自愈水凝胶
材料科学
纤维素
极限抗拉强度
复合材料
电导率
多孔性
抗压强度
电解质
离子电导率
钛
化学工程
化学
高分子化学
物理化学
工程类
冶金
电极
作者
Miaomiao Wu,Hu Liu,Xiong‐Fei Zhang,Mengjie Li,Jianfeng Yao
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-07-08
卷期号:41 (28): 18903-18910
被引量:1
标识
DOI:10.1021/acs.langmuir.5c02530
摘要
The development of cellulose-based hydrogels with integrated mechanical robustness, ionic conductivity, and environmental tolerance is critical for advancing wearable electronics. Herein, we report a dual-cross-linked cellulose hydrogel reinforced with attapulgite-derived titanium silicate (ATS). An acid-hydrothermal approach was used to transform attapulgite into ATS. ATS has a porous structure with uniform channels, and it can serve as a physical cross-linker to improve the mechanical robustness of the hydrogel. The as-prepared hydrogel demonstrated a high tensile strength (155 kPa), fracture elongation (177%), and compressive stress (0.58 MPa). Simultaneously, the ATS-engineered porous network facilitates rapid ion transport, yielding a high ionic conductivity of 2.45 S m-1. When assembled into a strain sensor, the hydrogel can realize the precise detection of human motions. This work provides a sustainable strategy for designing sensors through inorganic filler engineering to tune the mechanical and conductive properties of hydrogels.
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