Origin of additional capacities in metal oxide lithium-ion battery electrodes

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作者
机构
[1] Hu, Yan-Yan
[2] Liu, Zigeng
[3] Nam, Kyung-Wan
[4] Borkiewicz, Olaf J.
[5] Cheng, Jun
[6] Hua, Xiao
[7] Dunstan, Matthew T.
[8] Yu, Xiqian
[9] Wiaderek, Kamila M.
[10] Du, Lin-Shu
[11] Chapman, Karena W.
[12] Chupas, Peter J.
[13] Yang, Xiao-Qing
[14] 1,Grey, Clare P.
来源
| 1600年 / Nature Publishing Group卷 / 12期
关键词
Conversion reactions - Higher energy density - In-situ synchrotrons - Intercalation reaction - Reversible capacity - Reversible reaction - Theoretical calculations - Theoretical capacity;
D O I
10.1038/nmat3784
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摘要
Metal fluorides/oxides (MFx/MxOy) are promising electrodes for lithium-ion batteries that operate through conversion reactions. These reactions are associated with much higher energy densities than intercalation reactions. The fluorides/oxides also exhibit additional reversible capacity beyond their theoretical capacity through mechanisms that are still poorly understood, in part owing to the difficulty in characterizing structure at the nanoscale, particularly at buried interfaces. This study employs high-resolution multinuclear/multidimensional solid-state NMR techniques, with in situ synchrotron-based techniques, to study the prototype conversion material RuO 2. The experiments, together with theoretical calculations, show that a major contribution to the extra capacity in this system is due to the generation of LiOH and its subsequent reversible reaction with Li to form Li 2 O and LiH. The research demonstrates a protocol for studying the structure and spatial proximities of nanostructures formed in this system, including the amorphous solid electrolyte interphase that grows on battery electrodes. © 2013 Macmillan Publishers Limited. All rights reserved.
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