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Self-supporting and dual-active 3D Co-S nanosheets constructed by ligand replacement reaction from MOF for rechargeable Al battery

阴极 材料科学 法拉第效率 化学工程 电池(电) 多孔性 惰性 电导率 电极 复合材料 电化学 化学 有机化学 工程类 物理 物理化学 量子力学 功率(物理)
作者
Aijing Lv,Songle Lu,Mingyong Wang,Haotian Shi,Wenjing Yan,Shuqiang Jiao
出处
期刊:Journal of Energy Chemistry [Elsevier BV]
卷期号:69: 35-43 被引量:22
标识
DOI:10.1016/j.jechem.2021.12.022
摘要

A novel self-supporting 3D Co-S/CC cathode without binder for Al battery is designed, and reveals high capability and good cycling stability due to capacity contribution of double active elements and high mass utilization. Metal sulfides with high theoretical capacities are expected as promising cathode materials of Al batteries (AIBs). However, powdery active materials are mainly synthesized and loaded on current collector by insulating binder without capacity. Meanwhile, S as inert element in metal sulfides can not usually provide capacity. So, powdery metal sulfides only exhibit limiting practical capacity and poor cycling stability due to weak conductivity and low mass utilization. Herein, the novel self-supporting and dual-active Co-S nanosheets on carbon cloth (i.e. Co-S/CC) with hierarchically porous structure are constructed as cathode of AIBs . Co-S nanosheets are derived from ZIF-67 nanosheets on CC by a facile ligand replacement reaction. As a result, the binder-free Co-S/CC cathode with good conductivity delivers excellent initial discharge capacity of 383.4 mAh g −1 (0.211 mAh cm −2 ) at current density of 200 mA g −1 and maintain reversible capacity of 156.9 mAh g −1 (0.086 mAh cm −2 ) with Coulombic efficiency of 95.8% after 500 cycles, which are much higher than those of the traditional slurry-coating cathodes. Both Co and S as active elements in Co-S/CC contribute to capacity, which leads to a high mass utilization. This work provides a significant strategy for the construction of self-supporting metallic cathode for advanced high-energy density Al battery.
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