MoS2 encapsulated FeS2 composite anchored on graphite substrate for high-performance sodium-ion batteries

K Kai Shi (State Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences) K Kai Zhou J Jun Ma Q Qingtian Li P Pengfei Hou (Nankai University , , ,) Y Yuning Cui (State Key Laboratory of Metastable Materials Science and Technology, School of Materials Science and Engineering, Yanshan University 1 , Qinhuangdao 066004,) X Xing Meng (Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education), College of Physics, Jilin University 2 , Changchun 130012,) H Hailong Qiu D Di Jin (State Key Laboratory of Metastable Materials Science, School of Science, Yanshan University 3 , Qinhuangdao 066004,)

Abstract

Transition metal sulfides (TMSs) are currently recognized as promising anode materials for sodium-ion batteries owing to their high theoretical capacities and relatively weak M–S bonds. However, TMSs face significant challenges during cycling, particularly poor electronic conductivity and severe volume expansion, impeding their practical applications. In this study, FeS2–MoS2/C multicomponent composite materials are synthesized through a molten salt synthesis route, followed by high-temperature sulfurization. The FeS2–MoS2 heterostructure significantly improves both ion and electron transfer, offering a wealth of active sites. The graphite carbon layer acts as a robust support and conductive framework for FeS2–MoS2, ensuring uniform dispersion of active components. This unique architecture, combined with the asynchronous redox behavior of FeS2 and MoS2, effectively mitigates volume expansion during sodium insertion/extraction, maintaining structural stability and improving the cycling stability of the electrode material. The FeS2–MoS2/C composite exhibits exceptional electrochemical performance, achieving a sustained specific capacity of 478.5 mA h g−1 after 3000 cycles at 5000 mA g−1, with an impressive capacity retention rate of 97.2%. Additionally, it demonstrates excellent rate capability and high-temperature adaptability. Even at 60 °C, the electrode delivers a reversible discharge capacity of 515.6 mA h g−1 after 600 cycles at 2 A g−1.

Article Details

Volume / Issue Vol. 126, Issue 26
Published June 30, 2025
ISSN 0003-6951
Publisher American Institute of Physics

Journal Info

Applied Physics Letters

American Institute of Physics

ISSN: 0003-6951 Physical Sciences

Authors (9)

K

Kai Shi

State Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences

K

Kai Zhou

J

Jun Ma

Q

Qingtian Li

P

Pengfei Hou

Nankai University , , ,

Y

Yuning Cui

State Key Laboratory of Metastable Materials Science and Technology, School of Materials Science and Engineering, Yanshan University 1 , Qinhuangdao 066004,

X

Xing Meng

Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education), College of Physics, Jilin University 2 , Changchun 130012,

H

Hailong Qiu

D

Di Jin

State Key Laboratory of Metastable Materials Science, School of Science, Yanshan University 3 , Qinhuangdao 066004,