Issue 17, 2011

Graphene-like MoS2/amorphous carbon composites with high capacity and excellent stability as anode materials for lithium ion batteries

Abstract

A facile process to synthesize graphene-like MoS2/amorphous carbon (a-C) composites was developed. MoS2/C composites were firstly prepared by hydrothermal method employing sodium molybdate, sulfocarbamide and glucose as starting materials. The graphene-like MoS2/a-C composites were obtained after annealing at 800 °C in H2/N2. The samples were characterized by XRD, SEM, EDS and HRTEM. It was confirmed that in the composites MoS2 has a structure of single-layer, which is named graphene-like nanostructure. The graphene-like MoS2 nanosheets were uniformly dispersed in amorphous carbon. The interlaminar distance of the adjacent graphene-like MoS2 nanosheets in the composites measured was ∼1.0 nm. The mechanism of the formation of the graphene-like MoS2/a-C composites was investigated. The graphene-like MoS2/a-C composites exhibited high capacity and excellent cyclic stability used as anode materials for Li-ion batteries. The composite prepared by adding 1.0 g of glucose in hydrothermal solution exhibited the highest reversible capacity (962 mAh g−1) and excellent cyclic stability. After 100 cycles, it still retained 912 mAh g−1. The significant improvements in the electrochemical properties of the graphene-like MoS2/a-C composites could be attributed to the graphene-like structure of the MoS2 nanosheets and the synergistic effects of graphene-like MoS2 and amorphous carbon.

Graphical abstract: Graphene-like MoS2/amorphous carbon composites with high capacity and excellent stability as anode materials for lithium ion batteries

Article information

Article type
Paper
Submitted
12 Jan 2011
Accepted
18 Feb 2011
First published
23 Mar 2011

J. Mater. Chem., 2011,21, 6251-6257

Graphene-like MoS2/amorphous carbon composites with high capacity and excellent stability as anode materials for lithium ion batteries

K. Chang, W. Chen, L. Ma, H. Li, H. Li, F. Huang, Z. Xu, Q. Zhang and J. Lee, J. Mater. Chem., 2011, 21, 6251 DOI: 10.1039/C1JM10174A

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