堆积
电化学
阴极
材料科学
氧化物
相变
离子
过渡金属
结晶学
化学工程
化学
电极
物理化学
冶金
有机化学
催化作用
热力学
工程类
物理
作者
Kun Luo,Ming Chen,Mengdan Tian,Wenhui Li,Yang Jiang,Zhihao Yuan
标识
DOI:10.1016/j.cej.2023.142101
摘要
Layered P2-type sodium manganese oxide materials (NaxMnO2) attract substantial interest due to their low cost and high security. However, the staircase-like electrochemical profiles in P2-type NaxMnO2 caused by unfavorable phase transitions and layer gliding upon sodium extraction/re-insertion, particularly from P-type stacking to O-type stacking (e. g. P2 to O2 or OP4), are difficult to be eliminated. In this work, the staircase-like electrochemical profiles induced by PO transition are effectively suppressed in P’2-type Na2/3Mn0.8Ti0.2O2 by a solid-solution reaction with continuous structural evolution during the charge/discharge processes. P’2-Na2/3Mn0.8Ti0.2O2 exhibits smooth voltage profiles and delivers a high specific capacity of 153 mA h g−1 within 2.0–4.0 V. Structural characterizations indicate that P’2-Na2/3Mn0.8Ti0.2O2 undergoes a solid-solution reaction with continuous phase transition from P’2 phase to so-called “Z” phase, considered as an intergrowth of P-type stacking and O-type stacking in the layered lattice. The structural evolution mechanism described in this work provides a solution to suppress the staircase-like electrochemical profiles induced by PO transition in P2-type oxide cathode materials and a versatile strategy for boosting the performance of P2-type cathode materials.
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