氧化还原
阴极
离子
化学物理
氧化物
材料科学
氧气
电池(电)
电极
化学工程
无机化学
纳米技术
化学
物理化学
热力学
物理
功率(物理)
有机化学
冶金
工程类
作者
Robert A. House,John‐Joseph Marie,Miguel A. Pérez‐Osorio,Gregory J. Rees,Édouard Boivin,Peter G. Bruce
出处
期刊:Nature Energy
[Springer Nature]
日期:2021-03-01
卷期号:6 (8): 781-789
被引量:231
标识
DOI:10.1038/s41560-021-00780-2
摘要
The energy density of Li-ion batteries can be improved by storing charge at high voltages through the oxidation of oxide ions in the cathode material. However, oxidation of O2− triggers irreversible structural rearrangements in the bulk and an associated loss of the high voltage plateau, which is replaced by a lower discharge voltage, and a loss of O2 accompanied by densification at the surface. Here we consider various models for oxygen redox that are proposed in the literature and then describe a single unified model involving O2− oxidation to form O2, most of which is trapped in the bulk and the remainder of which evolves from the surface. The model extends the O2 formation and evolution at the surface, which is well known and well characterized, into the electrode particle bulk as caged O2 that can be reversibly reduced and oxidized. This converged understanding enables us to propose practical strategies to avoid oxygen-redox-induced instability and provide potential routes towards more reversible, high energy density Li-ion cathodes. Oxygen redox in Li-rich oxide cathodes is of both fundamental and practical interest in Li-ion battery development. Bruce and team examine the current understanding of oxygen-redox processes, especially those concerning O2 formation, and discuss strategies that can harness oxygen redox with suppressed side effects.
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