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Organizing the colloidal particles into 3D superstructures is a promising strategy for fabricating functional metamaterials with novel optical, electric, and catalytic properties. The rich surface properties of the colloidal particles provide many ways to manipulate their assembly behavior. Emulsion droplets are ideal microspaces for confining colloidal self-assembly, offering many advantages such as versatility, scalability, and controllability over size, shape, and composition. In this review, we first introduce recently developed strategies for the emulsion-confined assembly of colloidal particles into 3D superstructures by manipulating the interfacial properties of the emulsion droplets and colloidal particles, then demonstrate the novel collective properties of the assembled superstructures and highlight some of their unique optical and catalytic properties and applications in bioimaging, diagnosis, drug delivery, and therapy.
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Directed colloidal assembly and banding via DC electrokinetics
Manipulating the transport and assembly of colloidal particles to form segregated bands or ordered supracolloidal structures plays an important role in many aspects of science and technology, from understanding the origin of life to synthesizing new materials for next-generation manufacturing, electronics, and therapeutics. One commonly used method to direct colloidal transport and assembly is the application of electric fields, either AC or DC, due to its feasibility. However, as colloidal segregation and assembly both require active redistribution of colloidal particles across multiple length scales, it is not apparent at first sight how a DC electric field, either externally applied or internally induced, can lead to colloidal structuring. In this Perspective, we briefly review and highlight recent advances and standing challenges in colloidal transport and assembly enabled by DC electrokinetics.
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- PAR ID:
- 10429433
- Date Published:
- Journal Name:
- Biomicrofluidics
- Volume:
- 17
- Issue:
- 3
- ISSN:
- 1932-1058
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1063/5.0133871
