High‐Entropy Doped P'2 Mn‐Based Layered Oxide with Superior Stability and High Capacity for Sodium‐Ion Batteries

X Xiaoyu Gui (Guangdong Provincial Key Laboratory of Fuel Cell Technology School of Chemistry and Chemical Engineering South China University of Technology Guangzhou 510641 China) Z Zhipeng Xiang (Materials Genome Institute, Shanghai University 1 , 200444 Shanghai,) T Tianlu Ren (Guangdong Provincial Key Laboratory of Fuel Cell Technology School of Chemistry and Chemical Engineering South China University of Technology Guangzhou 510641 China) W Wenbo Liu (Institute of Physics) Z Zhongyuan Pei (Guangdong Provincial Key Laboratory of Fuel Cell Technology School of Chemistry and Chemical Engineering South China University of Technology Guangzhou 510641 China) G Guifa Long (Dalian National Laboratory for Clean Energy) Z Zhiyong Fu K Kai Wan (Guangdong Provincial Key Laboratory of Fuel Cell Technology School of Chemistry and Chemical Engineering South China University of Technology Guangzhou People's Republic of China) Z Zhenxing Liang (School of Chemistry and Chemical Engineering South China University of Technology Guangzhou Guangdong Province China)

Abstract

Abstract P'2‐Na x MnO 2 (NMO) features an ultra‐high specific capacity in sodium‐ion batteries, which, however, suffers from a fast capacity decay. To improve the stability, a high‐entropy doped P'2‐Na 0.59 Mn 0.90 Ti 0.02 Cu 0.02 Ni 0.02 Co 0.02 Fe 0.02 O 1.95 F 0.05 (NMHE 0.1 OF) is developed to lessen the Jahn‐Teller distortion and address the multiple phase transition issue. Physicochemical characterizations reveal that the NMHE 0.1 OF yields a lower anisotropy in the Mn─O bond than does the undoped NMO. Theoretical calculations indicate that the cation doping enhances the coordination ability of oxygen and the F doping breaks the electronic symmetry of Mn. The in situ X‐ray diffraction result reveals that the NMO experiences a more abrupt and irreversible OP4‐P'2‐P″2 tri‐phase transition; and the NMHE 0.1 OF features a mild and reversible OP4‐P'2 bi‐phase transition, which originates from the alleviation in the contraction/expansion of the transition metal slabs evidenced by ex situ extended X‐ray absorption fine structure. The bi‐phase transition favors the compatibility between the NMHE 0.1 OF and the ether‐based electrolyte at high voltages. As a result, the NMHE 0.1 OF yields a superior cyclability (97.8% capacity retention after 100 cycles at 100 mA g −1 ) with a notable specific capacity of 224 mAh g −1 at 10 mA g −1 . This work provides an effective strategy for the rational design of cathode materials with high capacity and superior stability.

Article Details

Volume / Issue Vol. 37, Issue 20
Published May 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (9)

X

Xiaoyu Gui

Guangdong Provincial Key Laboratory of Fuel Cell Technology School of Chemistry and Chemical Engineering South China University of Technology Guangzhou 510641 China

Z

Zhipeng Xiang

Materials Genome Institute, Shanghai University 1 , 200444 Shanghai,

T

Tianlu Ren

Guangdong Provincial Key Laboratory of Fuel Cell Technology School of Chemistry and Chemical Engineering South China University of Technology Guangzhou 510641 China

W

Wenbo Liu

Institute of Physics

Z

Zhongyuan Pei

Guangdong Provincial Key Laboratory of Fuel Cell Technology School of Chemistry and Chemical Engineering South China University of Technology Guangzhou 510641 China

G

Guifa Long

Dalian National Laboratory for Clean Energy

Z

Zhiyong Fu

K

Kai Wan

Guangdong Provincial Key Laboratory of Fuel Cell Technology School of Chemistry and Chemical Engineering South China University of Technology Guangzhou People's Republic of China

Z

Zhenxing Liang

School of Chemistry and Chemical Engineering South China University of Technology Guangzhou Guangdong Province China