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Flexible Polymer-Assisted Mesoscale Self-Assembly of Colloidal CsPbBr3 Perovskite Nanocrystals into Higher Order Superstructures with Strong Inter-Nanocrystal Electronic Coupling.
Yang, Yang; Lee, Jacob T; Liyanage, Thakshila; Sardar, Rajesh.
Afiliação
  • Yang Y; Department of Chemistry and Chemical Biology , Indiana University-Purdue University Indianapolis , Indianapolis , Indiana 46202 , United States.
  • Lee JT; Department of Chemistry and Chemical Biology , Indiana University-Purdue University Indianapolis , Indianapolis , Indiana 46202 , United States.
  • Liyanage T; Department of Chemistry and Chemical Biology , Indiana University-Purdue University Indianapolis , Indianapolis , Indiana 46202 , United States.
  • Sardar R; Department of Chemistry and Chemical Biology , Indiana University-Purdue University Indianapolis , Indianapolis , Indiana 46202 , United States.
J Am Chem Soc ; 141(4): 1526-1536, 2019 Jan 30.
Article em En | MEDLINE | ID: mdl-30608690
Surface-passivating ligands, although ubiquitous to colloidal nanocrystal (NC) syntheses, play a role in assembling NCs into higher order structures and hierarchical superstructures, which has not been demonstrated yet for colloidal CsPbX3 (X = Cl, Br, and I) NCs. In this work, we report that functional poly(ethylene glycols) (PEG6-Y, Y = -COOH and -NH2) represent unique surface-passivating ligands enabling the synthesis of near-uniform CsPbBr3 NCs with diameters of 3.0 nm. The synthesized NCs are assembled into individual pearl necklaces, bundled pearl necklaces, lamellar, and nanorice superstructures, in situ. It is believed a variety of forces, including van der Waals attractions between hydrophilic PEG tails in a nonpolar solvent and dipole-dipole attraction between NCs, drive mesoscale assembly to form superstructures. Furthermore, postsynthetic ligand treatment strengthens the argument for polymer-assisted mesoscale assembly as pearl necklace assemblies can be successfully converted into either lamellar or nanorice structures. We observe an ∼240 meV bathochromic shift in the lowest energy absorption peak of CsPbBr3 NCs when they are present in the lamellar and nanorice assemblies, representing strong inter-NC electronic coupling. Moreover, pearl necklace structures are spontaneously assembled into micrometer length scale twisted ribbon hierarchical superstructures during storage of colloidal CsPbBr3 NCs. The results show that the self-assembled superstructures of CsPbBr3 NCs are now feasible to prepare via template-free synthesis, as self-assembled structures emerge in the bulk solvent, a process that mimics biological systems except for the use of nonbiological surface ligands (PEG6-Y). Taken together, emergent optoelectronic properties and higher order superstructures of CsPbBr3 NCs should aid their potential use in solid-state devices and simplify scalable manufacturing.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos