过电位
材料科学
成核
阳极
法拉第效率
阴极
电解质
化学工程
氧化物
复合材料
纳米技术
电流密度
电化学
冶金
物理化学
电极
工程类
物理
化学
有机化学
量子力学
作者
Chengbin Jin,Ouwei Sheng,Yun Lu,Jianmin Luo,Huadong Yuan,Wenkui Zhang,Hui Huang,Yongping Gan,Yang Xia,Chu Liang,Jun Zhang,Xinyong Tao
出处
期刊:Nano Energy
[Elsevier]
日期:2018-01-02
卷期号:45: 203-209
被引量:158
标识
DOI:10.1016/j.nanoen.2017.12.055
摘要
Lithium (Li) metal has been regarded as promising candidate anode to upgrade the energy density of Li secondary batteries. However, uncontrollable formation of Li dendrite, serious volumetric change, undesirable side reaction and poor mechanical properties of solid electrolyte interphase (SEI) layer impede the commercialization of this technology. By ex-situ observing the initial Li deposition process and conducting electrochemical test, we firstly confirm the prior nucleation behavior of Li metal at the step edge area. We thus employ a balsa wood derived porous carbon matrix as Li host and metal oxide nanoparticles are introduced to increase the nanoscale step amounts for Li nucleation. Hence, the Li nucleation overpotential is reduced and Li can be well accommodated within carbon matrix. Moreover, this step-edge-guided effect could promise the Li striping/plating to happen mainly around the steps area within channels, achieving a dendrite-free anode. Consequently, the modified Li anode is capable of working under an ultrahigh current density of 15 mA cm−2 with a Coulombic efficiency of ~ 96% and exhibit lower nucleation overpotential, more satisfactory cycling stability. And when in pair with commercial LiCoO2 cathode, it shows better rate performance and higher capacity compared with bare Li foil.
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