{"title":"氢氧化铜纳米带/氧化石墨烯纳米片衍生的 Cu-Cu2O/rGO 催化剂选择性电解 CO2 制乙烯†。","authors":"Chenxiang Peng, Bing Yao, Lei Wang and Xinyi Wan","doi":"10.1039/D4RA07259F","DOIUrl":null,"url":null,"abstract":"<p >Electrolyzing CO<small><sub>2</sub></small> into ethylene (C<small><sub>2</sub></small>H<small><sub>4</sub></small>) is a promising strategy for CO<small><sub>2</sub></small> utilization and carbon neutrality since C<small><sub>2</sub></small>H<small><sub>4</sub></small> is an important industrial feedstock. However, selectively converting CO<small><sub>2</sub></small> into C<small><sub>2</sub></small>H<small><sub>4</sub></small> <em>via</em> the CO<small><sub>2</sub></small> electro-reduction reaction (CO<small><sub>2</sub></small> ERR) is still a great challenge. Herein, Cu–Cu<small><sub>2</sub></small>O nanoparticles anchored on reduced graphene oxide nanosheets (Cu–Cu<small><sub>2</sub></small>O/rGO) were prepared from copper hydroxide nanostrands (CHNs) and graphene oxide (GO) nanosheets <em>via in situ</em> electrochemical reduction. Cu–Cu<small><sub>2</sub></small>O nanoparticles with diameter less than 10 nm were formed on the surface of rGO nanosheets. After assembling the Cu–Cu<small><sub>2</sub></small>O/rGO catalyst into a flow cell, it demonstrated high Faraday efficiencies (FEs) of 55.4%, 37.6%, and 6.7% for C<small><sub>2</sub></small>H<small><sub>4</sub></small>, C<small><sub>2</sub></small>H<small><sub>6</sub></small>, and H<small><sub>2</sub></small>, respectively, and a total 93% FE for C<small><sub>2</sub></small> at −1.3 V <em>vs.</em> the standard hydrogen electrode (SHE). Moreover, its FE was 68.2% for C<small><sub>2</sub></small>H<small><sub>4</sub></small>, 10.2% for C<small><sub>2</sub></small>H<small><sub>6</sub></small>, and 20.5% for H<small><sub>2</sub></small> at −1.4 (<em>vs.</em> SHE). Besides, no liquid carbon product was detected. This high selectivity is attributed to the synergistic effect arising from the small diameter of Cu–Cu<small><sub>2</sub></small>O NPs with the combination of Cu<small><sup>0</sup></small>–Cu<small><sup>+</sup></small> and rGO nanosheets, which promotes the activation of CO<small><sub>2</sub></small> molecules, facilitates C–C coupling, and enhances stability. This may provide a facile way for designing an efficient catalyst for selectively electrolyzing CO<small><sub>2</sub></small> into valuable C<small><sub>2</sub></small> chemicals.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 49","pages":" 36602-36609"},"PeriodicalIF":3.9000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ra/d4ra07259f?page=search","citationCount":"0","resultStr":"{\"title\":\"Selectively electrolyzing CO2 to ethylene by a Cu–Cu2O/rGO catalyst derived from copper hydroxide nanostrands/graphene oxide nanosheets†\",\"authors\":\"Chenxiang Peng, Bing Yao, Lei Wang and Xinyi Wan\",\"doi\":\"10.1039/D4RA07259F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Electrolyzing CO<small><sub>2</sub></small> into ethylene (C<small><sub>2</sub></small>H<small><sub>4</sub></small>) is a promising strategy for CO<small><sub>2</sub></small> utilization and carbon neutrality since C<small><sub>2</sub></small>H<small><sub>4</sub></small> is an important industrial feedstock. However, selectively converting CO<small><sub>2</sub></small> into C<small><sub>2</sub></small>H<small><sub>4</sub></small> <em>via</em> the CO<small><sub>2</sub></small> electro-reduction reaction (CO<small><sub>2</sub></small> ERR) is still a great challenge. Herein, Cu–Cu<small><sub>2</sub></small>O nanoparticles anchored on reduced graphene oxide nanosheets (Cu–Cu<small><sub>2</sub></small>O/rGO) were