Comparative Study of Different Polymeric Binders in Electrochemical CO Reduction

Abstract

Electrochemical reduction of carbon monoxide offers a possible route to produce valuable chemicals (such as acetate, ethanol or ethylene) from CO 2 in two consecutive electrochemical reactions. Such deeply reduced products are formed via the transfer of 4−6 electrons per CO molecule. Assuming similar-sized CO 2 and CO electrolyzers, 2−3-times larger current densities are required in the latter case to match the molar fluxes. Such high reaction rates can be ensured by tailoring the structure of the gas diffusion electrodes. Here, the structure of the cathode catalyst layer was systematically varied using different polymeric binders to achieve high reaction rates. Simple linear polymers, bearing the same backbone but different functional groups were compared to highlight the role of different structural motifs. The comparison was also extended to simple linear, partially fluorinated polymers. Interestingly, in some cases similar results were obtained as with the current state-of-the-art binders. Using different surface-wetting characterization techniques, we show that the hydrophobicity of the catalyst layer�provided by the binder� is a prerequisite for high-rate CO electrolysis. The validity of this notion was demonstrated by performing CO electrolysis experiments at high current density (1 A cm −2 ) for several hours using PVDF as the catalyst binder.