School of Molecular Sciences, Arizona State University , P.O. Box 871604, Tempe, Arizona 85287, United States.
Department of Chemistry and Biochemistry, University of Delaware , Newark, Delaware 19716, United States.
ACS Appl Mater Interfaces. 2017 Nov 29;9(47):41246-41257. doi: 10.1021/acsami.7b12810. Epub 2017 Nov 14.
Type I silicon clathrates based on BaAlSi (8 < y < 12) have been studied as potential anodes for lithium-ion batteries and display electrochemical properties that are distinct from those found in conventional silicon anodes. Processing steps such as ball-milling (typically used to reduce the particle size) and acid/base treatment (used to remove nonclathrate impurities) may modify the clathrate surface structure or introduce defects, which could affect the observed electrochemical properties. In this work, we perform a systematic investigation of BaAlSi clathrates with y ≈ 16, i.e, having a composition near BaAlSi, which perfectly satisfies the Zintl condition. The roles of ball-milling and acid/base treatment were investigated using electrochemical, X-ray diffraction, electron microscopy, X-ray photoelectron and Raman spectroscopy analysis. The results showed that acid/base treatment removed impurities from the synthesis, but also led to formation of a surface oxide layer that inhibited lithiation. Ball-milling could remove the surface oxide and result in the formation of an amorphous surface layer, with the observed charge storage capacity correlated with the thickness of this amorphous layer. According to the XRD and electrochemical analysis, all lithiation/delithiation processes are proposed to occur in single phase reactions at the surface with no discernible changes to the crystal structure in the bulk. Electrochemical impedance spectroscopy results suggest that the mechanism of lithiation is through surface-dominated, Faradaic processes. This suggests that for off-stoichiometric clathrates, as we studied in our previous work, Li insertion at defects or vacancies on the framework may be the origin of reversible Li cycling. However, for clathrates BaAlSi with y ≈ 16, Li insertion in the structure is unfavorable and low capacities are observed unless amorphous surface layers are introduced by ball-milling.
基于 BaAlSi(8 < y < 12)的 I 型硅笼合物已被研究作为锂离子电池的潜在阳极,其电化学性能与传统硅阳极明显不同。球磨(通常用于减小粒径)和酸碱处理(用于去除非笼合物杂质)等加工步骤可能会改变笼合物的表面结构或引入缺陷,从而影响观察到的电化学性能。在这项工作中,我们对 y ≈ 16 的 BaAlSi 笼合物进行了系统研究,即具有接近 BaAlSi 的组成,完美满足 Zintl 条件。使用电化学、X 射线衍射、电子显微镜、X 射线光电子能谱和拉曼光谱分析研究了球磨和酸碱处理的作用。结果表明,酸碱处理去除了合成中的杂质,但也导致形成了抑制锂化的表面氧化层。球磨可以去除表面氧化物并形成非晶态表面层,观察到的电荷存储容量与该非晶态层的厚度相关。根据 XRD 和电化学分析,所有的锂化/脱锂过程都被认为是在表面上发生单相反应,而在体相中没有明显的晶体结构变化。电化学阻抗谱结果表明,锂化的机制是通过表面主导的法拉第过程。这表明对于非化学计量的笼合物,正如我们在前一项工作中研究的那样,Li 可能是在框架上的缺陷或空位中插入,从而实现可逆的 Li 循环。然而,对于 y ≈ 16 的 BaAlSi 笼合物,Li 插入结构中是不利的,除非通过球磨引入非晶态表面层,否则观察到的容量较低。