材料科学
导电体
离子键合
纳米技术
自愈水凝胶
相变
电解质
复合材料
离子
化学
电极
高分子化学
量子力学
物理
有机化学
物理化学
作者
Ying Liu,Chan Wang,Zhuo Liu,Xuecheng Qu,Yansong Gai,Jiangtao Xue,Shengyu Chao,Jing Huang,Yuxiang Wu,Yusheng Li,Dan Luo,Zhou Li
标识
DOI:10.1038/s41467-024-44848-5
摘要
Abstract Ionically conductive fibers have promising applications; however, complex processing techniques and poor stability limit their practicality. To overcome these challenges, we proposed a stress-induced adaptive phase transition strategy to conveniently fabricate self-encapsulated hydrogel-based ionically conductive fibers (se-HICFs). se-HICFs can be produced simply by directly stretching ionic hydrogels with ultra-stretchable networks (us-IHs) or by dip-drawing from molten us-IHs. During this process, stress facilitated the directional migration and evaporation of water molecules in us-IHs, causing a phase transition in the surface layer of ionic fibers to achieve self-encapsulation. The resulting sheath-core structure of se-HICFs enhanced mechanical strength and stability while endowing se-HICFs with powerful non-contact electrostatic induction capabilities. Mimicking nature, se-HICFs were woven into spider web structures and camouflaged in wild environments to achieve high spatiotemporal resolution 3D depth-of-field sensing for different moving media. This work opens up a convenient route to fabricate stable functionalized ionic fibers.
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