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用于水系锌离子储能装置的高速二维聚芳酰亚胺共价有机骨架阳极

A High-Rate Two-Dimensional Polyarylimide Covalent Organic Framework Anode for Aqueous Zn-Ion Energy Storage Devices.

作者信息

Yu Minghao, Chandrasekhar Naisa, Raghupathy Ramya Kormath Madam, Ly Khoa Hoang, Zhang Haozhe, Dmitrieva Evgenia, Liang Chaolun, Lu Xihong, Kühne Thomas D, Mirhosseini Hossein, Weidinger Inez M, Feng Xinliang

机构信息

Center for Advancing Electronics Dresden (cfaed) & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062 Dresden, Germany.

Dynamics of Condensed Matter and Center for Sustainable Systems Design, Chair of Theoretical Chemistry, University of Paderborn, Warburger Strasse 100, 33098 Paderborn, Germany.

出版信息

J Am Chem Soc. 2020 Nov 18;142(46):19570-19578. doi: 10.1021/jacs.0c07992. Epub 2020 Nov 9.

Abstract

Rechargeable aqueous Zn-ion energy storage devices are promising candidates for next-generation energy storage technologies. However, the lack of highly reversible Zn-storage anode materials with low potential windows remains a primary concern. Here, we report a two-dimensional polyarylimide covalent organic framework (PI-COF) anode with high-kinetics Zn-storage capability. The well-organized pore channels of PI-COF allow the high accessibility of the build-in redox-active carbonyl groups and efficient ion diffusion with a low energy barrier. The constructed PI-COF anode exhibits a specific capacity (332 C g or 92 mAh g at 0.7 A g), a high rate capability (79.8% at 7 A g), and a long cycle life (85% over 4000 cycles). Raman investigation and first-principle calculations clarify the two-step Zn-storage mechanism, in which imide carbonyl groups reversibly form negatively charged enolates. Dendrite-free full Zn-ion devices are fabricated by coupling PI-COF anodes with MnO cathodes, delivering excellent energy densities (23.9 ∼ 66.5 Wh kg) and supercapacitor-level power densities (133 ∼ 4782 W kg). This study demonstrates the feasibility of covalent organic framework as Zn-storage anodes and shows a promising prospect for constructing reliable aqueous energy storage devices.

摘要

可充电水系锌离子储能装置是下一代储能技术的有潜力的候选者。然而,缺乏具有低电位窗口的高可逆性锌存储负极材料仍然是一个主要问题。在此,我们报道了一种具有高动力学锌存储能力的二维聚酰亚胺共价有机框架(PI-COF)负极。PI-COF 有序的孔道使得内置的氧化还原活性羰基具有高可及性,并能以低能垒实现高效离子扩散。构建的 PI-COF 负极表现出比容量(在 0.7 A g 时为 332 C g 或 92 mAh g)、高倍率性能(在 7 A g 时为 79.8%)和长循环寿命(在 4000 次循环后保持 85%)。拉曼研究和第一性原理计算阐明了两步锌存储机制,其中酰亚胺羰基可逆地形成带负电荷的烯醇盐。通过将 PI-COF 负极与 MnO 正极耦合制备了无枝晶的全锌离子装置,其具有优异的能量密度(23.9 ∼ 66.5 Wh kg)和超级电容器级别的功率密度(133 ∼ 4782 W kg)。这项研究证明了共价有机框架作为锌存储负极的可行性,并展示了构建可靠水系储能装置的广阔前景。

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