复合数
法拉第效率
阳极
沸石咪唑盐骨架
材料科学
碳纤维
化学工程
电解质
聚乙烯醇
纳米技术
复合材料
金属有机骨架
化学
电极
工程类
有机化学
吸附
物理化学
作者
Yanchun Xue,Mingyue Gao,Mengrong Wu,Dongqin Su,Xingmei Guo,Jing Shi,Mengting Duan,Jiale Chen,Junhao Zhang,Qinghong Kong
标识
DOI:10.1002/celc.202000932
摘要
Abstract Hard carbon anodes are the most promising candidates for sodium‐ion batteries due to lower sodium‐embedded platform and higher specific capacity. However, pure hard carbon carbons usually show very low initial coulombic efficiency, low electronic conductance, et al . Herein, hard carbon‐soft carbon (HC‐SC) composites composed of carbon nanotubes (CNTs) blooming on porous hard carbon, which were synthesized through thermal decomposition of zeolitic imidazolate framework‐67 (ZIF‐67) and polyvinyl alcohol (PVA) composite. This unique structure could greatly promote the sodium‐ion diffusion and electron transport due to the increased electrode/electrolyte contact area and enlarged pores. As expected, the HC‐SC delivers a high capacity (306.8 mAh g −1 at 500 mA g −1 ), impressive cycling stability (256.8 mAh g −1 after 1000 cycles) and enhanced rate performance (144.9 mAh g −1 at 20 C), which are far superior to those of both individual hard carbon and soft carbon. This encouraging performance may benefit from the synergistic effect of the modified defect concentration and interlayer distance in hard carbon by soft carbon, as well as the unique hierarchical structure. This work provides an exemplary strategy to develop optimized carbon materials for sodium‐ion batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI