Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4214
Title: Chemical Exfoliation as a Controlled Route to Enhance the Anodic Performance of COF in LIB
Authors: HALDAR, SATTWICK
ROY, KINGSHUK
KUSHWAHA, RINKU
OGALE, SATISHCHANDRA
VAIDHYANATHAN, RAMANATHAN
Dept. of Chemistry
Dept. of Physics
Keywords: Anodic Covalent Organic Nanosheets
Chemical Exfoliation
Full Cell Lithium Ion Batteries
Functionalizing Exfoliation Agents
Lithium Storage
TOC-NOV-2019
2019
Issue Date: Dec-2019
Publisher: Wiley
Citation: Advanced Energy Materials, 9(48).
Abstract: A covalent organic framework (COF), built from light atoms with a graphitic structure, could be an excellent anodic candidate for lightweight batteries, which can be of use in portable devices. But to replace the commercial graphite anode, they need more Li‐interactive sites/unit‐cell and all such sites should be made to participate. The compromise made in the volumetric density to gain the gravimetric advantage should be minimal. Exfoliation enhances surface/functional group accessibility yielding high capacity and rapid charge storage. A chemical strategy for simultaneous exfoliation and increase of Li‐loving active‐pockets can deliver a lightweight Li‐ion battery (LIB). Here, anthracene‐based COFs are chemically exfoliated into few‐layer‐thick nanosheets using maleic anhydride as a functionalizing exfoliation agent. It not only exfoliates but also introduces multiple Li‐interactive carbonyl groups, leading to a loading of 30 Li/unit‐cell (vs one Li per C6). The exfoliation enhances the specific capacity by ≈4 times (200–790 mAh g−1 @100 mA g−1). A realistic full‐cell, made using the exfoliated COF against a LiCoO2 cathode, delivers a specific capacity of 220 mAh g−1 over 200 cycles. The observed capacity stands highest among all organic polymers. For the first report of a COF derived full‐cell LIB, this is a windfall.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4214
https://doi.org/10.1002/aenm.201902428
ISSN: 1614-6832
1614-6840
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