In Situ Hydrogen Bonding-Mediated Self-Synthesis of Graphene-Coated SnO2 as Anode Materials for Lithium-Ion Batteries

被引:0
|
作者
Li, Hui [1 ,2 ]
Zhuang, Yi [1 ]
Qi, Haoyu [1 ]
Zheng, Chuanbo [1 ,2 ]
Wang, Zhiteng [2 ]
Yao, Huan [2 ]
Liu, Zhiqiang [2 ]
Li, Yingying [1 ]
He, Jiaqi [1 ]
Zou, Wenkai [1 ]
Zhu, Jin [2 ]
Yin, Shiyi [2 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Met Engn, Zhangjiagang 215600, Jiangsu, Peoples R China
[2] Jiangsu Univ Sci & Technol, Suzhou Inst Technol, Zhangjiagang 215600, Jiangsu, Peoples R China
关键词
graphene; hydrogen bonding self-assembly; lithium-ion batteries; SnO2; nanoparticles; COMPOSITE; FABRICATION; STORAGE; FACILE;
D O I
10.1002/ente.202400042
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Tin(IV) oxide (SnO2) has been recognized as the next frontier in innovative anode materials, set to revolutionize lithium-ion batteries. Anticipated to replace graphite anodes, SnO2 boasts an ideal capacity of 782 mAh g(-1) and an appropriate operating potential conducive to advanced battery technology. Nonetheless, the challenges posed by volume expansion and intricate synthesis route of Sn-based anode materials have impeded their commercial viability. Herein, SnO2@graphene nanoparticles are synthesized through hydrogen bonding-mediated self-assembly process, utilizing polyethylene glycol (PEG) and tin tetrachloride as starting materials. The resultant nanoparticles exhibit uniform distribution, forming a sandwich structure with graphene. Sample SP-0.3, obtained by incorporating 6 g of PEG, demonstrates remarkable capacity for reversible energy storage. It retains a capacity of 703.1 mAh g(-1) even after 900 cycles at a current density of 0.5 A g(-1). Coupled with the straightforward, convenient, and expeditious preparation method, the proposed technique positions the composite material as an invaluable candidate for commercialization.
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页数:10
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