材料科学
纳米技术
电导率
纤维素
离子键合
表面电荷
纳米纤维
离子电导率
生物电子学
离子
Zeta电位
生物相容性
化学工程
生物传感器
化学
纳米颗粒
电极
有机化学
冶金
物理化学
工程类
电解质
作者
Chengwei Wang,Sha Wang,Guang Chen,Weiqing Kong,Weiwei Ping,Jiaqi Dai,Glenn Pastel,Hua Xie,Shuaiming He,Siddhartha Das,Liangbing Hu
标识
DOI:10.1021/acs.chemmater.8b03006
摘要
Ion transport in nanochannels has unique behaviors such as charge selectivity and high ionic conductivity. Due to their simple structure, the photolithographic nanochannels have been widely used to understand the fundamentals of nanofluidic ion transport. However, for practical applications, especially biorelated applications, a scalable, flexible, mechanically stable, and biocompatible nanofluidic device engineered with charge selectivity and high ionic conductivity is more desirable. Herein, we report a scalable biomass material, namely, bacterial cellulose (BC), with excellent mechanical strength, flexibility, and biocompatibility for nanofluidic ion transport. The BC film is a 3-dimensional (3D) interconnected network of 10–30 nm thick cellulose nanofibers, containing 1–2 nm nanochannels with large negatively charged surface groups. After a facile TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl radical) oxidation treatment, the zeta potential of the cellulose nanofibers significantly improves from −13 mV to −45 mV, and the ionic conductivity increases 40 times from 2.5 × 10–5 S/cm to 1.0 × 10–3 S/cm at low salt concentrations. As a proof of concept, we successfully demonstrate an ultrasensitive humidity sensor with the BC nanofluidic film for wearable health monitor applications.
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