Hexadecapolar colloids
arXiv:1612.06502 · doi:10.1038/ncomms10659
Abstract
Outermost occupied electron shells of chemical elements can have symmetries resembling that of monopoles, dipoles, quadrupoles and octupoles corresponding to filled s-, p-, d- and forbitals. Theoretically, elements with hexadecapolar outer shells could also exist, but none of the known elements have filled g-orbitals. On the other hand, the research paradigm of "colloidal atoms" displays complexity of particle behaviour exceeding that of atomic counterparts, which is driven by DNA functionalization, geometric shape and topology and weak external stimuli. Here we describe elastic hexadecapoles formed by polymer microspheres dispersed in a liquid crystal, a nematic fluid of orientationally ordered molecular rods. Because of conically degenerate boundary conditions, the solid microspheres locally perturb the alignment of the nematic host, inducing hexadecapolar distortions that drive anisotropic colloidal interactions. We uncover physical underpinnings of formation of colloidal elastic hexadecapoles and describe the ensuing bonding inaccessible to elastic dipoles, quadrupoles and other nematic colloids studied previously.
References in corpus (3)
Cited by in corpus (8)
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- Colloidal Surfaces with Boundaries, Apex Boojums and Nested Elastic Self-Assembly of Nematic Colloids
- Transformation between elastic dipoles, quadrupoles, octupoles and hexadecapoles driven by surfactant self-assembly in nematic emulsion
- Repulsion-attraction switching of nematic colloids formed by liquid crystal dispersions of polygonal prisms
- Colloidal interactions and unusual crystallization versus de-mixing of elastic multipoles formed by gold mesoflowers
- Key-Lock Colloids in a Nematic Liquid Crystal