Dr. Wanfeng Yang, Dr. Yong Zhao, Yiqing Chen, Hangjuan Ren, Jiameng Sun, Zhangsheng Shi, Xindie Jin, Prof. Zhonghua Zhang, Prof. Xin Wang
{"title":"限制铜上的CO2覆盖促进强酸条件下CO2电还原生成多碳产物","authors":"Dr. Wanfeng Yang, Dr. Yong Zhao, Yiqing Chen, Hangjuan Ren, Jiameng Sun, Zhangsheng Shi, Xindie Jin, Prof. Zhonghua Zhang, Prof. Xin Wang","doi":"10.1002/anie.202422082","DOIUrl":null,"url":null,"abstract":"<p>Electrocatalytic CO<sub>2</sub> reduction (CO<sub>2</sub>R) to multi-carbon (C<sub>2+</sub>) products in strong acid presents a promising approach to mitigate the CO<sub>2</sub> loss commonly encountered in alkaline and neutral systems. However, this process often suffers from low selectivity for C<sub>2+</sub> products due to the competing C<sub>1</sub> (e.g., CO and HCOOH) formation and complex C−C coupling kinetics. In this work, we report a CO<sub>2</sub> coverage constraining strategy by diluting CO<sub>2</sub> reactant feed to modulate the intermediate distribution and C−C coupling pathways for an enhanced electrosynthesis of C<sub>2+</sub> products in strong acid. Lowering the CO<sub>2</sub> feed concentration reduces CO<sub>2</sub> coverage on copper catalyst, enriching the surface coverage and optimizing the adsorption configuration of the key CO intermediate for C−C coupling. This approach efficiently suppresses the formation of undesired C<sub>1</sub> products. By employing a 20 % CO<sub>2</sub> feed, we achieved a significant improvement in C<sub>2+</sub> Faradaic efficiency, reaching 68 % at 100 mA cm<sup>−2</sup>, approximately 1.7 times higher than the 41 % obtained using pure CO<sub>2</sub>. We demonstrated the direct electroreduction of a 30 % CO<sub>2</sub> feed—representative CO<sub>2</sub> concentration of typical industrial flue gases—in a full electrolyzer, achieving a C<sub>2+</sub> selectivity of 78 % and an energy efficiency of 23 % at 200 mA cm<sup>−2</sup>.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"64 12","pages":""},"PeriodicalIF":16.1000,"publicationDate":"2024-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Constraining CO2 Coverage on Copper Promotes CO2 Electroreduction to Multi-carbon Products in Strong Acid\",\"authors\":\"Dr. Wanfeng Yang, Dr. Yong Zhao, Yiqing Chen, Hangjuan Ren, Jiameng Sun, Zhangsheng Shi, Xindie Jin, Prof. Zhonghua Zhang, Prof. Xin Wang\",\"doi\":\"10.1002/anie.202422082\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Electrocatalytic CO<sub>2</sub> reduction (CO<sub>2</sub>R) to multi-carbon (C<sub>2+</sub>) products in strong acid presents a promising approach to mitigate the CO<sub>2</sub> loss commonly encountered in alkaline and neutral systems. However, this process often suffers from low selectivity for C<sub>2+</sub> products due to the competing C<sub>1</sub> (e.g., CO and HCOOH) formation and complex C−C coupling kinetics. In this work, we report a CO<sub>2</sub> coverage constraining strategy by diluting CO<sub>2</sub> reactant feed to modulate the intermediate distribution and C−C coupling pathways for an enhanced electrosynthesis of C<sub>2+</sub> products in strong acid. Lowering the CO<sub>2</sub> feed concentration reduces CO<sub>2</sub> coverage on copper catalyst, enriching the surface coverage and optimizing the adsorption configuration of the key CO intermediate for C−C coupling. This approach efficiently suppresses the formation of undesired C<sub>1</sub> products. By employing a 20 % CO<sub>2</sub> feed, we achieved a significant improvement in C<sub>2+</sub> Faradaic efficiency, reaching 68 % at 100 mA cm<sup>−2</sup>, approximately 1.7 times higher than the 41 % obtained using pure CO<sub>2</sub>. We demonstrated the direct electroreduction of a 30 % CO<sub>2</sub> feed—representative CO<sub>2</sub> concentration of typical industrial flue gases—in a full electrolyzer, achieving a C<sub>2+</sub> selectivity of 78 % and an energy efficiency of 23 % at 200 mA cm<sup>−2</sup>.</p>\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\"64 12\",\"pages\":\"\"},\"PeriodicalIF\":16.1000,\"publicationDate\":\"2024-12-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie International Edition\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/anie.202422082\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anie.202422082","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
在强酸中,电催化CO2还原(CO2R)为多碳(C2+)产物提供了一种很有前途的方法,可以减轻碱性和中性体系中常见的CO2损失。然而,由于竞争性的C1(如CO和HCOOH)形成和络合物C - C耦合动力学,该过程通常存在C2+产物选择性低的问题。在这项工作中,我们报告了一种CO2覆盖限制策略,通过稀释CO2反应物进料来调节中间分布和C - C偶联途径,以增强强酸中C2+产物的电合成。降低CO2进料浓度可降低铜催化剂上的CO2覆盖率,增加铜催化剂的表面覆盖率,优化C - C偶联过程中关键CO中间体的吸附构型。这种方法有效地抑制了不需要的C1产物的形成。通过使用20%的CO2进料,我们实现了C2+法拉第效率的显著提高,在100 mA cm‐2时达到68%,比使用纯CO2获得的41%高出约1.7倍。我们演示了在全电解槽中直接电还原30%的CO2进料(典型工业烟气的CO2浓度代表),在200 mA cm‐2下实现了78%的C2+选择性和23%的能源效率。
Constraining CO2 Coverage on Copper Promotes CO2 Electroreduction to Multi-carbon Products in Strong Acid
Electrocatalytic CO2 reduction (CO2R) to multi-carbon (C2+) products in strong acid presents a promising approach to mitigate the CO2 loss commonly encountered in alkaline and neutral systems. However, this process often suffers from low selectivity for C2+ products due to the competing C1 (e.g., CO and HCOOH) formation and complex C−C coupling kinetics. In this work, we report a CO2 coverage constraining strategy by diluting CO2 reactant feed to modulate the intermediate distribution and C−C coupling pathways for an enhanced electrosynthesis of C2+ products in strong acid. Lowering the CO2 feed concentration reduces CO2 coverage on copper catalyst, enriching the surface coverage and optimizing the adsorption configuration of the key CO intermediate for C−C coupling. This approach efficiently suppresses the formation of undesired C1 products. By employing a 20 % CO2 feed, we achieved a significant improvement in C2+ Faradaic efficiency, reaching 68 % at 100 mA cm−2, approximately 1.7 times higher than the 41 % obtained using pure CO2. We demonstrated the direct electroreduction of a 30 % CO2 feed—representative CO2 concentration of typical industrial flue gases—in a full electrolyzer, achieving a C2+ selectivity of 78 % and an energy efficiency of 23 % at 200 mA cm−2.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.