Sb/C composite embedded in SiOC buffer matrix via dispersion property control for novel anode material in sodium-ion batteries

Authors
Park, JeongeunKim, MinjunChoi, MinsuKu, MinkyeongKam, DayoungKim, Sang-OkChoi, Wonchang
Issue Date
2023-06
Publisher
Elsevier BV
Citation
Journal of Power Sources, v.568
Abstract
Due to vast sodium reserves, sodium-ion batteries (SIBs) are more cost-efficient to produce than lithium-ion batteries. Therefore, they are actively researched as next-generation energy storage materials. Antimony is a promising anode material for SIB owing to its high theoretical capacity (660 mA h g-1) and an appropriate sodiation voltage. However, due to the rapid volume change during sodium intercalation and deintercalation, cycling stability is poor, presenting a significant obstacle to the practical application of SIBs. Alleviating the Sb volume expansion throughout the charging and discharging processes is the key to the practical implementation of Sb-based anodes. Herein, Sb/C-SiOC composites are prepared using the hydrogen bonding-based adsorption properties of metal-organic frameworks (MOFs). The final product, the Sb/C-SiOC composites, exhibited significantly improved cycle performance, such as maintaining the initial capacity after 200 cycles by the SiOC matrix acting as a conductive buffer. Additionally, the presence of MOF-derived mesoporous carbon and SiOC contributed to the improved rate performance. The hydrogen bond-based adsorption properties of the MOFs used in this study can be effectively applied to uniformly introduce a matrix or coating layer that relieves the volume expansion of high-capacity composite anodes, making it an effective strategy for developing alloy-based energy storage materials.
Keywords
HIGH-PERFORMANCE ANODE; LITHIUM-ION; SILICONE OIL; LI-ION; CARBON; NANOCOMPOSITE; OXIDES; CYCLE; Anode; Antimony; Energy storage materials; Hydrogen -bonding; Metal -organic framework; Sodium -ion battery
ISSN
0378-7753
URI
https://pubs.kist.re.kr/handle/201004/113699
DOI
10.1016/j.jpowsour.2023.232908
Appears in Collections:
KIST Article > 2023
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