Effects of UV irradiation on Ce<sub>1-x</sub>Pr<sub>x</sub>O<sub>2</sub> nanocrystals
ORAL
Abstract
Wei Min Tu1, Peng-Chun Wang1, Tai-Sing Wu2, and Yun-Liang Soo1,2
1Department of Physics, National Tsing Hua University, Hsinchu, Taiwan
2National Synchrotron Radiation Research Center, Hsinchu, Taiwan
We have investigated the effects of ultra-violet (UV) irradiation on the structures and electronic properties of CeO2, Pr6O11, and Ce1-xPrxO2 nanocrystals with x=0.1~0.7 prepared using a polyol method. The crystal structure, microstructure, bandgap, cation valence states of the samples before and after UV irradiation were determined by x-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), UV-vis diffuse reflectance spectra, and x-ray absorption near edge structure (XANES) measurements, respectively. After UV irradiation, the bandgaps of the CeO2 and Ce1-xPrxO2 samples were slightly narrowed, as opposed to the widened Pr6O11 bandgap. Also, the reduction of Ce4+ ions to Ce3+ in CeO2 and the reduction of Pr4+ ions to Pr3+ in Pr6O11 due to UV irradiation were observed. While substantial reduction of Pr⁴⁺ occurred, the reduction of Ce⁴⁺ was largely suppressed in the Ce₁₋ₓPrₓO₂ sample after UV irradiation. Our results demonstrate that it is easier to create oxygen vacancies around Pr than around Ce, while the bandgap variation follows the trends of Ce oxides rather than Pr oxides under UV irradiation in Ce₁₋ₓPrₓO₂ nanocrystals. Variations in catalyst activity due to UV irradiation in Ce₁₋ₓPrₓO₂ nanocrystals for photocatalysis applications will also be discussed.
1Department of Physics, National Tsing Hua University, Hsinchu, Taiwan
2National Synchrotron Radiation Research Center, Hsinchu, Taiwan
We have investigated the effects of ultra-violet (UV) irradiation on the structures and electronic properties of CeO2, Pr6O11, and Ce1-xPrxO2 nanocrystals with x=0.1~0.7 prepared using a polyol method. The crystal structure, microstructure, bandgap, cation valence states of the samples before and after UV irradiation were determined by x-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), UV-vis diffuse reflectance spectra, and x-ray absorption near edge structure (XANES) measurements, respectively. After UV irradiation, the bandgaps of the CeO2 and Ce1-xPrxO2 samples were slightly narrowed, as opposed to the widened Pr6O11 bandgap. Also, the reduction of Ce4+ ions to Ce3+ in CeO2 and the reduction of Pr4+ ions to Pr3+ in Pr6O11 due to UV irradiation were observed. While substantial reduction of Pr⁴⁺ occurred, the reduction of Ce⁴⁺ was largely suppressed in the Ce₁₋ₓPrₓO₂ sample after UV irradiation. Our results demonstrate that it is easier to create oxygen vacancies around Pr than around Ce, while the bandgap variation follows the trends of Ce oxides rather than Pr oxides under UV irradiation in Ce₁₋ₓPrₓO₂ nanocrystals. Variations in catalyst activity due to UV irradiation in Ce₁₋ₓPrₓO₂ nanocrystals for photocatalysis applications will also be discussed.
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Presenters
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Yun-Liang Soo
National Tsing Hua University
Authors
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Yun-Liang Soo
National Tsing Hua University
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Wei Min Tu
National Tsing Hua University
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Peng-Chun Wang
National Tsing Hua University
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Tai-Sing Wu
Natl Tsing Hua Univ