• Applied Science and Convergence Technology
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• v.25 no.6
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• pp.162-165
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• 2016

APhotocatalysis process uses ambient oxygen from air and irradiation, fundamentally UV light, to generate oxidation and reduction which can degrade almost all harmful organic and inorganic compounds to nontoxic substances. This study was focused on enhancement of photocatalytic activity which improves the photocatlytic efficiency with $TiO_2$ particle by mixing of certain amounts of Zn particles. We analyzed degradation of organic pollutant materials such as toluene and phenol with the mixed photocatalysis by using UV-visible spectrophotometer and obtained a result that photocatalytic activity is increased with increasing amount of Zn particle. Especially, in the case of $TiO_2$ (1 mmol) and Zn (0.1 mmol) mixture photocatalyst, we obtained at least 2 times higher photocatalytic activity compared with the commercially available $TiO_2$ photocatalyst (Degussa P-25), indicating that our mixed photocatalyts (Zn-doped $TiO_2$) is very effective of removing both organic dye and pollutants and the conversion rate of toluene is much faster than that of phenol.

• Proceedings of the Korean Vacuum Society Conference
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• 2010.02a
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• pp.349-349
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• 2010

$TiO_2$ thin films were prepared on C fibers, and photocatalytic activity of these films for removing gas-phase toluene was studied. $TiO_2$ films were deposited on C fiber with 0.5 A-per-cycle growth rate by Atomic Layer Deposition (ALD) using TTIP (titanium tetra-isopropoxide) and $H_2O$ as precursors. The catalysts were characterized by Brunauer-Emmett-Teller (BET) for surface area and Scanning Electron Microscope (SEM) for morphology, respectively. Moreover, the samples were further characterized by X-ray Photoelectron Spectroscopy (XPS). As a function of $TiO_2$ thickness, no significant change in the photocatalytic activity could be identified. Interestingly, the bare-carbon fiber showed an even higher photocatalytic activity than the $TiO_2$ thin films for removing toluene. Origin of the high photocatalytic activity of the bare C fiber is discussed.

• Journal of the Korean Vacuum Society
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• v.22 no.3
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• pp.138-143
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• 2013

Recently, ZnO nanoparticles have been studied in various application fields due to their physico-chemical properties. In this study, we have researched on the ZnO photocatalytic activity by redox reaction. ZnO nanoparticles have low photocatalytic activity in comparison with $TiO_2$ nanoparticles because it has the disadvantage that the formation of $Zn(OH)_2$ in water solvent. Therefore, we were synthesized ZnO nanoparticles by spray-pyrolysis method, and then studied on stability in water solvent. At the results, the water treated-ZnO nanoparticles showed higher photocatalytic activity than non-treated ZnO nanoparticles because molecular $H_2O$ was increased onto the ZnO surface under the water treatment. Also, we confirmed that the ZnO nanoparticles synthesized by spray-pyrolysis method is very stable in the water solvent.

• Journal of Powder Materials
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• v.23 no.6
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• pp.458-465
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• 2016

A $TiO_2$/CNT nanohybrid photocatalyst is synthesized via sol-gel route, with titanium (IV) isopropoxide and multi-walled carbon nanotubes (MWCNTs) as the starting materials. The microstructures and phase constitution of the nanohybrid $TiO_2$/CNT (0.005wt%) samples after calcination at $450^{\circ}C$, $550^{\circ}C$ and $650^{\circ}C$ in air are compared with those of pure $TiO_2$ using field-emission scanning electron microscopy and X-ray diffraction, respectively. In addition, the photocatalytic activity of the nanohybrid is compared with that of pure $TiO_2$ with regard to the degradation of methyl orange under visible light irradiation. The $TiO_2$/CNT composite exhibits a fast grain growth and phase transformation during calcination. The nanocomposite shows enhanced photocatalytic activity under visible light irradiation in comparison to pure $TiO_2$ owing to not only better adsorption capability of CNT but also effective electron transfer between $TiO_2$ and CNTs. However, the high calcination temperature of $650^{\circ}C$, regardless of addition of CNT, causes a decrease in photocatalytic activity because of grain growth and phase transformation to rutile. These results such as fast phase transformation to rutile and effective electron transfer are related to carbon doping into $TiO_2$.

