电解质
阳极
材料科学
电池(电)
纳米线
电极
电化学电池
电化学
锂(药物)
透射电子显微镜
纳米技术
纳米线电池
半电池
锂离子电池
离子液体
化学
工作电极
磷酸钒锂电池
催化作用
物理
内分泌学
物理化学
功率(物理)
医学
量子力学
生物化学
作者
Meng Gu,Lucas R. Parent,B. Layla Mehdi,Raymond R. Unocic,Matthew T. McDowell,Robert L. Sacci,Wu Xu,Justin G. Connell,Pinghong Xu,Patricia Abellán,Xilin Chen,Yaohui Zhang,Daniel E. Perea,James Evans,Lincoln J. Lauhon,Ji‐Guang Zhang,Jun Liu,Nigel D. Browning,Yi Cui,Ilke Arslan
出处
期刊:Nano Letters
[American Chemical Society]
日期:2013-11-13
卷期号:13 (12): 6106-6112
被引量:289
摘要
Over the past few years, in situ transmission electron microscopy (TEM) studies of lithium ion batteries using an open-cell configuration have helped us to gain fundamental insights into the structural and chemical evolution of the electrode materials in real time. In the standard open-cell configuration, the electrolyte is either solid lithium oxide or an ionic liquid, which is point-contacted with the electrode. This cell design is inherently different from a real battery, where liquid electrolyte forms conformal contact with electrode materials. The knowledge learnt from open cells can deviate significantly from the real battery, calling for operando TEM technique with conformal liquid electrolyte contact. In this paper, we developed an operando TEM electrochemical liquid cell to meet this need, providing the configuration of a real battery and in a relevant liquid electrolyte. To demonstrate this novel technique, we studied the lithiation/delithiation behavior of single Si nanowires. Some of lithiation/delithation behaviors of Si obtained using the liquid cell are consistent with the results from the open-cell studies. However, we also discovered new insights different from the open cell configuration—the dynamics of the electrolyte and, potentially, a future quantitative characterization of the solid electrolyte interphase layer formation and structural and chemical evolution.
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