Surface-modification-assisted synthesis of in-situ graphene-doped carbon substrate coated silicon nanoparticles for boosting lithium storage performanceopen access
- Authors
- Shi, Jian; Li, Ruiqian; Li, Jingwei; Liu, Guicheng
- Issue Date
- Dec-2023
- Publisher
- Elsevier B.V.
- Keywords
- Co-pyrolysis method; In-situ graphene; Multilayer architecture; Silicon/carbon anode; Surface modification
- Citation
- Powder Technology, v.430, pp 1 - 11
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- Powder Technology
- Volume
- 430
- Start Page
- 1
- End Page
- 11
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/21032
- DOI
- 10.1016/j.powtec.2023.118988
- ISSN
- 0032-5910
1873-328X
- Abstract
- Improving the electrical conductivity and structural integrity of Si/C anodes is of great concern for lithium-ion batteries which can be effectively achieved by doping graphene. However, it is difficult to achieve graphene-doped Si/C composites with good interface contact and conductive architecture. Herein, an in-situ graphene-doped carbon coated silicon nanoparticles (SiNPs) with multilayer architecture is designed. SiNPs is firstly modified and coated by polymethyl methacrylate (PMMA) shell. Multilayer carbon architecture is constructed via co-pyrolysis method using PMMA and citric acid as carbon sources. It displays an excellent lithium storage performance with a reversible discharge capacity of 2117.5 mAhg−1 at 200 mAg−1. These impressive anodic properties are chiefly benefited from the ingenious carbon architecture coated SiNPs involving in-situ graphene with a strong interfacial bonding interaction. Overall, this investigation can not only broaden the application potential in LIBs for advanced Si/C anodes but also provide an alternative route on designing a graphene-related material. © 2023
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Natural Science > Division of Physics & Semiconductor Science > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.