Title of article
Effects of samarium dopant on photocatalytic activity of TiO2 nanocrystallite for methylene blue degradation
Author/Authors
Qi Xiao، نويسنده , , Zhichun Si، نويسنده , , Jiang Zhang، نويسنده , , Chong Xiao، نويسنده , , Zhiming Yu، نويسنده , , Guanzhou Qiu، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2007
Pages
6
From page
9194
To page
9199
Abstract
Sm3+-doped TiO2 nanocrystalline was synthesized
by a sol–gel auto-combustion method and characterized
by X-ray diffraction, Brunauer-Emmett-Teller
method (BET), UV–vis diffuse reflectance spectroscopy
(DRS), and also photoluminescence (PL) emission spectroscopy.
The photocatalytic activity of Sm3+–TiO2 catalyst
was evaluated by measuring degradation rates of
methylene blue (MB) under either UV or visible light. The
results showed that doping with the samarium ions significantly
enhanced the photocatalytic activity for MB
degradation under UV or visible light irradiation. This was
ascribed to the fact that a small amount of samarium
dopant simultaneously increased MB adsorption capacity
and separation efficiency of electron-hole pairs. The results
of DRS showed that Sm3+-doped TiO2 had significant
absorption between 400 nm and 500 nm, which increased
with the increase of samarium ion content. The adsorption
experimental demonstrated that Sm3+–TiO2 had a higher
MB adsorption capacity than undoped TiO2 and adsorption
capacity of MB increased with the increase of samarium
ion content. It is found that the stronger the PL intensity,
the higher the photocatalytic activity. This could be
explained by the points that PL spectra mainly resulted
from surface oxygen vacancies and defects during the
process of PL, while surface oxygen vacancies and defects
could be favorable in capturing the photoinduced electrons
during the process of photocatalytic reactions, so that the
recombination of photoinduced electrons and holes could
be effectively inhibited.
Journal title
Journal of Materials Science
Serial Year
2007
Journal title
Journal of Materials Science
Record number
833667
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