阴极
电化学
插层(化学)
材料科学
降级(电信)
格子(音乐)
离子
化学工程
相变
钾离子电池
过渡金属
无机化学
化学
电极
催化作用
物理化学
热力学
电气工程
磷酸钒锂电池
工程类
物理
有机化学
生物化学
声学
作者
Yan‐Song Xu,Yong‐Ning Zhou,Qinghua Zhang,Mu‐Yao Qi,Sijie Guo,Jin‐Min Luo,Yonggang Sun,Lin Gu,Amin Cao,Li‐Jun Wan
标识
DOI:10.1016/j.cej.2021.128735
摘要
The development of high-performance potassium-ion batteries (PIBs) is challenged by the availability of stable cathode materials, which are known to undergo complex phase transitions and irreversible structural degradation especially charged to high voltage. Here, we reported a P2-type cathode in formula of K0.6Mn0.8Ni0.1Ti0.1O2 (KMNT), which exhibited a highly reversible K+ (de)intercalation capability up to 4.2 V. We demonstrated that the coexistence of Ni and Ti was able to not only suppress the structural damage related to the Jahn-Teller effect of Mn3+, a critical factor accounting for the performance degradation of Mn-based PIBs cathodes, but also restrain the detrimental lattice sliding of transition metal layers at high voltage. Accordingly, the structurally engineered KMNT showed a much favored solid-solution reaction with a successful elimination of the destructive phase degradation at deep depotassiation state. Our results highlighted the essential role played by the lattice design of cathode materials in modulating their electrochemical behavior for stable and high-performance PIBs.
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