氧化还原
材料科学
阴极
歧化
阳极
锰
析氧
氧气
钠离子电池
溶解
相变
钠
无机化学
离子
电化学
化学工程
电极
物理化学
化学
热力学
催化作用
有机化学
生物化学
冶金
法拉第效率
工程类
物理
作者
Feng Wang,Bo Peng,Suyuan Zeng,Liping Zhao,Xiaolei Zhang,Guanglin Wan,Hongli Zhang,Genqiang Zhang
标识
DOI:10.1002/adfm.202202665
摘要
Abstract P2‐type layered Na x MnO 2 cathode shows great potential in practical sodium ion batteries, especially for grid‐level applications due to its eco‐friendly and cost‐effective sodium and manganese resources, and high theoretical specific capacity. However, several obstacles including severe phase transitions of P2‐O2 and P2‐P2′, low redox potential of Mn 3+ /Mn 4+ , disproportionation reaction and Jahn‐Teller distortion of Mn 3+ , and deficient behavior have already hindered its practical applications. Herein, a Li, Cu co‐doping strategy to tackle the mentioned obstacles by activating the oxygen redox is presented. The Li, Cu co‐doped material exhibits solid solution reaction without any phase transitions as proved by in situ X‐ray diffraction measurement and reduces the dissolution of active manganese element. With this modification treatment, it can dramatically raise the cycling stability from 30.4% to 80.1% after 150 cycles and simultaneously improves the deficient behavior due to the capacity contribution of oxygen redox at high voltage. More importantly, the coin‐cell type sodium ion full cell assembled with this cathode and commercial hard carbon anode delivers a promising energy density of 225.1 Wh kg –1 .
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