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Electrocatalytic CO2 reduction offers a means to produce value-added multi-carbon products and mitigate CO2 emissions. However, the stability of CO2 electrolyzers for C2+ products has not exceeded 200 h—well below that of CO- and H2-producing electrolyzers—and the most stable systems employ low-conductivity substrates incompatible with scale. Current gas diffusion electrodes (GDEs) become filled with salt precipitate and electrolyte, which limits CO2 availability at the catalyst beyond 30 h. We develop a GDE architecture that is resistant to flooding and maintains stable performance for >400 h. Using a combination of focused ion beam scanning electron microscopy, micro-computed tomography, and a purpose-built array tomography technique, we determine that the enhanced stability is due to a percolating network of polytetrafluoroethylene in the microporous layer that retains hydrophobicity. We scale this approach in an 800 cm2 cell and an 8,000 cm2 stack and transfer >108 C, the largest reported CO2 electrolysis demonstration.
O’Brien et al. (Thu,) studied this question.