异质结
材料科学
电化学
电场
离子
硫化
电极
纳米技术
扩散
化学工程
光电子学
化学
物理化学
工程类
物理
热力学
有机化学
冶金
量子力学
硫黄
作者
Haidong Bian,Zebiao Li,Jie Pan,Wenchao Liao,Zhangjian Li,Binbin Zhou,Zheming Zhang,Junwei Wu,Chen Liu
标识
DOI:10.1016/j.jcis.2022.08.011
摘要
Heterostructure materials, as newborn electrode materials for rechargeable batteries, are attracting increasing attention due to their robust architectures and superior electrochemical performances. It is widely believed that the inner electric field induced at the interface can improve the electric conductivity and ion diffusion kinetics, thus enhancing the long-term stability and high-rate performance of the batteries. Although much progress is made on heterostructure construction, the performance of the batteries is still far from satisfying the commercial applications. In this work, a new type of SnO2/SnSx (x = 1, 1.5) heterostructure embedded in carbon framework (C@SnO2/SnSx) is constructed via a facile sulfidation process. Compared to a single heterojunction, the multi-heterojunctions generated at SnO2/SnSx interface can induce an intensified built-in electric field, which promotes charge transportation and reaction kinetics of the electrode for Na-ions storage. Upon the sodiation process, the induced intensified electric field drives Na ions from Sn2S3 or SnO2 to SnS, while an inverse transportation of Na ions are accelerated upon the desodation process. As a result, C@SnO2/SnSx exhibits an outstanding reversible capacity of 510 mA h g-1 after 300 cycles at 200 mA g-1.
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