High Entropy-Induced Kinetics Improvement and Phase Transition Suppression in K-Ion Battery Layered Cathodes

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作者
Chu, Shiyong [1 ,2 ]
Shao, Caoyang [1 ,2 ]
Tian, Jiaming [1 ,2 ]
Wang, Jingyang [1 ]
Rao, Yuan [1 ,2 ]
Xu, Chengrong [1 ,2 ]
Zhou, Haoshen [1 ]
Guo, Shaohua [1 ,2 ]
机构
[1] College of Engineering and Applied Sciences, Jiangsu Key Laboratory of Artificial Functional Materials, National Laboratory of Solid-State Microstructures, Collaborative Innovation Center of Advanced Microstructures, Frontiers Science Center for Critical E
[2] Lab of Power and Energy Storage Batteries, Shenzhen Research Institute of Nanjing University, Shenzhen,518000, China
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Kinetics;
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摘要
Layered oxides are widely accepted to be promising cathode candidate materials for K-ion batteries (KIBs) in terms of their rich raw materials and low price, while their further applications are restricted by sluggish kinetics and poor structural stability. Here, the high-entropy design concept is introduced into layered KIB cathodes to address the above issues, and an example of high-entropy layered K0.45Mn0.60Ni0.075Fe0.075Co0.075Ti0.10Cu0.05Mg0.025O2 (HE-KMO) is successfully prepared. Benefiting from the high-entropy oxide with multielement doping, the developed HE-KMO exhibits half-metallic oxide features with a narrow bandgap of 0.19 eV. Increased entropy can also reduce the surface energy of the {010} active facets, resulting in about 2.6 times more exposure of the {010} active facets of HE-KMO than the low-entropy K0.45MnO2 (KMO). Both can effectively improve the kinetics in terms of electron conduction and K+ diffusion. Furthermore, high entropy can inhibit space charge ordering during K+ (de)insertion, and the transition metal-oxygen covalent interaction of HE-KMO is also enhanced, leading to suppressed phase transition of HE-KMO in 1.5-4.2 V and better electrochemical stability of HE-KMO (average capacity drop of 0.20%, 200 cycles) than the low-entropy KMO (average capacity drop of 0.41%, 200 cycles) in the wide voltage window. © 2023 American Chemical Society.
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页码:337 / 346
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