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High rate capabilities Fe3O4-based Cu nano-architectured electrodes for lithium-ion battery applications

机译:锂离子电池应用的高速率功能基于Fe3O4的Cu纳米结构电极

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摘要

All battery technologies are known to suffer from kinetic problems linked to the solid-state diffusion of Li in intercalation electrodes, the conductivity of the electrolyte in some cases and the quality of interfaces. For Li-ion technology the latter effect is especially acute when conversion rather than intercalation electrodes are used. Nano-architectured electrodes are usually suggested to enhance kinetics, although their realization is cumbersome. To tackle this issue for the conversion electrode material Fe3O4, we have used a two-step electrode design consisting of the electrochemically assisted template growth of Cu nanorods onto a current collector followed by electrochemical plating of Fe3O4. Using such electrodes, we demonstrate a factor of six improvement in power density over planar electrodes while maintaining the same total discharge time. The capacity at the 8C rate was 80% of the total capacity and was sustained over 100 cycles. The origin of the large hysteresis between charge and discharge, intrinsic to conversion reactions, is discussed and approaches to reduce it are proposed. We hope that such findings will help pave the way for the use of conversion reaction electrodes in future-generation Li-ion batteries.
机译:已知所有电池技术都遭受与锂在嵌入电极中的固态扩散,某些情况下电解质的电导率以及界面质量有关的动力学问题。对于锂离子技术,当使用转换电极而不是插入电极时,后一种效应尤其严重。通常建议使用纳米结构的电极来增强动力学,尽管实现起来很麻烦。为了解决转换电极材料Fe3O4的这一问题,我们采用了两步电极设计,包括电化学辅助模板生长Cu纳米棒到集电器上,然后电化学镀Fe3O4。使用这种电极,我们证明了在保持相同的总放电时间的同时,功率密度比平面电极提高了六倍。 8C速率下的容量为总容量的80%,并持续100个循环。讨论了转换反应所固有的充放电之间大磁滞的起源,并提出了降低磁滞的方法。我们希望这些发现将有助于在下一代锂离子电池中使用转换反应电极。

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