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Plasmonic silver nanoparticles loaded titania nanotube arrays exhibiting enhanced photoelectrochemical and photocatalytic activities
被引:31
|作者:
Nishanthi, S. T.
[1
]
Iyyapushpam, S.
[1
]
Sundarakannan, B.
[1
]
Subramanian, E.
[2
]
Padiyan, D. Pathinettam
[1
]
机构:
[1] Manonmaniam Sundaranar Univ, Dept Phys, Tirunelveli 627012, Tamil Nadu, India
[2] Manonmaniam Sundaranar Univ, Dept Chem, Tirunelveli 627012, Tamil Nadu, India
关键词:
Anodization;
Surface plasmon resonance;
Photocurrent density;
Electron-hole recombination;
Methyl orange;
TIO2;
AG;
DEGRADATION;
WATER;
NANOCOMPOSITES;
PHOTOCHROMISM;
GENERATION;
LAYERS;
D O I:
10.1016/j.jpowsour.2014.10.186
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A combination of electrochemical anodization and photochemical reduction is employed to fabricate highly ordered silver loaded titania nanotubes (Ag/TNT) arrays. The Ag/TNT samples show an extended optical absorbance from UV to visible region owing to the surface plasmon resonance effect of Ag. The photoluminescence intensity of Ag/TNT is significantly lower than that of pure titania revealing a decrease in charge carrier recombination. The photoelectrochemical properties of the prepared samples are studied using linear sweep and transient photocurrent measurements. Compared with pure TNT, the Ag loaded samples show a higher photoelectrochemical activity. The results demonstrate an efficient separation of photogenerated electron-hole pairs and the consequent increase in lifetime of charge carriers by Ag/TNT. The photocatalytic results of methyl orange dye degradation show that the Ag/11\1T-3-O5 sample exhibits the maximum degradation efficiency of 98.85% with kinetic rate constant of 0.0236(5) min(-1) for 180 min light illumination. (C) 2014 Elsevier B.V. All rights reserved.
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页码:885 / 893
页数:9
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