材料科学
聚酰亚胺
柔性电子器件
数码产品
纳米技术
可伸缩电子设备
图层(电子)
电气工程
工程类
作者
Yanyu Gao,Yan Sui,Ziyang Liu,Zhe Tang,Xinyu Zeng,Xiao Su,Cheng Wang,Qianqian Yu,Linge Wang
标识
DOI:10.1002/adfm.202513521
摘要
Abstract The development of high‐performance colorless polyimides (CPIs) demands a paradigm shift to overcome the mutual exclusivity of optical transparency, thermal stability, and mechanical strength. Drawing inspiration from nacre's hierarchical coordination motifs, a biomimetic strategy is presented that integrates molecular engineering with Zn 2+ ‐mediated crosslinking. Six pyridine‐containing diamines are synthesized to suppress charge transfer complexes and copolymerized with 6FDA, forming tunable polyimide backbones. Subsequent Zn 2 ⁺ coordination generates a dynamic N─Zn─N network, which rigidifies chains and delivers synergistic enhancements: an excellent T g of 338.5 °C (+16.6%), ultralow charge transfer complexes of 45.8 ppm K⁻¹ (−20.6%), and tensile strength of 138 MPa (+46.8%) while retaining 89.3% transmittance. The film enable cytocompatible wearable sensors with 38 ms response times and stable signal output after 10 000 bending cycles. Moreover, its relevance to foldable ACEL devices highlights the potential for industrial scalability. This work reimagines CPI design through coordination chemistry, offering a blueprint for multifunctional polymers in next‐generation electronics.
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