阳极
法拉第效率
材料科学
介孔材料
碳化
储能
化学工程
纳米结构
碳纤维
钴
多孔性
金属有机骨架
纳米技术
扩散
电极
催化作用
化学
复合材料
吸附
有机化学
冶金
量子力学
复合数
功率(物理)
物理化学
热力学
扫描电子显微镜
工程类
物理
作者
Xiaoni Liu,Shenghao Zhang,Yaqi Fan,Qichun Zhang,Caixia Li,Bo Ye,Minge Tian,Mengyu Liu,Lei Wang
标识
DOI:10.1002/ente.202300150
摘要
Cobalt‐based compounds have been extensively studied due to their relatively high theoretical capacity as anode materials for sodium‐ion batteries (SIBs). However, the requirement for strong conductivity and excellent cycling stability is still an urgent challenge for the energy‐storage system. To address these problems, metal–organic‐framework‐74‐derived porous rod‐shaped nanostructure Co/C materials are designed as advanced anode materials for SIBs, which is beneficial for the reaction kinetics of SIBs. Moreover, the efficient synergistic utility of the nanostructure and the rich mesopores of Co/C materials provides the ion‐diffusion paths and active sites for the transfer and storage of Na + , which contributes to the energy‐storage ability. The indurative structure of the carbonization electrode material can alleviate the influence of volume change due to Na + insertion/extraction. Therefore, the Co/C anode exhibits a high Coulombic efficiency of 94.3% at 0.1 A g −1 . After 300 cycles, the Na + ‐storage capacity is 200.4 mAh g −1 , and the Coulombic efficiency is 99.0%, where the capacity retention rate is up to 88.2%. Herein, insight is provided into the role of porous Co/C material in improving the kinetics of Na + reaction, supplying an effective strategy for the rational design of key materials for high‐performance rechargeable batteries.
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