{"title":"用于将二氧化碳电还原为醋酸或丙醇的自加压纳米级胶囊催化剂","authors":"Yanming Cai, Ruixin Yang, Jiaju Fu, Zhe Li, Liangyiqun Xie, Kai Li, Yu-Chung Chang, Shichao Ding, Zhaoyuan Lyu, Jian-Rong Zhang, Jun-Jie Zhu, Yuehe Lin, Wenlei Zhu","doi":"10.1038/s44160-024-00552-2","DOIUrl":null,"url":null,"abstract":"The selective one-step CO2 electroreduction reaction (CO2RR) to acetate and propanol has garnered intense interest. Here we report the design of self-pressurizing nanoscale capsule catalysts for the CO2RR. A high-pressure CO intermediate environment is created around copper catalysts by a permselective enclosure. Microkinetic modelling, 13CO2/12CO co-feed experiments and in situ Raman spectroscopy confirm that a unique CO–CO2 coupling path is involved, which is only initiated at high CO intermediate pressure. This pathway benefits acetate production due to the kinetic and energetic advantages of COCO2*. The acetate Faradaic efficiency is 38.5 ± 2.2% (8 times higher than that achieved without enclosure) and the acetate partial current density is 328 ± 19 mA cm−2, which surpasses the performance of previous CO2RR catalysts. In situ investigation indicates that the CO pressure inside the nanoscale capsule catalysts can reach 8 ± 3 bar. Furthermore, self-pressurizing nanoscale capsule catalysts with a CuI-derived core can reduce CO2 to propanol with a Faradaic efficiency of 25.7 ± 1.2% and a conversion rate of 155 ± 3 mA cm−2. CO2 electroreduction to multicarbon products is desirable but challenging. Now, self-pressurizing nanoscale capsule catalysts are synthesized. The self-pressurising capsules harness high-pressure CO environments for selective acetate or propanol production via a CO–CO2 coupling pathway.","PeriodicalId":74251,"journal":{"name":"Nature synthesis","volume":"3 7","pages":"891-902"},"PeriodicalIF":0.0000,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-pressurizing nanoscale capsule catalysts for CO2 electroreduction to acetate or propanol\",\"authors\":\"Yanming Cai, Ruixin Yang, Jiaju Fu, Zhe Li, Liangyiqun Xie, Kai Li, Yu-Chung Chang, Shichao Ding, Zhaoyuan Lyu, Jian-Rong Zhang, Jun-Jie Zhu, Yuehe Lin, Wenlei Zhu\",\"doi\":\"10.1038/s44160-024-00552-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The selective one-step CO2 electroreduction reaction (CO2RR) to acetate and propanol has garnered intense interest. Here we report the design of self-pressurizing nanoscale capsule catalysts for the CO2RR. A high-pressure CO intermediate environment is created around copper catalysts by a permselective enclosure. Microkinetic modelling, 13CO2/12CO co-feed experiments and in situ Raman spectroscopy confirm that a unique CO–CO2 coupling path is involved, which is only initiated at high CO intermediate pressure. This pathway benefits acetate production due to the kinetic and energetic advantages of COCO2*. The acetate Faradaic efficiency is 38.5 ± 2.2% (8 times higher than that achieved without enclosure) and the acetate partial current density is 328 ± 19 mA cm−2, which surpasses the performance of previous CO2RR catalysts. In situ investigation indicates that the CO pressure inside the nanoscale capsule catalysts can reach 8 ± 3 bar. Furthermore, self-pressurizing nanoscale capsule catalysts with a CuI-derived core can reduce CO2 to propanol with a Faradaic efficiency of 25.7 ± 1.2% and a conversion rate of 155 ± 3 mA cm−2. CO2 electroreduction to multicarbon products is desirable but challenging. Now, self-pressurizing nanoscale capsule catalysts are synthesized. The self-pressurising capsules harness high-pressure CO environments for selective acetate or propanol production via a CO–CO2 coupling pathway.\",\"PeriodicalId\":74251,\"journal\":{\"name\":\"Nature synthesis\",\"volume\":\"3 7\",\"pages\":\"891-902\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature synthesis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.nature.com/articles/s44160-024-00552-2\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"0\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature synthesis","FirstCategoryId":"1085","ListUrlMain":"https://www.nature.com/articles/s44160-024-00552-2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"0","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
一步法选择性 CO2 电还原反应(CO2RR)生成醋酸酯和丙醇引起了人们的浓厚兴趣。在此,我们报告了用于 CO2RR 的自加压纳米级胶囊催化剂的设计。铜催化剂周围通过包覆选择性形成了高压 CO 中间环境。微动力学建模、13CO2/12CO 共馈实验和原位拉曼光谱证实,其中涉及一种独特的 CO-CO2 耦合途径,该途径仅在高 CO 中间压力下启动。由于 COCO2* 在动力学和能量方面的优势,这一途径有利于醋酸盐的生产。醋酸酯法拉第效率为 38.5 ± 2.2%(是无封闭情况下的 8 倍),醋酸酯部分电流密度为 328 ± 19 mA cm-2,超过了以往 CO2RR 催化剂的性能。原位研究表明,纳米胶囊催化剂内部的 CO 压力可达 8 ± 3 巴。此外,以 CuI 为核心的自加压纳米级胶囊催化剂可将二氧化碳还原为丙醇,其法拉第效率为 25.7 ± 1.2%,转化率为 155 ± 3 mA cm-2。将 CO2 电还原为多碳产品是一种理想但具有挑战性的方法。现在,我们合成了自加压纳米级胶囊催化剂。自加压胶囊利用高压 CO 环境,通过 CO-CO2 偶联途径选择性地生产醋酸或丙醇。
Self-pressurizing nanoscale capsule catalysts for CO2 electroreduction to acetate or propanol
The selective one-step CO2 electroreduction reaction (CO2RR) to acetate and propanol has garnered intense interest. Here we report the design of self-pressurizing nanoscale capsule catalysts for the CO2RR. A high-pressure CO intermediate environment is created around copper catalysts by a permselective enclosure. Microkinetic modelling, 13CO2/12CO co-feed experiments and in situ Raman spectroscopy confirm that a unique CO–CO2 coupling path is involved, which is only initiated at high CO intermediate pressure. This pathway benefits acetate production due to the kinetic and energetic advantages of COCO2*. The acetate Faradaic efficiency is 38.5 ± 2.2% (8 times higher than that achieved without enclosure) and the acetate partial current density is 328 ± 19 mA cm−2, which surpasses the performance of previous CO2RR catalysts. In situ investigation indicates that the CO pressure inside the nanoscale capsule catalysts can reach 8 ± 3 bar. Furthermore, self-pressurizing nanoscale capsule catalysts with a CuI-derived core can reduce CO2 to propanol with a Faradaic efficiency of 25.7 ± 1.2% and a conversion rate of 155 ± 3 mA cm−2. CO2 electroreduction to multicarbon products is desirable but challenging. Now, self-pressurizing nanoscale capsule catalysts are synthesized. The self-pressurising capsules harness high-pressure CO environments for selective acetate or propanol production via a CO–CO2 coupling pathway.