Development of P3-type K0.70[Cr0.86Sb0.14]O2 cathode for high-performance K-ion batteries

被引:6
作者
Ko, Wonseok [1 ,2 ,5 ]
Kim, Junseong [1 ,2 ,5 ]
Kang, Jungmin [1 ,2 ]
Park, Hyunyoung [1 ,2 ]
Lee, Yongseok [1 ,2 ]
Ahn, Jinho [1 ,2 ]
Ku, Bonyoung [1 ,2 ]
Choi, Myungeun [1 ,2 ]
Ahn, Hobin [1 ,2 ]
Oh, Gwangeon [4 ]
Hwang, Jang-Yeon [4 ,5 ]
Kim, Jongsoon [1 ,2 ,3 ]
机构
[1] Sungkyunkwan Univ, Dept Energy Sci, Suwon 440746, South Korea
[2] Sungkyunkwan Univ, SKKU Inst Energy Sci & Technol SIEST, Suwon 440746, South Korea
[3] Sungkyunkwan Univ, KIST SKKU Carbon Neutral Res Ctr, Suwon 16419, South Korea
[4] Hanyang Univ, Dept Energy Engn, Seoul 04763, South Korea
[5] Hanyang Univ, Dept Battery Engn, Seoul 04763, South Korea
基金
新加坡国家研究基金会;
关键词
Cathode material; Layered-type structure; Potassium-ion battery; First-principles calculation; SODIUM; GRAPHITE; POTENTIALS;
D O I
10.1016/j.mtener.2023.101356
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Potassium-ion batteries (KIBs) are one of the most promising alternatives to lithium-ion batteries because of the high standard hydrogen electrode of K+/K, which is the second lowest after lithium. However, the large ionic size of K+ generally hinders the reversible intercalation and results in the undesirable structural changes during charge-discharge process. Thus, it is very important to develop stable cathode materials that accommodate K+ into their crystal structure with minimal structural changes. Here we propose P3-type K0.70 [Cr0.86Sb0.14]O2 as a potential cathode material for highperformance KIBs. The P3-type K0.70 [Cr0.86Sb0.14]O2 was successfully fabricated via electrochemical ion-exchange of Na+/K+. At a current density of 15 mA/g, P3-K0.70 [Cr0.86Sb0.14]O2 delivered a reversible capacity of 126.1 mAh/g with a high coulombic efficiency of 98.7%, corresponding to the de/intercalation of 0.57 mol of K+ ions from/into the structure. In addition, P3-type K0.70 [Cr0.86Sb0.14]O2 showed excellent cycling stability over 200 cycles at a current density of 150 mA/g and power capability even at high current rate of 750 mA/g. In contrast, P3-KxCrO2 demonstrates inferior electrochemical properties; this comparison implies that substitution of 0.14 mol Sb into Cr sites significantly improves structural stability with reversible Cr3+/4+ redox reaction during charge-discharge process.(c) 2023 Elsevier Ltd. All rights reserved.
引用
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页数:8
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