佩多:嘘
材料科学
共价有机骨架
导电聚合物
储能
纳米技术
化学工程
氧化还原
聚合物
多孔性
复合材料
图层(电子)
工程类
量子力学
物理
冶金
功率(物理)
作者
Edon Vitaku,Cara N. Gannett,Keith Carpenter,Luxi Shen,Héctor D. Abruña,William R. Dichtel
标识
DOI:10.26434/chemrxiv.9185948
摘要
Redox-active covalent organic frameworks (COFs) are promising materials for energy storage devices because of their high density of redox sites, permanent and controlled porosity, high surface areas, and tunable structures. However, the low electrochemical accessibility of their redox-active sites has limited COF-based devices either to thin films (<250 nm) grown on conductive substrates, or to thicker films (1 µm) when a conductive polymer is introduced into the COF pores. Electrical energy storage devices constructed from bulk microcrystalline COF powders, eliminating the need for both thin-film formation and conductive polymer guests, would offer both improved capacity and potentially scalable fabrication processes. Here we report on the synthesis and electrochemical evaluation of a new phenazine-based 2D COF (DAPH-TFP COF), as well as its composite with poly(3,4-ethylenedioxythiophene) (PEDOT). Both the COF and its PEDOT composite were evaluated as powders that were solution-cast onto bulk electrodes serving as current collectors. The unmodified DAPH-TFP COF exhibited excellent electrical access to its redox sites, even without PEDOT functionalization, and outperformed the PEDOT composite of a previously reported anthraquinone-based system. Devices containing DAPH-TFP COF were able to deliver both high energy (250 Wh/kg) and power densities (2950 W/kg), validating the promise of unmodified redox-active COFs that are easily incorporated into electrical energy storage devices.
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