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超越薄膜:阐明-LiSi形成对薄膜、纳米颗粒和多孔硅电极的影响。

Beyond Thin Films: Clarifying the Impact of -LiSi Formation in Thin Film, Nanoparticle, and Porous Si Electrodes.

作者信息

Woodard Jasper C, Kalisvaart W Peter, Sayed Sayed Youssef, Olsen Brian C, Buriak Jillian M

机构信息

Department of Chemistry, University of Alberta, 11227 Saskatchewan Drive, Edmonton, AB T6G 2G2, Canada.

出版信息

ACS Appl Mater Interfaces. 2021 Aug 18;13(32):38147-38160. doi: 10.1021/acsami.1c04293. Epub 2021 Aug 6.

Abstract

The formation of the -LiSi phase has well-established detrimental effects on the capacity retention of thin film silicon electrodes. However, the role of this crystalline phase with respect to the loss of capacity is somewhat ambiguous in nanoscale morphologies. In this work, three silicon-based morphologies are examined, including planar films, porous planar films, and silicon nanoparticle composite powder electrodes. The cycling conditions are used as the lever to induce, or not induce, the formation of -LiSi through application of constant-current (CC) or constant-current constant-voltage (CCCV) steps. In this manner, the role of this phase on capacity retention and Coulombic efficiency can be determined with few other convoluting factors such as alteration of the composition or morphology of the silicon electrodes themselves. The results here confirm that the -LiSi phase increases the rate of capacity decay in planar films but has no major effect on capacity retention in half-cells based on porous silicon films or silicon nanoparticle composite powder electrodes, although this conclusion is nuanced. Besides using a constant-voltage step, formation of the -LiSi phase is influenced by the dimensions of the Si material and the lithiation cutoff voltage. Porous Si films, which, in this work, comprise primary Si particle sizes that are smaller than those in the preformed Si nanoparticle slurries, do not undergo the formation of -LiSi at 50 mV, whereas Si nanoparticle slurries are accompanied by the formation of -LiSi up to 80 mV. The solid-electrolyte interphase (SEI) formed from reaction of the -LiSi with the carbonate-based electrolyte causes polarization in both nanoparticle and porous film silicon electrodes and lowers the average Coulombic efficiency. A comparison of the cumulative irreversibilities due to SEI formation between different lithiation cutoff voltages in silicon nanoparticle slurry electrodes confirmed the connection between higher SEI buildup and formation of the -LiSi phase. This work indicates that concerns about the -LiSi phase in silicon nanoparticles and porous silicon electrodes should mainly focus on the stability of the SEI and a reduction of irreversible electrolyte reactions.

摘要

-LiSi相的形成对薄膜硅电极的容量保持率具有公认的不利影响。然而,在纳米尺度形态下,这种晶相在容量损失方面所起的作用尚有些模糊。在本工作中,研究了三种硅基形态,包括平面薄膜、多孔平面薄膜和硅纳米颗粒复合粉末电极。通过施加恒流(CC)或恒流恒压(CCCV)步骤,将循环条件用作诱导或不诱导-LiSi形成的杠杆。通过这种方式,可以在几乎没有其他复杂因素(如硅电极自身组成或形态的改变)的情况下,确定该相对容量保持率和库仑效率的作用。此处结果证实,-LiSi相增加了平面薄膜中容量衰减的速率,但对基于多孔硅薄膜或硅纳米颗粒复合粉末电极的半电池中的容量保持率没有重大影响,尽管这一结论存在细微差别。除了使用恒压步骤外,-LiSi相的形成还受硅材料尺寸和锂化截止电压的影响。在本工作中,多孔硅薄膜的初级硅颗粒尺寸小于预制硅纳米颗粒浆料中的尺寸,在50 mV时不会形成-LiSi,而硅纳米颗粒浆料在高达80 mV时会伴随-LiSi的形成。由-LiSi与碳酸盐基电解质反应形成的固体电解质界面(SEI)在纳米颗粒和多孔薄膜硅电极中都会引起极化,并降低平均库仑效率。对硅纳米颗粒浆料电极中不同锂化截止电压下因SEI形成导致的累积不可逆性进行比较,证实了较高的SEI积累与-LiSi相形成之间的联系。这项工作表明,对硅纳米颗粒和多孔硅电极中-LiSi相的关注应主要集中在SEI的稳定性和不可逆电解质反应的减少上。

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