Anlin Feng , Chaoyu Lin , Huiqin Zhou , Weihong Jin , Yidong Hu , Dongyang Li , Qingyang Li
{"title":"ZnO纳米线阵列修饰Cu纳米颗粒催化4-硝基苯酚转化为4-氨基苯酚","authors":"Anlin Feng , Chaoyu Lin , Huiqin Zhou , Weihong Jin , Yidong Hu , Dongyang Li , Qingyang Li","doi":"10.1016/j.gce.2023.03.003","DOIUrl":null,"url":null,"abstract":"<div><p>To realize economical and effective removal of hazardous 4-nitrophenol from the environment, we developed an easily recyclable ZnO nanowire array decorated with Cu nanoparticles. Its salix argyracea-shaped structure not only provides a platform to achieve stable and good dispersion of Cu nanoparticles, but also offers a great deal of catalytically active sites. The density functional theory calculations reveal that ZnO and Cu have a very beneficial synergistic effect on their catalytic capability. This synergy is ascribed to the electronic localization occurring at ZnO/Cu interface, which helps improve Cu nanoparticle's ability to adsorb electro-negatively 4-nitrophenolate ions and to capture hydrogen radicals, thereby accelerating the hydrogen transfer from metal hydride complex to 4-nitrophenol. Benefiting from these characteristics, it exhibits high efficiency and reusability towards the catalytic reduction of waste 4-nitrophenol to valuable 4-aminophenol with a rate constant of 43.02 × 10<sup>−3</sup> s<sup>−1</sup> and an average conversion of 96.5% in 90 s during 10 cycles. This activity is superior to that of most reported noble- or non-noble-metal powder, bulk, coating, and array catalysts, indicating its competitive advantages in cost and efficiency, as well as enticing application prospects.</p></div>","PeriodicalId":66474,"journal":{"name":"Green Chemical Engineering","volume":null,"pages":null},"PeriodicalIF":9.1000,"publicationDate":"2023-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666952823000092/pdfft?md5=14c640bf4d755654c412c8e3b6653a4f&pid=1-s2.0-S2666952823000092-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Catalytic transformation of 4-nitrophenol into 4-aminophenol over ZnO nanowire array-decorated Cu nanoparticles\",\"authors\":\"Anlin Feng , Chaoyu Lin , Huiqin Zhou , Weihong Jin , Yidong Hu , Dongyang Li , Qingyang Li\",\"doi\":\"10.1016/j.gce.2023.03.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>To realize economical and effective removal of hazardous 4-nitrophenol from the environment, we developed an easily recyclable ZnO nanowire array decorated with Cu nanoparticles. Its salix argyracea-shaped structure not only provides a platform to achieve stable and good dispersion of Cu nanoparticles, but also offers a great deal of catalytically active sites. The density functional theory calculations reveal that ZnO and Cu have a very beneficial synergistic effect on their catalytic capability. This synergy is ascribed to the electronic localization occurring at ZnO/Cu interface, which helps improve Cu nanoparticle's ability to adsorb electro-negatively 4-nitrophenolate ions and to capture hydrogen radicals, thereby accelerating the hydrogen transfer from metal hydride complex to 4-nitrophenol. Benefiting from these characteristics, it exhibits high efficiency and reusability towards the catalytic reduction of waste 4-nitrophenol to valuable 4-aminophenol with a rate constant of 43.02 × 10<sup>−3</sup> s<sup>−1</sup> and an average conversion of 96.5% in 90 s during 10 cycles. This activity is superior to that of most reported noble- or non-noble-metal powder, bulk, coating, and array catalysts, indicating its competitive advantages in cost and efficiency, as well as enticing application prospects.</p></div>\",\"PeriodicalId\":66474,\"journal\":{\"name\":\"Green Chemical Engineering\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":9.1000,\"publicationDate\":\"2023-03-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2666952823000092/pdfft?md5=14c640bf4d755654c412c8e3b6653a4f&pid=1-s2.0-S2666952823000092-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Chemical Engineering\",\"FirstCategoryId\":\"1089\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666952823000092\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemical Engineering","FirstCategoryId":"1089","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666952823000092","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Catalytic transformation of 4-nitrophenol into 4-aminophenol over ZnO nanowire array-decorated Cu nanoparticles
To realize economical and effective removal of hazardous 4-nitrophenol from the environment, we developed an easily recyclable ZnO nanowire array decorated with Cu nanoparticles. Its salix argyracea-shaped structure not only provides a platform to achieve stable and good dispersion of Cu nanoparticles, but also offers a great deal of catalytically active sites. The density functional theory calculations reveal that ZnO and Cu have a very beneficial synergistic effect on their catalytic capability. This synergy is ascribed to the electronic localization occurring at ZnO/Cu interface, which helps improve Cu nanoparticle's ability to adsorb electro-negatively 4-nitrophenolate ions and to capture hydrogen radicals, thereby accelerating the hydrogen transfer from metal hydride complex to 4-nitrophenol. Benefiting from these characteristics, it exhibits high efficiency and reusability towards the catalytic reduction of waste 4-nitrophenol to valuable 4-aminophenol with a rate constant of 43.02 × 10−3 s−1 and an average conversion of 96.5% in 90 s during 10 cycles. This activity is superior to that of most reported noble- or non-noble-metal powder, bulk, coating, and array catalysts, indicating its competitive advantages in cost and efficiency, as well as enticing application prospects.