4.8 Article

Lithium/Boron Co-doped Micrometer SiOx as Promising Anode Materials for High-Energy-Density Li-Ion Batteries

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 24, Pages 27854-27860

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c04983

Keywords

lithium-ion batteries; anode; silicon monoxide; co-doping strategy; initial Coulombic efficiency

Funding

  1. National Key R&D Program of China [2019YFA0705602, 2021YFB2400200]
  2. Innovation Team for R&D and Industrialization of High Energy Density Si-based Power batteries [2018607219003]
  3. Basic Science Center Project of National Natural Science Foundation of China [51788104]
  4. Transformational Technologies for Clean Energy and Demonstration
  5. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA21070300]
  6. National Science Foundation of China [52002374]
  7. Natural Science Foundation of Shandong Province [ZR2020ME057]
  8. National Natural Science Foundation of China [22005314]

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In this study, a Li/B co-doping strategy was developed to enhance the initial Coulombic efficiency and cycling stability of SiOx@C anodes, while alleviating volume expansion and pulverization. The findings are significant for the practical application of high-energy-density lithium-ion batteries.
The carbon-coated silicon monoxide (SiOx@C) has been considered as one of the most promising high-capacity anodes for the next-generation high-energy-density lithium-ion batteries (LIBs). However, the relatively low initial Coulombic efficiency (ICE) and the still existing huge volume expansion during repeated lithiation/delithiation cycling remain the greatest challenges to its practical application. Here, we developed a lithium and boron (Li/B) co-doping strategy to efficiently enhance the ICE and alleviate the volume expansion or pulverization of SiOx@C anodes. The in situ generated Li silicates (LixSiOy) by Li doping will reduce the active Li loss during the initial cycling and enhance the ICE of SiOx@C anodes. Meanwhile, B doping works to promote the Li+ diffusion and strengthen the internal bonding networks within SiOx@C, enhancing its resistance to cracking and pulverization during cycling. As a result, the enhanced ICE (83.28%), suppressed volume expansion, and greatly improved cycling (85.4% capacity retention after 200 cycles) and rate performance could be achieved for the Li/B co-doped SiOx@C (Li/B-SiOx@C) anodes. Especially, the Li/B-SiOx@C and graphite composite anodes with a capacity of 531.5 mA h g(-1) were demonstrated to show an ICE of 90.1% and superior cycling stability (90.1% capacity retention after 250 cycles), which is significant for the practical application of high-energy-density LIBs.

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