Key points are not available for this paper at this time.
Regulating competitive reaction pathways to enhance the selectivity of C 2 H 4 production in electrochemical CO 2 reduction reactions is crucial yet remains challenging, primarily due to the limited understanding of the active sites. In this study, we propose oxygen vacancy bridged Cu–Ce pairs to construct an adjustable atomic interface, which enables a Faradaic efficiency of C 2 H 4 as high as 55.6% and stability for 60 h at 300 mA cm –2 . Advanced characterizations revealed that the introduction of Ce causes local lattice distortion, breaking the original symmetric coordination structure and promoting the formation of oxygen vacancies. In situ infrared spectroscopy combined with density functional theory calculations show that the redox ion pairs of synergistic interactions of Ce species and oxygen vacancies can accelerate the *CO protonation through facilitating water dissociation, reduce the energy barrier of asymmetric *CO–*CHO coupling, and improve the Faradaic efficiency of electrocatalytic CO 2 reduction to C 2 H 4 .
Zhang et al. (Thu,) studied this question.