TY - JOUR
T1 - Synthesis of three-dimensional rare-earth ions doped CNTs-GO-Fe3O4 hybrid structures using one-pot hydrothermal method
AU - Gao, Guo
AU - Zhang, Qiang
AU - Cheng, Xin-Bing
AU - Sun, Rongjin
AU - Shapter, Joseph
AU - Yin, Ting
AU - Cui, Daxiang
PY - 2015
Y1 - 2015
N2 - Abstract Rechargeable lithium ion batteries (LIBs) are currently the dominant power source for all sorts of electronic devices due to their low cost and high energy density. The cycling stability of LIBs is significantly compromised due to the broad satellite peak for many anode materials. Herein, we develop a facile hydrothermal process for preparing rare-earth (Er, Tm) ions doped three-dimensional (3D) transition metal oxides/carbon hybrid nanocomposites, namely CNTs-GO-Fe3O4, CNTs-GO-Fe3O4-Er and CNTs-GO-Fe3O4-Tm. The GO sheets and CNTs are interlinked by ultrafine Fe3O4 nanoparticles forming three-dimensional (3D) architectures. When evaluated as anode materials for LIBs, the CNTs-GO-Fe3O4 hybrid composites have a bigger broad satellite peak. As for the CNTs-GO-Fe3O4-Er and CNTs-GO-Fe3O4-Tm hybrid composites, the broad satellite peak can be completely eliminated. When the current density changes from 5 C back to 0.1 C, the capacity of CNTs-GO-Fe3O4-Tm hybrid composites can recover to 1023.9 mAhg-1, indicating an acceptable rate capability. EIS tests show that the charge transfer resistance does not change significantly after 500 cycles, demonstrating that the cycling stability of CNTs-GO-Fe3O4-Tm hybrid composites are superior to CNTs-GO-Fe3O4 and CNTs-GO-Fe3O4-Er hybrid structures.
AB - Abstract Rechargeable lithium ion batteries (LIBs) are currently the dominant power source for all sorts of electronic devices due to their low cost and high energy density. The cycling stability of LIBs is significantly compromised due to the broad satellite peak for many anode materials. Herein, we develop a facile hydrothermal process for preparing rare-earth (Er, Tm) ions doped three-dimensional (3D) transition metal oxides/carbon hybrid nanocomposites, namely CNTs-GO-Fe3O4, CNTs-GO-Fe3O4-Er and CNTs-GO-Fe3O4-Tm. The GO sheets and CNTs are interlinked by ultrafine Fe3O4 nanoparticles forming three-dimensional (3D) architectures. When evaluated as anode materials for LIBs, the CNTs-GO-Fe3O4 hybrid composites have a bigger broad satellite peak. As for the CNTs-GO-Fe3O4-Er and CNTs-GO-Fe3O4-Tm hybrid composites, the broad satellite peak can be completely eliminated. When the current density changes from 5 C back to 0.1 C, the capacity of CNTs-GO-Fe3O4-Tm hybrid composites can recover to 1023.9 mAhg-1, indicating an acceptable rate capability. EIS tests show that the charge transfer resistance does not change significantly after 500 cycles, demonstrating that the cycling stability of CNTs-GO-Fe3O4-Tm hybrid composites are superior to CNTs-GO-Fe3O4 and CNTs-GO-Fe3O4-Er hybrid structures.
KW - CNTs
KW - Fe O
KW - Hydrothermal
KW - LIBs
UR - http://www.scopus.com/inward/record.url?scp=84938340726&partnerID=8YFLogxK
U2 - 10.1016/j.jallcom.2015.06.130
DO - 10.1016/j.jallcom.2015.06.130
M3 - Article
SN - 0925-8388
VL - 649
SP - 82
EP - 88
JO - JOURNAL OF ALLOYS AND COMPOUNDS
JF - JOURNAL OF ALLOYS AND COMPOUNDS
M1 - 34483
ER -