阳极
材料科学
法拉第效率
电化学
电极
电池(电)
背景(考古学)
锂(药物)
导电体
纳米复合材料
离子
复合数
锂离子电池
纳米技术
化学工程
复合材料
物理化学
热力学
有机化学
化学
工程类
内分泌学
物理
古生物学
功率(物理)
生物
医学
作者
Bing Han,Yu Yang,Xiaobo Shi,Guangzhao Zhang,Lu Gong,Dongwei Xu,Hongbo Zeng,Chaoyang Wang,Meng Gu,Yonghong Deng
出处
期刊:Nano Energy
[Elsevier BV]
日期:2018-05-19
卷期号:50: 359-366
被引量:109
标识
DOI:10.1016/j.nanoen.2018.05.044
摘要
Silicon is a promising candidate for negative electrodes due to its high theoretical specific capacity (~ 3579 mA h g−1) and low lithiation potential (~ 0.40 V vs. Li). However, its practical applications in battery have been inhibited by the large volume change (~ 400%) induced by Li+-insertion into Si lattices. Here, we attempt to resolve this issue at a fundamental level, and report for the first time a novel liquid metal (LM)-mediated spontaneous repairing conductive-additive-free Si anode for Li-ion battery. The fluidity of LM ensures the eternal contact between Si and the conducting-network during its repeated electrochemical reactions. The as-prepared nano-composite of LM/Si leads to superior performances as characterized by high capacity utilization (2300 mA h g−1 at 500 mA g−1), long-term stability (968 mA h g−1 after 1500 charge-discharge cycles at 8 A g−1 with 81.3% retention), high rate capability (360 mA h g−1 at 20 A g−1, equivalence of 55 C, or full charge/discharge in 65 s), and, in particular, an extra-ordinarily high initial coulombic efficiency (95.92%), which is not only the highest reported for Si to the best of our knowledge, but also higher than the mature graphitic carbon anodes. The unique approach described in this work not only resolves the basic stress challenges faced by the promising but often problematic alloy-type materials; in broader context it also provides a universal inspiration to all electrode materials whose electric properties suffer from extreme mechanic upheavals induced by the electrochemical strains during the cell reactions.
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