Photovoltaic-driven electrocatalytic upcycling for polyethylene terephthalate plastic waste from simulated electrolysis to photovoltaic direct-driven electrolysis†

IF 3.1 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Jiyi Sun, Sen Yang, Chengcheng Cai, Xin Li, Huijing Ma, Yichan Wen, Yan Fang, Hongyu Song, Xufang Qian, Yixin Zhao and Tianfu Wang
{"title":"Photovoltaic-driven electrocatalytic upcycling for polyethylene terephthalate plastic waste from simulated electrolysis to photovoltaic direct-driven electrolysis†","authors":"Jiyi Sun, Sen Yang, Chengcheng Cai, Xin Li, Huijing Ma, Yichan Wen, Yan Fang, Hongyu Song, Xufang Qian, Yixin Zhao and Tianfu Wang","doi":"10.1039/D5RE00166H","DOIUrl":null,"url":null,"abstract":"<p >The photovoltaic (PV)-driven electrolysis of polyethylene terephthalate (PET) plastic waste represents a sustainable pathway for resource recovery. Current research predominantly focuses on simulated electrolysis systems or integrated energy storage configurations, while practical implementation under real solar irradiation conditions remains insufficiently investigated. Herein, we report a direct PV-driven electrocatalytic strategy, capable of continuously and simultaneously upcycling PET using a NiOOH electrocatalyst. Remarkably, the catalyst exhibits stable operation for over 500 hours at 300 mA cm<small><sup>−2</sup></small> in the laboratory, and it retains a Faradaic efficiency above 86% within 36 hours under real solar light PV-driven conditions. Through catalyst characterization, we reveal that current fluctuations inherent to solar intermittency induce structural degradation of active catalytic species, highlighting the critical need for enhanced stability optimization. This study provides a pioneering proof-of-concept direct PV-driven electrocatalytic strategy and presents a chemical engineering guideline for scaling PV-powered plastic upcycling technologies.</p>","PeriodicalId":101,"journal":{"name":"Reaction Chemistry & Engineering","volume":" 9","pages":" 2114-2120"},"PeriodicalIF":3.1000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Chemistry & Engineering","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/re/d5re00166h","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The photovoltaic (PV)-driven electrolysis of polyethylene terephthalate (PET) plastic waste represents a sustainable pathway for resource recovery. Current research predominantly focuses on simulated electrolysis systems or integrated energy storage configurations, while practical implementation under real solar irradiation conditions remains insufficiently investigated. Herein, we report a direct PV-driven electrocatalytic strategy, capable of continuously and simultaneously upcycling PET using a NiOOH electrocatalyst. Remarkably, the catalyst exhibits stable operation for over 500 hours at 300 mA cm−2 in the laboratory, and it retains a Faradaic efficiency above 86% within 36 hours under real solar light PV-driven conditions. Through catalyst characterization, we reveal that current fluctuations inherent to solar intermittency induce structural degradation of active catalytic species, highlighting the critical need for enhanced stability optimization. This study provides a pioneering proof-of-concept direct PV-driven electrocatalytic strategy and presents a chemical engineering guideline for scaling PV-powered plastic upcycling technologies.

Abstract Image

光伏驱动电催化对聚对苯二甲酸乙二醇酯塑料废物从模拟电解到光伏直接驱动电解的升级回收
光伏(PV)驱动的电解聚对苯二甲酸乙二醇酯(PET)塑料废物代表了资源回收的可持续途径。目前的研究主要集中在模拟电解系统或集成储能配置上,而在真实太阳辐射条件下的实际实施仍然没有得到充分的研究。在此,我们报告了一种直接的pv驱动电催化策略,能够使用NiOOH电催化剂连续和同时升级PET。值得注意的是,该催化剂在实验室中在300 mA cm−2下稳定运行超过500小时,在实际太阳能光pv驱动条件下,36小时内保持86%以上的法拉第效率。通过催化剂表征,我们揭示了太阳能间歇性固有的电流波动诱导活性催化物种的结构降解,突出了增强稳定性优化的迫切需要。这项研究提供了一个开创性的概念验证,直接由光伏驱动的电催化策略,并为扩大光伏驱动的塑料升级回收技术提供了一个化学工程指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Reaction Chemistry & Engineering
Reaction Chemistry & Engineering Chemistry-Chemistry (miscellaneous)
CiteScore
6.60
自引率
7.70%
发文量
227
期刊介绍: Reaction Chemistry & Engineering is a new journal reporting cutting edge research into all aspects of making molecules for the benefit of fundamental research, applied processes and wider society. From fundamental, molecular-level chemistry to large scale chemical production, Reaction Chemistry & Engineering brings together communities of chemists and chemical engineers working to ensure the crucial role of reaction chemistry in today’s world.
×
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:604180095
Book学术官方微信