract

Heterostructured oxides with versatile active sites, as a class of efficient catalysts for CO₂ electrochemical reduction (CO₂ ER), are prone to undergo structure reconstruction under working conditions, thus bringing challenges to understanding the reaction mechanism and rationally designing catalysts. Herein, we for the first time elucidate the structural reconstruction of CuO/SnO₂ under electrochemical potentials and reveal the intrinsic relationship between CO₂ ER product selectivity and the in situ evolved heterostructures. At -0.85 V_RHE , the CuO/SnO₂ evolves to Cu₂ O/SnO₂ with high selectivity to HCOOH (Faradaic efficiency of 54.81 %). Mostly interestingly, it is reconstructed to Cu/SnO_2-x at -1.05 V_RHE with significantly improved Faradaic efficiency to ethanol of 39.8 %. In situ Raman spectra and density functional theory (DFT) calculations reveal that the synergetic absorption of *COOH and *CHOCO intermediates at the interface of Cu/SnO_2-x favors the formation of *CO and decreases the energy barrier of C-C coupling, leading to high selectivity to ethanol.