材料科学
菱形
阴极
电化学
电池(电)
金属有机骨架
钠离子电池
离子
共轭体系
拓扑(电路)
纳米技术
金属
化学工程
无机化学
电极
有机化学
物理化学
吸附
化学
复合材料
冶金
聚合物
功率(物理)
物理
量子力学
法拉第效率
工程类
几何学
数学
组合数学
作者
Meiling Qi,Linqi Cheng,Heng‐guo Wang,Fengchao Cui,Qingyuan Yang,Лонг Чэн
标识
DOI:10.1002/adma.202401878
摘要
Abstract Two‐dimensional conjugated metal–organic frameworks (2D c ‐MOFs) have garnered significant attention as promising electroactive materials for energy storage. However, their further applications have been hindered by low capacity, limited cycling life, and underutilization of the active sites. Herein, we introduce Cu‐TBA (TBA = octahydroxyl tetrabenzoanthracene) with large conjugation units (narrow energy gap) and a unique rhombus topology as the cathode material for sodium‐ion batteries (SIBs). Notably, Cu‐TBA with a rhombus topology exhibits a high specific surface area (613 m 2 g −1 ) and metallic band structure. Additionally, Cu‐TBA outperforms its hexagonal counterpart, Cu‐HHTP (HHTP = 2,3,6,7,10,11‐hexahydroxyphenanthrene), demonstrating superior reversible capacity (153.6 mAh g −1 at 50 mA g −1 ) and outstanding cyclability with minimal capacity decay even after 3,000 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. This article is protected by copyright. All rights reserved
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