Xiaoshuang Qi, Yikai Yang, Yupeng Lan, Xiuming Bu, Siwei Yang, Di Yin, Hongwen Huang, Johnny C. Ho, Xianying Wang
{"title":"通过增强活性吸氢优化Cu0/Cu+/Ga界面上的C─C耦合,实现优异的CO2-to-C2+电合成","authors":"Xiaoshuang Qi, Yikai Yang, Yupeng Lan, Xiuming Bu, Siwei Yang, Di Yin, Hongwen Huang, Johnny C. Ho, Xianying Wang","doi":"10.1002/smll.202500538","DOIUrl":null,"url":null,"abstract":"<p>The electrocatalytic reduction of CO<sub>2</sub> (CO<sub>2</sub>RR) to high-value chemicals and fuels offers a promising route for a clean carbon cycle. However, it often suffers from low catalytic activity and poor selectivity. Heterostructure construction has been shown to be an effective strategy for producing multi-carbon products, but the synergistic mechanisms between multiple active sites resulting from the reconstruction process remain unclear. In this study, a Ga<sub>2</sub>O<sub>3</sub>/CuO heterostructure is established via a simple sol–gel method to produce C<sub>2+</sub> products. Experimental results demonstrate that Ga<sub>2</sub>O<sub>3</sub> stabilizes Cu<sup>+</sup> to form Cu<sup>0</sup>/Cu<sup>+</sup>/Ga active centers and enhances water-splitting ability during the reaction. The improved hydrogen absorption on the Ga site shifts the C─C coupling reaction pathway from <sup>*</sup>OCCO to the asymmetric <sup>*</sup>OCCHO coupling path with a lower energy barrier. As a result, the catalysts exhibit superior CO<sub>2</sub>RR performance, achieving a 70.1% C<sub>2+</sub> Faradaic efficiency at −1.2 V<sub>RHE</sub> in a flow cell, with ethylene Faradaic efficiency reaching 58.3% and remaining stable for 10 h.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 15","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimizing C─C Coupling on Cu0/Cu+/Ga Interfaces by Enhancing Active Hydrogen Absorption for Excellent CO2-to-C2+ Electrosynthesis\",\"authors\":\"Xiaoshuang Qi, Yikai Yang, Yupeng Lan, Xiuming Bu, Siwei Yang, Di Yin, Hongwen Huang, Johnny C. Ho, Xianying Wang\",\"doi\":\"10.1002/smll.202500538\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The electrocatalytic reduction of CO<sub>2</sub> (CO<sub>2</sub>RR) to high-value chemicals and fuels offers a promising route for a clean carbon cycle. However, it often suffers from low catalytic activity and poor selectivity. Heterostructure construction has been shown to be an effective strategy for producing multi-carbon products, but the synergistic mechanisms between multiple active sites resulting from the reconstruction process remain unclear. In this study, a Ga<sub>2</sub>O<sub>3</sub>/CuO heterostructure is established via a simple sol–gel method to produce C<sub>2+</sub> products. Experimental results demonstrate that Ga<sub>2</sub>O<sub>3</sub> stabilizes Cu<sup>+</sup> to form Cu<sup>0</sup>/Cu<sup>+</sup>/Ga active centers and enhances water-splitting ability during the reaction. The improved hydrogen absorption on the Ga site shifts the C─C coupling reaction pathway from <sup>*</sup>OCCO to the asymmetric <sup>*</sup>OCCHO coupling path with a lower energy barrier. As a result, the catalysts exhibit superior CO<sub>2</sub>RR performance, achieving a 70.1% C<sub>2+</sub> Faradaic efficiency at −1.2 V<sub>RHE</sub> in a flow cell, with ethylene Faradaic efficiency reaching 58.3% and remaining stable for 10 h.</p>\",\"PeriodicalId\":228,\"journal\":{\"name\":\"Small\",\"volume\":\"21 15\",\"pages\":\"\"},\"PeriodicalIF\":12.1000,\"publicationDate\":\"2025-03-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/smll.202500538\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202500538","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Optimizing C─C Coupling on Cu0/Cu+/Ga Interfaces by Enhancing Active Hydrogen Absorption for Excellent CO2-to-C2+ Electrosynthesis
The electrocatalytic reduction of CO2 (CO2RR) to high-value chemicals and fuels offers a promising route for a clean carbon cycle. However, it often suffers from low catalytic activity and poor selectivity. Heterostructure construction has been shown to be an effective strategy for producing multi-carbon products, but the synergistic mechanisms between multiple active sites resulting from the reconstruction process remain unclear. In this study, a Ga2O3/CuO heterostructure is established via a simple sol–gel method to produce C2+ products. Experimental results demonstrate that Ga2O3 stabilizes Cu+ to form Cu0/Cu+/Ga active centers and enhances water-splitting ability during the reaction. The improved hydrogen absorption on the Ga site shifts the C─C coupling reaction pathway from *OCCO to the asymmetric *OCCHO coupling path with a lower energy barrier. As a result, the catalysts exhibit superior CO2RR performance, achieving a 70.1% C2+ Faradaic efficiency at −1.2 VRHE in a flow cell, with ethylene Faradaic efficiency reaching 58.3% and remaining stable for 10 h.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.