阳极
材料科学
碳纳米管
锂(药物)
碳化
化学工程
电化学
无定形碳
锡
纳米技术
碳纤维
多孔性
无定形固体
电极
复合材料
化学
扫描电子显微镜
冶金
有机化学
工程类
物理化学
复合数
医学
内分泌学
作者
Chunwei Dong,Yongjin Xia,Zhijiang Su,Zhihua Han,Yang Dong,Jingyun Chen,Hao Fei,Qiyao Yu,Qing Jiang,Jiaye Ye
标识
DOI:10.1016/j.jechem.2024.06.055
摘要
Tin disulfide (SnS2), due to large interlayer spacing and high theoretical capacity, is regarded as a prospective anode material for lithium-ion batteries. Nevertheless, the poor electron conductivity of SnS2 and huge volumetric change during the lithiation/delithiation process lead to a rapid capacity decay of the battery, hindering its commercialization. To address these issues, herein, SnS2 is in-situ grown on the surface of carbon nanotubes (CNT) and then encapsulated with a layer of porous amorphous carbon (CNT/SnS2@C) by simple solvothermal and further carbonization treatment. The synergistic effect of CNT and porous carbon layer not only enhances the electrical conductivity of SnS2 but also limits the huge volumetric change to avoid the pulverization and detachment of SnS2. Density functional theory calculations show that CNT/SnS2@C has high Li+ adsorption and lithium storage capacity achieving high reaction kinetics. Consequently, cells with the CNT/SnS2@C anode exhibit a high lithium storage capacity of 837 mAh/g after 100 cycles at 0.1 A/g and retaining a capacity of 529.8 mAh/g under 1.0 A/g after 1000 cycles. This study provides a fundamental understanding of the electrochemical processes and beneficial guidance to design high-performance SnS2-based anodes for LIBs.
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