Please use this identifier to cite or link to this item:
|Title:||CTAB-assisted synthesis of single-layer MoS2-graphene composites as anode materials of Li-ion batteries|
|Citation:||Wang, Z., Chen, T., Chen, W., Chang, K., Ma, L., Huang, G., Chen, D., Lee, J.Y. (2013-02-14). CTAB-assisted synthesis of single-layer MoS2-graphene composites as anode materials of Li-ion batteries. Journal of Materials Chemistry A 1 (6) : 2202-2210. ScholarBank@NUS Repository. https://doi.org/10.1039/c2ta00598k|
|Abstract:||A facile and scalable process was developed for the synthesis of single-layer MoS2-graphene nanosheet (SL-MoS2-GNS) composites based on the concurrent reduction of (NH4) 2MoS4 and graphene oxide sheets by hydrazine in the presence of cetyltrimethylammonium bromide (CTAB), followed by annealing in a N2 atmosphere. The morphology and microstructure of the composites were examined by X-ray diffraction, field emission scanning electron microscopy, high-resolution transmission electron microscopy and Raman spectroscopy. The formation process for the SL-MoS2-GNS composites was also investigated. The SL-MoS2-GNS composites delivered a large reversible capacity and good cycle stability as a Li-ion battery anode. In particular, the composites easily surpassed MoS2 in terms of rate performance and cycle stability at high current densities. Electrochemical impedance spectroscopy revealed that the GNS in the composite not only reduced the contact resistance in the electrode but also significantly facilitated the electron transfer in lithiation and delithiation reactions. The good electrochemical performance of the composites for reversible Li+ storage could be attributed to the synergy between the functions of SL-MoS2 and GNS. This journal is © The Royal Society of Chemistry 2013.|
|Source Title:||Journal of Materials Chemistry A|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jul 22, 2018
WEB OF SCIENCETM
checked on Jul 4, 2018
checked on Jun 14, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.