prepared from copper hydroxide nanostrands (CHNs) and graphene oxide (GO) nanosheets <em>via in situ</em> electrochemical reduction. Cu–Cu<small><sub>2</sub></small>O nanoparticles with diameter less than 10 nm were formed on the surface of rGO nanosheets. After assembling the Cu–Cu<small><sub>2</sub></small>O/rGO catalyst into a flow cell, it demonstrated high Faraday efficiencies (FEs) of 55.4%, 37.6%, and 6.7% for C<small><sub>2</sub></small>H<small><sub>4</sub></small>, C<small><sub>2</sub></small>H<small><sub>6</sub></small>, and H<small><sub>2</sub></small>, respectively, and a total 93% FE for C<small><sub>2</sub></small> at −1.3 V <em>vs.</em> the standard hydrogen electrode (SHE). Moreover, its FE was 68.2% for C<small><sub>2</sub></small>H<small><sub>4</sub></small>, 10.2% for C<small><sub>2</sub></small>H<small><sub>6</sub></small>, and 20.5% for H<small><sub>2</sub></small> at −1.4 (<em>vs.</em> SHE). Besides, no liquid carbon product was detected. This high selectivity is attributed to the synergistic effect arising from the small diameter of Cu–Cu<small><sub>2</sub></small>O NPs with the combination of Cu<small><sup>0</sup></small>–Cu<small><sup>+</sup></small> and rGO nanosheets, which promotes the activation of CO<small><sub>2</sub></small> molecules, facilitates C–C coupling, and enhances stability. This may provide a facile way for designing an efficient catalyst for selectively electrolyzing CO<small><sub>2</sub></small> into valuable C<small><sub>2</sub></small> chemicals.</p>\",\"PeriodicalId\":102,\"journal\":{\"name\":\"RSC Advances\",\"volume\":\" 49\",\"pages\":\" 36602-36609\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-11-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ra/d4ra07259f?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC Advances\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ra/d4ra07259f\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Advances","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ra/d4ra07259f","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Selectively electrolyzing CO2 to ethylene by a Cu–Cu2O/rGO catalyst derived from copper hydroxide nanostrands/graphene oxide nanosheets†
Electrolyzing CO2 into ethylene (C2H4) is a promising strategy for CO2 utilization and carbon neutrality since C2H4 is an important industrial feedstock. However, selectively converting CO2 into C2H4via the CO2 electro-reduction reaction (CO2 ERR) is still a great challenge. Herein, Cu–Cu2O nanoparticles anchored on reduced graphene oxide nanosheets (Cu–Cu2O/rGO) were prepared from copper hydroxide nanostrands (CHNs) and graphene oxide (GO) nanosheets via in situ electrochemical reduction. Cu–Cu2O nanoparticles with diameter less than 10 nm were formed on the surface of rGO nanosheets. After assembling the Cu–Cu2O/rGO catalyst into a flow cell, it demonstrated high Faraday efficiencies (FEs) of 55.4%, 37.6%, and 6.7% for C2H4, C2H6, and H2, respectively, and a total 93% FE for C2 at −1.3 V vs. the standard hydrogen electrode (SHE). Moreover, its FE was 68.2% for C2H4, 10.2% for C2H6, and 20.5% for H2 at −1.4 (vs. SHE). Besides, no liquid carbon product was detected. This high selectivity is attributed to the synergistic effect arising from the small diameter of Cu–Cu2O NPs with the combination of Cu0–Cu+ and rGO nanosheets, which promotes the activation of CO2 molecules, facilitates C–C coupling, and enhances stability. This may provide a facile way for designing an efficient catalyst for selectively electrolyzing CO2 into valuable C2 chemicals.
期刊介绍:
An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.