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Environment Tolerant Conductive Nanocomposite Organohydrogels as Flexible Strain Sensors and Power Sources for Sustainable Electronics
Author(s) -
Sun Hongling,
Zhao Yi,
Jiao Sulin,
Wang Chunfeng,
Jia Yunpeng,
Dai Kun,
Zheng Guoqiang,
Liu Chuntai,
Wan Pengbo,
Shen Changyu
Publication year - 2021
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202101696
Subject(s) - materials science , nanotechnology , flexible electronics , electronics , nanocomposite , conductivity , electrical conductor , self healing hydrogels , electrode , triboelectric effect , optoelectronics , composite material , electrical engineering , chemistry , polymer chemistry , engineering
Conductive hydrogels (CHs) have been highlighted in the design of flexible strain sensors and stretchable triboelectric nanogenerators (TENGs) on the basis of their excellent physicochemical properties such as large stretchability and high conductivity. Nevertheless, the incident freezing and drying behaviors of CHs by using water solvent as the dispersion medium limit their application scopes significantly. Herein, an environment tolerant and ultrastretchable organohydrogel is demonstrated by a simple solvent‐replacement strategy, in which the partial water in the as‐synthesized polyacrylamide/montmorillonite/carbon nanotubes hydrogel is replaced with the glycerol, leading to excellent temperature toleration (−60 to 60 °C) and good stability (30 days under normal environment) without sacrificing the stretchability and conductivity. The organohydrogel exhibits an ultrawide strain sensing range (0–4196%) with a high sensitivity of 8.5, enabling effective detection and discrimination of human activities that are gentle or drastic under various conditions. Furthermore, the organohydrogel is assembled in a single‐electrode TENG, which displays excellent energy harvesting ability even under a stretchability of 500% and robustness to directly power wearable electronics in harsh cold conditions. This work inspires a simple route for multifunctional organohydrogel and promises the practical application of flexible and self‐powered wearable devices in extreme environments.