{"title":"“Parallel+uniaxial” conjugated electrospinning for dual-function analogous-tricolor microfiber film with multicolor emission and magnetism","authors":"Xintong Huo, Yunrui Xie, Yuqi Sheng, Yaolin Hu, Haina Qi, Hong Shao, Qianli Ma, Wensheng Yu, Guixia Liu, Xiangting Dong","doi":"10.1016/j.matt.2024.101946","DOIUrl":null,"url":null,"abstract":"Innovative “parallel+uniaxial” conjugated electrospinning is advanced and utilized to synthesize a unique {[CsPbBr<sub>3</sub>/polystyrene (PS)]//[CoFe<sub>2</sub>O<sub>4</sub>/PS]}||[CsPb(Br<sub>0.06</sub>/I<sub>0.94</sub>)<sub>3</sub>/PS] analogous-tricolor microfiber film (ATMF) with multicolor emission and tunable magnetism. This analogous-tricolor microfiber as a structural element accomplishes three independent microcosmic partitions to assemble CsPbBr<sub>3</sub> perovskite quantum dots (QDs) with green fluorescence, CsPb(Br<sub>0.06</sub>/I<sub>0.94</sub>)<sub>3</sub> QDs with red fluorescence, and magnetic CoFe<sub>2</sub>O<sub>4</sub> into their respective partitions. As a result, the adverse impacts of dark-colored CoFe<sub>2</sub>O<sub>4</sub> on the fluorescence of the two perovskite QDs are shunned, and the microcosmic spatial separation of the two kinds of perovskite QDs fully addresses infaust halogen anion exchange between them to receive super fluorescence-magnetic bifuction. The light-emitting diodes (LEDs) packaged using blue chips and ATMF as phosphor exhibit white-light fluorescence. The formation mechanisms of the analogous-tricolor microfiber and ATMF are advanced, and corresponding facile construction techniques are established to shun complex processes. This work provides support for the design and preparation of other multifunctional materials.","PeriodicalId":388,"journal":{"name":"Matter","volume":"8 1","pages":""},"PeriodicalIF":17.3000,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Matter","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.matt.2024.101946","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Innovative “parallel+uniaxial” conjugated electrospinning is advanced and utilized to synthesize a unique {[CsPbBr3/polystyrene (PS)]//[CoFe2O4/PS]}||[CsPb(Br0.06/I0.94)3/PS] analogous-tricolor microfiber film (ATMF) with multicolor emission and tunable magnetism. This analogous-tricolor microfiber as a structural element accomplishes three independent microcosmic partitions to assemble CsPbBr3 perovskite quantum dots (QDs) with green fluorescence, CsPb(Br0.06/I0.94)3 QDs with red fluorescence, and magnetic CoFe2O4 into their respective partitions. As a result, the adverse impacts of dark-colored CoFe2O4 on the fluorescence of the two perovskite QDs are shunned, and the microcosmic spatial separation of the two kinds of perovskite QDs fully addresses infaust halogen anion exchange between them to receive super fluorescence-magnetic bifuction. The light-emitting diodes (LEDs) packaged using blue chips and ATMF as phosphor exhibit white-light fluorescence. The formation mechanisms of the analogous-tricolor microfiber and ATMF are advanced, and corresponding facile construction techniques are established to shun complex processes. This work provides support for the design and preparation of other multifunctional materials.
期刊介绍:
Matter, a monthly journal affiliated with Cell, spans the broad field of materials science from nano to macro levels,covering fundamentals to applications. Embracing groundbreaking technologies,it includes full-length research articles,reviews, perspectives,previews, opinions, personnel stories, and general editorial content.
Matter aims to be the primary resource for researchers in academia and industry, inspiring the next generation of materials scientists.