4.8 Article

Highly Stretchable, Ultra-Soft, and Fast Self-Healable Conductive Hydrogels Based on Polyaniline Nanoparticles for Sensitive Flexible Sensors

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 32, 期 33, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202204366

关键词

conductive hydrogels; flexible sensors; highly stretchable; polyaniline nanoparticles; self-healable; ultra-soft

资金

  1. National Natural Science Foundation of China [52103074, 21875033]
  2. Natural Science Foundation of Shanghai [21ZR1402800]
  3. Innovation Program of Shanghai Municipal Education Commission [2021-01-07-00-03-E00108]
  4. China Postdoctoral Science Foundation [2021M690597]

向作者/读者索取更多资源

In this study, novel conductive composite hydrogels with high stretchability, ultra-softness, excellent conductivity, and good self-healing ability were developed. The hydrogels were formed by incorporating polyaniline nanoparticles (PANI-NPs) into poly(poly(ethylene glycol) methacrylate-co-acrylic acid) (P(PEG-co-AA)) scaffolds through dynamically electrostatic interactions and hydrogen bonds. The PANI-NPs served as conductive fillers, while the enhanced interactions between PANI-NPs and P(PEG-co-AA) matrix imparted high stretchability, low modulus, excellent elasticity, and fast self-healing ability to the hydrogel. The introduction of a binary solvent system also allowed for ideal anti-freezing properties. Composite hydrogel-based sensors were proposed, demonstrating states-independent properties, low detection limit, high linearity, and excellent anti-fatigue performance.
Herein, novel conductive composite hydrogels are developed with high stretchability, ultra-softness, excellent conductivity, and good self-healing ability. The hydrogels are formed in the water/glycerol binary solvent system, in which the polyaniline nanoparticles (PANI-NPs) are incorporated into the poly(poly(ethylene glycol) methacrylate-co-acrylic acid) (P(PEG-co-AA)) scaffolds via the dynamically electrostatic interactions and hydrogen bonds. The PANI-NPs serve as conductive fillers to assign conductivity to the hydrogel, while the enhanced interfacial interactions between the PANI-NPs and P(PEG-co-AA) matrix endow the hydrogel with high stretchability (>1000%), low modulus (approximate to 6 kPa), excellent elasticity (eta = 0.07, energy loss coefficient at 500% strain), and fast self-healing ability (93.3% after 10 mins). Particularly, the desirable anti-freezing property is achieved by introducing a binary solvent system. The composite hydrogel-based sensors are proposed, with the states-independent properties, low detection limit (0.5% strain and 25 Pa), highly linear dependence, and excellent anti-fatigue performance (>1000 cycles). In addition, during the practical wearable sensing tests, various external stimulus and human motions can be detected, including speaking, writing, joint movement, or even small water droplets, indicating the potential applications for the next generation of epidermal sensors.

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