4.8 Article

Assembling Ordered Crystals with Disperse Building Blocks

Journal

NANO LETTERS
Volume 19, Issue 8, Pages 5774-5780

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.9b02508

Keywords

Nanoparticles; self-assembly; dispersity; polymer brushes; supramolecular chemistry

Funding

  1. NSF CAREER Grant [CHE-1653289]
  2. NSF [DMR 14-19807, DMR-0520547]
  3. NSF Graduate Research Fellowship Program [1122374]
  4. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  5. European Union's Horizon 2020 research and innovation program under the SINE2020 project [654000]

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Conventional colloidal crystallization techniques typically require low dispersity building blocks in order to make ordered particle arrays, resulting in a practical challenge for studying or scaling these materials. Nano particles covered in a polymer brush therefore may be predicted to be challenging building blocks in the formation of high-quality particle superlattices, as both the nanoparticle core and polymer brush are independent sources of dispersity in the system. However, when supramolecular bonding between complementary functional groups at the ends of the polymer chains are used to drive particle assembly, these nanocomposite tectons can make high quality superlattices with polymer dispersities as large as 1.44 and particle diameter relative standard deviations up to 23% without any significant change to superlattice crystallinity. Here we demonstrate and explain how the flexible and dynamic nature of the polymer chains that comprise the particle brush allows them to deform to accommodate the irregularities in building block size and shape that arise from the inherent dispersity of their constituent components. Incorporating soft components into nanomaterials design therefore offers a facile and robust method for maintaining good control over organization when the materials themselves are imperfect.

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