纳米纤维素
聚乙烯醇
自愈水凝胶
乙烯醇
材料科学
化学工程
碳纤维
极限抗拉强度
硼酸
纤维素
电容感应
纳米技术
聚合物
复合材料
复合数
高分子化学
化学
有机化学
计算机科学
工程类
操作系统
作者
Zhiqi Wang,Fangchao Cheng,Hangchuan Cai,Xiurong Li,Jianping Sun,Yiqiang Wu,Nannan Wang,Yanqiu Zhu
标识
DOI:10.1016/j.carbpol.2021.117753
摘要
A new type of nanocellulose/poly(vinyl alcohol)/carbon dot (NPC) multifunctional hydrogel was successfully fabricated by an one-step in-situ hydrothermal method. The one-pot strategy led to the formation of a complex hydrogen bonding/dynamic boric acid ester/nitrogen-doped carbon dots network, and endowed the hydrogel with multifunctionality. The hydrogel underwent self-healing at room temperature (25 °C) and exhibited double-emission fluorescence and high mechanical strength (tensile strength of up to 2.98 MPa). An NPC hydrogel-based capacitive sensor exhibited remarkable linear capacitance responsiveness toward pressure, strain, and glucose concentration, and enabled real-time synchronous quantitative pressure/glucose sensing with multiple linear correlations, which was a key performance criteria for biomechanical sensors. The versatility and multiple advantages of the as-prepared hydrogel demonstrate the potential of biological–mechanical sensing materials using natural cellulosic biomass.
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