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Article: Programming Self-Assembled Materials With DNA-Coated Colloids

TitleProgramming Self-Assembled Materials With DNA-Coated Colloids
Authors
KeywordsDNA colloidal crystals
patchy particle
anisotropic particle
programmable self-assembly
self-assembly
Issue Date2021
PublisherFrontiers Research Foundation. The Journal's web site is located at http://www.frontiersin.org/physics/
Citation
Frontiers in Physics, 2021, v. 9, p. article no. 672375 How to Cite?
AbstractIntroducing the concept of programmability paves the way for designing complex and intelligent materials, where the materials’ structural information is pre-encoded in the components that build the system. With highly tunable interactions, DNA-coated particles are promising building elements to program materials at the colloidal scale, but several grand challenges have prevented them from assembling into the desired structures and phases. In recent years, the field has seen significant progress in tackling these challenges, which has led to the realization of numerous colloidal structures and dynamics previously inaccessible, including the desirable colloidal diamond structure, that are useful for photonic and various other applications. We review this exciting progress, focusing in detail on how DNA-coated colloids can be designed to have a sophisticatedly tailored surface, shape, patches, as well as controlled kinetics, which are key factors that allow one to program in principle a limitless number of structures. We also share our view on how the field may be directed in future.
Persistent Identifierhttp://hdl.handle.net/10722/306216
ISSN
2021 Impact Factor: 3.718
2020 SCImago Journal Rankings: 0.754
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhang, T-
dc.contributor.authorLyu, D-
dc.contributor.authorXu, W-
dc.contributor.authorMu, Y-
dc.contributor.authorWang, Y-
dc.date.accessioned2021-10-20T10:20:27Z-
dc.date.available2021-10-20T10:20:27Z-
dc.date.issued2021-
dc.identifier.citationFrontiers in Physics, 2021, v. 9, p. article no. 672375-
dc.identifier.issn2296-424X-
dc.identifier.urihttp://hdl.handle.net/10722/306216-
dc.description.abstractIntroducing the concept of programmability paves the way for designing complex and intelligent materials, where the materials’ structural information is pre-encoded in the components that build the system. With highly tunable interactions, DNA-coated particles are promising building elements to program materials at the colloidal scale, but several grand challenges have prevented them from assembling into the desired structures and phases. In recent years, the field has seen significant progress in tackling these challenges, which has led to the realization of numerous colloidal structures and dynamics previously inaccessible, including the desirable colloidal diamond structure, that are useful for photonic and various other applications. We review this exciting progress, focusing in detail on how DNA-coated colloids can be designed to have a sophisticatedly tailored surface, shape, patches, as well as controlled kinetics, which are key factors that allow one to program in principle a limitless number of structures. We also share our view on how the field may be directed in future.-
dc.languageeng-
dc.publisherFrontiers Research Foundation. The Journal's web site is located at http://www.frontiersin.org/physics/-
dc.relation.ispartofFrontiers in Physics-
dc.rightsThis Document is Protected by copyright and was first published by Frontiers. All rights reserved. It is reproduced with permission.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectDNA colloidal crystals-
dc.subjectpatchy particle-
dc.subjectanisotropic particle-
dc.subjectprogrammable self-assembly-
dc.subjectself-assembly-
dc.titleProgramming Self-Assembled Materials With DNA-Coated Colloids-
dc.typeArticle-
dc.identifier.emailWang, Y: wanglab@hku.hk-
dc.identifier.authorityWang, Y=rp02191-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3389/fphy.2021.672375-
dc.identifier.scopuseid_2-s2.0-85111936820-
dc.identifier.hkuros327600-
dc.identifier.volume9-
dc.identifier.issue330-
dc.identifier.spagearticle no. 672375-
dc.identifier.epagearticle no. 672375-
dc.identifier.isiWOS:000679850500001-
dc.publisher.placeSwitzerland-

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