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RISS 인기검색어
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- 저자 : Baibiao Huang (검색결과 3 건)
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Chaoyi Wu,Zhenggang Gao,Shanmin Gao,Qingyao Wang,Zeyan Wang,Baibiao Huang,Ying Dai 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2016 NANO Vol.11 No.8
Ti3+ self-doped TiO2 (TiO2-x)/N-doped carbon nanostructure composites were prepared via a facile one-step hydrothermal method to optimize the use of visible light and reduce recombination of photogenerated electrons and holes. The composites were characterized by X-ray diffraction, transmission electron microscopy (TEM), high-resolution TEM, X-ray photoelectron spectroscopy, and Fourier-transform infrared spectroscopy. The amounts of carbon and nitrogen sources affect the morphology and photocatalytic performance. At low amounts of the sources, the Ndoped carbon nanostructure is an amorphous film and is well-combined with TiO2-x nanoparticles through surface carbon–oxygen groups. At high amounts of the sources, N-doped carbon quantum dots (NCQDs) were obtained, and carbon atoms could substitute for oxygen atoms in the TiO2 lattice to form Ti–C structures, which are responsible for the high photocatalytic activity under visible light illumination. Transient photocurrent response and electrochemical impedance spectroscopy results indicate that the amorphous hybrid film becomes a trap for electrons and that NCQDs can accelerate electron transfer. The improved visible light photocatalytic property for the TiO2-x/NCQDs composite can be attributed to the enhancement of light absorption and inhibition of the photogenerated electron–hole recombination of anchored NCQDs.
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Liu, Chunping,Lin, Haili,Gao, Shanmin,Yin, Ping,Guo, Lei,Huang, Baibiao,Dai, Ying Korean Chemical Society 2014 Bulletin of the Korean Chemical Society Vol.35 No.2
$AgI/AgCl/H_2WO_4$ double heterojunctions photocatalyst was prepared via deposition-precipitation followed by ion exchange method. The structure, crystallinity, morphology, chemical content and other physical-chemical properties of the samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive x-ray spectra (EDX), UV-vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL). The photocatalytic activity of the $AgI/AgCl/H_2WO_4$ was evaluated by degrading methyl orange (MO) under visible light irradiation (${\lambda}$ > 400 nm). The double heterojunctions photocatalyst displayed more efficient photocatalytic activity than pure AgI, AgCl, $H_2WO_4$ and AgCl/$H_2WO_4$. Based on the reactive species and energy band structure, the enhanced photocatalytic activity mechanism of $AgI/AgCl/H_2WO_4$ was discussed in detail. The improved photocatalytic performance of $AgI/AgCl/H_2WO_4$ double heterojunctions could be ascribed to the enhanced interfacial charge transfer and the inhibited recombination of electron-hole pairs, which was in close relation with the $AgI/AgCl/H_2WO_4$ heterojunctions formed between AgI, AgCl and $H_2WO_4$.
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Chunping Liu,Haili Lin,Shanmin Gao,Ping Yin,Lei Guo,Baibiao Huang,Ying Dai 대한화학회 2014 Bulletin of the Korean Chemical Society Vol.35 No.2
AgI/AgCl/H2WO4 double heterojunctions photocatalyst was prepared via deposition-precipitation followed by ion exchange method. The structure, crystallinity, morphology, chemical content and other physical-chemical properties of the samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive x-ray spectra (EDX), UV–vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL). The photocatalytic activity of the AgI/AgCl/H2WO4 was evaluated by degrading methyl orange (MO) under visible light irradiation (λ> 400 nm). The double heterojunctions photocatalyst displayed more efficient photocatalytic activity than pure AgI, AgCl, H2WO4 and AgCl/H2WO4. Based on the reactive species and energy band structure, the enhanced photocatalytic activity mechanism of AgI/AgCl/H2WO4 was discussed in detail. The improved photocatalytic performance of AgI/AgCl/H2WO4 double heterojunctions could be ascribed to the enhanced interfacial charge transfer and the inhibited recombination of electron-hole pairs, which was in close relation with the AgI/AgCl/H2WO4 heterojunctions formed between AgI, AgCl and H2WO4.
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