将商品泡沫聚苯乙烯升级为氧化还原聚合物基电极。

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2025-03-19 DOI:10.1002/cssc.202500092
Algin Oh Biying, Sabrina Trano, Yi Jie Eng, Gabriele Lingua, Haritz Sardon, David Mecerreyes, Julian M W Chan
{"title":"将商品泡沫聚苯乙烯升级为氧化还原聚合物基电极。","authors":"Algin Oh Biying, Sabrina Trano, Yi Jie Eng, Gabriele Lingua, Haritz Sardon, David Mecerreyes, Julian M W Chan","doi":"10.1002/cssc.202500092","DOIUrl":null,"url":null,"abstract":"<p><p>Commodity polystyrene from styrofoam food boxes was chemically transformed into redox-active organic polymers via a two-step functionalization sequence. In the first step, controlled chloromethylation of the pendent phenyl rings was used to functionalize 30-50 % of the polymer chain. The degree of functionalization could be tuned by simply varying the reaction time (1-3 h). Next, phenothiazine or nitroxide radical moieties were introduced via nucleophilic displacement of the benzylic chlorides to afford polymers with redox-active pendent sidechains. These phenothiazine and TEMPO-functionalized polymers were then characterized electrochemically to demonstrate their redox properties and evaluate their performance as battery electrodes. Overall, this process serves as proof-of-concept for the rapid conversion of consumer-grade styrofoam into redox-active polymers with the potential to serve as metal-free electrodes in organic batteries.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":" ","pages":"e202500092"},"PeriodicalIF":7.5000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Upcycling Commodity Styrofoam into Redox Polymer-based Electrodes.\",\"authors\":\"Algin Oh Biying, Sabrina Trano, Yi Jie Eng, Gabriele Lingua, Haritz Sardon, David Mecerreyes, Julian M W Chan\",\"doi\":\"10.1002/cssc.202500092\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Commodity polystyrene from styrofoam food boxes was chemically transformed into redox-active organic polymers via a two-step functionalization sequence. In the first step, controlled chloromethylation of the pendent phenyl rings was used to functionalize 30-50 % of the polymer chain. The degree of functionalization could be tuned by simply varying the reaction time (1-3 h). Next, phenothiazine or nitroxide radical moieties were introduced via nucleophilic displacement of the benzylic chlorides to afford polymers with redox-active pendent sidechains. These phenothiazine and TEMPO-functionalized polymers were then characterized electrochemically to demonstrate their redox properties and evaluate their performance as battery electrodes. Overall, this process serves as proof-of-concept for the rapid conversion of consumer-grade styrofoam into redox-active polymers with the potential to serve as metal-free electrodes in organic batteries.</p>\",\"PeriodicalId\":149,\"journal\":{\"name\":\"ChemSusChem\",\"volume\":\" \",\"pages\":\"e202500092\"},\"PeriodicalIF\":7.5000,\"publicationDate\":\"2025-03-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemSusChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/cssc.202500092\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cssc.202500092","RegionNum":2,"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

摘要

从泡沫聚苯乙烯食品盒中的商品聚苯乙烯通过两步功能化顺序化学转化为氧化还原活性有机聚合物。在第一步中,对悬垂的苯基环进行控制氯甲基化,使30-50%的聚合物链功能化。只需改变反应时间(1-3小时)即可调整功能化程度。接下来,通过亲核取代苯基氯化物,引入吩噻嗪或氮氧化物自由基,得到具有氧化还原活性侧链的聚合物。然后对这些吩噻嗪和tempo功能化聚合物进行电化学表征,以证明它们的氧化还原特性并评估它们作为电池电极的性能。总的来说,这一过程证明了将消费级聚苯乙烯泡沫塑料快速转化为氧化还原活性聚合物的概念,并具有作为有机电池中无金属电极的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Upcycling Commodity Styrofoam into Redox Polymer-based Electrodes.

Commodity polystyrene from styrofoam food boxes was chemically transformed into redox-active organic polymers via a two-step functionalization sequence. In the first step, controlled chloromethylation of the pendent phenyl rings was used to functionalize 30-50 % of the polymer chain. The degree of functionalization could be tuned by simply varying the reaction time (1-3 h). Next, phenothiazine or nitroxide radical moieties were introduced via nucleophilic displacement of the benzylic chlorides to afford polymers with redox-active pendent sidechains. These phenothiazine and TEMPO-functionalized polymers were then characterized electrochemically to demonstrate their redox properties and evaluate their performance as battery electrodes. Overall, this process serves as proof-of-concept for the rapid conversion of consumer-grade styrofoam into redox-active polymers with the potential to serve as metal-free electrodes in organic batteries.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信