{"title":"铜锡双金属气凝胶合金,用于电还原CO2生成甲酸†","authors":"Baibin Ren, Jing Shao, Hongji Li and Qingming Xu","doi":"10.1039/D4NJ04703F","DOIUrl":null,"url":null,"abstract":"<p >The electrochemical reduction of CO<small><sub>2</sub></small> (CO<small><sub>2</sub></small>RR) enables the conversion of CO<small><sub>2</sub></small> into various value-added hydrocarbons, with formate garnering significant interest due to its high energy density and efficient conversion potential. Although tin (Sn)-based catalysts generally exhibit high selectivity for formate and effectively suppress the hydrogen evolution reaction (HER), the simultaneous presence of low selectivity and current density limits further applications. In this work, a series of bimetallic Cu–Sn aerogel catalysts were synthesized; the Cu–Sn (1 : 1) aerogel catalyst demonstrated superior CO<small><sub>2</sub></small> reduction performance, with higher cathodic reaction activity (35.61 mA cm<small><sup>−2</sup></small>) and a formate faradaic efficiency (FE) exceeding 90%, while maintaining stable CO<small><sub>2</sub></small> selectivity over a period of 7 hours. The high efficiency in generating formate is attributed to the high surface area provided by the bimetallic aerogel, which facilitates CO<small><sub>2</sub></small> transport and product desorption. Additionally, the high-energy interfaces formed during alloying and electronic synergistic effects increase the charge density at active sites. The self-supporting structure further optimizes electron transfer performance. This study provides new insights into the development of bimetallic catalysts for efficiently reducing CO<small><sub>2</sub></small> to formate.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 6","pages":" 2201-2208"},"PeriodicalIF":2.5000,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Copper–tin bimetallic aerogel alloy for the electroreduction of CO2 to formate†\",\"authors\":\"Baibin Ren, Jing Shao, Hongji Li and Qingming Xu\",\"doi\":\"10.1039/D4NJ04703F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The electrochemical reduction of CO<small><sub>2</sub></small> (CO<small><sub>2</sub></small>RR) enables the conversion of CO<small><sub>2</sub></small> into various value-added hydrocarbons, with formate garnering significant interest due to its high energy density and efficient conversion potential. Although tin (Sn)-based catalysts generally exhibit high selectivity for formate and effectively suppress the hydrogen evolution reaction (HER), the simultaneous presence of low selectivity and current density limits further applications. In this work, a series of bimetallic Cu–Sn aerogel catalysts were synthesized; the Cu–Sn (1 : 1) aerogel catalyst demonstrated superior CO<small><sub>2</sub></small> reduction performance, with higher cathodic reaction activity (35.61 mA cm<small><sup>−2</sup></small>) and a formate faradaic efficiency (FE) exceeding 90%, while maintaining stable CO<small><sub>2</sub></small> selectivity over a period of 7 hours. The high efficiency in generating formate is attributed to the high surface area provided by the bimetallic aerogel, which facilitates CO<small><sub>2</sub></small> transport and product desorption. Additionally, the high-energy interfaces formed during alloying and electronic synergistic effects increase the charge density at active sites. The self-supporting structure further optimizes electron transfer performance. This study provides new insights into the development of bimetallic catalysts for efficiently reducing CO<small><sub>2</sub></small> to formate.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 6\",\"pages\":\" 2201-2208\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-01-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04703f\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04703f","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
CO2的电化学还原(CO2RR)可以将CO2转化为各种增值碳氢化合物,甲酸盐因其高能量密度和高效转化潜力而备受关注。虽然锡基催化剂通常对甲酸盐具有高选择性,并能有效抑制析氢反应(HER),但同时存在的低选择性和电流密度限制了其进一步应用。本文合成了一系列双金属Cu-Sn气凝胶催化剂;Cu-Sn(1:1)气凝胶催化剂表现出优异的CO2还原性能,具有较高的阴极反应活性(35.61 mA cm−2)和甲酸faradaic效率(FE)超过90%,同时在7小时内保持稳定的CO2选择性。双金属气凝胶的高表面积有利于CO2的运输和产物的解吸,从而提高了生成甲酸盐的效率。此外,合金化过程中形成的高能界面和电子协同效应增加了活性位点的电荷密度。自支撑结构进一步优化了电子传递性能。该研究为开发高效还原CO2为甲酸盐的双金属催化剂提供了新的思路。
Copper–tin bimetallic aerogel alloy for the electroreduction of CO2 to formate†
The electrochemical reduction of CO2 (CO2RR) enables the conversion of CO2 into various value-added hydrocarbons, with formate garnering significant interest due to its high energy density and efficient conversion potential. Although tin (Sn)-based catalysts generally exhibit high selectivity for formate and effectively suppress the hydrogen evolution reaction (HER), the simultaneous presence of low selectivity and current density limits further applications. In this work, a series of bimetallic Cu–Sn aerogel catalysts were synthesized; the Cu–Sn (1 : 1) aerogel catalyst demonstrated superior CO2 reduction performance, with higher cathodic reaction activity (35.61 mA cm−2) and a formate faradaic efficiency (FE) exceeding 90%, while maintaining stable CO2 selectivity over a period of 7 hours. The high efficiency in generating formate is attributed to the high surface area provided by the bimetallic aerogel, which facilitates CO2 transport and product desorption. Additionally, the high-energy interfaces formed during alloying and electronic synergistic effects increase the charge density at active sites. The self-supporting structure further optimizes electron transfer performance. This study provides new insights into the development of bimetallic catalysts for efficiently reducing CO2 to formate.