30 Li+‐Accommodating Covalent Organic Frameworks as Ultralong Cyclable High‐Capacity Li‐Ion Battery Electrodes

Covalent organic frameworks (COFs) have attracted considerable attention as a facile and versatile design platform for advanced energy storage materials owing to their structural diversity, ordered porous structures, and chemical stability. In this study, a redox‐active COF (TP–OH–COF) that can acco...

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Vydané v:Advanced functional materials Ročník 32; číslo 9
Hlavní autori: Zhai, Lipeng, Li, Gaojie, Yang, Xiubei, Park, Sodam, Han, Diandian, Mi, Liwei, Wang, Yanjie, Li, Zhongping, Lee, Sang‐Young
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Hoboken Wiley Subscription Services, Inc 01.02.2022
Predmet:
Carbonyls
Chemical synthesis
covalent organic frameworks
Electrode materials
Energy storage
high capacity
Lithium-ion batteries
Materials science
redox‐active carbonyl sites
Tethering
ISSN:1616-301X, 1616-3028
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Shrnutí:Covalent organic frameworks (COFs) have attracted considerable attention as a facile and versatile design platform for advanced energy storage materials owing to their structural diversity, ordered porous structures, and chemical stability. In this study, a redox‐active COF (TP–OH–COF) that can accommodate 30 Li+ ions is synthesized for potential use as an ultralong cyclable high‐capacity lithium‐ion battery electrode material. The TP–OH–COF is synthesized using triformylpholoroglucinol and 2,5‐diaminohydroquinone dihydrochloride under solvothermal conditions. The accommodation of such exceptional Li+ ion content in the TP–OH–COF is achieved by alternately tethering redox‐active hydroxyl and carbonyl sites on the pore walls. Owing to this unique chemical/structural feature, the TP–OH–COF delivers a high specific capacity of 764.1 mAh g–1, and capacity retention of 63% after 8000 cycles at a fast current density of 5.0 A g–1. A redox‐active COF with alternate tethering of redox‐active hydroxyl and carbonyl sites on the pore walls is demonstrated as an organic‐based, ultralong cyclable high‐capacity LIB anode material. This COF electrode accommodated 30 Li+ ions owing to its unique framework structure and materials chemistry, which has never been reported in previous studies on COF‐based electrode materials.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 14
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202108798