Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/6823
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dc.contributor.authorSaikia, Lachit-
dc.contributor.authorSarkar, Tanmoy-
dc.contributor.authorThomas, Meera-
dc.contributor.authorRaghunathan, V.A.-
dc.contributor.authorSain, Anirban-
dc.contributor.authorSharma, Prerna-
dc.date.accessioned2018-01-08T07:53:20Z-
dc.date.available2018-01-08T07:53:20Z-
dc.date.issued2017-10-27-
dc.identifier.citationNature Communications, 2017, Vol. 18, p1160en_US
dc.identifier.issn2041-1723 (online)-
dc.identifier.urihttp://hdl.handle.net/2289/6823-
dc.descriptionOpen Accessen_US
dc.description.abstractBuckling and wrinkling instabilities are failure modes of elastic sheets that are avoided in the traditional material design. Recently, a new paradigm has appeared where these instabilities are instead being utilized for high-performance applications. Multiple approaches such as heterogeneous gelation, capillary stresses, and confinement have been used to shape thin macroscopic elastic sheets. However, it remains a challenge to shape two-dimensional self-assembled monolayers at colloidal or molecular length scales. Here, we show the existence of a curvature instability that arises during the crystallization of finite-sized monolayer membranes of chiral colloidal rods. While the bulk of the membrane crystallizes, its edge remains fluid like and exhibits chiral ordering. The resulting internal stresses cause the flat membrane to buckle macroscopically and wrinkle locally. Our results demonstrate an alternate pathway based on intrinsic stresses instead of the usual external ones to assemble non-Euclidean sheets at the colloidal length scale.en_US
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.relation.urihttp://dx.doi.org/10.1038/s41467-017-01441-3en_US
dc.rights2017 The authorsen_US
dc.titleCurvature instability of chiral colloidal membranes on crystallizationen_US
dc.typeArticleen_US
Appears in Collections:Research Papers (SCM)

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