2016
DOI: 10.1002/adma.201600480
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Extremely Stretchable and Fast Self‐Healing Hydrogels

Abstract: Dynamic crosslinking of extremely stretchable hydrogels with rapid self-healing ability is described. Using this new strategy, the obtained hydrogels are able to elongate 100 times compared to their initial length and to completely self-heal within 30 s without external energy input.

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Cited by 418 publications
(332 citation statements)
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“…Ionomers, a commercially available self-healing polymer, [45] require an external stimulus such as temperature to increase polymer chain mobility and activate self-healing. [4][5][6][7][8][9][10][11][12][13][14][15][16] The ability to rationally tune and add new functionality in materials can lead to transformative advances in emerging self-healing systems. This material tolerates extreme strains exceeding 5000%, features an ionic conductivity of 10 −4 S cm −1 , and shows high transparency across the visible spectrum with an average transmittance of 92%.…”
mentioning
confidence: 99%
“…Ionomers, a commercially available self-healing polymer, [45] require an external stimulus such as temperature to increase polymer chain mobility and activate self-healing. [4][5][6][7][8][9][10][11][12][13][14][15][16] The ability to rationally tune and add new functionality in materials can lead to transformative advances in emerging self-healing systems. This material tolerates extreme strains exceeding 5000%, features an ionic conductivity of 10 −4 S cm −1 , and shows high transparency across the visible spectrum with an average transmittance of 92%.…”
mentioning
confidence: 99%
“…9,10 Traditional chemically cross-linked hydrogels tend to display low mechanical strength and poor toughness, due to the inhomogeneity of the chemical crosslinking network and lack of effective energy dissipation under deformation. In order to get better mechanical properties, to date, a good deal of approaches have been proposed in an effort to obtain hydrogels with favourable mechanical properties, such as semi-IPN hydrogels, 11 slide-ring hydrogels, 12 hydrophobic association hydrogels (HA gels), [13][14][15] double-network (DN) hydrogels, [16][17][18] macromolecular microsphere composite (MMC) hydrogels 19 and nanocomposite hydrogels. [20][21][22] Among the various hydrogels, DN gels stand out, having gained tremendous attraction due to their remarkable comprehensive mechanical performance.…”
Section: Introductionmentioning
confidence: 99%
“…For example, by adding hygroscopic ions to the hydrogel, the hydrogel could self-hydrate by pulling water out of the ambient environment (Bai et al, 2014;Chen et al, 2014), ensuring that the actuator is always ready to self-heal. The high water concentration in hydrogels (when compared with the humidity of the surrounding air) can enable hydrogel polymers to heal much more rapidly than normal self-healing polymers, as demonstrated by Jeon et al (2016). However, one constant challenge that hydrogels face is ensuring that they remain sufficiently hydrated.…”
Section: Hydrogel Actuatorsmentioning
confidence: 99%
“…The hydraulic gripper was built with a highly deformable hydrogel that was simultaneously gentle and robust, capable of trapping a live fish without harming it. Highly stretchable, self-healing hydrogels such as the one recently presented by Jeon et al (2016) could potentially be used to create these types of hydrogel grippers. Their hydrogel can self-heal very quickly (in under 30 s, given ideal conditions) and can strain over 1,000% its original length ( Figure 2C).…”
Section: Hydrogel Actuatorsmentioning
confidence: 99%