离子键合
化学物理
离子
阴极
密度泛函理论
锂(药物)
电池(电)
材料科学
阳极
相(物质)
纳米技术
化学
分子物理学
计算化学
热力学
物理化学
物理
电极
功率(物理)
内分泌学
有机化学
医学
作者
Aaron Mascaro,Zi Wang,Pierre Hovington,Yoichi Miyahara,Andrea Paolella,Vincent Gariépy,Zimin Feng,Tyler Enright,C. P. Aiken,Karim Zaghib,Kirk H. Bevan,Peter Grütter
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-06-19
卷期号:17 (7): 4489-4496
被引量:32
标识
DOI:10.1021/acs.nanolett.7b01857
摘要
One of the main challenges in improving fast charging lithium-ion batteries is the development of suitable active materials for cathodes and anodes. Many materials suffer from unacceptable structural changes under high currents and/or low intrinsic conductivities. Experimental measurements are required to optimize these properties, but few techniques are able to spatially resolve ionic transport properties at small length scales. Here we demonstrate an atomic force microscope (AFM)-based technique to measure local ionic transport on LiFePO4 to correlate with the structural and compositional analysis of the same region. By comparing the measured values with density functional theory (DFT) calculations, we demonstrate that Coulomb interactions between ions give rise to a collective activation energy for ionic transport that is dominated by large phase boundary hopping barriers. We successfully measure both the collective activation energy and the smaller single-ion bulk hopping barrier and obtain excellent agreement with values obtained from our DFT calculations.
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