Carbon-Coated ZnS-FeS2 Heterostructure as an Anode Material for Lithium-Ion Battery Applications

被引:7
|
作者
Naveenkumar, Perumal [1 ]
Maniyazagan, Munisamy [2 ]
Kang, Nayoung [2 ]
Yang, Hyeon-Woo [1 ,2 ]
Kang, Woo-Seung [3 ]
Kim, Sun-Jae [1 ,2 ]
机构
[1] Sejong Univ, Met Organ Cpds Mat Res Ctr, 209 Neungdong Ro, Seoul 05006, South Korea
[2] Sejong Univ, Dept Nanotechnol & Adv Mat Engn, 209 Neungdong Ro, Seoul 05006, South Korea
[3] Inha Tech Coll, Dept Met & Mat Engn, Incheon 22212, South Korea
基金
新加坡国家研究基金会;
关键词
hydrothermal; carbon coating; heterostructure; lithium-ion battery; ZnS-FeS2@C; HIGH-PERFORMANCE LITHIUM; NITROGEN-DOPED CARBON; GRAPHENE OXIDE; CONSTRUCTION; COMPOSITES; POLYHEDRA;
D O I
10.3390/ijms232213945
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The construction of carbon-coated heterostructures of bimetallic sulfide is an effective technique to improve the electrochemical activity of anode materials in lithium-ion batteries. In this work, the carbon-coated heterostructured ZnS-FeS2 is prepared by a two-step hydrothermal method. The crystallinity and nature of carbon-coating are confirmed by the investigation of XRD and Raman spectroscopy techniques. The nanoparticle morphology of ZnS and plate-like morphology of FeS2 is established by TEM images. The chemical composition of heterostructure ZnS-FeS2@C is discovered by an XPS study. The CV results have disclosed the charge storage mechanism, which depends on the capacitive and diffusion process. The BET surface area (37.95 m(2)g(-1)) and lower R-ct value (137 ohm) of ZnS-FeS2@C are beneficial to attain higher lithium-ion storage performance. It delivered a discharge capacity of 821 mAh g(-1) in the 500th continuous cycle @ A g(-1), with a coulombic efficiency of around 100%, which is higher than the ZnS-FeS2 heterostructure (512 mAh g(-1)). The proposed strategy can improve the electrochemical performance and stability of lithium-ion batteries, and can be helpful in finding highly effective anode materials for energy storage devices.
引用
收藏
页数:13
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