CO2 electroreduction on Cu operates via an alternative chain growth mechanism to form C–C bonds at elevated temperature and pressure

作者：Rafaël E. Vos, Pengfei Sun, Daniel Schauermann, Hassan Javed, Selwyn Hanselman, Gang Fu, Marc T. M. Koper · 发表于：Nature Catalysis · 年份：2025 · DOI：10.1038/s41929-025-01451-1 · 被引用次数：29 · 研究领域：CO2 Reduction Techniques and Catalysts、Catalysts for Methane Reforming、Ammonia Synthesis and Nitrogen Reduction

Abstract Future practical applications of the electrochemical CO 2 reduction reaction will probably involve the use of higher pressures and temperatures. However, most research on the copper-catalysed electrochemical CO 2 reduction reaction—the most widely studied system due to its C–C coupling ability—is typically performed under ambient conditions, and hence the mechanistic conclusions drawn also pertain to those conditions. Using a custom high-pressure, high-temperature electrochemical cell, we show here that on copper electrodes, the C–C coupling mechanism changes from the typical CO dimerization mechanism at low temperatures to a Fischer–Tropsch-like chain growth mechanism at temperatures above 125 °C (also requiring higher pressure). These results show that temperature and pressure are crucial parameters to consider in applied and mechanistic studies of the electrochemical reduction of CO 2 because they can open up alternative reaction pathways and alter known mechanisms.