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Enhanced photocatalytic activity of Ce-doped β-Ga2O3 nanofiber fabricated by electrospinning method

Herein, β-Ga 2 O 3 photocatalyst was designed to improve the photocatalytic activity. Therefore, two strategies were employed: chemical modification by Ce doping and morphological control by formation of nanofibers. Therefore, Ce-doped β-Ga 2 O 3 nanofibers were successfully synthesized using a sol–...

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Published in:Journal of materials science. Materials in electronics 2021-02, Vol.32 (3), p.3402-3414
Main Authors: Kim, Young-Hun, Heo, Youn-Jung, Koh, Won-Gun, Shin, Gyojic, Choi, Kyung Ho
Format: Article
Language:English
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Summary:Herein, β-Ga 2 O 3 photocatalyst was designed to improve the photocatalytic activity. Therefore, two strategies were employed: chemical modification by Ce doping and morphological control by formation of nanofibers. Therefore, Ce-doped β-Ga 2 O 3 nanofibers were successfully synthesized using a sol–gel derived electrospinning. These synthesized nanofibers were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and UV–vis spectroscopy. The SEM and XRD results indicated that Ce doping slightly influence on the morphology and crystal structure of nanofibers. In addition, the UV–vis transmittance spectra result indicates that the bandgap energy of Ce-doped β-Ga 2 O 3 nanofibers was significantly reduced from 4.92 eV to 4.54 eV. In specific, the 0.7 mol % Ce-doped β-Ga 2 O 3 nanofibers exhibits the lowest optical band gap energy as 4.54 eV. Moreover, the photodegradation properties of β-Ga 2 O 3 nanofibers were evaluated by using the Methylene Blue (MB) under UV light. Interestingly, the β-Ga 2 O 3 nanofibers doped by 0.7 mol% cerium atom exhibited the highest photocatalytic activity than other synthesized nanofibers. Consequently, from the overall characterizations, it was found that improved activity of photocatalytic degradation will be attributed to the narrow optical bandgap energy and reduced recombination rate arising from the cerium doping.
ISSN:0957-4522
1573-482X
DOI:10.1007/s10854-020-05087-8