4.8 Article

Beyond Thin Films: Clarifying the Impact of c-Li15Si4 Formation in Thin Film, Nanoparticle, and Porous Si Electrodes

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 32, 页码 38147-38160

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c04293

关键词

silicon; porous silicon; films; lithium-ion batteries; anodes; nanoparticles; crystallization; Li15Si4

资金

  1. Future Energy Systems of the University of Alberta [T12-P04]
  2. NSERC [RGPIN-2018-04294]
  3. Alberta Innovates Technology Futures [AITF iCORE IC50-T1 G2013000198]
  4. Western Economic Diversification (WD) [000014328]
  5. Canada Research Chairs program [CRC 207142]

向作者/读者索取更多资源

The study reveals that the c-Li15Si4 phase accelerates capacity decay in planar films but has minimal impact on capacity retention in half-cells based on porous silicon films or silicon nanoparticle composite powder electrodes. Formation of the c-Li15Si4 phase is influenced by the dimensions of the Si material and the lithiation cutoff voltage, leading to differences in SEI formation and electrochemical behavior in different morphologies of silicon electrodes.
The formation of the c-Li15Si4 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 c-Li15Si4 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 c-Li15Si4 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 c-Li15Si4 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 c-Li15Si4 at 50 mV, whereas Si nanoparticle slurries are accompanied by the formation of c-Li15Si4 up to 80 mV. The solid-electrolyte interphase (SEI) formed from reaction of the c-Li15Si4 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 c-Li15Si4 phase. This work indicates that concerns about the c-Li15Si4 phase in silicon nanoparticles and porous silicon electrodes should mainly focus on the stability of the SEI and a reduction of irreversible electrolyte reactions.

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