A PEGylated deep eutectic solvent for "bubbling" synthesis of SnO2/SnS heterostructure for the stable lithium-ion storage

被引:1
|
作者
Liu, Zhiqiang [1 ]
Li, Hui [1 ,2 ]
Yao, Huan [2 ]
Zhuang, Yi [1 ]
Gao, Runbo [2 ]
Wang, Zhiteng [2 ]
Zhu, Zhenhe [1 ]
Lan, Huixin [1 ]
Li, Zeheng [4 ]
Cai, Wenlong [3 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Met Engn, Zhangjiagang 215600, Peoples R China
[2] Jiangsu Univ Sci & Technol, Suzhou Inst Technol, Zhangjiagang 215600, Peoples R China
[3] Sichuan Univ, Coll Mat Sci & Engn, Chengdu 610000, Peoples R China
[4] Zhejiang Univ, Coll Chem & Biol Engn, Hangzhou 310027, Peoples R China
关键词
Heterostructure; Lithium-ion batteries; High-performance; Synthesis mechanism; PERFORMANCE ANODE; CARBON; MICROSPHERES;
D O I
10.1016/j.jcis.2024.12.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Constructing heterostructures is an effective strategy for the synthesis of high-performance anode electrode materials for lithium-ion batteries (LIBs). In this study, a "bubbling" PEGylated deep eutectic solvent (DES) method is utilized to synthesize SnO2/SnS heterostructure nanodots anchored on carbon nanosheets (SnO2/ SnS@CN). A comprehensive investigation of the physical and chemical processes during the "bubbling" reaction offers in-depth insights into the underlying mechanism of the PEGylated DES approach. The carbon nanosheet structure enhances the electrical conductivity between SnO2 particle units and, due to its excellent mechanical properties, significantly contributes to material stability. The nanodot configuration of the heterostructure further improves electron transfer and lithium-ion (Li+) migration within the SnO2 units. The SnO2/SnS@CN material exhibits outstanding Li+ storage performance, achieving a high capacity of 675.6 mA h/g at 1 A/g after 1000 cycles. These findings establish a theoretical foundation for preparing heterostructure anode materials using the "bubbling" PEGylated DES method.
引用
收藏
页码:995 / 1005
页数:11
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