• Applied Science and Convergence Technology
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• v.24 no.4
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• pp.96-101
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• 2015

Quantitative evaluation of photocatalytic activity of oxide nanoparticles in aqueous solution is quite challenging in that the kinetic reaction rate is determined by a complicated interplay among various limiting factors such as light scattering and absorption, diffusion and adsorption of reactants in condensed liquid phase, photoexcited charge separation and recombination rate, and the exact nature of active sites determined by detailed morphology and crystallinity of nanocrystals. Here, we present our simple experimental results showing that the kinetic regime of a typical photocatalytic degradation experiment over UV-irradiated $TiO_2$ nanoparticles in aqueous solution is in that dominated by the photoactivity of $TiO_2$ and its concentration. This result lays a firm ground of using the measured kinetic reaction rate in evaluating photocatalytic efficiency of oxide nanocrystals under evaluation.

• Proceedings of the Materials Research Society of Korea Conference
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• 2003.11a
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• pp.141-141
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• 2003

Dichlorobenzen과 같은 휘발성 유기물질(Volatile Organic Compound)은 산업폐수 및 폐가스, 폐기물등이 다양한 형태로 대기 중에 존재하면서 심각한 환경문제를 유발시키고 있다 따라서, 본 연구에서는 TiO$_2$에 SiO$_2$를 첨가하여 열처리시 anatase상에서 rutile상으로 전이되는 것을 제어하며 비표면적을 크게 하여 휘발성유기 물질에 대한 광촉매 활성을 증진시키고자 두가지 합성방법, 즉 졸겔 공정과 수열합성 공정을 사용하여, 공정조건을 변화시키면서, 광촉매활성이 가장 우수한 실험조건을 결정하였다.

• Journal of the Korean Ceramic Society
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• v.22 no.4
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• pp.9-14
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• 1985

The quantum efficiency vs. wavelength curves with different reducing treatments for the 99.99% and 98.5% $TiO_2$ ceramic electrodes have been analyzed according to the Schottky barrier model of the semiconductor-elect-rolyte interface, The model allows the main physical parameters governing the photoelectrochemical properties of the semicon-ductor to be determined. According to these data the impurity ions as three valence state ($Fe^{3+})$ in the $TiO_2$ raw materials have great influence on the photoresponse and the $TiO_2$ ceramic electrodes show much lower quantum efficiency than the $TiO_2$ single crystal due to existence of the recombination centers.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.8 no.6
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• pp.1579-1582
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• 2007

The purpose of this study is to compare degrading performance of organic contaminants in aqueous solution using photocatalyst and find an optimal condition for decomposing non-degradable matters. The parameters of this research is light intensity and state of photocatalytic material within reactor. The results showed that Type 3 (terms of plastic beads : $500^{\circ}C$, 3hr) has the greatest reactivity.

• Bulletin of the Korean Chemical Society
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• v.22 no.12
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• pp.1371-1374
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• 2001

Metal doping was adopted to modify TiO2 (P-25) and enhance the photocatalytic degradation of harmful cyanides in aqueous solution. Ni, Cu, Co, and Ag doped TiO2 were found to be active photocatalysts for UV light induced degradation of aqueous cyanides generating cyanate, nitrate and ammonia as main nitrogen-containing products. The photoactivity of Ni doped TiO2 was greatly affected by the state of Ni, that is, the crystal size and the degree of reduction of Ni. The modification effects of some mixed oxides, that is, Ni-Cu/TiO2 were also studied. The activity of Ni-Cu/TiO2 for any ratio of Cu/Ni was higher than that of Ni- or Cu-doped TiO2, and the catalyst at the Cu/Ni ratio of 0.3 showed the highest activity for cyanide conversion.

