| Literature DB >> 28557296 |
Baolong Zhou1,2, Xiang Hu2, Guang Zeng2, Shiwu Li2, Zhenhai Wen2, Long Chen1.
Abstract
Two redox-active porous organic frameworks (POFs) with a built-in radical moiety (TEMPO) and hierarchical porous structures were synthesized through a facile bottom-up strategy and studied as cathode materials for lithium-sulfur (Li-S) batteries. The sulfur loading in these two POFs reached 61 %, benefitting from their large pore volumes. Owing to the highly dense docking sites of TEMPO, sulfur could be covalently immobilized within the porous networks and efficiently inhibit the shuttle effect, thereby significantly improving the cycling performance. The composites TPE-TEMPO-POF-S (TPE=tetraphenylethene) deliver a capacity in excess of 470 mAh g-1 after 200 cycles with a coulombic efficiency of around 100 % at a current rate of 0.1 C. Furthermore, TEMPO-POFs with sulfur embedded showed excellent rate capability with limited capacity loss at rates of 0.1-1 C.Entities:
Keywords: batteries; electrodes; microporous materials; polymers; radicals
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Year: 2017 PMID: 28557296 DOI: 10.1002/cssc.201700749
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928