材料科学
电化学
钠
氧化锰
插层(化学)
锰
兴奋剂
氧化钠
离子
无机化学
阴极
钠离子电池
价(化学)
氧化物
化学工程
电极
冶金
化学
物理化学
光电子学
有机化学
法拉第效率
工程类
作者
Munseok S. Chae,Hyojeong J. Kim,Jeyne Lyoo,Ran Attias,Yosef Gofer,Seung‐Tae Hong,Doron Aurbach
标识
DOI:10.1002/aenm.202002205
摘要
Abstract Various types of sodium manganese oxides are promising cathode materials for sodium storage systems. One of the most considerable advantages of this family of materials is their widespread natural abundance. So far, only a few host candidates have been reported and there is a need to develop new materials with improved practical electrochemical performance. Here, P2‐type Al/F‐doped sodium manganese oxide as well as its unique sodium storage mechanism is demonstrated by a combination of electrochemical characterization, structural analyses from powder X‐ray diffraction (XRD) data, and 3D bond valence energy level calculations for the sodium diffusion pathways. The material exhibits a high reversible capacity of 164.3 mAh g −1 (0.3C rate) and capacity retention of 89.1% after 500 cycles (5C rate). The study clearly unravels the beneficial effect of the doping and the unique sodium intercalation mechanism devoid of the low diffusion O3 transformation.
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