过电位
成核
枝晶(数学)
阳极
材料科学
电化学
电极
锂(药物)
电池(电)
化学工程
纳米技术
复合材料
化学
几何学
热力学
物理化学
医学
物理
工程类
内分泌学
功率(物理)
有机化学
数学
作者
Yuanliang Chen,Xingping Yuan,Cuiping He,Qingyi Gou,Ni Yang,Gang Xie,Keyu Zhang,Yaochun Yao,Yanqing Hou
出处
期刊:Energies
[Multidisciplinary Digital Publishing Institute]
日期:2023-04-27
卷期号:16 (9): 3745-3745
被引量:9
摘要
Li metal has been considered an ideal anode in lithium batteries due to its high theoretical capacity of 3860 mAh·g−1 and lowest negative reduction potential of −3.040 V among the standard hydrogen electrodes. However, lithium dendrites can easily grow on the surface of the negative electrode during charging, which results in a short circuit of the battery and reduces its efficiency. This paper investigated dendrite growth and inhibition mechanisms in lithium metal batteries to improve battery life. The impacts of the initial nucleation spacing, surface energy anisotropy strength, and interfacial electrochemical driving force on lithium dendrite growth were analyzed with electrochemical experiments and mathematical models. The results showed that the smaller nucleation spacing inhibits the growth of dendrite side branches and reduces the roughness of lithium metal deposition on the negative electrode. A lower interfacial energy anisotropy strength can slow down the growth of dendrite tips and improve the dendrite growth structure. The growth of the dendrites is influenced by the interfacial electrochemical driving force. Reducing the nucleation overpotential can effectively inhibit the growth of lithium dendrites.
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