材料科学
电极
中子衍射
过渡金属
相变
相(物质)
衍射
钠
吸收(声学)
化学工程
分析化学(期刊)
晶体结构
结晶学
复合材料
冶金
热力学
物理化学
化学
光学
物理
工程类
生物化学
催化作用
有机化学
色谱法
作者
Jun Wang,Dong Zhou,Xin He,Li Zhang,Xia Cao,De Ning,Bo Yan,Xin Qi,Jinke Li,Vadim Murzin,Elie Paillard,Xinzhi Liu,G. Schumacher,Martin Winter,Jie Li
标识
DOI:10.1021/acsami.9b18109
摘要
P2-type Fe- and Mn-based layered sodium transition metal oxides are promising positive electrode materials for sodium batteries due to their high energy density and low costs of the constituting transition metals. However, poor structural reversibility and fast capacity decay have prevented their breakthrough so far. Herein, the real-time dynamic phase transitions and capacity fading mechanism of the P2 Na0.67Fe0.5Mn0.5O2 positive electrode are revealed by operando X-ray diffraction, operando/ex situ X-ray absorption spectroscopy, neutron powder diffraction, and neutron pair distribution functions. Upon the desodiation process, a layered OP4 phase with long-range order is found as an intermediate state. With further deep desodiation, the formation of a Na-depleted ramsdellite phase with a short coherent length of 30 Å is observed for the first time. However, the transition from OP4 to ramsdellite is considered to be irreversible due to the breakdown of the layered structural characteristics, resulting in poor cycling performance in a variety of Fe-based layered sodium transition metal oxides. This work suggests that stabilizing the crystal structure by substitution or chemical modification can be a favorable strategy to avoid the degradation of positive electrodes and thus to improve the cycling performance.
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