氧化还原
电化学储能
锂(药物)
电化学
电池(电)
阴极
储能
有机自由基电池
纳米技术
阳离子聚合
化学
材料科学
无机化学
电极
物理
功率(物理)
心理学
高分子化学
超级电容器
物理化学
精神科
量子力学
作者
Gaurav Assat,Jean‐Marie Tarascon
出处
期刊:Nature Energy
[Springer Nature]
日期:2018-04-09
卷期号:3 (5): 373-386
被引量:1111
标识
DOI:10.1038/s41560-018-0097-0
摘要
Our increasing dependence on lithium-ion batteries for energy storage calls for continual improvements in the performance of their positive electrodes, which have so far relied solely on cationic redox of transition-metal ions for driving the electrochemical reactions. Great hopes have recently been placed on the emergence of anionic redox—a transformational approach for designing positive electrodes as it leads to a near-doubling of capacity. But questions have been raised about the fundamental origins of anionic redox and whether its full potential can be realized in applications. In this Review, we discuss the underlying science that triggers a reversible and stable anionic redox activity. Furthermore, we highlight its practical limitations and outline possible approaches for improving such materials and designing new ones. We also summarize their chances for market implementation in the face of the competing nickel-based layered cathodes that are prevalent today. The discovery of anionic redox chemistry in Li-rich cathode materials provides much hope for enhancing battery performance. Tarascon and Assat analyse the underlying science behind anionic redox and discuss its practical limitations as well as the routes to overcome the application barriers.
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