Fully bio-based ion-conductive organo-hydrogels with multi-functionalities such as high mechanical properties, self-healing, anti-freezing, and non-drying capabilities are still extremely rare so far, and achieving it remains a great challenge. In this work, a starch/natural rubber composite hydrogel is first obtained by a simple one-pot method, and then an ion-conductive organo-hydrogel composed of starch, natural rubber, lithium chloride, and glycerol with adjustable mechanical properties (ultimate tensile stress of 0.15-2.33 MPa with a failure strain of 675-1367%, elastic modulus of 0.087-15.2 MPa) is fabricated by a solvent replacement strategy. The organo-hydrogels exhibit excellent fatigue resistance, elasticity, and good self-healing, anti-freezing, non-drying properties (with no obvious change after 10 days at ambient environment). The obtained hydrogels are successfully applied to monitor human movement with high durability (over 1000 cycles) and low hysteresis. In addition, the sensors exhibit high stability in a wide temperature range from -20 °C to 100 °C that endows it with a wide range of potential applications in flexible sensing and wearable devices.
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http://dx.doi.org/10.1002/marc.202200890 | DOI Listing |
Small
January 2025
Institute of Biomass and Function Materials & National Demonstration Centre for Experimental Light Chemistry Engineering Education, College of Bioresources Chemistry and Materials Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, P. R. China.
As skin bioelectronics advances, hydrogel wearable devices have broadened perspectives in environment sensing and health monitoring. However, their application is severely hampered by poor mechanical and self-healing properties, environmental sensitivity, and limited sensory functions. Herein, inspired by the hierarchical structure and unique cross-linking mechanism of hagfish slime, a self-powered supramolecular hydrogel is hereby reported, featuring high stretchability (>2800% strain), ultrafast autonomous self-healing capabilities (electrical healing time: 0.
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January 2025
School of Materials Science and Engineering, Suzhou University of Science and Technology, Suzhou, 215009, China.
Eutectogels are recently emerged as promising alternatives to hydrogels owing to their good environmental stability derived from deep eutectic solvents (DES). However, construction of competent eutectogels with both high conductivity and mechanical toughness is still difficult to achieve yet highly demanded. In this work, new LMNP-PEDOT-CMC-AA (LPCA) eutectogels are prepared using acrylic acid (AA) and carboxymethylcellulose sodium (CMC) as polymeric networks, liquid metal nanoparticle-poly(3,4-ethylenedioxythiophene) (LMNP-PEDOT) are added as multifunctional soft fillers.
View Article and Find Full Text PDFMater Horiz
January 2025
Institute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu 610031, China.
Int J Biol Macromol
January 2025
"Petru Poni" Institute of Macromolecular Chemistry of Romanian Academy, 41 A Gr. Ghica Voda Alley, 700487, Iasi, Romania. Electronic address:
Conductive hydrogels are an appealing class of "smart" materials with great application potential, as they combine the stimuli-responsiveness of hydrogels with the conductivity of magnetic fillers. However, fabricating multifunctional conductive hydrogels that simultaneously exhibit conductivity, self-healing, adhesiveness, and anti-freezing properties remains a significant challenge. To address this issue, we introduce here a freeze-thawing approach to develop versatile, multiresponsive composite cryogels able to preserve their features under low-temperature conditions.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
College of Textile and Clothing Engineering, Soochow University, 199 Ren-ai Road, Suzhou 215123, China. Electronic address:
Conductive hydrogels have attracted intensive attention for their promising applications in flexible electronics, sensors, and electronic skins. However, extremely poor adaptability under cold or dry environmental conditions along with inferior repairability seriously hinders the development of hydrogels in wearable electronics. Here, a triple network conductive hydrogel (PBCP-MXene) was prepared by proportionally mixing polyvinyl alcohol (PVA), borax, chitosan (CS), phytic acid (PA), and MXene.
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