Phase-controlled synthesis, surface morphology, and photocatalytic activity of the perovskite AlFeO3
2
Science and technology on vacuum technology and physics laboratory, Lanzhou Institute of Physics, Lanzhou, China
|
3
Institute of Nuclear physics and chemistry, China Academy of Engineering Physics, Mianyang, China
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Тип публикации: Journal Article
Дата публикации: 2017-02-13
scimago Q2
wos Q1
БС1
SJR: 0.513
CiteScore: 4.8
Impact factor: 3.2
ISSN: 09280707, 15734846
Materials Chemistry
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Condensed Matter Physics
Biomaterials
Краткое описание
Perovskite-type AlFeO3 powders are synthesized by a modified polyacrylamide gel route using different chelating agents at different pHs. X-ray diffraction and Raman results indicate that the AlFeO3 powders synthesized with oxalic acid are rhombohedral structure, while the AlFeO3 powders fabricated by using the other chelating agents exhibit an orthorhombic structure. The scanning electron microscopic images indicate that the morphology of the AlFeO3 samples depend on the choice of chelating agent and pH value. In addition, the particle size of samples with rhombohedral structure is larger than that of the samples with orthorhombic structure. X-ray photoelectron spectroscopy and scanning electron microscopic analysis indicate that the AlFeO3 powders fabricated at pH = 7 have good phase purity and uniform size. Photocatalytic activities of the AlFeO3 samples are determined by the degradation of rhodamine B dye in the presence of hydrogen peroxide and the results show that the samples will probably be applicable in the development of highly efficient photocatalyst. In addition, the rhombohedral AlFeO3 samples exhibit better photocatalysis than the orthorhombic samples, which is probably because that the crystal structure of AlFeO3 samples play a more important role than particle size in photocatalytic activity. The as-prepared AlFeO3 photocatalyst exhibits a pronounced photocatalytic activity for the decomposition of rhodamine B under visible-light irradiation, which is expected to widen the potential applications for perovskite-type oxide AlFeO3. A novel perovskite-type photocatalyst AlFeO3 is synthesized by a modified polyacrylamide gel route using different chelating agents. The crystal structure of AlFeO3 sample depend on the choice of chelating agent and AlFeO3 photocatalyst, in the presence of hydrogen peroxide, exhibit a pronounced photocatalytic activity for the decomposition of rhodamine B under simulated sunlight.
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Li Q. et al. Phase-controlled synthesis, surface morphology, and photocatalytic activity of the perovskite AlFeO3 // Journal of Sol-Gel Science and Technology. 2017. Vol. 82. No. 2. pp. 500-508.
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Li Q., Wang S., YUAN Y., Gao H., Xia X. Phase-controlled synthesis, surface morphology, and photocatalytic activity of the perovskite AlFeO3 // Journal of Sol-Gel Science and Technology. 2017. Vol. 82. No. 2. pp. 500-508.
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TY - JOUR
DO - 10.1007/s10971-017-4325-z
UR - https://doi.org/10.1007/s10971-017-4325-z
TI - Phase-controlled synthesis, surface morphology, and photocatalytic activity of the perovskite AlFeO3
T2 - Journal of Sol-Gel Science and Technology
AU - Li, Qiang
AU - Wang, Shifa
AU - YUAN, YONGGANG
AU - Gao, Hui
AU - Xia, Xiang
PY - 2017
DA - 2017/02/13
PB - Springer Nature
SP - 500-508
IS - 2
VL - 82
SN - 0928-0707
SN - 1573-4846
ER -
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@article{2017_Li,
author = {Qiang Li and Shifa Wang and YONGGANG YUAN and Hui Gao and Xiang Xia},
title = {Phase-controlled synthesis, surface morphology, and photocatalytic activity of the perovskite AlFeO3},
journal = {Journal of Sol-Gel Science and Technology},
year = {2017},
volume = {82},
publisher = {Springer Nature},
month = {feb},
url = {https://doi.org/10.1007/s10971-017-4325-z},
number = {2},
pages = {500--508},
doi = {10.1007/s10971-017-4325-z}
}
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Li, Qiang, et al. “Phase-controlled synthesis, surface morphology, and photocatalytic activity of the perovskite AlFeO3.” Journal of Sol-Gel Science and Technology, vol. 82, no. 2, Feb. 2017, pp. 500-508. https://doi.org/10.1007/s10971-017-4325-z.