4.8 Article

Mechanosynthesis of polymer-stabilized lead bromide perovskites: Insight into the formation and phase conversion of nanoparticles

期刊

NANO RESEARCH
卷 14, 期 4, 页码 1078-1086

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-020-3152-7

关键词

lead bromide perovskites; mechanosynthesis; polymer ligands; polymer micelles; poly(ethyleneimine)-induced phase conversion

资金

  1. China Scholarship Council [201706740088, 201606340161]
  2. bilateral IB-BMBF-TUBITAK Project ColMiBack [01DL20002]
  3. DFG [EY 16/14-3]
  4. TUBITAK
  5. TUBA
  6. German Federal Ministry of Education of Research (BMBF) [03SF0451]
  7. Swiss National Science Foundation (SNF)
  8. German Research Foundation (DFG ) [DFG EY 16/18-2]
  9. Jiangsu Overseas Visiting Scholar Program for University Prominent Young & Middle-aged Teachers and Presidents
  10. National Natural Science Foundation of China [21701143]

向作者/读者索取更多资源

The study demonstrates a mechanosynthesis method of polymer-coordinated perovskite nanoparticles, showing green emission and high photoluminescence quantum yield. The polymer-stabilized NPs exhibit excellent durability and resistance to polar solvents, making them suitable for optical materials applications.
The application of polymers to replace oleylamine (OLA) and oleic acid (OA) as ligands for perovskite nanocrystals is an effective strategy to improve their stability and durability especially for the solution-based processing. Herein, we report a mechanosynthesis of lead bromide perovskite nanoparticles (NPs) stabilized by partially hydrolyzed poly(methyl methacrytate) (h-PMMA) and highmolecular-weight highly-branched poly(ethylenimine) (PEI-25K). The as-synthesized NP solutions exhibited green emission centered at 516 nm, possessing a narrow full-width at half-maximum of 17 nm and as high photoluminescence quantum yield (PLQY) as 85%, while showing excellent durability and resistance to polar solvents, e.g., methanol. The colloids of polymer-stabilized NPs were directly processable to form stable and strongly-emitting thin films and solids, making them attractive as gain media. Furthermore, the roles of h-PMMA and PEI-25K in the grinding process were studied in depth. The h-PMMA can form micelles in the grinding solvent of dichloromethane to act as size-regulating templates for the growth of NPs. The PEI-25K with large amounts of amino groups induced significant enrichment of PbBr2 in the reaction mixture, which in turn caused the formation of CsPb2Br5-mPbBr(2) and CsPbBr3-Os4PbBr6-nCsBr NPs. The presence of CsPbBr3-Cs4PbBr6-nCsBr NPs was responsible for the high PLQY, as the Cs4PbBr6 phase with a wide energy bandgap can passivate the surface defects of the CsPbBr3 phase. This work describes a direct and facile mechanosynthesis of polymer-coordinated perovskite NPs and promotes in-depth understanding of the formation and phase conversion for perovskite NPs in the grinding process.

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