尖晶石
电化学
电极
电子转移
氧化还原
阴极
氧化态
材料科学
离子
X射线光电子能谱
分析化学(期刊)
化学
无机化学
物理化学
金属
冶金
核磁共振
物理
有机化学
色谱法
作者
Ruimin Qiao,L. Andrew Wray,Jung Hyun Kim,Nicholas P. W. Pieczonka,Stephen J. Harris,Wanli Yang
标识
DOI:10.1021/acs.jpcc.5b07479
摘要
The LiNi0.5Mn1.5O4 spinel is an appealing cathode material for next generation rechargeable Li-ion batteries due to its high operating voltage of ∼4.7 V (vs Li/Li+). Although it is widely believed that the full range of electrochemical cycling involves the redox of Ni(II)/(IV), it has not been experimentally clarified whether Ni(III) exists as the intermediate state or a double-electron transfer takes place. Here, combined with theoretical calculations, we show unambiguous spectroscopic evidence of the Ni(III) state when the LiNi0.5Mn1.5O4 electrode is half charged. This provides a direct verification of single-electron-transfer reactions in LiNi0.5Mn1.5O4 upon cycling, namely, from Ni(II) to Ni(III), then to Ni(IV). Additionally, by virtue of its surface sensitivity, soft X-ray absorption spectroscopy also reveals the electrochemically inactive Ni2+ and Mn2+ phases on the electrode surface. Our work provides the long-awaited clarification of the single-electron transfer mechanism in LiNi0.5Mn1.5O4 electrodes. Furthermore, the experimental results serve as a benchmark for further spectroscopic characterizations of Ni-based battery electrodes.
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