| Project/Area Number |
22550184
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Inorganic industrial materials
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| Research Institution | Kitakyushu National College of Technology |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
OBATA Kenji 北九州工業高等専門学校, 物質化学工学科, 准教授 (70370046)
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| Project Period (FY) |
2010 – 2012
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| Project Status |
Completed (Fiscal Year 2012)
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| Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2012: ¥390,000 (Direct Cost: ¥300,000、Indirect Cost: ¥90,000)
Fiscal Year 2011: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2010: ¥3,380,000 (Direct Cost: ¥2,600,000、Indirect Cost: ¥780,000)
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| Keywords | 光触媒 / 無機微粒子の合成 / 機器分析 / 電子構造計算 / 複合酸化物 / 可視光応答 / CaO-Bi2O3系複合酸化物 / CaO-Bi_2O_3系複合酸化物 / CaO-Bi_2O_3複合酸化物 |
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| Research Abstract |
The single phase of Ca4Bi6O13 crystal was obtained at lower calcination temperature in a citric acid complex method in comparison with a solid-state reaction method. It was confirmed that the photocatalytic activity of Ca4Bi6O13 for the degradation of methylene blue (MB) was higher in a citric acid complex method than in a solid-state reaction under visible-light irradiation (λ ? 420 nm). When Sr was added to Ca4Bi6O13, the optical band gap of Ca4Bi6O13 decreases slightly and the photocatalytic activity was improved. Further, we performed first-principles band calculation of Ca4Bi6O13 to determine the type of the optical transition, the characters of valence and conduction bands, and the band-gap energy. Ca4Bi6O13 is a direct-gap oxide and the energy states near the valence band maximum (VBM) and conduction band minimum (CBM) show wide dispersion, indicating a higher mobility of holes and electrons generated by band gap excitation. In addition, Ca4Bi6O13 has a distorted local structure consisting of [BiO6] polyhedron and a consequent dipole moment. Thus, a high photocatalytic ability of Ca4Bi6O13 is attributable to both the wide band dispersion near the valence band maximum and the conduction band minimum and its distorted local crystal structure.
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