• Bulletin of the Korean Chemical Society
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• v.24 no.1
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• pp.49-54
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• 2003

TiO₂nanoparticles were synthesized using the metallorganic chemical vapor deposition process. Particles with and without metal ion dopants were obtained. X-ray photoelectron and energy dispersive X-ray spectroscopic measurements confirmed the stoichiometry of the TiO₂nanoparticles. X-ray diffraction patterns showed a polycrystalline anatase structure of TiO₂. Transmission electron microscopy revealed that these particles are of nanoscale dimensions. Exact particle size and size distribution analyses were carried out by dynamic light scattering. The average particle size was determined to be 22 nm. The nanosize particles provided large surface area for photocatalysis and a large number of free surface-charge carriers, which are crucial for the enhancement of photocatalytic activity. To improve the photocatalytic activity, metal ions, including transition metal ions $(Pd^{2+},\;Pt^{4+},\;Fe^{3+})$ and lanthanide ion $(Nd^{3+})$ were added to pure TiO₂nanoparticles. The effects of dopants on photocatalytic kinetics were investigated by the degradation of 2-chlorophenol under an ultraviolet light source. The results showed that the TiO₂nanoparticles with the metal ion dopants have higher photocatalytic activity than undoped TiO₂. The $Nd^{3+}$ ion of these dopant metal ions showed the highest catalytic activity. The difference in the photocatalytic activity with different dopants is related to the different ionic radii of the dopants.

• Korean Journal of Materials Research
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• v.20 no.3
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• pp.117-124
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• 2010

Titanium dioxide ($TiO_2$) particles deposited on different quantitative Fe-treated carbon nanotube (CNT) composites with high photocatalytic activity of visible light were prepared by a modified sol-gel method using TNB as a titanium source. The composites were characterized by BET, XRD, SEM, TEM and EDX, which showed that the BET surface area was related to the adsorption capacity for each composite. From TEM images, surface and structural characterization of for the CNT surface had been carried out. The XRD results showed that the Fe-ACF/$TiO_2$ composite mostly contained an anatase structure with a Fe-mediated compound. EDX results showed the presence of C, O, and Ti with Fe peaks in the Fe-CNT/$TiO_2$ composites. The photocatalytic activity of the composites was examined by degradation of methylene blue (MB) in aqueous solution under visible light, which was found to depend on the amount of CNT. The highest photocatalytic activity among the different composites was related to the optimal content of CNT in the Fe-CNT/$TiO_2$ composites. In particular, the photocatalytic activity of the Fe-CNT/$TiO_2$ composites under visible light was better than that of the CNT/$TiO_2$ composites due to the introduction of Fe particles.

• 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.

• Rapid Communication in Photoscience
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• v.4 no.1
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• pp.19-21
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• 2015

Zeolite is an ideal host material for encapsulating nano-size metal catalyst species because of its defined microporous structure, prominent adsorption/condensation properties, high surface area, chemical/thermal stability, and transparency to light. In this study, $TiO_2$ photocatalyst was incorporated in highly hydrophobic Y zeolite and its photocatalytic activity was examined in the photocatalytic oxidation of olefins under UV-light irradiation using molecular oxygen as an oxygen source. $TiO_2$ nanoparticles incorporated in hydrophobic Y zeolite exhibited a markedly enhanced photocatalytic activity compared with bare $TiO_2$ owing to its excellent affinity toward organic moieties, which facilitates the mass transfer of organic substrates and allows them to efficiently access to the neighboring active $TiO_2$ surface.

• Journal of the Korean Ceramic Society
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• v.48 no.3
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• pp.211-216
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• 2011

Nickel oxide-doped ACF and $TiO_2$ composites (NiO/ACF/$TiO_2$) were prepared by a sol-gel method. The composite obtained was characterized by BET surface area measurements, X-ray diffraction, transmission electron microscopy and energy dispersive X-ray analysis. A methylene blue (MB) solution under visible light irradiation was used to determine their photocatalytic activity. Excellent photocatalytic degradation of the MB solution was observed using the $TiO_2$, Ti-ACF and NiO/ACF/$TiO_2$ composite under visible light.

• Bulletin of the Korean Chemical Society
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• v.31 no.6
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• pp.1661-1664
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• 2010

The photocatalytic decomposition of toluene vapor by bare and $TiO_2$-coated carbon fibers was studied. Atomic layer deposition (ALD) was used to perform the $TiO_2$ coating. We show that, under our conditions, the photocatalytic activity of bare carbon fibers was comparable with that of $TiO_2$ films, which are known to be good photocatalysts. The origin of the high photocatalytic activity of bare carbon fibers is discussed.