• Bulletin of the Korean Chemical Society
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• v.31 no.5
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• pp.1128-1134
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• 2010

Nanocarbon supported Fe/$TiO_2$ composite catalysts were prepared using CNTs (carbon nanotubes) and $C_{60}$ (fullerene) as nanocarbon sources by a modified sol-gel method. The Fe/$TiO_2$-nanocarbon composites were characterized by the BET surface area, scanning electron microscope (SEM), Transmission Electron Microscope (TEM), X-ray diffraction (XRD), energy dispersive X-ray (EDX) and UV-vis spectra. In comparison with non-nanocarbon doped Fe/$TiO_2$ composites, the nanocarbon supported Fe/$TiO_2$ composites had higher absorption ability with a larger specific surface area, and showed higher photocatalytic activity during the degradation of methylene blue (MB) under visible light. The reasons for the obvious increase of photocatalytic activity indicated that the photoactivity not only benefits from nanocarbon introduced, but also relates to the cooperative effect of the Fe as a dopant.

• Journal of the Korean Ceramic Society
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• v.52 no.1
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• pp.9-12
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• 2015

Nano-structured electrodes were fabricated to develop efficient photoelectrochemical conversion systems for the synthesis of hydrogen from water and hydrocarbon fuels from $CO_2$. In this work, we compared the photoactivity of rutile $TiO_2$ nanorods grown on FTO and SEED/FTO by a hydrothermal method. An analysis of the microstructures showed that the density of nanorod/SEED/FTO samples, which showed only the (002) peak in their x-ray diffraction patterns, was two times higher than that of a nanorod/FTO sample. The photocurrent density of nanorod/SEED/FTO samples was increased by as much as 40% of the photocurrent density of the nanorod/FTO sample due to the increased specific density of the nanorods. However, the transient time for a recombination of photogenerated electrons and holes was 20 times faster in the nanorod/SEED/FTO. The seed layers are discussed as possible recombination sites.

• Transactions of the Korean hydrogen and new energy society
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• v.16 no.2
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• pp.130-135
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• 2005

Cadmium selenide is one of the group IIb-VI compounds, which is the promising semiconductor material due to its wide range of technological applications in optoelectronic devices such as photoelectrochemical cells, solid state solar cells, thin film photoconductors etc. CdSe has optical band gap of 1.7-1.8eV and proper conduction band edge for water splitting. CdSe films are coated with small thickness(20-50nm) nanocrystalline $TiO_2$ film by electrodeposition or chemical bath deposition methods and PEC properties of CdSe and CdSe/$TiO_2$ sandwich structure are studied. The photoactivity of CdSe and CdSe/$TiO_2$ films deposited on titanium substrate is studied in aqueous electrolyte of 1M NaOH solution. Photocurrent and photovoltage obtained were of the order of 2-4 mA/$cm^2$ and 0.5V, respectively, under the intensity of illumination of 100 mW/$cm^2$.

• Bulletin of the Korean Chemical Society
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• v.35 no.8
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• pp.2512-2518
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• 2014

The praseodymium-doped $TiO_2$ photocatalyst samples, which could degrade methyl orange under UV irradiation, were prepared by sol-microwave method for improving the photocatalytic activity of $TiO_2$. The resulting materials were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), Transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Raman spectra, Fourier transform infrared spectra (FTIR) and Ultraviolet-visible diffuse reflectance spectra (UV-vis DRS). It was found Pr doping retarded the growth of crystalline size and the phase transformation from anatase to rutile, and narrowed the band gap energy. Praseodymium doping brought about remarkable improvement in the photoactivity. The optimal dopant amount of Pr was 2% by molar of cement and the calcination temperature was $500^{\circ}C$ for the best photocatalytic activity. The improvement of photocatalytic activity was ascribed to the occurrence of lattice distortion and the effective containment of the recombination of the electron-hole by $Pr^{3+}$.

• 한국신재생에너지학회:학술대회논문집
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• 2009.11a
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• pp.222-225
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• 2009

In this paper, $TiO_2$ nanotube is prepared and the preparation is influenced by electrochemical etching rate and chemical dissolution rate. Especially, the chemical dissolution rate is lowered as the length $TiO_2$ nanotube increases. Titanium foil were anodized at various bias or current such as 20V, 55V and 0.1A (bath temperature $25^{\circ}C$) in organic electrolytes (ethylene glycol, glycerol) and then annealed at $450^{\circ}C$ and $650^{\circ}C$ to obtain the crystallized tubular $TiO_2$ on the Ti foil. Higher efficiency (89.1%) for the Cr(VI) reduction was obtained with the prepared sample compared to that (20.9%) with the sample in 0.5% HF electrolyte earlier studied.