材料科学
制作
电极
石墨烯
纳米技术
导电体
柔性电子器件
激光器
数码产品
光电子学
基质(水族馆)
选择性激光烧结
碳纳米管
聚合物
转印
热导率
作者
Zhe Yang,Zhimin Cai,Zhe Yu,Xiaofeng Chen,Jianjie Li,Cheng Zhang,Cheng Zhang,Zhiying Hu,Heng Deng,Ying Yi,Chi Zhang,Chi Zhang
标识
DOI:10.1002/adfm.202519191
摘要
Abstract Flexible electronics are pivotal for next‐generation technologies, yet their advancement is hindered by fabrication complexities, substrate limitations, and transfer‐reduced performance degradation. Herein, an innovative in situ transfer printing method integrated with Laser Shock Imprinting (LSI) is reported to directly synthesize laser‐induced graphene (LIG) on PET substrates. By using polyether sulfone (PES) as a dual‐functional medium—serving as both a binder for coal particles and a shock pressure generator via thermal decomposition—this approach enables simultaneous in situ graphenization of coal and PES and shock‐driven embedding of the produced graphene into softened PET. Moreover, PES‐derived LIG bridges graphenized coal particles, forming a seamlessly interconnected conductive network. The resulting flexible electrodes exhibit excellent conductivity (15 Ω □ −1 ), superior electromechanical performance (response/recovery times: 40/50 ms; GF = 516), and 3D customizability via PET's thermoplasticity‐an achievement unattainable with PI‐supported LIG or traditional transfer methods. Accordingly, the flexible electrode successfully demonstrates potential applications in motion monitoring, multidirectional strain sensing, and human‐computer interaction. This one‐step, transfer‐free method overcomes traditional limitations of complex procedures and resulting mechanical mismatches, providing a new strategy for synthesizing advanced flexible electronics.
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