Shilei Wei , Hang Hua , Qingxuan Ren , Jingshan Luo
{"title":"Enhanced electrochemical carbon dioxide reduction in membrane electrode assemblies with acidic electrolytes through a silicate buffer layer","authors":"Shilei Wei , Hang Hua , Qingxuan Ren , Jingshan Luo","doi":"10.1016/S1872-2067(24)60129-4","DOIUrl":null,"url":null,"abstract":"<div><div>The electrochemical reduction of CO<sub>2</sub> holds considerable promise in combating global climate change while yielding valuable chemical commodities. Membrane electrode assemblies operating within acidic electrolyte have exhibited noteworthy advancements in CO<sub>2</sub> utilization efficiency, albeit encountering formidable competition from the hydrogen evolution reaction. In our investigation, we introduced a silicate buffer layer, which yielded exceptional outcomes even using strong acid electrolyte. Notably, our approach yielded a CO Faradic efficiency of 90% and reached a substantial current density of 400 mA cm<sup>–2</sup>. Furthermore, our system displayed remarkable stability over a 12-hour duration, and achieved a high single-pass-conversion efficiency of 67%. Leveraging <em>in-situ</em> Raman analysis, we attributed these performance enhancements to the augmented CO<sub>2</sub> adsorption and localized alkaline environment facilitated by the incorporation of the silicate buffer layer. We think the addition of buffer layer to adjust the microenvironment is essential to achieve high performance and keep stable in acid condition.</div></div>","PeriodicalId":9832,"journal":{"name":"Chinese Journal of Catalysis","volume":"66 ","pages":"Pages 139-145"},"PeriodicalIF":15.7000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872206724601294","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
The electrochemical reduction of CO2 holds considerable promise in combating global climate change while yielding valuable chemical commodities. Membrane electrode assemblies operating within acidic electrolyte have exhibited noteworthy advancements in CO2 utilization efficiency, albeit encountering formidable competition from the hydrogen evolution reaction. In our investigation, we introduced a silicate buffer layer, which yielded exceptional outcomes even using strong acid electrolyte. Notably, our approach yielded a CO Faradic efficiency of 90% and reached a substantial current density of 400 mA cm–2. Furthermore, our system displayed remarkable stability over a 12-hour duration, and achieved a high single-pass-conversion efficiency of 67%. Leveraging in-situ Raman analysis, we attributed these performance enhancements to the augmented CO2 adsorption and localized alkaline environment facilitated by the incorporation of the silicate buffer layer. We think the addition of buffer layer to adjust the microenvironment is essential to achieve high performance and keep stable in acid condition.
期刊介绍:
The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.