Ultrafast lithium storage in TiO2-bronze nanowires/N-doped graphene nanocomposites
A TiO 2 -bronze/N-doped graphene nanocomposite (TiO 2 -B/NG) is prepared by a facile hydrothermal combined with hydrazine monohydrate vapor reduction method. The material exhibits macro- and meso-porosity with a high specific surface area of 163.4 m 2 g −1 . X-Ray photoelectron spectroscopy confirms...
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Sprache: | eng |
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Zusammenfassung: | A TiO
2
-bronze/N-doped graphene nanocomposite (TiO
2
-B/NG) is prepared by a facile hydrothermal combined with hydrazine monohydrate vapor reduction method. The material exhibits macro- and meso-porosity with a high specific surface area of 163.4 m
2
g
−1
. X-Ray photoelectron spectroscopy confirms the successful doping of nitrogen in the graphene sheets. In addition, the TiO
2
-B nanowires are substantially bonded to the NG sheets. Cyclic voltammetry and electrochemical impedance spectroscopy show that the N-doped graphene improves the electron and Li ion transport in the electrode which results in better electrochemical kinetics than that of the pristine TiO
2
-B nanowires. As a result, the charge transfer resistance of the TiO
2
-B/NG electrode is significantly reduced. In addition, the lithium diffusion coefficient of TiO
2
-B/NG increases by about five times with respect to that of pristine TiO
2
-B. The TiO
2
-B/NG composite exhibits a remarkably enhanced electrochemical performance compared to that of TiO
2
-B. It shows a discharge capacity of 220.7 mA h g
−1
at the 10C rate with a capacity retention of 96% after 1000 cycles. In addition, it can deliver a discharge capacity of 101.6 mA h g
−1
at an ultra high rate of 100C, indicating its great potential for use in high power lithium ion batteries.
A TiO
2
-bronze/N-doped graphene nanocomposite was prepared by a facile method. The material exhibits outstanding rate capacity. A high reversible capacity of 101.6 mA h g
−1
is obtained at the 100C rate, indicating its great potential for use in high power lithium ion batteries. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c4ta06361a |