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Dip-coating deposition of resistive BiVO4 thin film and evaluation of their photoelectrochemical parameters under distinct sources illumination
Resistive monoclinic bismuth vanadate (BiVO 4 ) nanocrystals in the form of thin films were obtained by the solution combustion synthesis coupled with the dip-coating deposition process. The structure, morphology, and optical properties of BiVO 4 nanocrystals were characterized by means of x-ray dif...
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Published in: | Journal of solid state electrochemistry 2016-06, Vol.20 (6), p.1527-1538 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Resistive monoclinic bismuth vanadate (BiVO
4
) nanocrystals in the form of thin films were obtained by the solution combustion synthesis coupled with the dip-coating deposition process. The structure, morphology, and optical properties of BiVO
4
nanocrystals were characterized by means of x-ray diffraction (XRD), scanning electron microscopy (SEM), and UV-Vis spectroscopy. The photoelectrochemical properties were obtained by cyclic voltammetry and chronoamperometry techniques in potassium chloride (KCl) electrolyte solution under distinct visible light sources irradiation condition. Under blue InGaN light emitting diode (LED) irradiation, the electrode has a better efficiency, faster response time (260 ms), and faster decay time (65 ms), when compared with the irradiation by dichroic lamp. Besides, the photocurrent density (
j
ph
) is approximately 39 times higher than
j
ph
obtained under dichroic lamp. The performance analysis based on the methylene blue degradation reaction has shown that the BiVO
4
material has higher electroactivity under InGaN LED irradiation condition, with estimated
k
obs
value of 200 × 10
−4
min
−1
, which is a little higher than the value obtained with dichroic lamp illumination. In the dark condition, the BiVO
4
presented much lower photocatalytic activity. |
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ISSN: | 1432-8488 1433-0768 |
DOI: | 10.1007/s10008-016-3166-y |