Gas diffusion electrodes (GDEs) are
extensively used
for high current
density electrochemical CO2 electrolysis (ECO2R), enabled by significantly reducing mass transfer resistance of
CO2 to the catalyst layer. Conventionally, these GDEs are
based upon hydrophobic carbon-based gas-diffusion layers (GDLs) that
facilitate the gas transport; however, these supports are prone to
flood with electrolyte during electrolysis. This potential-induced
flooding, known as electrowetting, is related to the inherent conductivity
of carbon and limits the activity of ECO2R. To investigate
the effect of electrical conductivity more carefully, a GDE is constructed
based on a Cu mesh with a nonconductive microporous GDL applied to
this substrate, the latter composed of a mixture of metal oxide and
polytetrafluoroethylene. With alumina as the metal oxide, a stable
operation is obtained at −200 mA cm–2 with
70% selectivity for ECO2R (with over half toward C2+ products) without flooding as observed by in situ microscopy. On the contrary, with a Vulcan carbon-based GDL, the
initial activity is rapidly lost as severe flooding ensues. It is
reasoned that electrowetting is averted by virtue of the nonconductive
nature of alumina, providing a new perspective on alternative GDL
compositions and their influence on ECO2R performance.