Oxygen deficient, carbon coated self-organized TiO2 nanotubes as anode material for Li-ion intercalationElectronic supplementary information (ESI) available. See DOI: 10.1039/c5ta03621f
Since several years, research for high capacity anode materials in Li-ion batteries is addressed to titanium dioxide (TiO 2 ), which offers important advantages in terms of cost effectiveness, safety and environmental compatibility. This work reports on the lithiation and delithiation characteristic...
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Main Authors | , , , , , |
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Format | Journal Article |
Language | English |
Published |
04.08.2015
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Online Access | Get full text |
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Summary: | Since several years, research for high capacity anode materials in Li-ion batteries is addressed to titanium dioxide (TiO
2
), which offers important advantages in terms of cost effectiveness, safety and environmental compatibility. This work reports on the lithiation and delithiation characteristics of anodically grown, self-organized TiO
2
nanotubes annealed in Ar (TiO
2−
x
) and Ar/C
2
H
2
(TiO
2−
x
-C). The systems are used as model composite electrodes for the anode in Li-ion batteries. Anatase TiO
2−
x
-C nanotubes demonstrate a superior Li storage capacity as high as 320(±68) mA h g
−1
(Li
0.96
TiO
2
) compared to 180(±38) mA h g
−1
(Li
0.54
TiO
2
) for TiO
2−
x
. This is comparable to the highest reported capacities for TiO
2
nanotubes to date. The double layer capacities are estimated from cyclic voltammetry measurements to 85 μF cm
−
² for TiO
2−
x
and 20 μF cm
−
² for TiO
2−
x
-C nanotubes respectively. Additionally, electrochemical impedance spectroscopy reveals smaller charge transfer resistances for TiO
2−
x
-C nanotubes at the solid/liquid interface which improves the transfer of Li
+
-ions from the electrolyte into the electrode.
Anatase TiO
2−
x
-C nanotubes demonstrate a superior Li storage capacity as high as 320(±68) mA h g
−1
compared to 180(±38) mA h g
−1
for TiO
2−
x
. |
---|---|
Bibliography: | 10.1039/c5ta03621f Electronic supplementary information (ESI) available. See DOI |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c5ta03621f |