Affiliation:
1. State Key Laboratory of Supramolecular Structure and Materials College of Chemistry Jilin University Changchun 130012 China
2. College of Materials Science and Engineering Shenzhen University Shenzhen 518060 China
3. Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education and Faculty of Chemistry Northeast Normal University Changchun 130024 China
4. State Key Laboratory of Organic–Inorganic Composites Beijing University of Chemical Technology Beijing 100029 China
Abstract
Abstract2D conjugated metal–organic frameworks (2D c‐MOFs) have garnered significant attention as promising electroactive materials for energy storage. However, their further applications are hindered by low capacity, limited cycling life, and underutilization of the active sites. Herein, Cu‐TBA (TBA = octahydroxyltetrabenzoanthracene) with large conjugation units (narrow energy gap) and a unique rhombus topology is introduced as the cathode material for sodium‐ion batteries (SIBs). Notably, Cu‐TBA with a rhombus topology exhibits a high specific surface area (613 m2 g−1) and metallic band structure. Additionally, Cu‐TBA outperforms its hexagonal counterpart, Cu‐HHTP (HHTP = 2,3,6,7,10,11‐hexahydroxyltriphenylene), demonstrating superior reversible capacity (153.6 mAh g−1 at 50 mA g−1) and outstanding cyclability with minimal capacity decay even after 3000 cycles at 1 A g−1. This work elucidates a new strategy to enhance the electrochemical performance of 2D c‐MOFs cathode materials by narrowing the energy gap of organic linkers, effectively expanding the utilization of 2D c‐MOFs for SIBs.
Funder
National Natural Science Foundation of China
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献