Dataset Information

Ultra-Tough Self-Healing Hydrogel via Hierarchical Energy Associative Dissipation.

ABSTRACT: Owing to high water content and homogeneous texture, conventional hydrogels hardly reach satisfactory mechanical performance. Tensile-resistant groups and structural heterogeneity are employed to fabricate tough hydrogels. However, those techniques significantly increase the complexity and cost of material synthesis, and have only limited applicability. Here, it is shown that ultra-tough hydrogels can be obtained via a unique hierarchical architecture composed of chemically coupled self-assembly units. The associative energy dissipation among them may be rationally engineered to yield libraries of tough gels with self-healing capability. Tunable tensile strength, fracture strain, and toughness of up to 19.6 MPa, 20 000%, and 135.7 MJ cm⁻³ are achieved, all of which exceed the best known records. The results demonstrate a universal strategy to prepare desired ultra-tough hydrogels in predictable and controllable manners.

SUBMITTER: Zhao Z

PROVIDER: S-EPMC10520617 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Ultra-Tough Self-Healing Hydrogel via Hierarchical Energy Associative Dissipation.

Zhao Zhi Z Li Yurong Y Wang Haibin H Shan Yupeng Y Liu Xuemei X Wu Mengfei M Zhang Xinping X Song Xiaoyan X

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20230728 27

Owing to high water content and homogeneous texture, conventional hydrogels hardly reach satisfactory mechanical performance. Tensile-resistant groups and structural heterogeneity are employed to fabricate tough hydrogels. However, those techniques significantly increase the complexity and cost of material synthesis, and have only limited applicability. Here, it is shown that ultra-tough hydrogels can be obtained via a unique hierarchical architecture composed of chemically coupled self-assembly ...[more]

PMID: 37505367

Similar Datasets

Project description:Currently, hydrogels simultaneously featuring high strength, high toughness, superior recoverability, and benign anti-fatigue properties have demonstrated great application potential in broad fields; thus, great efforts have been made by researchers to develop satisfactory hydrogels. Inspired by the double network (DN)-like theory, we previously reported a novel high-strength/high-toughness hydrogel which had two consecutive energy-dissipation systems, namely, the unzipping of coordinate bonds and the dissociation of the crystalline network. However, this structural design greatly damaged its stretchability, toughness recoverability, shape recoverability, and anti-fatigue capability. Thus, we realized that a soft/ductile matrix is indispensable for an advanced strong tough hydrogel. On basis of our previous work, we herein reported a modified energy-dissipation model, namely, a "binary DN-like structure" for strong tough hydrogel design for the first time. This structural model comprises three interpenetrated polymer networks: a covalent/ionic dually crosslinked tightened polymer network (stiff, first order network), a constrictive crystalline polymer network (sub-stiff, second order network), and a ductile/flexible polymer network (soft, third order network). We hypothesized that under low tension, the first order network served as the sacrificing phase through decoordination of ionic crosslinks, while the second order and third order networks together functioned as the elastic matrix phase; under high tension, the second order network worked as the energy dissipation phase (ionic crosslinks have been destroyed at the time), while the third order network played the role of the elastic matrix phase. Owing to the "binary DN-like" structure, the as-prepared hydrogel, in principle, should demonstrate enhanced energy dissipation capability, toughness/shape recoverability, and anti-fatigue/anti-tearing capability. Finally, through a series of characterizations, the unique "binary DN-like" structure was proved to fit well with our initial theoretical assumption. Moreover, compared to other energy-dissipation models, this structural design showed a significant advantage regarding comprehensive properties. Therefore, we think this design philosophy would inspire the development of advanced strong tough hydrogel in the future.

Project description:In this study, a self-healing hydrogel was prepared that is transparent to visible (Vis) light while absorbing ultraviolet (UV), infrared (IR), and microwave. The optothermal features of the hydrogel were explored by monitoring temperature using an IR thermometer under an IR source. The hydrogel was synthesized using sodium tetraborate decahydrate (borax) and polyvinyl alcohol (PVA) as raw materials based on a facile thermal route. More significantly, graphene oxide (GO) and graphite-like carbon nitride (g-C3N4) nanostructures as well as carbon microsphere (CMS) were applied as guests to more dissect their influence on the microwave and optical characteristics. The morphology of the fillers was evaluated using field emission scanning electron microscopy (FE-SEM). Fourier transform infrared (FTIR) attested that the chemical functional groups of the hydrogel have been formed and the result of diffuse reflection spectroscopy (DRS) confirmed that the hydrogel absorbs UV while is transparent in Vis light. The achieved result implied that the hydrogel acts as an essential IR absorber due to its functional groups desirable for energy efficiency and harvesting. Interestingly, the achieved results have testified that the self-healing hydrogels had the proper self-healing efficiency and self-healing time. Eventually, microwave absorbing properties and shielding efficiency of the hydrogel, hydrogel/GO, g-C3N4, or CMS were investigated, demonstrating the salient microwave characteristics, originated from the established ionic conductive networks and dipole polarizations. The efficient bandwidth of the hydrogel was as wide as 3.5 GHz with a thickness of 0.65 mm meanwhile its maximum reflection loss was 75.10 dB at 14.50 GHz with 4.55 mm in thickness. Particularly, the hydrogel illustrated total shielding efficiency (SET) > 10 dB from 1.19 to 18 and > 20 dB from 4.37 to 18 GHz with 10.00 mm in thickness. The results open new windows toward improving the shielding and energy efficiency using practical ways.

Dataset Information

Ultra-Tough Self-Healing Hydrogel via Hierarchical Energy Associative Dissipation.

Publications

Ultra-Tough Self-Healing Hydrogel via Hierarchical Energy Associative Dissipation.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets