Meiling QiLinqi ChengHeng‐guo WangFengchao CuiQingyuan YangLong Chen
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.
Lu LiuYu GongYifan TongHao TianXubo WangYiming HuShaofeng HuangWeiwei HuangSandeep SharmaJingnan CuiYinghua JinWeitao GongWei Zhang
Shaonan GuZhaowen BaiSoumyadip MajumderBaoling HuangGuohua Chen
Meiling QiLong ChenXupeng ZhangYuzhao GuoXi SuXiaoxiao SunYi LiuLei WangHeng‐guo WangLong Chen
Shuai LiuPuiki LeungYong ZuoMeng SunLei WeiFrank C. WalshTianshou ZhaoQiang Liao
Hongxia LiJunwei LangShulai LeiJiangtao ChenYingde WangLingyang LiuTianyun ZhangWeisheng LiuXingbin Yan