The scaling-up of electrochemical CO reduction requires circumventing the CO loss as carbonates under alkaline conditions. Zero-gap cell configurations with a reverse-bias bipolar membrane (BPM) represent a possible solution, but the catalyst layer in direct contact with the acidic environment of a BPM usually leads to H evolution dominating. Here we show that using acid-tolerant Ni molecular electrocatalysts selective (>60%) CO reduction can be achieved in a zero-gap BPM device using a pure water and CO feed. At a higher current density (100 mA cm), CO selectivity decreases, but was still >30%, due to reversible product inhibition. This study demonstrates the importance of developing acid-tolerant catalysts for use in large-scale CO reduction devices.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074102 | PMC |
http://dx.doi.org/10.1021/jacs.1c13024 | DOI Listing |
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