材料科学
阳极
铜
多孔性
集电器
电解质
金属
枝晶(数学)
电化学
化学工程
锂(药物)
复合材料
纳米技术
电极
冶金
物理化学
内分泌学
化学
数学
工程类
医学
几何学
作者
Rui Li,Jianxu Wang,Liangdong Lin,Hao Wang,Chunming Wang,Chenghui Zhang,Chunhua Song,Fang Tian,Jian Yang,Yitai Qian
标识
DOI:10.1016/j.mtener.2019.100367
摘要
The applications of Li metal anode in next-generation batteries, have been impeded by virtually infinite volume change and inevitable side reactions between Li metal and electrolytes. To address the issues, current collectors have to possess a porous structure and a lithiophilic surface. However, how to achieve a tunable porous structure in a simple and cost-effective way is a great challenge. Here, mechanical pressure is proposed to tune the porosity of surface-oxidized copper foams that realize the tunable porosity and surface affinity to lithium simultaneously. These foams exhibit enhanced electrochemical performances as the host for Li metal anodes. They can run 5000 cycles at 5 mA cm−2 for 1 mAh cm−2 in symmetrical cells, much better than the cases without pressure regulation or without surface oxidization. It is one of the best results reported so far using copper structures as the current collector for Li metal anodes. The full cells paired with LiFePO4 or with LiNi0.5Co0.3Mn0.2O2 also demonstrate their advantages than those without surface oxidization or without compression. These results indicate the promising potential of these foams as a host for dendrite-free Li metal anodes.
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