Hai-lin Ren, Yang Su, Shuai Zhao, Cheng-wei Li, Xiao-min Wang, Bo-han Li
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引用次数: 0
摘要
SiOx (0 <;x & lt;2)由于其高容量和更稳定的循环充放电性能,被认为是最有前途的锂离子电池阳极之一,但与石墨相比,它仍然存在固有电导率较低和体积膨胀较大的缺点。为此,本文选择了Si的同源元素Sn,采用简单的溶剂热法和煅烧法在SiOx表面构建SiOx@SnO2异质结构。DFT分析与实验结果相结合表明,SiOx的非均相结构增强了SiOx的Si-O键强度,加之SiOx与SnO2晶格差异引起的局域应力减轻了SiOx在锂化/去锂化过程中的体积变化。在1C下循环300次后的可逆容量为536.8 mAh g-1,在0.5C下循环200次后的可逆容量为1152.4 mAh g-1。SiOx@SnO2异质结的构建也将费米能级带入价带,使材料表现出一定的金属性质,并提高了电导率,增强了Li+的扩散。
Construction of SiOx-SnO2 heterojunction and surface coating to achieve high-performance anode materials for lithium-ion batteries
SiOx (0 < x < 2) has been considered as one of the most promising anodes for lithium-ion batteries due to its high capacity and more stable cyclic charging and discharging performance, but it still has the drawbacks of lower intrinsic conductivity and larger volume expansion compared to graphite. For this purpose, Sn, a homologous element of Si, is selected in this paper, and the SiOx@SnO2 heterostructure is constructed on the SiOx surface using simple solvothermal and calcination methods. The combination of DFT analysis and experimental results shows that the heterogeneous structure enhances the Si-O bond strength in SiOx, and coupled with the localised stresses due to the lattice differences between SiOx and SnO2 alleviates the volume change of SiOx during lithiation /de-lithiation. The reversible capacity was 536.8 mAh g-1 after 300 cycles at 1C and 1152.4 mAh g-1 after 200 cycles at 0.5C. The construction of SiOx@SnO2 heterojunction will also bring the Fermi energy levels into the valence band, which makes the material exhibit some metallic properties and improves the electrical conductivity enhancing the Li+ diffusion.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.