Rongxing Qiu, Linxiao Cui, Li Peng, Olga Syzgantseva, Jiaran Li, Nan Fang, Maria Syzgantseva, Yuan Jiang, Jie Zhang, Bingxing Zhang, Ling-Zhi Ding, Yangyang Dong, Tianwei Xue, Cheng Li, Jin-Chao Dong, Jin-Yu Ye, Isil Akpinar, Shuliang Yang, Jun Li, Jianling Zhang, Jian-Feng Li, Buxing Han
{"title":"Cooperative promotion of electroreduction of CO to n-propanol by *CO enrichment and proton regulation","authors":"Rongxing Qiu, Linxiao Cui, Li Peng, Olga Syzgantseva, Jiaran Li, Nan Fang, Maria Syzgantseva, Yuan Jiang, Jie Zhang, Bingxing Zhang, Ling-Zhi Ding, Yangyang Dong, Tianwei Xue, Cheng Li, Jin-Chao Dong, Jin-Yu Ye, Isil Akpinar, Shuliang Yang, Jun Li, Jianling Zhang, Jian-Feng Li, Buxing Han","doi":"10.1039/d5sc00274e","DOIUrl":null,"url":null,"abstract":"The CO2/CO electroreduction reaction (CO2RR/CORR) to liquid products presents an enticing pathway to store intermittent renewable electricity. However, the selectivity for desirable high-value C3 products, such as n-propanol, remains unsatisfactory in CO2RR/CORR. Here, we report that *CO enrichment and proton regulation cooperatively enhance C1-C2 coupling by increasing CO pressure and utilizing proton sponge modification, promoting the production of n-propanol over a Cu0/Cu⁺ nanosheet catalyst in the CORR. We obtain an impressive Faradaic efficiency (FE) of 44.0% ± 2.3% for n-propanol at a low potential of −0.44 V vs. reversible hydrogen electrode (RHE) under 3 bar CO. Experimental results demonstrated that *H intermediates could be regulated by proton sponge modification. In situ characterizations combined with density functional theory (DFT) calculations validate that Cu+ species exist stably in proton sponge-modified Cu-based catalysts along with appropriate *CO coverage. This design facilitates the potential-determining C1-C1 and C1-C2 coupling steps and contributes to the n-propanol production.","PeriodicalId":9909,"journal":{"name":"Chemical Science","volume":"217 1","pages":""},"PeriodicalIF":7.6000,"publicationDate":"2025-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Science","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5sc00274e","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
Abstract
The CO2/CO electroreduction reaction (CO2RR/CORR) to liquid products presents an enticing pathway to store intermittent renewable electricity. However, the selectivity for desirable high-value C3 products, such as n-propanol, remains unsatisfactory in CO2RR/CORR. Here, we report that *CO enrichment and proton regulation cooperatively enhance C1-C2 coupling by increasing CO pressure and utilizing proton sponge modification, promoting the production of n-propanol over a Cu0/Cu⁺ nanosheet catalyst in the CORR. We obtain an impressive Faradaic efficiency (FE) of 44.0% ± 2.3% for n-propanol at a low potential of −0.44 V vs. reversible hydrogen electrode (RHE) under 3 bar CO. Experimental results demonstrated that *H intermediates could be regulated by proton sponge modification. In situ characterizations combined with density functional theory (DFT) calculations validate that Cu+ species exist stably in proton sponge-modified Cu-based catalysts along with appropriate *CO coverage. This design facilitates the potential-determining C1-C1 and C1-C2 coupling steps and contributes to the n-propanol production.
期刊介绍:
Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.