In situ preparation of novel p-n junction photocatalyst BiOI/(BiO)2CO3 with enhanced visible light photocatalytic activity
Novel p–n junction photocatalysts BiOI/(BiO)2CO3 with different contents of BiOI were in situ synthesized by etching (BiO)2CO3 precursor with hydroiodic acid (HI) solution. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectrometry (FT-IR),...
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2012
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curtin-20.500.11937-161202017-09-13T15:03:20Z In situ preparation of novel p-n junction photocatalyst BiOI/(BiO)2CO3 with enhanced visible light photocatalytic activity Cao, J. Li, Xin Yong Lin, H. Chen, S. Fu, X. Novel p–n junction photocatalysts BiOI/(BiO)2CO3 with different contents of BiOI were in situ synthesized by etching (BiO)2CO3 precursor with hydroiodic acid (HI) solution. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectrometry (FT-IR), energy-dispersive spectroscopy (EDS) and UV–vis diffuse reflectance spectroscopy (DRS) were employed to study the structures, morphologies and optical properties of the as-prepared samples. Under visible light (λ > 420 nm), BiOI/(BiO)2CO3 hybrid displayed much higher photocatalytic activity than pure (BiO)2CO3 and BiOI for the degradation of methyl orange (MO). The increased photocatalytic activity of BiOI/(BiO)2CO3 could be attributed to the formation of the p–n junction between p-BiOI and n-(BiO)2CO3, which effectively suppresses the recombination of photoinduced electron–hole pairs. Moreover, the tests of radical scavengers confirmed that radical dotO2− and h+ were the main reactive species for the degradation of MO. 2012 Journal Article http://hdl.handle.net/20.500.11937/16120 10.1016/j.jhazmat.2012.08.078 restricted |
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Curtin University Malaysia |
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Curtin Institutional Repository |
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Online Access |
description |
Novel p–n junction photocatalysts BiOI/(BiO)2CO3 with different contents of BiOI were in situ synthesized by etching (BiO)2CO3 precursor with hydroiodic acid (HI) solution. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectrometry (FT-IR), energy-dispersive spectroscopy (EDS) and UV–vis diffuse reflectance spectroscopy (DRS) were employed to study the structures, morphologies and optical properties of the as-prepared samples. Under visible light (λ > 420 nm), BiOI/(BiO)2CO3 hybrid displayed much higher photocatalytic activity than pure (BiO)2CO3 and BiOI for the degradation of methyl orange (MO). The increased photocatalytic activity of BiOI/(BiO)2CO3 could be attributed to the formation of the p–n junction between p-BiOI and n-(BiO)2CO3, which effectively suppresses the recombination of photoinduced electron–hole pairs. Moreover, the tests of radical scavengers confirmed that radical dotO2− and h+ were the main reactive species for the degradation of MO. |
format |
Journal Article |
author |
Cao, J. Li, Xin Yong Lin, H. Chen, S. Fu, X. |
spellingShingle |
Cao, J. Li, Xin Yong Lin, H. Chen, S. Fu, X. In situ preparation of novel p-n junction photocatalyst BiOI/(BiO)2CO3 with enhanced visible light photocatalytic activity |
author_facet |
Cao, J. Li, Xin Yong Lin, H. Chen, S. Fu, X. |
author_sort |
Cao, J. |
title |
In situ preparation of novel p-n junction photocatalyst BiOI/(BiO)2CO3 with enhanced visible light photocatalytic activity |
title_short |
In situ preparation of novel p-n junction photocatalyst BiOI/(BiO)2CO3 with enhanced visible light photocatalytic activity |
title_full |
In situ preparation of novel p-n junction photocatalyst BiOI/(BiO)2CO3 with enhanced visible light photocatalytic activity |
title_fullStr |
In situ preparation of novel p-n junction photocatalyst BiOI/(BiO)2CO3 with enhanced visible light photocatalytic activity |
title_full_unstemmed |
In situ preparation of novel p-n junction photocatalyst BiOI/(BiO)2CO3 with enhanced visible light photocatalytic activity |
title_sort |
in situ preparation of novel p-n junction photocatalyst bioi/(bio)2co3 with enhanced visible light photocatalytic activity |
publishDate |
2012 |
url |
http://hdl.handle.net/20.500.11937/16120 |
first_indexed |
2018-09-06T19:32:46Z |
last_indexed |
2018-09-06T19:32:46Z |
_version_ |
1610887846875365376 |