Self-Assembly of Quantum Dot–Gold Heterodimer Nanocrystals with Orientational Order

The self-assembly of nanocrystals into ordered superlattices is a powerful strategy for the production of functional nanomaterials. The assembly of well-ordered target structures, however, requires control over the building blocks’ size and shape as well as their interactions. While nanocrystals wit...

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Published inNano letters Vol. 18; no. 8; pp. 5049 - 5056
Main Authors Zhu, Hua, Fan, Zhaochuan, Yuan, Yucheng, Wilson, Mitchell A., Hills-Kimball, Katie, Wei, Zichao, He, Jie, Li, Ruipeng, Grünwald, Michael, Chen, Ou
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 08.08.2018
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Summary:The self-assembly of nanocrystals into ordered superlattices is a powerful strategy for the production of functional nanomaterials. The assembly of well-ordered target structures, however, requires control over the building blocks’ size and shape as well as their interactions. While nanocrystals with homogeneous composition are now routinely synthesized with high precision and assembled into various ordered structures, high-quality multicomponent nanocrystals and their ordered assemblies are rarely reported. In this paper, we demonstrate the synthesis of quantum dot–gold (QD-Au) heterodimers. These heterodimers possess a uniform shape and narrow size distribution and are capped with oleylamine and do­decyl­tri­methyl­am­monium bromide (DTAB). Assembly of the heterodimers results in a superlattice with long-range orientational alignment of dimers. Using synchrotron-based X-ray measurements, we characterize the complex superstructure formed from the dimers. Molecular dynamics simulations of a coarse-grained model suggest that anisotropic interactions between the quantum dot and gold components of the dimer drive superlattice formation. The high degree of orientational order demonstrated in this work is a potential route to nanomaterials with useful optoelectronic properties.
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BNL-209103-2018-JAAM
USDOE Office of Science (SC), Basic Energy Sciences (BES)
SC0012704
ISSN:1530-6984
1530-6992
DOI:10.1021/acs.nanolett.8b01860