Water-Stable Perovskite Nanocrystals to Overcome the Photocatalysis–Stability Trade-Off in Aqueous Photo-RAFT Polymerization

光催化 聚合 链式转移 钙钛矿(结构) 水溶液 光化学 分散性 催化作用 可逆加成-断裂链转移聚合 材料科学 木筏 化学工程 化学 自由基聚合 高分子化学 聚合物 有机化学 工程类 复合材料
作者
Mengqiang Zhang,Jingyi Hao,Chengli Wang,Yue Zhang,Xiaomeng Zhang,Zhe Cui,Peng Fu,Minying Liu,Ge Shi,Xiaoguang Qiao,Yajing Chang,Yanjie He,Xinchang Pang
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:14 (21): 16313-16323 被引量:15
标识
DOI:10.1021/acscatal.4c03407
摘要

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 3 NCs stabilized on Al 2 O 3 nanoflowers (denoted as A-CsPbBr 3 NCs) are utilized as water-stable photocatalysts for aqueous photomediated reversible addition–fragmentation chain transfer (photo-RAFT) polymerization. The A-CsPbBr 3 NCs exhibited exceptional water stability and photostability owing to the stabilization effect endowed by Al 2 O 3 nanoflowers without sacrificing their charge/carrier transport properties. Consequently, aqueous photo-RAFT polymerization was successfully performed by leveraging A-CsPbBr 3 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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