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用于高导电性和储能的共价有机框架纳米通道中的电子高速公路。

Electron Highways into Nanochannels of Covalent Organic Frameworks for High Electrical Conductivity and Energy Storage.

机构信息

Department of Chemistry and Integrated Research Consortium on Chemical Sciences (IRCCS) , Nagoya University , Furo-cho, Chikusa-ku , Nagoya 464-8602 , Japan.

出版信息

ACS Appl Mater Interfaces. 2019 Feb 27;11(8):7661-7665. doi: 10.1021/acsami.8b21696. Epub 2019 Feb 4.

Abstract

To enhance the electron transfer within the covalent organic frameworks (COFs), we obtained a nanocomposite of conductive poly(3,4-ethylenedioxythiophene) (PEDOT) and redox-active AQ-COF by performing a facile in situ solid-state polymerization inside the nanochannels of COFs. The PEDOT chains functioned like electron highways within the nanochannels, resulting in a PEDOT@AQ-COF nanocomposite with an excellent electrical conductivity of 1.1 S cm and a remarkably improved performance in faradaic energy storage. The all-organic PEDOT@AQ-COF electrode showed specific capacitance as high as 1663 F g (at 1 A g), ultrafast charge/discharge rate performance (998 F g at 500 A g), and excellent stability for 10 000 cycles. This research demonstrates a promising strategy for increasing the conductivity of COF-based materials and broadening their applications.

摘要

为了增强共价有机框架(COFs)内的电子转移,我们通过在 COFs 的纳米通道内进行简便的原位固态聚合,获得了导电聚(3,4-乙二氧基噻吩)(PEDOT)和氧化还原活性 AQ-COF 的纳米复合材料。PEDOT 链在纳米通道内充当电子高速公路,导致 PEDOT@AQ-COF 纳米复合材料具有 1.1 S cm 的优异电导率和显著改善的法拉第储能性能。全有机 PEDOT@AQ-COF 电极表现出高达 1663 F g 的比电容(在 1 A g 下)、超快速的充放电率性能(在 500 A g 下为 998 F g)和 10000 次循环的优异稳定性。这项研究为提高基于 COF 的材料的电导率和拓宽其应用提供了一种很有前途的策略。

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