TY - JOUR
T1 - Development of P3-type K0.70[Cr0.86Sb0.14]O2 cathode for high-performance K-ion batteries
AU - Ko, Wonseok
AU - Kim, Junseong
AU - Kang, Jungmin
AU - Park, Hyunyoung
AU - Lee, Yongseok
AU - Ahn, Jinho
AU - Ku, Bonyoung
AU - Choi, Myungeun
AU - Ahn, Hobin
AU - Oh, Gwangeon
AU - Hwang, Jang Yeon
AU - Kim, Jongsoon
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/8
Y1 - 2023/8
N2 - 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 high-performance 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.
AB - 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 high-performance 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.
KW - Cathode material
KW - First-principles calculation
KW - Layered-type structure
KW - Potassium-ion battery
UR - https://www.scopus.com/pages/publications/85165348023
U2 - 10.1016/j.mtener.2023.101356
DO - 10.1016/j.mtener.2023.101356
M3 - Article
AN - SCOPUS:85165348023
SN - 2468-6069
VL - 36
JO - Materials Today Energy
JF - Materials Today Energy
M1 - 101356
ER -