Covalent-assisted seeding of Si nanoparticles into a dual-matrix design toward advanced Si-based Li-ion batteries
- Authors
- Do, Kwanghyun; Park, Changyong; Hwang, Jeonguk; Kim, Sucheol; Jung, Yeju; Lee, Se Hun; Lim, Hee-Dae; Ahn, Heejoon
- Issue Date
- May-2024
- Publisher
- Royal Society of Chemistry
- Citation
- Journal of Materials Chemistry A, v.12, no.18, pp 11062 - 11074
- Pages
- 13
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Materials Chemistry A
- Volume
- 12
- Number
- 18
- Start Page
- 11062
- End Page
- 11074
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/202105
- DOI
- 10.1039/d3ta07989a
- ISSN
- 2050-7488
2050-7496
- Abstract
- Silicon oxycarbide (SiOC) holds enormous promise as a buffer matrix material in Si-based composites owing to its outstanding electro-chemo-mechanical stability and cost-effectiveness. However, there is an urgent need to develop a new approach for establishing robust chemical bonds or interactions between Si nanoparticles (NPs) and SiOC. This study introduces a novel silicon alkoxide-based sol–gel method for synthesizing Si-NP-seeded SiOC (Si@SiOC), resulting in the covalent-assisted seeding (CAS) of Si NPs into the matrix. As a result, the Si@SiOC composites exhibited improved reversible capacity and coulombic efficiency compared to bare SiOC. Nevertheless, an inherent trade-off exists between capacity and cycling stability with increasing Si NP content. To address this challenge, a dual-matrix design is proposed by integrating Sn nanocrystals into a Si@SiOC matrix. The introduction of Sn as a pore trigger led to the creation of internal artificial voids and simultaneously enhanced both the ionic and electronic conductivities. Consequently, the SiSn@SiOC composites demonstrated superior reversible capacities, initial coulombic efficiencies, and cycling stabilities compared to Si@SiOC. This study not only introduces an innovative method for establishing robust bonds between Si NPs and the SiOC host but also represents a novel approach by employing Sn as a pore-inducing agent to further
enhance electrochemical performance.
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