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Issue 40, 2014
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Highly ordered 2D microgel arrays: compression versus self-assembly

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Monolayers of micro- and nanoparticles at fluid interfaces are a key component in a variety of applications, ranging from particle lithography to stabilizers in foams or emulsions. In addition to commonly used “hard” colloids, soft polymeric particles like microgels are attracting increasing attention due to their potential in the fabrication of tailored and responsive assemblies. In particular, regular hexagonal arrays of microgels have been previously deposited after assembly at a fluid interface. While the arrangement cannot be easily controlled after adsorption and self-assembly from the bulk phase, specific structures can be achieved by compressing an interfacial microgel monolayer spread in a Langmuir trough and by transferring it onto substrates at distinct compression states. The degree of ordering after compression surpasses the one that is reached after self-assembly from the bulk and is, in general, independent from the presence of charges and different microgel morphologies. As a consequence, by monitoring the surface pressure during compression it is possible to produce highly ordered microgel arrays where the interparticle distance can be systematically and externally controlled.

Graphical abstract: Highly ordered 2D microgel arrays: compression versus self-assembly

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Publication details

The article was received on 29 May 2014, accepted on 23 Jul 2014 and first published on 24 Jul 2014

Article type: Paper
DOI: 10.1039/C4SM01166J
Citation: Soft Matter, 2014,10, 7968-7976

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    Highly ordered 2D microgel arrays: compression versus self-assembly

    K. Geisel, W. Richtering and L. Isa, Soft Matter, 2014, 10, 7968
    DOI: 10.1039/C4SM01166J

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