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Constructing heterostructured FeS2/CuS nanospheres as high rate performance lithium ion battery anodes

Abstract

Iron sulfides have been considered as a promising anode material in recent years, characterized by higher theoretical capacities, non-toxicity, and abundant reserves in nature. Nevertheless, they suffer from large volume changes during cycling and severe irreversible capacity loss because of their weak electronic conductivity as well as the poor stability. In this work, the heterostructured FeS2 /CuS nanospheres (HFCSs) are successfully synthesized by a facile hydrothermal method and vapor phase vulcanization at mild temperature. The copper ions are uniformly distributed in the HFCSs composites, endowing to continuously high conductivity during the constant electrochemical process. When applied to lithium ion batteries, the composites exhibit impressive electrochemical performance. As expected, the assembled HFCSs electrodes possess a high reversible capacity of 843.3 mAh g−1 even after 600 cycles at 1.0 A g−1 and a surprising rate capability of 530.4 mAh g−1 at 10.0 A g−1, which are superior to most of the reported FeS2 or CuS anode materials. The assembled HFCSs electrodes possess both high conductivity and porous structure, which is beneficial to the interior electron transport, reaction kinetics, lower volume changes and pulverization, significantly achieving improved rate capability as well as remarkable long-term cycling stability. This approach is feasible for fabricating heterogeneous porous structure and may shed some light on designing metal sulfide-based anode materials with high rate performance for energy storage applications.

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Supplementary files

Article information


Submitted
24 Dec 2019
Accepted
01 Mar 2020
First published
09 Mar 2020

Inorg. Chem. Front., 2020, Accepted Manuscript
Article type
Research Article

Constructing heterostructured FeS2/CuS nanospheres as high rate performance lithium ion battery anodes

X. Xu, L. Li, H. Chen, X. Guo, Z. Zhang, J. Liu, G. Li and C. Mao, Inorg. Chem. Front., 2020, Accepted Manuscript , DOI: 10.1039/C9QI01674K

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