Electrocatalytic Reduction of Low Concentrations of CO2Gas in a Membrane Electrode Assembly Electrolyzer

Authors
Kim, D.Choi, W.Lee, H.W.Lee, S.Y.Choi, Y.Lee, D.K.Kim, W.Na, J.Lee, U.Hwang, Y.J.Won, D.H.
Issue Date
2021-10
Publisher
American Chemical Society
Citation
ACS Energy Letters, v.6, no.10, pp.3488 - 3495
Abstract
The direct conversion of low concentrations of CO2 is an essential approach, considering the expensive gas conditioning process for pure CO2, but has not yet been intensely studied in a membrane electrode assembly (MEA) electrolyzer. Herein, we explored the CO2 reduction with various CO2 concentrations in a zero-gap MEA electrolyzer and found that suppressing the hydrogen evolution reaction (HER) became more critical at low concentrations of CO2. We demonstrate that a Ni single-atom (Ni-N/C) catalyst exhibits a high tolerance toward low CO2 partial pressure (PCO2) because of the intrinsically large activation energy of the HER. Ni-N/C outperformed the CO productivity of Ag nanoparticles, especially at low concentrations of CO2 in the zero-gap MEA. When the PCO2 was lowered from 1.0 to 0.1 atm, Ni-N/C maintained >93% of CO Faradaic efficiency (FECO), but Ag nanoparticles showed a decrease in FECO from 94% to 40%. Furthermore, on the basis of a computational fluid dynamics simulation, we developed extrinsic operating conditions controlling the water transfer from the anolyte to the catalyst layer and improved CO selectivity at low CO2 concentrations in the MEA electrolyzer. ? 2021 American Chemical Society.
Keywords
Activation energy; Binary alloys; Catalyst selectivity; Cobalt alloys; Computational fluid dynamics; Electrodes; Electrolytic cells; Ethanolamines; Metal nanoparticles; More electric aircraft; Silver nanoparticles; CO2 concentration; CO2 reduction; Conditioning process; Direct conversion; Electrocatalytic reduction; Electrolyzers; Gas conditioning; Hydrogen evolution reactions; Low concentrations; Membrane electrode assemblies; Carbon dioxide
ISSN
2380-8195
URI
https://pubs.kist.re.kr/handle/201004/116346
DOI
10.1021/acsenergylett.1c01797
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KIST Article > 2021
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