CsPbBr3 Nanocrystals Prepared Using Block Copolymer Micelles for LEDs

IF 5.3 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY ACS Applied Nano Materials Pub Date : 2024-11-22 DOI:10.1021/acsanm.4c0612210.1021/acsanm.4c06122
Belda Amelia Junisu, Ya-Sen Sun*, Cindy Mutiara Septani and Orion Shih, 
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Abstract

We systematically investigated how block copolymer (BCP) templating influences CsPbBr3 nanocrystals inside polystyrene-block-poly(2-vinylpyridine) (PSm-b-P2VPn) micelles in benzene (BEN), toluene (TOL), oxylene (OXY), and 1,3,5-trimethylbenzene (TMB) for light-emitting diode (LED) applications. Each organic solvent features a benzene ring attached to different numbers of methyl groups, thus providing varying solvent qualities for the formation of CsPbBr3 nanocrystals. We found that solvent quality plays a crucial role in fabricating CsPbBr3 nanocrystals with a superior photoluminescence (PL) performance and long-term stability. The micellization strength of PSm-b-P2VPn is strongest in TMB but weakest in BEN, suggesting that increasing the number of methyl groups attached to benzene enhances micellization. Furthermore, increasing the number of methyl groups attached to benzene also yields three positive effects: increased dissociation, complexation, and coordination interaction of PbBr2 with P2VP cores. Consequently, each PSm-b-P2VPn micelle can capture a higher content of [PbBr3] complexes in TMB. Complexation of PbBr2 followed by coordination interaction with P2VP is also critical because the growth of CsPbBr3 nanocrystals inside individual micelles involves binding of Cs+ cations with [PbBr3] complexes rather than with PbBr2 nanocrystals. However, [PbBr3] complexes are not crystalline but amorphous and are not uniformly distributed within the P2VP cores. When a small amount of CsBr was added, a portion of [PbBr3] complexes transformed to form CsPbBr3 perovskite nanocrystals (PNCs) with small size and polydisperse size distribution, coexisting with abundant active [PbBr3] and [PbBr4]2– complexes. Furthermore, variations in the molecular weights and compositions of PSm-b-P2VPn have minimal influence on the size of the CsPbBr3 nanoparticles. Instead, the CsBr content plays a more decisive role in controlling nanoparticle size, primarily due to the limited solubility of CsBr, an all-inorganic precursor, in methanol.

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我们系统地研究了嵌段共聚物 (BCP) 模板如何影响聚苯乙烯-嵌段-聚(2-乙烯基吡啶)(PSm-b-P2VPn)胶束内用于发光二极管 (LED) 应用的铯硼三纳米晶体在苯(BEN)、甲苯(TOL)、二甲苯(OXY)和 1,3,5 三甲基苯(TMB)中的形成。每种有机溶剂的苯环上都附有不同数量的甲基,从而为形成 CsPbBr3 纳米晶体提供了不同的溶剂质量。我们发现,溶剂质量在制造具有优异光致发光(PL)性能和长期稳定性的 CsPbBr3 纳米晶体中起着至关重要的作用。PSm-b-P2VPn 在 TMB 中的胶束化强度最强,而在 BEN 中的胶束化强度最弱,这表明增加附着在苯上的甲基数量可增强胶束化。此外,增加苯上附着的甲基数还会产生三个积极影响:增加 PbBr2 与 P2VP 核心的解离、络合和配位相互作用。因此,每个 PSm-b-P2VPn 胶束都能捕获 TMB 中更高含量的 [PbBr3]- 复合物。PbBr2 与 P2VP 发生配位作用后的络合也很关键,因为 CsPbBr3 纳米晶体在单个胶束内的生长涉及 Cs+ 阳离子与 [PbBr3]- 复合物的结合,而不是与 PbBr2 纳米晶体的结合。不过,[PbBr3]- 复合物不是晶体而是无定形的,在 P2VP 核心内的分布也不均匀。当加入少量铯硼时,一部分[PbBr3]- 复合物转变为 CsPbBr3 包晶石纳米晶体(PNC),其尺寸较小,且呈多分散粒度分布,与丰富的活性[PbBr3]- 和[PbBr4]2- 复合物共存。此外,PSm-b-P2VPn 的分子量和成分变化对 CsPbBr3 纳米粒子的尺寸影响极小。相反,CsBr 的含量在控制纳米粒子大小方面起着决定性作用,这主要是由于全无机前体 CsBr 在甲醇中的溶解度有限。
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来源期刊
CiteScore
8.30
自引率
3.40%
发文量
1601
期刊介绍: ACS Applied Nano Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics and biology relevant to applications of nanomaterials. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important applications of nanomaterials.
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