材料科学
阴极
电化学
电池(电)
钠
钠离子电池
有机自由基电池
离子
共轭体系
纳米技术
金属
化学工程
无机化学
电极
有机化学
物理化学
化学
复合材料
冶金
聚合物
功率(物理)
法拉第效率
工程类
物理
量子力学
作者
Meiling Qi,Linqi Cheng,Heng‐guo Wang,Fengchao Cui,Qingyuan Yang,Long Chen
标识
DOI:10.1002/adma.202401878
摘要
Abstract 2D 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 m 2 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.
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