4.8 Article

Electrostatic co-assembly of nanoparticles with oppositely charged small molecules into static and dynamic superstructures

Journal

NATURE CHEMISTRY
Volume 13, Issue 10, Pages 940-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41557-021-00752-9

Keywords

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Funding

  1. European Research Council (ERC) [820008, 818776]
  2. Minerva Foundation
  3. Federal German Ministry for Education and Research
  4. Swiss National Science Foundation [200021_175735, IZLIZ2_183336]
  5. European Union's Horizon 2020 Research and Innovation Program under the Marie Skodowska-Curie grant [812868]
  6. Planning and Budgeting Committee of the Council for Higher Education
  7. Koshland Foundation
  8. McDonald-Leapman grant
  9. DOE Office of Science by Argonne National Laboratory [DE-AC02-06CH11357]
  10. Coronavirus CARES Act
  11. Swiss National Science Foundation (SNF) [IZLIZ2_183336, 200021_175735] Funding Source: Swiss National Science Foundation (SNF)
  12. European Research Council (ERC) [818776, 820008] Funding Source: European Research Council (ERC)

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The use of small molecules with electric charges can effectively induce attractive interactions between oppositely charged nanoparticles in water, guiding their assembly into colloidal crystals. This approach offers a facile way to fabricate, manipulate, and investigate nanostructured materials in aqueous environments.
Coulombic interactions can be used to assemble charged nanoparticles into higher-order structures, but the process requires oppositely charged partners that are similarly sized. The ability to mediate the assembly of such charged nanoparticles using structurally simple small molecules would greatly facilitate the fabrication of nanostructured materials and harnessing their applications in catalysis, sensing and photonics. Here we show that small molecules with as few as three electric charges can effectively induce attractive interactions between oppositely charged nanoparticles in water. These interactions can guide the assembly of charged nanoparticles into colloidal crystals of a quality previously only thought to result from their co-crystallization with oppositely charged nanoparticles of a similar size. Transient nanoparticle assemblies can be generated using positively charged nanoparticles and multiply charged anions that are enzymatically hydrolysed into mono- and/or dianions. Our findings demonstrate an approach for the facile fabrication, manipulation and further investigation of static and dynamic nanostructured materials in aqueous environments.

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