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Ultrathin thermoresponsive self-folding 3D graphene

Graphene and other two-dimensional materials have unique physical and chemical properties of broad relevance. It has been suggested that the transformation of these atomically planar materials to three-dimensional (3D) geometries by bending, wrinkling, or folding could significantly alter their prop...

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Autores principales: Xu, Weinan, Qin, Zhao, Chen, Chun-Teh, Kwag, Hye Rin, Ma, Qinli, Sarkar, Anjishnu, Buehler, Markus J., Gracias, David H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630237/
https://www.ncbi.nlm.nih.gov/pubmed/28989963
http://dx.doi.org/10.1126/sciadv.1701084
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author Xu, Weinan
Qin, Zhao
Chen, Chun-Teh
Kwag, Hye Rin
Ma, Qinli
Sarkar, Anjishnu
Buehler, Markus J.
Gracias, David H.
author_facet Xu, Weinan
Qin, Zhao
Chen, Chun-Teh
Kwag, Hye Rin
Ma, Qinli
Sarkar, Anjishnu
Buehler, Markus J.
Gracias, David H.
author_sort Xu, Weinan
collection PubMed
description Graphene and other two-dimensional materials have unique physical and chemical properties of broad relevance. It has been suggested that the transformation of these atomically planar materials to three-dimensional (3D) geometries by bending, wrinkling, or folding could significantly alter their properties and lead to novel structures and devices with compact form factors, but strategies to enable this shape change remain limited. We report a benign thermally responsive method to fold and unfold monolayer graphene into predesigned, ordered 3D structures. The methodology involves the surface functionalization of monolayer graphene using ultrathin noncovalently bonded mussel-inspired polydopamine and thermoresponsive poly(N-isopropylacrylamide) brushes. The functionalized graphene is micropatterned and self-folds into ordered 3D structures with reversible deformation under a full control by temperature. The structures are characterized using spectroscopy and microscopy, and self-folding is rationalized using a multiscale molecular dynamics model. Our work demonstrates the potential to design and fabricate ordered 3D graphene structures with predictable shape and dynamics. We highlight applicability by encapsulating live cells and creating nonlinear resistor and creased transistor devices.
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spelling pubmed-56302372017-10-08 Ultrathin thermoresponsive self-folding 3D graphene Xu, Weinan Qin, Zhao Chen, Chun-Teh Kwag, Hye Rin Ma, Qinli Sarkar, Anjishnu Buehler, Markus J. Gracias, David H. Sci Adv Research Articles Graphene and other two-dimensional materials have unique physical and chemical properties of broad relevance. It has been suggested that the transformation of these atomically planar materials to three-dimensional (3D) geometries by bending, wrinkling, or folding could significantly alter their properties and lead to novel structures and devices with compact form factors, but strategies to enable this shape change remain limited. We report a benign thermally responsive method to fold and unfold monolayer graphene into predesigned, ordered 3D structures. The methodology involves the surface functionalization of monolayer graphene using ultrathin noncovalently bonded mussel-inspired polydopamine and thermoresponsive poly(N-isopropylacrylamide) brushes. The functionalized graphene is micropatterned and self-folds into ordered 3D structures with reversible deformation under a full control by temperature. The structures are characterized using spectroscopy and microscopy, and self-folding is rationalized using a multiscale molecular dynamics model. Our work demonstrates the potential to design and fabricate ordered 3D graphene structures with predictable shape and dynamics. We highlight applicability by encapsulating live cells and creating nonlinear resistor and creased transistor devices. American Association for the Advancement of Science 2017-10-06 /pmc/articles/PMC5630237/ /pubmed/28989963 http://dx.doi.org/10.1126/sciadv.1701084 Text en Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Xu, Weinan
Qin, Zhao
Chen, Chun-Teh
Kwag, Hye Rin
Ma, Qinli
Sarkar, Anjishnu
Buehler, Markus J.
Gracias, David H.
Ultrathin thermoresponsive self-folding 3D graphene
title Ultrathin thermoresponsive self-folding 3D graphene
title_full Ultrathin thermoresponsive self-folding 3D graphene
title_fullStr Ultrathin thermoresponsive self-folding 3D graphene
title_full_unstemmed Ultrathin thermoresponsive self-folding 3D graphene
title_short Ultrathin thermoresponsive self-folding 3D graphene
title_sort ultrathin thermoresponsive self-folding 3d graphene
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630237/
https://www.ncbi.nlm.nih.gov/pubmed/28989963
http://dx.doi.org/10.1126/sciadv.1701084
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