{"title":"在水性光-RAFT 聚合过程中克服光催化-稳定性权衡的水稳定性 Perovskite 纳米晶体","authors":"Mengqiang Zhang, Jingyi Hao, Chengli Wang, Yue Zhang, Xiaomeng Zhang, Zhe Cui, Peng Fu, Minying Liu, Ge Shi, Xiaoguang Qiao, Yajing Chang, Yanjie He* and Xinchang Pang*, ","doi":"10.1021/acscatal.4c0340710.1021/acscatal.4c03407","DOIUrl":null,"url":null,"abstract":"<p >Metal halide perovskite nanocrystals (PNCs) have demonstrated remarkable photocatalytic properties in diverse photochemical reactions owing to their high absorption coefficients and long photogenerated carrier lifetimes. However, their catalytic applications have been severely hindered by their structural incompatibility with polar solvents, water in particular, due to the labile ionic nature of the perovskite. Realization of the photocatalytic performance of PNCs in an aqueous medium would significantly expand their potential in photocatalysis. Herein, judiciously designed CsPbBr<sub>3</sub> NCs stabilized on Al<sub>2</sub>O<sub>3</sub> nanoflowers (denoted as A-CsPbBr<sub>3</sub> NCs) are utilized as water-stable photocatalysts for aqueous photomediated reversible addition–fragmentation chain transfer (photo-RAFT) polymerization. The A-CsPbBr<sub>3</sub> NCs exhibited exceptional water stability and photostability owing to the stabilization effect endowed by Al<sub>2</sub>O<sub>3</sub> nanoflowers without sacrificing their charge/carrier transport properties. Consequently, aqueous photo-RAFT polymerization was successfully performed by leveraging A-CsPbBr<sub>3</sub> NCs as photocatalysts under visible light illumination, which was inaccessible to conventional short-ligand-capped PNCs. The effects of the excitation wavelength, catalyst loading, and architectures of PNCs on the visible-light-mediated polymerization were scrutinized to reveal the polymerization via a photoinduced electron-/energy-transfer mechanism, yielding polymers/copolymers with well-defined compositions, well-controlled molecular weights, low polydispersity, and high chain-end fidelity.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"14 21","pages":"16313–16323 16313–16323"},"PeriodicalIF":11.3000,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Water-Stable Perovskite Nanocrystals to Overcome the Photocatalysis–Stability Trade-Off in Aqueous Photo-RAFT Polymerization\",\"authors\":\"Mengqiang Zhang, Jingyi Hao, Chengli Wang, Yue Zhang, Xiaomeng Zhang, Zhe Cui, Peng Fu, Minying Liu, Ge Shi, Xiaoguang Qiao, Yajing Chang, Yanjie He* and Xinchang Pang*, \",\"doi\":\"10.1021/acscatal.4c0340710.1021/acscatal.4c03407\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Metal halide perovskite nanocrystals (PNCs) have demonstrated remarkable photocatalytic properties in diverse photochemical reactions owing to their high absorption coefficients and long photogenerated carrier lifetimes. However, their catalytic applications have been severely hindered by their structural incompatibility with polar solvents, water in particular, due to the labile ionic nature of the perovskite. Realization of the photocatalytic performance of PNCs in an aqueous medium would significantly expand their potential in photocatalysis. Herein, judiciously designed CsPbBr<sub>3</sub> NCs stabilized on Al<sub>2</sub>O<sub>3</sub> nanoflowers (denoted as A-CsPbBr<sub>3</sub> NCs) are utilized as water-stable photocatalysts for aqueous photomediated reversible addition–fragmentation chain transfer (photo-RAFT) polymerization. The A-CsPbBr<sub>3</sub> NCs exhibited exceptional water stability and photostability owing to the stabilization effect endowed by Al<sub>2</sub>O<sub>3</sub> nanoflowers without sacrificing their charge/carrier transport properties. Consequently, aqueous photo-RAFT polymerization was successfully performed by leveraging A-CsPbBr<sub>3</sub> NCs as photocatalysts under visible light illumination, which was inaccessible to conventional short-ligand-capped PNCs. The effects of the excitation wavelength, catalyst loading, and architectures of PNCs on the visible-light-mediated polymerization were scrutinized to reveal the polymerization via a photoinduced electron-/energy-transfer mechanism, yielding polymers/copolymers with well-defined compositions, well-controlled molecular weights, low polydispersity, and high chain-end fidelity.</p>\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"14 21\",\"pages\":\"16313–16323 16313–16323\"},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2024-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acscatal.4c03407\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acscatal.4c03407","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Water-Stable Perovskite Nanocrystals to Overcome the Photocatalysis–Stability Trade-Off in Aqueous Photo-RAFT Polymerization
Metal halide perovskite nanocrystals (PNCs) have demonstrated remarkable photocatalytic properties in diverse photochemical reactions owing to their high absorption coefficients and long photogenerated carrier lifetimes. However, their catalytic applications have been severely hindered by their structural incompatibility with polar solvents, water in particular, due to the labile ionic nature of the perovskite. Realization of the photocatalytic performance of PNCs in an aqueous medium would significantly expand their potential in photocatalysis. Herein, judiciously designed CsPbBr3 NCs stabilized on Al2O3 nanoflowers (denoted as A-CsPbBr3 NCs) are utilized as water-stable photocatalysts for aqueous photomediated reversible addition–fragmentation chain transfer (photo-RAFT) polymerization. The A-CsPbBr3 NCs exhibited exceptional water stability and photostability owing to the stabilization effect endowed by Al2O3 nanoflowers without sacrificing their charge/carrier transport properties. Consequently, aqueous photo-RAFT polymerization was successfully performed by leveraging A-CsPbBr3 NCs as photocatalysts under visible light illumination, which was inaccessible to conventional short-ligand-capped PNCs. The effects of the excitation wavelength, catalyst loading, and architectures of PNCs on the visible-light-mediated polymerization were scrutinized to reveal the polymerization via a photoinduced electron-/energy-transfer mechanism, yielding polymers/copolymers with well-defined compositions, well-controlled molecular weights, low polydispersity, and high chain-end fidelity.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.