Programmable Colloidal Approach to Hierarchical Structures of Methylammonium Lead Bromide Perovskite Nanocrystals with Bright Photoluminescent Properties

dc.contributor.authorTeunis, Meghan B.
dc.contributor.authorJohnson, Merrell A.
dc.contributor.authorMuhoberac, Barry B.
dc.contributor.authorSeifert, Soenke
dc.contributor.authorSardar, Rajesh
dc.contributor.departmentChemistry and Chemical Biology, School of Scienceen_US
dc.date.accessioned2017-12-28T18:45:11Z
dc.date.available2017-12-28T18:45:11Z
dc.date.issued2017-04
dc.description.abstractSystematic tailoring of nanocrystal architecture could provide unprecedented control over their electronic, photophysical, and charge transport properties for a variety of applications. However, at present, manipulation of the shape of perovskite nanocrystals is done mostly by trial-and-error-based experimental approaches. Here, we report systematic colloidal synthetic strategies to prepare methylammonium lead bromide quantum platelets and quantum cubes. In order to control the nucleation and growth processes of these nanocrystals, we appropriately manipulate the solvent system, surface ligand chemistry, and reaction temperature causing syntheses into anisotropic shapes. We demonstrate that both the presence of chlorinated solvent and a long chain aliphatic amine in the reaction mixture are crucial for the formation of ultrathin quantum platelets (∼2.5 nm in thickness), which is driven by mesoscale-assisted growth of spherical seed nanocrystals (∼1.6 nm in diameter) through attachment of monomers onto selective crystal facets. A combined surface and structural characterization, along with small-angle X-ray scattering analysis, confirm that the long hydrocarbon of the aliphatic amine is responsible for the well ordered hierarchical stacking of the quantum platelets of 3.5 nm separation. In contrast, the formation of ∼12 nm edge-length quantum cubes is a kinetically driven process in which a high flux of monomers is achieved by supplying thermal energy. The photoluminescence quantum yield of our quantum platelets (∼52%) is nearly 2-fold higher than quantum cubes. Moreover, the quantum platelets display a lower nonradiative rate constant than that found with quantum cubes, which suggests less surface trap states. Together, our research has the potential both to improve the design of synthetic methods for programmable control of shape and assembly and to provide insight into optoelectronic properties of these materials for solid-state device fabrication, e.g., light-emitting diodes, solar cells, and lasing materials.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationTeunis, M. B., Johnson, M. A., Muhoberac, B. B., Seifert, S., & Sardar, R. (2017). Programmable Colloidal Approach to Hierarchical Structures of Methylammonium Lead Bromide Perovskite Nanocrystals with Bright Photoluminescent Properties. Chemistry of Materials, 29(8), 3526–3537. https://doi.org/10.1021/acs.chemmater.6b05393en_US
dc.identifier.urihttps://hdl.handle.net/1805/14914
dc.language.isoenen_US
dc.publisherACSen_US
dc.relation.isversionof10.1021/acs.chemmater.6b05393en_US
dc.relation.journalChemistry of Materialsen_US
dc.rightsAttribution-NonCommercial 3.0 United States
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/us
dc.sourcePublisheren_US
dc.subjectnanocrystal architectureen_US
dc.subjectsystematic tailoringen_US
dc.subjectperovskite nanocrystalsen_US
dc.titleProgrammable Colloidal Approach to Hierarchical Structures of Methylammonium Lead Bromide Perovskite Nanocrystals with Bright Photoluminescent Propertiesen_US
dc.typeArticleen_US
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