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高容量微米级 Li2S 颗粒作为先进可充电锂离子电池的阴极材料。

High-capacity micrometer-sized Li2S particles as cathode materials for advanced rechargeable lithium-ion batteries.

机构信息

Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, USA.

出版信息

J Am Chem Soc. 2012 Sep 19;134(37):15387-94. doi: 10.1021/ja3052206. Epub 2012 Sep 10.

Abstract

Li(2)S 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(2)S 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(2)S. By applying a higher voltage cutoff, this barrier can be overcome and Li(2)S 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(2)S 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(2)S and electrolyte without polysulfide and (b) lithium-ion diffusion in Li(2)S. These results demonstrate a simple and scalable approach to utilizing Li(2)S as the cathode material for rechargeable lithium-ion batteries with high specific energy.

摘要

Li(2)S 是一种用于无金属锂可再充电电池的高容量阴极材料。它具有 1166 mAh/g 的理论容量,比传统的金属氧化物/磷酸盐阴极高近 1 个数量级。然而,由于 Li(2)S 的高电子电阻率和低锂离子扩散率,通常认为它是电化学惰性的。在本文中,我们发现 Li(2)S 在充电初期存在一个大的势垒(约 1 V)。通过施加更高的电压截止,这个势垒可以被克服,Li(2)S 变得活跃。此外,这个势垒在随后的循环中不再出现。随后的循环表明,该材料的行为类似于具有高能量效率的常见硫阴极。即使是 10 μm 的 Li(2)S 颗粒,初始放电容量也大于 800 mAh/g。此外,经过 10 次循环后,容量稳定在 500-550 mAh/g 左右,容量衰减率仅为每循环约 0.25%。初始势垒的起源被发现是多硫化物的相成核,但势垒的幅度主要归因于两个因素:(a)Li(2)S 和电解质之间没有多硫化物的直接电荷转移,以及(b)Li(2)S 中的锂离子扩散。这些结果表明了一种简单且可扩展的方法,可将 Li(2)S 用作具有高比能的可再充电锂离子电池的阴极材料。

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