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首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Structural Evolution of Disordered LixV2O5 Bronzes in V2O5 Cathodes for Li-Ion Batteries
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Structural Evolution of Disordered LixV2O5 Bronzes in V2O5 Cathodes for Li-Ion Batteries

机译:锂离子电池V2O5阴极无序Lixv2O5铜结构的结构演变

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摘要

Vanadium pentaoxide, V2O5, is an attractive cathode material for Li-ion batteries, which can store up to three Li ion per formula unit. At deep discharge, an irreversible reconstructive phase transition occurs with formation of the disordered omega-LixV2O5 bronze, which, despite the lack of long-range order, exhibits a high reversible capacity (similar to 310 mAh/g) without regaining the crystallinity upon recharge. Here, we utilize operando powder X-ray diffraction and total scattering (i.e., pair distribution function analysis) to investigate the atomic-scale structures of the deep-discharge phase omega-LixV2O5 (x similar to 3) and, for the first time, the highly disordered phase beta-LixV2O5 (x similar to 0.3) formed during subsequent Li-extraction. Our studies reveal that the deep discharge omega-Li3V2O5 phase consists of similar to 60 angstrom domains rock salt structure with a local cation ordering on an similar to 15 angstrom length scale. The charged beta-LixV2O5 phase only exhibits very short-range ordering (similar to 10 angstrom ). The phase transition between these phases is structurally reversible and appears unexpectedly to occur via a two-phase transition mechanism.
机译:钒五氧化物V2O5是一种用于锂离子电池的有吸引力的阴极材料,可以每种配方单元存储最多三个LI离子。在深度放电时,发生不可逆的重建相转变,形成无序的ω-lixv2O5青铜,尽管缺乏远程顺序,但呈现高可逆容量(类似于310mAh / g),而不会在充电后重新获得结晶度。在此,我们利用Operando粉末X射线衍射和总散射(即,一对分布函数分析)来研究深放电阶段OMEGA-LIXV2O5(x类似于3)的原子级结构,并首次进行在随后的Li萃取期间形成的高度无序相β-LiXV2O5(类似于0.3)。我们的研究表明,深度放电Omega-Li3V2O5阶段包括与60埃域岩石盐结构类似,其局部阳离子排序在类似于15埃长度尺度上。收费的Beta-Lixv2O5阶段仅表现出非常短的排序(类似于10埃)。这些相之间的相位转变在结构上是可逆的并且意外地出现通过两相转变机制发生。

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