Shang Yinghui, Wei Junjie, He Xian, Zhao Jie, Shen Hongdou, Wu Dongbei, Wu Tong, Wang Qigang
Frontiers Science Center for Intelligent Autonomous Systems, School of Chemical Science and Engineering, Tongji University, Shanghai, 200092, P. R. China.
Translational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People's Hospital, School of Medicine, Tongji University, Shanghai, 200434, P. R. China.
Adv Mater. 2023 Mar;35(12):e2208443. doi: 10.1002/adma.202208443. Epub 2023 Feb 8.
Flexible energy-storage devices lay the foundation for a convenient, advanced, fossil fuel-free society. However, the fabrication of flexible energy-storage devices remains a tremendous challenge due to the intrinsic dissimilarities between electrode and electrolyte. In this study, a strategy is proposed for fabricating a flexible electrode and electrolyte entirely inside a matrix. First, a nest-structural and redox-active ionohydrogel with excellent stretchability (up to 3000%) and conductivity (167.9 mS cm ) is designed using a hydrated ionic liquid (HIL) solvent and chemical foaming strategy. The nest-structure ionohydrogel provides sufficient "highways" and "service area", and the cation in HIL facilitates the reaction, transportation, and deposition of benzoquinone. Subsequently, in situ, a novel benzoquinone crystal-gel interface (CGI) is in situ fabricated on the surface of the ionohydrogel through electrochemical deposition of benzoquinone. Thus, an integrated CGI-gel platform is successfully achieved with a middle body as an electrolyte and the surficial redox-active CGI membrane for electrochemical energy conversion and storage. Based on the CGI-gel platform, an extreme simple and effective "stick-to-use" strategy is proposed for constructing flexible energy-storage devices and then a series of flexible supercapatteries are fabricated with high stretchability and capacitance (5222.1 mF cm at 600% strain), low self-discharge and interfacial resistance and a wearable, self-power and intelligent display.
柔性储能装置为构建一个便捷、先进且无化石燃料的社会奠定了基础。然而,由于电极和电解质之间存在本质差异,柔性储能装置的制造仍然面临巨大挑战。在本研究中,我们提出了一种在基质内部完全制造柔性电极和电解质的策略。首先,使用水合离子液体(HIL)溶剂和化学发泡策略设计了一种具有出色拉伸性(高达3000%)和导电性(167.9 mS cm)的巢状结构且具有氧化还原活性的离子水凝胶。巢状结构的离子水凝胶提供了足够的“高速公路”和“服务区”,HIL中的阳离子促进了苯醌的反应、传输和沉积。随后,通过苯醌的电化学沉积在离子水凝胶表面原位制备了一种新型的苯醌晶体 - 凝胶界面(CGI)。因此,成功实现了一个集成的CGI - 凝胶平台,其中间主体作为电解质,表面的氧化还原活性CGI膜用于电化学能量转换和存储。基于CGI - 凝胶平台,提出了一种极其简单有效的“即贴即用”策略来构建柔性储能装置,随后制造了一系列具有高拉伸性和电容(在600%应变下为5222.1 mF cm)、低自放电和界面电阻以及可穿戴、自供电和智能显示功能的柔性超级电容器。