Scalable Synthesis of Ultrathin Polyimide Covalent Organic Framework Nanosheets for High-Performance Lithium−Sulfur Batteries



Wu, Xiaofeng, Duan, Haiyan, Li, Ke, Xie, Mo, Chen, Jiaming, Zhou, Hougan, Ning, Guohong, Cooper, Andrew and Li, Dan
(2021) Scalable Synthesis of Ultrathin Polyimide Covalent Organic Framework Nanosheets for High-Performance Lithium−Sulfur Batteries. Journal of the American Chemical Society, 143 (46). pp. 19446-19453.

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Abstract

Development of new porous materials as hosts to suppress the dissolution and shuttle of lithium polysulfides is beneficial for constructing highly efficient lithium-sulfur batteries (LSBs). Although 2D covalent organic frameworks (COFs) as host materials exhibit promising potential for LSBs, their performance is still not satisfactory. Herein, we develop polyimide COFs (PI-COF) with a well-defined lamellar structure, which can be exfoliated into ultrathin (∼1.2 nm) 2D polyimide nanosheets (PI-CONs) with a large size (∼6 μm) and large quantity (40 mg/batch). Explored as new sulfur host materials for LSBs, PI-COF and PI-CONs deliver high capacities (1330 and 1205 mA h g<sup>-1</sup> at 0.1 C, respectively), excellent rate capabilities (620 and 503 mA h g<sup>-1</sup> at 4 C, respectively), and superior cycling stability (96% capacity retention at 0.2 C for PI-CONs) by virtue of the synergy of robust conjugated porous frameworks and strong oxygen-lithium interactions, surpassing the vast majority of organic/polymeric lithium-sulfur battery cathodes ever reported. Our finding demonstrates that ultrathin 2D COF nanosheets with carbonyl groups could be promising host materials for LSBs with excellent electrochemical performance.

Item Type: Article
Uncontrolled Keywords: 40 Engineering, 4016 Materials Engineering, 34 Chemical Sciences, 3406 Physical Chemistry, 7 Affordable and Clean Energy
Divisions: Faculty of Science and Engineering > School of Physical Sciences
Depositing User: Symplectic Admin
Date Deposited: 04 Nov 2021 08:25
Last Modified: 21 Jun 2024 06:11
DOI: 10.1021/jacs.1c08675
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3142721