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

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-10-22 DOI:10.1021/acscatal.4c0340710.1021/acscatal.4c03407
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*, 
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引用次数: 0

摘要

由于具有高吸收系数和长光生载流子寿命,金属卤化物过氧化物纳米晶体(PNCs)在各种光化学反应中表现出显著的光催化特性。然而,由于其结构与极性溶剂不相容,特别是与水不相容,从而严重阻碍了它们的催化应用。实现 PNCs 在水介质中的光催化性能将大大拓展其在光催化领域的潜力。在此,我们利用经过合理设计、稳定在 Al2O3 纳米流体上的 CsPbBr3 NCs(称为 A-CsPbBr3 NCs)作为水稳定性光催化剂,用于水介质光催化可逆加成-断裂链转移(photo-RAFT)聚合反应。由于 Al2O3 纳米流体的稳定作用,A-CsPbBr3 NCs 在不牺牲其电荷/载体传输特性的前提下,表现出优异的水稳定性和光稳定性。因此,在可见光照射下,利用 A-CsPbBr3 NCs 作为光催化剂,成功实现了传统短配体封端 PNCs 无法实现的水性光-RAFT 聚合。研究人员仔细观察了激发波长、催化剂负载量和 PNCs 结构对可见光介导聚合的影响,发现聚合是通过光诱导电子/能量转移机制进行的,从而产生了成分明确、分子量控制良好、多分散性低和链端保真度高的聚合物/共聚物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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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.

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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
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.
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