通过 PdCu-TiO2 光催化剂在流动中选择性氧化聚酯。

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Journal of the American Chemical Society Pub Date : 2024-11-20 Epub Date: 2024-11-05 DOI:10.1021/jacs.4c11973
Shuai Zhang, Bernt Johannessen, Bingquan Xia, Xintong Gao, Kenneth Davey, Jingrun Ran, Shi-Zhang Qiao
{"title":"通过 PdCu-TiO2 光催化剂在流动中选择性氧化聚酯。","authors":"Shuai Zhang, Bernt Johannessen, Bingquan Xia, Xintong Gao, Kenneth Davey, Jingrun Ran, Shi-Zhang Qiao","doi":"10.1021/jacs.4c11973","DOIUrl":null,"url":null,"abstract":"<p><p>Catalytic upcycling of plastic wastes offers a sustainable circular economy. Selective conversion of the most widely used polyester, polyethylene terephthalate (PET), under ambient conditions is practically attractive because of low energy consumption and carbon footprint. Here, we report selective, aerobic conversion of PET in a flow reactor using TiO<sub>2</sub> photocatalyst modified with atomic Pd and metallic PdCu (Pd<sub>1</sub>Cu<sub>0.4</sub>-TiO<sub>2</sub>) under ambient conditions. We demonstrate that atomically synergistic Pd<sub>1</sub>Cu<sub>0.4</sub>-TiO<sub>2</sub> exhibits a formate evolution of 4707 μmol g<sup>-1</sup> h<sup>-1</sup> with a selectivity of 92.3% together with trace CO<sub><i>x</i></sub> released. Importantly, we show that this corresponds to 10-10<sup>3</sup> times greater activity than reported photocatalytic systems. We confirm that synergy between atomic Pd and metallic PdCu boosts directional charge transfer and oxygen-induced C-C cleavage and inhibits product decomposition. We conclude that photocatalytic waste plastic-to-chemical conversion is sustainable via targeted engineering of atomically synergistic catalysts and reaction systems.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":" ","pages":"32003-32012"},"PeriodicalIF":14.4000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Selective Oxidation of Polyesters via PdCu-TiO<sub>2</sub> Photocatalysts in Flow.\",\"authors\":\"Shuai Zhang, Bernt Johannessen, Bingquan Xia, Xintong Gao, Kenneth Davey, Jingrun Ran, Shi-Zhang Qiao\",\"doi\":\"10.1021/jacs.4c11973\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Catalytic upcycling of plastic wastes offers a sustainable circular economy. Selective conversion of the most widely used polyester, polyethylene terephthalate (PET), under ambient conditions is practically attractive because of low energy consumption and carbon footprint. Here, we report selective, aerobic conversion of PET in a flow reactor using TiO<sub>2</sub> photocatalyst modified with atomic Pd and metallic PdCu (Pd<sub>1</sub>Cu<sub>0.4</sub>-TiO<sub>2</sub>) under ambient conditions. We demonstrate that atomically synergistic Pd<sub>1</sub>Cu<sub>0.4</sub>-TiO<sub>2</sub> exhibits a formate evolution of 4707 μmol g<sup>-1</sup> h<sup>-1</sup> with a selectivity of 92.3% together with trace CO<sub><i>x</i></sub> released. Importantly, we show that this corresponds to 10-10<sup>3</sup> times greater activity than reported photocatalytic systems. We confirm that synergy between atomic Pd and metallic PdCu boosts directional charge transfer and oxygen-induced C-C cleavage and inhibits product decomposition. We conclude that photocatalytic waste plastic-to-chemical conversion is sustainable via targeted engineering of atomically synergistic catalysts and reaction systems.</p>\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\" \",\"pages\":\"32003-32012\"},\"PeriodicalIF\":14.4000,\"publicationDate\":\"2024-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/jacs.4c11973\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c11973","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

塑料废料的催化升级再循环技术提供了一种可持续的循环经济。在环境条件下选择性转化最广泛使用的聚酯--聚对苯二甲酸乙二酯(PET),由于能耗低、碳足迹小,因此具有实际吸引力。在此,我们报告了在流动反应器中使用经原子钯和金属钯铜修饰的二氧化钛光催化剂(Pd1Cu0.4-TiO2)在环境条件下对 PET 进行选择性好氧转化的情况。我们证明,原子协同 Pd1Cu0.4-TiO2 的甲酸盐进化速度为 4707 μmol g-1 h-1,选择性为 92.3%,同时释放出微量 COx。重要的是,我们发现这比已报道的光催化系统的活性高出 10-103 倍。我们证实,原子钯和金属钯铜之间的协同作用促进了定向电荷转移和氧诱导的 C-C 裂解,并抑制了产物分解。我们的结论是,通过有针对性地设计原子协同催化剂和反应体系,光催化废塑料转化为化学品的过程是可持续的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Selective Oxidation of Polyesters via PdCu-TiO<sub>2</sub> Photocatalysts in Flow.

Selective Oxidation of Polyesters via PdCu-TiO2 Photocatalysts in Flow.

Catalytic upcycling of plastic wastes offers a sustainable circular economy. Selective conversion of the most widely used polyester, polyethylene terephthalate (PET), under ambient conditions is practically attractive because of low energy consumption and carbon footprint. Here, we report selective, aerobic conversion of PET in a flow reactor using TiO2 photocatalyst modified with atomic Pd and metallic PdCu (Pd1Cu0.4-TiO2) under ambient conditions. We demonstrate that atomically synergistic Pd1Cu0.4-TiO2 exhibits a formate evolution of 4707 μmol g-1 h-1 with a selectivity of 92.3% together with trace COx released. Importantly, we show that this corresponds to 10-103 times greater activity than reported photocatalytic systems. We confirm that synergy between atomic Pd and metallic PdCu boosts directional charge transfer and oxygen-induced C-C cleavage and inhibits product decomposition. We conclude that photocatalytic waste plastic-to-chemical conversion is sustainable via targeted engineering of atomically synergistic catalysts and reaction systems.

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
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
×
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