4.8 Article

Morphological Transitions in Patchy Nanoparticles

Journal

ACS NANO
Volume 14, Issue 4, Pages 4577-4584

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c00108

Keywords

nanoparticles; patches; polymer ligands; nanopatterning; gold-thiol bond

Funding

  1. National Science and Engineering Research Council of Canada (NSERC Canada)
  2. Connaught International Scholarship
  3. Ministry of Research and Education of the Russian Federation [14.W03.31.0022]
  4. Alexander von Humboldt Foundation (Feodor Lynen Research Fellowship)
  5. Leopoldina Fellowship Program, German National Academy of Sciences Leopoldina [LPDR 2019-01]
  6. NSERC Canada

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Nanoparticles (NPs) decorated with topographically or chemically distinct surface patches are an emerging class of colloidal building blocks of functional hierarchical materials. Surface segregation of polymer ligands into pinned micelles offers a strategy for the generation of patchy NPs with controlled spatial distribution and number of patches. The thermodynamic nature of this approach poses a question about the stability of multiple patches on the NP surface, as the lowest energy state is expected for NPs carrying a single patch. In the present work, for gold NPs end-grafted with thiol-terminated polymer molecules, we show that the patchy surface morphology is preserved under conditions of strong grafting of the thiol groups to the NP surface (i.e., up to a temperature of 40 degrees C), although the patch shape changes over time. At higher temperatures (e.g., at 80 degrees C), the number of patches per NP decreases, due to the increased lateral mobility and coalescence of the patches as well as the ultimate loss of the polymer ligands due to desorption at enhanced solvent quality. The experimental results were rationalized theoretically, using a scaling approach. The results of this work offer insight into the surface science of patchy nanocolloids and specify the time and temperature ranges of the applications of patchy NPs.

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