Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/106358
Title: Li3V2(PO4)3 nanocrystals embedded in a nanoporous carbon matrix supported on reduced graphene oxide sheets : binder-free and high rate cathode material for lithium-ion batteries
Authors: Liu, Weiling
Xu, Chen
Tan, Huiteng
Xiao, Ni
Hng, Huey Hoon
Yan, Qingyu
Lim, Tuti Mariana
Rui, Xianhong
Sim, Daohao
Wong, Kangming
Zhu, Jixin
Issue Date: 2012
Source: Rui, X., Sim, D., Wong, K., Zhu, J., Liu, W., Xu, C., et al. (2012). Li3V2(PO4)3 nanocrystals embedded in a nanoporous carbon matrix supported on reduced graphene oxide sheets: Binder-free and high rate cathode material for lithium-ion batteries. Journal of Power Sources, 214, 171-177.
Series/Report no.: Journal of power sources
Abstract: Li3V2(PO4)3 nanocrystals (5–8 nm) embedded in a nanoporous carbon matrix attached onto reduced graphene oxide nanosheets (LVP-NC@NPCM@rGO) are synthesized by a facile approach. The rGO sheets not only form the interconnected conducting scaffold to enhance the charge transfer but also act as the heterogeneous nucleation site to facilitate the growth of nanograins of LVP. The nanoporous carbon acts as the nanocontainer to enhance the electrolyte/active material interaction and also inhibit the grain growth of Li3V2(PO4)3. This leads to the fast kinetics of the Li ion transfer and the excellent cathode performance, especially at high current densities. Binder-free cathodes can be prepared based such LVP-NC@NPCM@rGO sample, which shows high specific capacities, stable cyclabilities and excellent rate capabilities in the voltage ranges of 3.0–4.3 and 3.0–4.8 V.
URI: https://hdl.handle.net/10356/106358
http://hdl.handle.net/10220/11356
ISSN: 0378-7753
DOI: 10.1016/j.jpowsour.2012.03.113
Schools: School of Civil and Environmental Engineering 
School of Materials Science & Engineering 
Organisations: TUM CREATE Centre for Electromobility
Research Centres: Energy Research Institute @ NTU (ERI@N) 
Rights: © 2012 Elsevier B.V.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:CEE Journal Articles
ERI@N Journal Articles
MSE Journal Articles

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