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dc.contributor.authorGuo, Jingjing
dc.contributor.authorLiu, Xinyue
dc.contributor.authorJiang, Nan
dc.contributor.authorYetisen, Ali K.
dc.contributor.authorYuk, Hyunwoo
dc.contributor.authorYang, Changxi
dc.contributor.authorKhademhosseini, Ali
dc.contributor.authorZhao, Xuanhe
dc.contributor.authorYun, Seok-Hyun
dc.date.accessioned2019-01-16T17:26:06Z
dc.date.available2019-01-16T17:26:06Z
dc.date.issued2016-06
dc.date.submitted2016-10
dc.identifier.issn0935-9648
dc.identifier.issn1521-4095
dc.identifier.urihttp://hdl.handle.net/1721.1/120088
dc.description.abstractThe design and fabrication of highly stretchable and tough optical fibers made of optically optimized alginate-polyacrylamide hydrogel materials in a core/clad step-index structure was reported. To characterize the swelling properties, hydrogels were fabricated at different AAm concentrations, and their weights were measured immediately after crosslinking (pre-swelling state) and later after they have been immersed in Dulbecco's Modified Eagle Medium (DMEM) at 37°C and 5% CO2 for 3 d. The weights of postswelling samples increased by a factor of 1.53 1.62 with respect to the preswelling states almost independent of the AAM concentration. First, the core was fabricated by injecting a Ca2+ containing alginate-polyacrylamide precursor solution into a platinum-cured silicone tube mold with a syringe and curing the solution by UV light irradiation. After polymerization, the core was extracted from the mold by swelling the tube in dichloromethane for 20 min. Next, the clad was formed on the core fiber by a two-step dip-coating method. The ionic cross-linking of alginate chains by Ca2+ results in high viscosity and makes it hard to dip the core and coat a cladding layer on it. Using various tube molds of different inner diameters and varying the clad dipping time, hydrogel fibers with various core and clad diameters were fabricated. The diameter of the crosslinked core when taken out of the mold is identical to the inner diameter of the mold (pre-swelling), but it increases by a factor of 1.5 1.7 at fully swollen states. The strain accuracy was ±1% in short- and long-term measurements in the moist environment, but the readout was sensitive to the variation of swelling state of the hydrogels. Keywords: absorbance spectroscopy; fiber optics; hydrogels; strain sensingen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01‐AI123312)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant P41‐EB015903)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01‐CA192878)en_US
dc.description.sponsorshipUnited States. Department of Defense (Grant FA9550‐11‐1‐0331)en_US
dc.publisherWiley Blackwellen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/ADMA.201603160en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleHighly Stretchable, Strain Sensing Hydrogel Optical Fibersen_US
dc.typeArticleen_US
dc.identifier.citationGuo, Jingjing et al. “Highly Stretchable, Strain Sensing Hydrogel Optical Fibers.” Advanced Materials 28, 46 (October 2016): 10244–10249 © 2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.mitauthorLiu, Xinyue
dc.contributor.mitauthorYuk, Hyunwoo
dc.contributor.mitauthorZhao, Xuanhe
dc.relation.journalAdvanced Materialsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-01-15T19:10:44Z
dspace.orderedauthorsGuo, Jingjing; Liu, Xinyue; Jiang, Nan; Yetisen, Ali K.; Yuk, Hyunwoo; Yang, Changxi; Khademhosseini, Ali; Zhao, Xuanhe; Yun, Seok-Hyunen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1187-493X
dc.identifier.orcidhttps://orcid.org/0000-0003-1710-9750
dc.identifier.orcidhttps://orcid.org/0000-0001-5387-6186
mit.licenseOPEN_ACCESS_POLICYen_US


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