6533b82cfe1ef96bd128f770

RESEARCH PRODUCT

Controlled assembly of single colloidal crystals using electro-osmotic micro-pumps.

Erdal C. OğuzHartmut LöwenRan NiuAlexander ReinmüllerHannah MüllerDenis BotinThomas Palberg

subject

Void (astronomy)Materials scienceIon exchangedigestive oral and skin physiologyGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyColloidal crystalCondensed Matter - Soft Condensed Matter010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencescomplex mixtures0104 chemical sciencesCrystalCondensed Matter::Soft Condensed MatterColloidChemical physicsBrownian dynamicsSoft Condensed Matter (cond-mat.soft)SPHERESPhysical and Theoretical ChemistrySingle domain0210 nano-technology

description

We assemble charged colloidal spheres at deliberately chosen locations on a charged unstructured glass substrate utilizing ion exchange based electro-osmotic micro-pumps. Using microscopy, a simple scaling theory and Brownian Dynamics simulations, we systematically explore the control parameters of crystal assembly and the mechanisms through which they depend on the experimental boundary conditions. We demonstrate that crystal quality depends crucially on the assembly distance of the colloids. This is understood as resulting from the competition between inward transport by the electro-osmotic pump flow and the electro-phoretic outward motion of the colloids. Optimized conditions include substrates of low and colloids of large electro-kinetic mobility. Then a sorting of colloids by size is observed in binary mixtures with larger particles assembling closer to the ion exchanger beads. Moreover, mono-sized colloids form defect free single domain crystals which grow outside a colloid-free void with facetted inner crystal boundaries centred on the ion exchange particle. This works remarkably well, even with irregularly formed ion exchange resin splinters.

10.1039/c6cp07231chttps://pubmed.ncbi.nlm.nih.gov/28079208