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On the electrochemistry of tin oxide coated tin electrodes in lithium-ion batteries

机译:锂离子电池中氧化锡包覆锡电极的电化学研究

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摘要

As tin based electrodes are of significant interest in the development of improved lithium-ion batteries it is important to understand the associated electrochemical reactions. In this work it is shown that the electrochemical behavior of SnO2 coated tin electrodes can be described based on the SnO2 and SnO conversion reactions, the lithium tin alloy formation and the oxidation of tin generating SnF2. The CV, XPS and SEM data, obtained for electrodeposited tin crystals on gold substrates, demonstrates that the capacity loss often observed for SnO2 is caused by the reformed SnO2 layer serving as a passivating layer protecting the remaining tin. Capacities corresponding up to about 80% of the initial SnO2 capacity could, however, be obtained by cycling to 3.5 V vs. Li+/Li. It is also shown that the oxidation of the lithium tin alloy is hindered by the rate of the diffusion of lithium through a layer of tin with increasing thickness and that the irreversible oxidation of tin to SnF2 at potentials larger than 2.8V vs. Li+/Li is due to the fact that SnF2 is formed below the SnO2 layer. This improved electrochemical understanding of the SnO2/Sn system should be valuable in the development of tin based electrodes for lithium-ion batteries. (C) 2015 Elsevier Ltd. All rights reserved.
机译:由于锡基电极在改进的锂离子电池的开发中具有重大意义,因此了解相关的电化学反应非常重要。在这项工作中表明,可以基于SnO2和SnO的转化反应,锂锡合金的形成以及锡的生成SnF2的氧化来描述SnO2涂覆的锡电极的电化学行为。对于在金基底上电沉积锡晶体获得的CV,XPS和SEM数据表明,经常观察到的SnO2容量损失是由重整后的SnO2层作为保护剩余锡的钝化层引起的。然而,通过将其循环至相对于Li + / Li的3.5 V,可以获得相当于初始SnO2容量约80%的容量。还显示锂锡合金的氧化受到锂通过厚度增加的锡层的扩散速率的阻碍,并且在大于2.8V vs. Li + / Li的电势下锡不可逆氧化为SnF2这是由于在SnO2层下方形成了SnF2。改进的对SnO2 / Sn系统的电化学理解在开发锂离子电池锡基电极中应该是有价值的。 (C)2015 Elsevier Ltd.保留所有权利。

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