碳包裹自组装三维花状ZnO制备稳定锂金属阳极

IF 2.4 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ionics Pub Date : 2023-08-15 DOI:10.1007/s11581-023-05161-1
Yue Yu, Ping Li, Tianying Wang, Qiwei Tan, Jie Shi, Qi Wan, Xuanhui Qu
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引用次数: 0

摘要

采用简单的水热法合成了碳包覆的花状ZnO,然后进行了碳化(ZnO@C),并首次利用ZnO的亲锂性作为载体材料,促进锂的均匀沉积和溶解。具有分层多孔结构和大比表面积的花状ZnO可以为锂的调控沉积提供丰富的位点,同时抑制锂枝晶的生长。当在对称电池中测试时,ZnO@C-500电极可以在1.0 mA cm−2下稳定循环3000 h以上,过电位低至13 mV,并显示出令人满意的倍率性能。当与LiFePO4阴极耦合时,电池在1℃下循环300次后仍能保持103 mAh·g−1的高比容量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Self-assembled three-dimensional flower-like ZnO encased by carbon toward stable lithium metal anode

Self-assembled three-dimensional flower-like ZnO encased by carbon toward stable lithium metal anode

The carbon-encased flower-like ZnO was synthesized through a facile hydrothermal method, then followed with carbonization (ZnO@C), and for the first time utilized as a host material to facilitate uniform deposition and dissolution of lithium by taking advantage of the lithiophilic nature of ZnO. Flower-like ZnO with hierarchically porous structures and large specific surface area could provide abundant sites for regulated lithium deposition and simultaneously inhibit lithium dendrite growth. When tested in symmetric cells, the ZnO@C-500 electrode could maintain stable cycling at 1.0 mA cm−2 for over 3000 h with a low overpotential of 13 mV and display satisfactory rate performance. When coupled with LiFePO4 cathode, the full cell could still hold a high specific capacity of 103 mAh·g−1 after 300 cycles at 1 C.

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来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
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