Breaking the Activity–Hydrophobicity Trade-off via Fluorinated Silane-Modified Cu for Efficient CO2-to-C2 Conversion
Dong Hyeon Kim a, Hyun Su Kim a, Youngha Kweon a, Ara Cho a, Minho Kim a, Min Hyung Lee a
a Kyunghee university
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS Fall 2026 Conference (MATSUSFall26)
E4 Advances and Innovations in (Photo)Electrochemical CO2 and N2 Conversion and Water Splitting
Palma, Spain, 2026 October 26th - 30th
Organizer: Guillermo Díaz-Sainz
Poster, Dong Hyeon Kim, 530
Publication date: 22nd July 2026

The electrochemical reduction of CO2 to multi-carbon products on Cu catalysts is often limited by the difficulty of maintaining a hydrophobic reaction interface without blocking catalytically active sites. Here, we demonstrate a vapor-phase fluorinated silane modification of Cu that provides a hydrophobic yet electrochemically accessible interface for enhanced C2 production under high-current-density flow-cell conditions. The modified Cu electrode achieves a C2 Faradaic efficiency of approximately 75% and a C2 partial current density of 122 mA cm-2, exceeding those of pristine Cu while maintaining a comparable total current density. Experimental characterization, together with density functional theory and classical molecular dynamics simulations, indicates that the fluorinated silane layer enhances *CO retention, suppresses CO desorption, and reorganizes the interfacial water environment, thereby promoting C-C coupling and C2 product formation. The hydrophobic interface also contributes to stable CO2 reduction during prolonged operation by preserving a favorable gas-liquid-solid reaction environment. These results highlight vapor-phase fluorinated silane modification as an effective approach for controlling the Cu/electrolyte interface and improving multi-carbon selectivity without compromising catalytic accessibility.

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