TY - JOUR
T1 - A facile one-pot synthesis of TiO2/nitrogen-doped reduced graphene oxide nanocomposite as anode materials for high-rate lithium-ion batteries
AU - Wang, Jie
AU - Shen, Laifa
AU - Li, Hongsen
AU - Wang, Xiaoyan
AU - Nie, Ping
AU - Ding, Bing
AU - Xu, Guiyin
AU - Dou, Hui
AU - Zhang, Xiaogang
N1 - Funding Information:
This work was supported by the National Basic Research Program of China (973 Program) (No. 2014CB239701), National Natural Science Foundation of China (No. 21173120, 21103091, 51372116), Natural Science Foundation of Jiangsu Province (BK2011030), and Fundamental Research Funds for the Central Universities (NP2014403).
PY - 2014/7/1
Y1 - 2014/7/1
N2 - TiO2/nitrogen-doped reduced graphene oxide nanocomposite (TiO2/N-RGO) is prepared via a facile one-pot hydrothermal method, in which ethylene glycol and ammonia are used as the reducing agent and nitrogen precursor, respectively. The reducing and nitrating process was accompanied by the generation of TiO2 nanoparticles. Various state-of-the-art techniques, including field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, thermogravimetric (TG) analysis and X-ray photoelectron spectroscopy (XPS) are performed to characterize the morphologies, structures and compositions. The introduced nitrogen atoms into graphene skeleton could enhance nucleation and growth kinetics and thus resulted in the nano-sized TiO2 uniformly anchoring on the N-RGO surface. Electrochemical tests show that the TiO2/N-RGO nanocomposite exhibits superior rate capability and outstanding capacity retention. The reversible capacity of the TiO2/N-RGO electrode is up to 126.8 mAh g-1 at 10 C and still remains at 118.4 mAh g-1 after 100 cycles. The excellent electrochemical performances can be attributed to electronic structure modification of graphene, which promoting intrinsic electron transfer between the host substrate and electroactive materials. Moreover, the high contact area between the electrolyte/electrode facilitates the transportation of electrolyte ion into the inner region of the electrode. Therefore, the TiO2/N-RGO nanocomposite can be a promising candidate anode material for high-rate lithium ion batteries.
AB - TiO2/nitrogen-doped reduced graphene oxide nanocomposite (TiO2/N-RGO) is prepared via a facile one-pot hydrothermal method, in which ethylene glycol and ammonia are used as the reducing agent and nitrogen precursor, respectively. The reducing and nitrating process was accompanied by the generation of TiO2 nanoparticles. Various state-of-the-art techniques, including field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, thermogravimetric (TG) analysis and X-ray photoelectron spectroscopy (XPS) are performed to characterize the morphologies, structures and compositions. The introduced nitrogen atoms into graphene skeleton could enhance nucleation and growth kinetics and thus resulted in the nano-sized TiO2 uniformly anchoring on the N-RGO surface. Electrochemical tests show that the TiO2/N-RGO nanocomposite exhibits superior rate capability and outstanding capacity retention. The reversible capacity of the TiO2/N-RGO electrode is up to 126.8 mAh g-1 at 10 C and still remains at 118.4 mAh g-1 after 100 cycles. The excellent electrochemical performances can be attributed to electronic structure modification of graphene, which promoting intrinsic electron transfer between the host substrate and electroactive materials. Moreover, the high contact area between the electrolyte/electrode facilitates the transportation of electrolyte ion into the inner region of the electrode. Therefore, the TiO2/N-RGO nanocomposite can be a promising candidate anode material for high-rate lithium ion batteries.
KW - Lithium ion batteries
KW - Nitrogen-doped reduced graphene oxide
KW - One-pot hydrothermal
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U2 - 10.1016/j.electacta.2014.03.095
DO - 10.1016/j.electacta.2014.03.095
M3 - Article
AN - SCOPUS:84899806607
SN - 0013-4686
VL - 133
SP - 209
EP - 216
JO - Electrochimica Acta
JF - Electrochimica Acta
ER -