Xiaoguang Qiao, Xinchang Pang, Mengna Feng, Mengjie Zhou, Wenjie Zhang, Yanjie He, Ge Shi
{"title":"Carbon dots driven near infrared light induced miniemulsion atom transfer radical polymerization","authors":"Xiaoguang Qiao, Xinchang Pang, Mengna Feng, Mengjie Zhou, Wenjie Zhang, Yanjie He, Ge Shi","doi":"10.1039/d5py00873e","DOIUrl":null,"url":null,"abstract":"Photoinduced polymerization methods are increasingly valued for their mild operating conditions, precise spatiotemporal control, and operational simplicity. Beyond homogeneous systems, adapting photopolymerization to emulsions offers a greener and more practical approach. Nevertheless, the poor penetration of short-wavelength light sources commonly adopted in prior studies, combined with the opacity inherent to heterogeneous systems, led to inefficient light energy utilization. This work presents an efficient near-infrared (NIR) light induced miniemulsion atom transfer radical polymerization (mini-ATRP), by utilizing phosphorus and nitrogen codoped carbon dots (PN-CDs) as the photocatalyst. Owing to the absorption in the NIR region, PN-CDs can generate electrons under excitation by an 808 nm laser, thereby initiating mini-ATRP through electron transfer with Cu(II)/surfactant ion-pair at the interface of oil/water droplets. This NIR induced mini-ATRP system successfully produced polymers with low dispersity (Đ<1.25) and high monomer conversion (~86%) within 2 hour. Excellent temporal control of the polymerization and the chain fidelity of polymers were illustrated by light-switching experiment and chain extension, separately. This research establishes new pathways for robust emulsion photopolymerization techniques, providing enhanced control, efficiency, and a more sustainable process.","PeriodicalId":100,"journal":{"name":"Polymer Chemistry","volume":"573 1","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5py00873e","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Photoinduced polymerization methods are increasingly valued for their mild operating conditions, precise spatiotemporal control, and operational simplicity. Beyond homogeneous systems, adapting photopolymerization to emulsions offers a greener and more practical approach. Nevertheless, the poor penetration of short-wavelength light sources commonly adopted in prior studies, combined with the opacity inherent to heterogeneous systems, led to inefficient light energy utilization. This work presents an efficient near-infrared (NIR) light induced miniemulsion atom transfer radical polymerization (mini-ATRP), by utilizing phosphorus and nitrogen codoped carbon dots (PN-CDs) as the photocatalyst. Owing to the absorption in the NIR region, PN-CDs can generate electrons under excitation by an 808 nm laser, thereby initiating mini-ATRP through electron transfer with Cu(II)/surfactant ion-pair at the interface of oil/water droplets. This NIR induced mini-ATRP system successfully produced polymers with low dispersity (Đ<1.25) and high monomer conversion (~86%) within 2 hour. Excellent temporal control of the polymerization and the chain fidelity of polymers were illustrated by light-switching experiment and chain extension, separately. This research establishes new pathways for robust emulsion photopolymerization techniques, providing enhanced control, efficiency, and a more sustainable process.
期刊介绍:
Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.