{"title":"Tailoring the Product Selectivity of Electrochemical CO2 Reduction at Copper-Tin Composite Oxide Nanofibers","authors":"Subin Choi, Taehui Kwon, Youngmi Lee","doi":"10.1016/j.jallcom.2025.178574","DOIUrl":null,"url":null,"abstract":"Electrochemical reduction of carbon dioxide (CO<sub>2</sub>RR) has been receiving attention as an attractive technique to convert CO<sub>2</sub> into various useful resources. Because CO<sub>2</sub>RR generally produces diverse products and competes with hydrogen reduction reaction (HER), the development of efficient electrocatalysts exhibiting high product selectivity is required. This paper demonstrates a simple approach to synthesize Cu-Sn bimetallic oxide nanofibers with various Cu/Sn composition ratios using electrospinning and post-calcination. The prepared nanofibers (denoted as Cu<sub>1</sub>Sn<sub><em>x</em></sub>O<sub><em>y</em></sub>, <em>x</em> = 0.5, 1, 2) showed excellent electrocatalytic activity and product selectivity for CO<sub>2</sub>RR, which were drastically improved from those of single metal oxides (i.e, CuO and SnO<sub>2</sub>). Of great importance, the product selectivity could be finely controlled by changing the Cu/Sn content ratio in Cu<sub>1</sub>Sn<sub><em>x</em></sub>O<sub><em>y</em></sub> nanofibers. In fact, Cu-enriched Cu<sub>1</sub>Sn<sub>0.5</sub>O<sub><em>y</em></sub> showed nearly exclusive faradaic efficiency (FE) for carbon monoxide (CO) at −0.8 V<sub>RHE</sub> (~95%); and Sn-enriched Cu<sub>1</sub>Sn<sub>2</sub>O<sub><em>y</em></sub> exhibited high FE for formic acid at −0.9 V<sub>RHE</sub> (~91%), supporting the exceptionally high selectivity to CO and formic acid, respectively. In addition, both Cu<sub>1</sub>Sn<sub>0.5</sub>O<sub><em>y</em></sub> and Cu<sub>1</sub>Sn<sub>2</sub>O<sub><em>y</em></sub> nanofibers barely generated hydrogen during CO<sub>2</sub>RR, suppressing HER successfully.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"67 1","pages":""},"PeriodicalIF":5.8000,"publicationDate":"2025-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alloys and Compounds","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.jallcom.2025.178574","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Electrochemical reduction of carbon dioxide (CO2RR) has been receiving attention as an attractive technique to convert CO2 into various useful resources. Because CO2RR generally produces diverse products and competes with hydrogen reduction reaction (HER), the development of efficient electrocatalysts exhibiting high product selectivity is required. This paper demonstrates a simple approach to synthesize Cu-Sn bimetallic oxide nanofibers with various Cu/Sn composition ratios using electrospinning and post-calcination. The prepared nanofibers (denoted as Cu1SnxOy, x = 0.5, 1, 2) showed excellent electrocatalytic activity and product selectivity for CO2RR, which were drastically improved from those of single metal oxides (i.e, CuO and SnO2). Of great importance, the product selectivity could be finely controlled by changing the Cu/Sn content ratio in Cu1SnxOy nanofibers. In fact, Cu-enriched Cu1Sn0.5Oy showed nearly exclusive faradaic efficiency (FE) for carbon monoxide (CO) at −0.8 VRHE (~95%); and Sn-enriched Cu1Sn2Oy exhibited high FE for formic acid at −0.9 VRHE (~91%), supporting the exceptionally high selectivity to CO and formic acid, respectively. In addition, both Cu1Sn0.5Oy and Cu1Sn2Oy nanofibers barely generated hydrogen during CO2RR, suppressing HER successfully.
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.