1 Ocak 2021 Dergi makalesi Açık Erişim

Jiang, Guocan; Erdem, Onur; Hubner, Rene; Georgi, Maximilian; Wei, Wei; Fan, Xuelin; Wang, Jin; Demir, Hilmi Volkan; Gaponik, Nikolai

DataCite XML

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/232588</identifier>
  <creators>
    <creator>
      <creatorName>Jiang, Guocan</creatorName>
      <givenName>Guocan</givenName>
      <familyName>Jiang</familyName>
      <affiliation>Tech Univ Dresden, Phys Chem, Zellescher Weg 19, D-01069 Dresden, Germany</affiliation>
    </creator>
    <creator>
      <creatorName>Erdem, Onur</creatorName>
      <givenName>Onur</givenName>
      <familyName>Erdem</familyName>
    </creator>
    <creator>
      <creatorName>Hubner, Rene</creatorName>
      <givenName>Rene</givenName>
      <familyName>Hubner</familyName>
      <affiliation>Helmholtz Zentrum Dresden Rossendorf, Inst Ion Beam Phys &amp; Mat Res, Bautzner Landstr 400, D-01328 Dresden, Germany</affiliation>
    </creator>
    <creator>
      <creatorName>Georgi, Maximilian</creatorName>
      <givenName>Maximilian</givenName>
      <familyName>Georgi</familyName>
      <affiliation>Tech Univ Dresden, Phys Chem, Zellescher Weg 19, D-01069 Dresden, Germany</affiliation>
    </creator>
    <creator>
      <creatorName>Wei, Wei</creatorName>
      <givenName>Wei</givenName>
      <familyName>Wei</familyName>
      <affiliation>Tech Univ Dresden, Phys Chem, Zellescher Weg 19, D-01069 Dresden, Germany</affiliation>
    </creator>
    <creator>
      <creatorName>Fan, Xuelin</creatorName>
      <givenName>Xuelin</givenName>
      <familyName>Fan</familyName>
      <affiliation>Tech Univ Dresden, Phys Chem, Zellescher Weg 19, D-01069 Dresden, Germany</affiliation>
    </creator>
    <creator>
      <creatorName>Wang, Jin</creatorName>
      <givenName>Jin</givenName>
      <familyName>Wang</familyName>
      <affiliation>Zhejiang Normal Univ, Key Lab, Minist Educ Adv Catalysis Mat, Jinhua 321004, Zhejiang, Peoples R China</affiliation>
    </creator>
    <creator>
      <creatorName>Demir, Hilmi Volkan</creatorName>
      <givenName>Hilmi Volkan</givenName>
      <familyName>Demir</familyName>
    </creator>
    <creator>
      <creatorName>Gaponik, Nikolai</creatorName>
      <givenName>Nikolai</givenName>
      <familyName>Gaponik</familyName>
      <affiliation>Tech Univ Dresden, Phys Chem, Zellescher Weg 19, D-01069 Dresden, Germany</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Mechanosynthesis Of Polymer-Stabilized Lead Bromide Perovskites: Insight Into The Formation And Phase Conversion Of Nanoparticles</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2021</publicationYear>
  <dates>
    <date dateType="Issued">2021-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/232588</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1007/s12274-020-3152-7</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">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.</description>
  </descriptions>
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