Real‐time Monitoring Reveals Dissolution/Redeposition Mechanism in Cu Nanocatalysts during the Initial Stages of the CO2 Reduction Reaction

Size, morphology and surface sites of electrocatalysts have a major impact on their performance. Understanding how, when, and why these parameters change under operating conditions is of uttermost importance for designing stable, active, and selective catalysts. Here, we study the reconstruction of a Cu-based nanocatalysts during the startup phase of the electrochemical CO 2 reduction reaction by combining results from electrochemical in-situ transmission electron microscopy with operando X-ray absorption spectroscopy. We reveal that dissolution followed by redeposition, rather than coalescence, is the mechanism responsible for the size increase and morphology change of the electrocatalyst. Furthermore, we point out the key role played by the formation of copper oxides in the process. Understanding of the underlying processes opens a pathway to rational design of Cu electro (re)deposited catalysts and to stability improvement for catalysts fabricated by other methods.