Stretchable, self-adhesive, and conductive hemicellulose-based hydrogels as wearable strain sensors

被引:3
|
作者
Zhao, Lihui [1 ]
Luo, Banxin [3 ]
Gao, Shishuai [1 ,2 ]
Liu, Yupeng [1 ,2 ]
Lai, Chenhuan [2 ]
Zhang, Daihui [1 ,2 ]
Guan, Wenxian [3 ]
Wang, Chunpeng [1 ,2 ]
Chu, Fuxiang [1 ,2 ]
机构
[1] Chinese Acad Forestry, Inst Chem Ind Forest Prod, Natl Engn Lab Biomass Chem Utilizat,Key Lab Biomas, Key Lab Chem Engn Forest Prod Natl Forestry & Gras, Nanjing 210042, Jiangsu, Peoples R China
[2] Nanjing Forestry Univ, Coinnovat Ctr Efficient Proc & Utilizat Forest Res, Nanjing 210037, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Nanjing Drum Tower Hosp, Drum Tower Clin Med Coll, Dept Gen Surg, Nanjing 210008, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogel; Hemicellulose; Sensor;
D O I
10.1016/j.ijbiomac.2024.137313
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Conductive hydrogels have recently gained impressive attention in flexible sensing. However, their low sensing limit and poor interface matching have raised great concern during the practical application. Therefore, incorporating excellent stretchability and adhesiveness into conductive hydrogel is highly desirable but still be a huge challenge. In this study, we synthesized composite hydrogels with desired properties by utilizing the synergistic role of hemicellulose (HC) and conductive two-dimensional material MXene. As a result, the synthesized hydrogels showed good self-adhesion (3.12 KPa on the skin), great stretchability (>1700 %), and satisfactory electrical conductivity. These multifunctional hydrogels operated as adaptable sensors, adeptly capturing the nuanced signals emanating from an array of human motions. They exhibited an expansive strain tolerance, swift reactivity, and an enhanced acuity in detecting even the slightest deformations (GF = 2.1). Our research provides new insights for creating stretchable, self-adhesive, and functional hydrogels for sensing applications.
引用
收藏
页数:9
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