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Anisotropic hydrogel based on bilayers: color, strength, toughness, and fatigue resistance

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Title: Anisotropic hydrogel based on bilayers: color, strength, toughness, and fatigue resistance
Authors: Haque, Md. Anamul Browse this author
Kurokawa, Takayuki Browse this author →KAKEN DB
Gong, Jian Ping Browse this author →KAKEN DB
Keywords: Self-assembly
Non-equilibrium chemistry
Lamellar structure
One-dimensional swelling
Stress sensor
Issue Date: 21-Aug-2012
Publisher: Royal Society of Chemistry
Journal Title: Soft Matter
Volume: 8
Issue: 31
Start Page: 8008
End Page: 8016
Publisher DOI: 10.1039/c2sm25670c
Abstract: In this highlight, we introduce a novel anisotropic hydrogel with a perfect 1D photonic crystal structure based on the uni-axial alignment of lamellar bilayers. The gel was synthesized in a one-pot polymerization from a precursor solution containing polymerizable surfactant (dodecyl glyceryl itaconate: DGI), acrylamide, and a cross-linker. By applying shear flow to the precursor solution, lamellar bilayers of self-assembled DGI were aligned in one direction parallel to the substrate surface. The polymerized lamellar bilayers were stacked periodically and entrapped in the polyacrylamide matrix to give a hydrogel with 1D photonic crystal structure. This hydrogel, containing 94-95 wt% water and 1.0-1.5 wt% bilayer molecules, shows perfect one-dimensional swelling, strong anisotropy in the elastic modulus, and magnificent structural color by multilayer interference according to Bragg's law of diffraction. Owing to the softness and large deformability, the color of the gel can be reversibly tuned by both compressive and tensile mechanical stimuli over the entire wavelength range of visible color. The single-domain lamellar bilayer not only diffracts light, but also serves as a reversible sacrificial bonds that dissociates upon deformation, exhibiting large hysteresis as an energy dissipation mechanism, which gives the gel high tensile strength and fatigue resistance. Both the molecular dissociation and lipid-like mobile nature of DGI molecules in the bilayers dramatically enhance the resistance against crack propagation by the formation of extra-ordinary blunting, which gives the gel an extraordinarily high toughness.
Rights: Soft Matter, 2012,8, 8008-8016 - Reproduced by permission of The Royal Society of Chemistry (RSC)
Type: article (author version)
Appears in Collections:生命科学院・先端生命科学研究院 (Graduate School of Life Science / Faculty of Advanced Life Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 龔 剣萍 (Gong Jian Ping)

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