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High-Capacity Micrometer-Sized Li 2 S Particles as Cathode Materials for Advanced Rechargeable Lithium-Ion Batteries

机译:大容量微米级Li 2 S颗粒作为高级可充电锂离子电池的阴极材料

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摘要

Li 2S is a high-capacity cathode material for lithium metal-free rechargeable batteries. It has a theoretical capacity of 1166 mAh/g, which is nearly 1 order of magnitude higher than traditional metal oxides/phosphates cathodes. However, Li 2S is usually considered to be electrochemically inactive due to its high electronic resistivity and low lithium-ion diffusivity. In this paper, we discover that a large potential barrier (∼1 V) exists at the beginning of charging for Li 2S. By applying a higher voltage cutoff, this barrier can be overcome and Li 2S becomes active. Moreover, this barrier does not appear again in the following cycling. Subsequent cycling shows that the material behaves similar to common sulfur cathodes with high energy efficiency. The initial discharge capacity is greater than 800 mAh/g for even 10 μm Li 2S particles. Moreover, after 10 cycles, the capacity is stabilized around 500-550 mAh/g with a capacity decay rate of only ∼0.25% per cycle. The origin of the initial barrier is found to be the phase nucleation of polysulfides, but the amplitude of barrier is mainly due to two factors: (a) charge transfer directly between Li 2S and electrolyte without polysulfide and (b) lithium-ion diffusion in Li 2S. These results demonstrate a simple and scalable approach to utilizing Li 2S as the cathode material for rechargeable lithium-ion batteries with high specific energy. © 2012 American Chemical Society.
机译:Li 2S是用于无锂金属可充电电池的高容量正极材料。它的理论容量为1166 mAh / g,比传统的金属氧化物/磷酸盐阴极高出近1个数量级。然而,由于Li 2S的高电阻率和低锂离子扩散率,通常被认为是电化学惰性的。在本文中,我们发现Li 2S充电开始时存在较大的势垒(〜1 V)。通过施加更高的电压截止值,可以克服该势垒,并激活Li 2S。此外,在随后的循环中该障碍不再出现。随后的循环表明,该材料的行为类似于普通的硫阴极,具有高能效。甚至10μm的Li 2S颗粒的初始放电容量也大于800 mAh / g。此外,经过10个循环后,容量稳定在500-550 mAh / g左右,每个循环的容量衰减率仅为约0.25%。发现初始势垒的起源是多硫化物的相核化,但势垒的幅度主要归因于两个因素:(a)电荷在Li 2S和电解质之间直接转移而没有多硫化物;(b)锂离子扩散李2S。这些结果证明了一种简单且可扩展的方法,可将Li 2S用作具有高比能的可再充电锂离子电池的正极材料。 ©2012美国化学学会。

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