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基于二维共价有机框架的水系锌离子电池中的锌离子相互作用

Zinc ion interactions in a two-dimensional covalent organic framework based aqueous zinc ion battery.

作者信息

Khayum M Abdul, Ghosh Meena, Vijayakumar Vidyanand, Halder Arjun, Nurhuda Maryam, Kumar Sushil, Addicoat Matthew, Kurungot Sreekumar, Banerjee Rahul

机构信息

Academy of Scientific and Innovative Research (AcSIR) , Sector 19, Kamla Nehru Nagar , Ghaziabad , Uttar Pradesh-201002 , India.

Physical and Materials Chemistry Division , CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road , Pune-411008 , India . Email:

出版信息

Chem Sci. 2019 Aug 6;10(38):8889-8894. doi: 10.1039/c9sc03052b. eCollection 2019 Oct 14.

Abstract

The two-dimensional structural features of covalent organic frameworks (COFs) can promote the electrochemical storage of cations like H, Li, and Na through both faradaic and non-faradaic processes. However, the electrochemical storage of cations like Zn ion is still unexplored although it bears a promising divalent charge. Herein, for the first time, we have utilized hydroquinone linked β-ketoenamine COF acting as a Zn anchor in an aqueous rechargeable zinc ion battery. The charge-storage mechanism comprises of an efficient reversible interlayer interaction of Zn ions with the functional moieties in the adjacent layers of COF (-182.0 kcal mol). Notably, due to the well-defined nanopores and structural organization, a constructed full cell, displays a discharge capacity as high as 276 mA h g at a current rate of 125 mA g.

摘要

共价有机框架(COFs)的二维结构特征可通过法拉第和非法拉第过程促进H、Li和Na等阳离子的电化学存储。然而,尽管Zn离子带有二价电荷,但其电化学存储仍未得到探索。在此,我们首次利用对苯二酚连接的β-酮烯胺COF作为水系可充电锌离子电池中的锌锚定体。电荷存储机制包括Zn离子与COF相邻层中的功能基团之间高效的可逆层间相互作用(-182.0 kcal mol)。值得注意的是,由于具有明确的纳米孔和结构组织,构建的全电池在125 mA g的电流速率下显示出高达276 mA h g的放电容量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb07/6855258/c42208601b27/c9sc03052b-f1.jpg

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