Molecule-Copper Interface for Efficient Electrochemical CO<sub>2</sub>-to-Ethylene in Acidic Media.
basic_science · Level V
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- Record sourced from PubMed, PMID 41950078.
- Also identified by DOI 10.1021/acs.nanolett.6c00241.
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Abstract
Acidic electrochemical CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) offers an attractive route to store intermittent renewables as valuable chemicals with high carbon efficiency but suffers from low selectivity due to predominant hydrogen evolution reaction. Utilizing concentrated alkali cations steers the acidic CO<sub>2</sub>RR to multicarbon (C<sub>2+</sub>) products but leads to salt precipitation. Here we report a molecular tuning strategy to facilitate acidic CO<sub>2</sub>RR to ethylene under a low K<sup>+</sup> concentration by modifying tetraphenylporphyrin-based molecules onto a Cu surface. At 200 mA cm<sup>-2</sup>, we achieve a record ethylene Faradaic efficiency (FE) of 53% on 5,10,15,20-tetraphenyl-21<i>H</i>,23<i>H</i>-porphine zinc functionalized Cu catalysts (a 1.2× improvement compared to the best reports at above 100 mA cm<sup>-2</sup> under an acidic electrolyte having a low alkali cation concentration) and a high C<sub>2+</sub> FE of 85%, as well as a high CO<sub>2</sub> single-pass utilization of 72%. This work presents a catalyst design strategy for efficient acidic CO<sub>2</sub>-to-ethylene electrolysis under low alkali-cation availability.