Elaborate interface design of SnS2/SnO2@C/rGO nanocomposite as a high-performance anode for lithium-ion batteries

•Tightly contacted SnS2/SnO2 heterostructure is formed by in-situ oxidation of SnS2.•The amorphous carbon can strongly anchor SnS2/SnO2 nanoparticles on rGO sheets.•N and S heteroatoms are co-doped into rGO by using thiourea as N and S sources.•The reaction reversibility and kinetics are enhanced at...

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Veröffentlicht in:Electrochimica acta 2022-02, Vol.405, p.139799, Article 139799
Hauptverfasser: Jin, Shuangling, Gu, Feijiao, Wang, Jitong, Ma, Xia, Qian, Chenliang, Lan, Yaxin, Han, Qi, Li, Junqiang, Wang, Xiaorui, Zhang, Rui, Qiao, Wenming, Ling, Licheng, Jin, Minglin
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Sprache:eng
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Zusammenfassung:•Tightly contacted SnS2/SnO2 heterostructure is formed by in-situ oxidation of SnS2.•The amorphous carbon can strongly anchor SnS2/SnO2 nanoparticles on rGO sheets.•N and S heteroatoms are co-doped into rGO by using thiourea as N and S sources.•The reaction reversibility and kinetics are enhanced at SnS2/SnO2 heterojunctions.•The carbon and rGO guarantee the electrical connection and structural stability. The practical application of Sn-based anode materials is limited by their low electrical conductivity and large volume expansion during cycling. To overcome these challenges, a novel SnS2/SnO2@C/rGO nanocomposite is synthesized by in-situ H2O2 oxidation of SnS2@C/rGO that is prepared via a hydrothermal reaction using SnCl2, thiourea, L-ascorbic acid and GO as the reactants. Tightly contacted SnS2/SnO2 heterostructured nanoparticles are encapsulated by the amorphous carbon derived from L-ascorbic acid, which are further firmly anchored on the rGO sheets through the chemical interactions between the hydroxyl groups of L-ascorbic acid and hydroxyl/carbonyl groups of rGO. The amorphous carbon layer can act as a spacer to prevent the stacking of rGO sheets to retain the ion transport pathway. Meanwhile, the N and S heteroatoms are co-doped into the rGO sheets by using thiourea as N and S sources, which can enhance the electrical conductivity and provide more active sites for Li+ insertion/extraction. The obtained nanocomposite exhibits a specific capacity of 689 mA h g−1 after 300 cycles at a current density of 0.1 C (1 C = 783 mA g−1) and a moderate capacity of 619 mA h g−1 up to 500 cycles at a large current rate of 0.5 C. [Display omitted]
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2021.139799