Yuwen Zhang, Alessio Lo Bocchiaro, Xiaolei Hu, Carlos Pavon, Cristian Pezzato, Krzysztof Matyjaszewski*, Francesca Lorandi* and Edmondo M. Benetti*,
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Herein, we report a red-light-driven SI-photoATRP process enabled by a catalytic system composed of methylene blue (MB<sup>+</sup>) and a Cu-based ATRP catalyst, which achieves efficient polymer brush growth under fully open-air conditions. Systematic variation of reaction parameters─including light intensity, composition of the catalytic system, and solvent─enabled rapid growth of compositionally different brushes with high and tunable thickness. The deep penetration capability of red light was exploited to decorate microporous three-dimensional materials with polymer brushes. Spatially defined brush growth was demonstrated by shifting the wavelength of light irradiation, alternatively stimulating surface-initiated polymerization in the outer volumes of the support or uniformly across the entire microporous material.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 26","pages":"38773–38782"},"PeriodicalIF":8.2000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acsami.5c08584","citationCount":"0","resultStr":"{\"title\":\"Open-Air Growth of Polymer Brushes by Surface-Initiated PhotoATRP under Red-Light Irradiation\",\"authors\":\"Yuwen Zhang, Alessio Lo Bocchiaro, Xiaolei Hu, Carlos Pavon, Cristian Pezzato, Krzysztof Matyjaszewski*, Francesca Lorandi* and Edmondo M. Benetti*, \",\"doi\":\"10.1021/acsami.5c08584\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The translation of polymer brushes into technologically relevant coatings hinges on the development of scalable and robust fabrication strategies that are tolerant of environmental conditions. Surface-initiated photoinduced atom transfer radical polymerization (SI-photoATRP) has emerged as a powerful tool for synthesizing functional brushes with precise control over their architectural parameters. However, traditional SI-photoATRP requires high-energy light and confined setups to mitigate oxygen inhibition within nondeoxygenated mixtures, limiting substrate versatility and process scalability. Herein, we report a red-light-driven SI-photoATRP process enabled by a catalytic system composed of methylene blue (MB<sup>+</sup>) and a Cu-based ATRP catalyst, which achieves efficient polymer brush growth under fully open-air conditions. Systematic variation of reaction parameters─including light intensity, composition of the catalytic system, and solvent─enabled rapid growth of compositionally different brushes with high and tunable thickness. The deep penetration capability of red light was exploited to decorate microporous three-dimensional materials with polymer brushes. Spatially defined brush growth was demonstrated by shifting the wavelength of light irradiation, alternatively stimulating surface-initiated polymerization in the outer volumes of the support or uniformly across the entire microporous material.</p>\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"17 26\",\"pages\":\"38773–38782\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-06-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acsami.5c08584\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsami.5c08584\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsami.5c08584","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Open-Air Growth of Polymer Brushes by Surface-Initiated PhotoATRP under Red-Light Irradiation
The translation of polymer brushes into technologically relevant coatings hinges on the development of scalable and robust fabrication strategies that are tolerant of environmental conditions. Surface-initiated photoinduced atom transfer radical polymerization (SI-photoATRP) has emerged as a powerful tool for synthesizing functional brushes with precise control over their architectural parameters. However, traditional SI-photoATRP requires high-energy light and confined setups to mitigate oxygen inhibition within nondeoxygenated mixtures, limiting substrate versatility and process scalability. Herein, we report a red-light-driven SI-photoATRP process enabled by a catalytic system composed of methylene blue (MB+) and a Cu-based ATRP catalyst, which achieves efficient polymer brush growth under fully open-air conditions. Systematic variation of reaction parameters─including light intensity, composition of the catalytic system, and solvent─enabled rapid growth of compositionally different brushes with high and tunable thickness. The deep penetration capability of red light was exploited to decorate microporous three-dimensional materials with polymer brushes. Spatially defined brush growth was demonstrated by shifting the wavelength of light irradiation, alternatively stimulating surface-initiated polymerization in the outer volumes of the support or uniformly across the entire microporous material.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.