DocumentCode :
22994
Title :
Formation and catalytic performance of novel colourful BiOI photocatalysts with adjustable bandgap under visible light
Author :
Jian Yang ; Feng-Jun Zhang ; Fa-Zhi Xie ; Wen-Jie Xie ; Han-Mei Hu ; Lei Zhu ; Won-Chun Oh
Author_Institution :
Key Lab. of Functional Molecule Design & Interface Process, Anhui Jianzhu Univ., Hefei, China
Volume :
9
Issue :
10
fYear :
2014
fDate :
10 2014
Firstpage :
702
Lastpage :
706
Abstract :
A series of novel colourful BiOI photocatalysts have been synthesised by a simple oil bath method at 160°C. Several characterisation tools including X-ray diffraction, a scanning electron microscope, energy-dispersive X-ray spectroscopy and ultraviolet-visible diffuse reflectance spectroscopy were used to study the phase structure, morphologies, bandgap and catalytic performance of the prepared samples. The results show that BiOI exhibited higher photocatalytic efficiency under visible light (λ > 420 nm) in the degradation of methyl orange. This result could be because of the narrow bandgap, for which Eg is about 1.4-2.25 eV, and a number of active positions for catalysts. h+ acts as the main active species during methyl orange degradation.
Keywords :
X-ray chemical analysis; X-ray diffraction; bismuth compounds; catalysis; catalysts; crystal growth from solution; crystal structure; dyes; energy gap; photochemistry; reflectivity; scanning electron microscopy; semiconductor growth; semiconductor materials; ultraviolet spectra; visible spectra; BiOI; X-ray diffraction; band gap; energy-dispersive X-ray spectroscopy; methyl orange degradation; morphological properties; oil bath method; phase structure; photocatalytic efficiency; photocatalytic mechanism; photocatalytic properties; scanning electron microscopy; temperature 160 degC; ultraviolet-visible diffuse reflectance spectroscopy; visible light irradiation;
fLanguage :
English
Journal_Title :
Micro & Nano Letters, IET
Publisher :
iet
ISSN :
1750-0443
Type :
jour
DOI :
10.1049/mnl.2014.0337
Filename :
6942334
Link To Document :
بازگشت