Selective colloidal bonds via polymer-mediated interactions

Joeri Opdam, Remco Tuinier (Corresponding author), Theodore Hueckel, Thom J. Snoeren, Stefano Sacanna (Corresponding author)

Research output: Contribution to journalArticleAcademicpeer-review

14 Citations (Scopus)

Abstract

Regioselectivity in colloidal self-assembly typically requires specific chemical interactions to guide particle binding. In this paper, we describe a new method to form selective colloidal bonds that relies solely on polymer adsorption. Mixtures of polymer-coated and bare particles are initially stable due to long-ranged electrostatic repulsion. When their charge is screened, the two species can approach each other close enough for polymer bridges to form, binding the particles together. By utilizing colloidal dumbbells, where each lobe is coated with polymer brushes of differing lengths, we demonstrate that the Debye screening length serves as a selective switch for the assembly of bare tracer particles onto the two lobes. We model the interaction using numerical self-consistent field lattice computations and show how regioselectivity arises from just a few nanometers difference in polymer brush length.

Original languageEnglish
Pages (from-to)7438-7446
Number of pages9
JournalSoft Matter
Volume16
Issue number32
DOIs
Publication statusPublished - 19 Aug 2020

Funding

This work was supported by the NSF CAREER award DMR-1653465. The Zeiss Merlin FESEM was acquired through the support of the NSF under award number DMR-0923251. J. O. and R. T. are grateful for financial support from the Dutch Ministry of Economic Affairs of the Netherlands via The Top-consortium Knowledge and Innovation (TKI) roadmap Chemistry of Advanced Materials (CHEMIE.PGT.2018.006).

FundersFunder number
Ministerie van Economische Zaken en Klimaat
National Science Foundation1653465, DMR-1653465, DMR-0923251

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