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用于CO还原反应的膜电极组件电解槽中阴极表面碱金属阳离子的定量分析与调控

Quantitative Analysis and Manipulation of Alkali Metal Cations at the Cathode Surface in Membrane Electrode Assembly Electrolyzers for CO Reduction Reactions.

作者信息

Kato Shintaro, Ito Shotaro, Nakahata Shoko, Kurihara Ryo, Harada Takashi, Nakanishi Shuji, Kamiya Kazuhide

机构信息

Research Center for Solar Energy Chemistry, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka, Osaka, 560-8531, Japan.

Innovative Catalysis Science Division, Institute for Open and Transdisciplinary Research Initiatives (ICS-OTRI), Osaka University, Suita, Osaka, 565-0871, Japan.

出版信息

ChemSusChem. 2024 Nov 25;17(22):e202401013. doi: 10.1002/cssc.202401013. Epub 2024 Aug 7.

DOI:10.1002/cssc.202401013
PMID:38899491
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11587695/
Abstract

The stable operation of the CO reduction reaction (CORR) in membrane electrode assembly (MEA) electrolyzers is known to be hindered by the accumulation of bicarbonate salt, which are derived from alkali metal cations in anolytes, on the cathode side. In this study, we conducted a quantitative evaluation of the correlation between the CORR activity and the transported alkali metal cations in MEA electrolyzers. As a result, although the presence of transported alkali metal cations on the cathode surface significantly contributes to the generation of C compounds, the rate of K ion transport did not match the selectivity of C, suggesting that a continuous supply of high amount of K to the cathode surface is not required for C formation. Based on these findings, we achieved a faradaic efficiency (FE) and a partial current density for C of 77 % and 230 mA cm, respectively, even after switching the anode solution from 0.1 M KHCO to a dilute K solution (<7 mM). These values were almost identical to those when 0.1 M KHCO was continuously supplied. Based on this insight, we successfully improved the durability of the system against salt precipitation by intermittently supplying concentrated KHCO, compared with the continuous supply.

摘要

已知膜电极组件(MEA)电解槽中一氧化碳还原反应(CORR)的稳定运行会受到阴极侧碳酸氢盐积累的阻碍,这些碳酸氢盐源自阳极电解液中的碱金属阳离子。在本研究中,我们对MEA电解槽中CORR活性与传输的碱金属阳离子之间的相关性进行了定量评估。结果表明,尽管阴极表面传输的碱金属阳离子的存在对C化合物的生成有显著贡献,但K离子的传输速率与C的选择性不匹配,这表明形成C并不需要持续向阴极表面供应大量的K。基于这些发现,即使将阳极溶液从0.1 M KHCO切换为稀K溶液(<7 mM)后,我们仍分别实现了77%的法拉第效率(FE)和230 mA cm的C的分电流密度。这些值与持续供应0.1 M KHCO时的值几乎相同。基于这一认识,与持续供应相比,我们通过间歇性供应浓KHCO成功提高了系统对盐沉淀的耐久性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/b1be8af6ae76/CSSC-17-e202401013-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/ee4b53dd6439/CSSC-17-e202401013-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/822a4edf5c8f/CSSC-17-e202401013-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/1a9be675d715/CSSC-17-e202401013-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/b94c91fed7db/CSSC-17-e202401013-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/b1be8af6ae76/CSSC-17-e202401013-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/ee4b53dd6439/CSSC-17-e202401013-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/822a4edf5c8f/CSSC-17-e202401013-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/1a9be675d715/CSSC-17-e202401013-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/b94c91fed7db/CSSC-17-e202401013-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f7/11587695/b1be8af6ae76/CSSC-17-e202401013-g006.jpg

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