Blaž Tomc, Mitja Kostelec, Matic Plut, Primož Šket, Matjaž Finšgar, Martin Šala, Mejrema Nuhanović, Francisco Ruiz‐Zepeda, Dušan Strmčnik, Marjan Bele, Nejc Hodnik
Pulsed electrolysis is known to enhance the stability of electrochemical CO 2 reduction (ECO 2 R) on copper, yet the mechanistic origin of this effect remains poorly understood. Using identical-location electron microscopy in combination with operando impedance spectroscopy, we show that pulsed operation induces continuous and dynamic restructuring of the copper surface. Over 23 h of electrolysis, the catalyst evolved from its initial morphology into a grain-like architecture decorated with dendritic features enriched in high-index facets. This structural evolution was accompanied by a steady increase in the ethylene-to-hydrogen selectivity ratio. Quantitative analysis of the electrolyte during pulsed electrolysis revealed an approximately 30-fold increase in dissolved copper species compared to static operation, identifying redirected dissolution–redeposition of copper as the central mechanistic pathway by which pulsing governs morphology evolution and, consequently, ECO 2 R selectivity. ● Pulsed CO₂ electroreduction redirects copper dissolution–redeposition dynamics. ● Operando EIS and IL-SEM link copper restructuring to stability and selectivity. ● Pulsing sustains ethylene selectivity for one day without activity loss. ● Oxidation–reduction cycles induce dendritic copper growth. ● Stability arises from controlled catalyst instability, not structural suppression.