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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
Author(s) -
Yang Yang,
Jacob T. Lee,
Thakshila Liyanage,
Rajesh Sardar
Publication year - 2019
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.8b10083
Subject(s) - nanocrystal , chemistry , lamellar structure , nanotechnology , van der waals force , colloid , polymer , self assembly , chemical physics , crystallography , chemical engineering , materials science , molecule , organic chemistry , engineering
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 CsPbX 3 (X = Cl, Br, and I) NCs. In this work, we report that functional poly(ethylene glycols) (PEG 6 -Y, Y = -COOH and -NH 2 ) represent unique surface-passivating ligands enabling the synthesis of near-uniform CsPbBr 3 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 CsPbBr 3 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 CsPbBr 3 NCs. The results show that the self-assembled superstructures of CsPbBr 3 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 (PEG 6 -Y). Taken together, emergent optoelectronic properties and higher order superstructures of CsPbBr 3 NCs should aid their potential use in solid-state devices and simplify scalable manufacturing.

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