材料科学
阳极
锡
电池(电)
兴奋剂
锂(药物)
多孔性
形态学(生物学)
锂离子电池
纳米技术
化学工程
复合材料
冶金
光电子学
电极
工程类
化学
功率(物理)
物理化学
内分泌学
物理
生物
医学
量子力学
遗传学
作者
Jun‐Xia Li,Qinxing Xie,Yingqiang Zhao,Peng Zhao,Shoumin Zhang,Wei-Ping Huang
标识
DOI:10.1016/j.est.2024.111605
摘要
The widespread application of lithium-ion batteries (LiBs) has driven an increasing demand for advanced anodes with high-energy density and high-power density. Electroactive transition metal oxides (TMOs) are considered as promising candidates due to their high theoretical capacity. However, practical application has been hampered by their low conductivity and poor stability. In this study, tin-doped Co3O4 porous nanoarrays were successfully assembled on stainless steel mesh (SSM) using Co/Sn bimetallic organic frameworks as precursors. The resulting (Co/Sn)3O4@SSM was employed as a free-standing anode for LiBs. The lattice doping with tin atoms significantly enhances the internal conductivity of Co3O4, as confirmed by first-principle calculations. Benefiting from its hybrid advantages, such as a binder-free porous architecture and the improved conductivity, (Co/Sn)3O4@SSM exhibits dramatically enhanced energy storage capability, including high specific capacity, excellent cycling stability, and superior rate performance.
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