4.6 Article

Polloidal Chains from Self-Assembly of Flattened Particles

Journal

LANGMUIR
Volume 29, Issue 33, Pages 10340-10345

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la401232g

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Funding

  1. National Science Foundation (CBET) [1033851]
  2. Division Of Materials Research [1062691] Funding Source: National Science Foundation
  3. Div Of Chem, Bioeng, Env, & Transp Sys [1033851] Funding Source: National Science Foundation

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Chains of micrometer-size colloidal particles have been self-assembled that are flexible, mechanically stable, and observable in optical microscopy. The chains sometimes have more than 30 particles, and we call them polloidal chains. A key aspect of the work is the careful modeling of the interparticle forces between partially flattened polystyrene spheres. This modeling helped us to identify a narrow window of system conditions that produce interparticle physical bonds with a bond energy greater than 15kT, as well as a gap of fluid between particles that enables freely rotating bonds and flexible chains. The formation of the chains is well-modeled using linear condensation growth from classical polymer theory, suggesting that the chains might be used experimentally as large-scale, relatively slow moving models for polymer chains.

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