We used an etching process to control the line-width of screen printed Ag paste patterns. Ag paste was printed on anodized Al substrate to produce a high power LED. In general, Ag paste spreads or diffuses on anodized Al substrate in the process of screen printing; therefore, the line-width of the printed Ag paste pattern increases in contrast with the ideal line-width of the pattern. Smudges of Ag paste on anodized Al substrate were removed by neutral etching process without surface damage of the anodized Al substrate. Accordingly, the line-width of the printed Ag paste pattern was controlled as close as possible to the ideal line-width. When the etched Ag paste pattern was used as a seed layer for electroless Ni plating, the line width of the plated Ni film was similar to the line-width of the etched Ag paste pattern. Finally, in pattern formation by Ag paste screen printing, we found that the accuracy of the line-width of the pattern can be effectively improved by using an etching process before electroless Ni plating.

This study was carried out to investigate the characterization of iron oxide nanotubes (INTs) by anodization method and applied adsorption isotherms and kinetic models for phosphate adsorption. SEM analysis was conducted to examine the INTs surface formation. Further XRD and XPS analysis were performed to observe the crystal structure of INTs before and after phosphate adsorption. AFM analysis was conducted to determine of Fe foil surface before and after anodization. Phosphate stock solution for adsorption experiment was prepared by KH2PO4. The batch experiment was conducted using 20 ml phosphate stock solution and 40 cm3 of INTs in 50 ml conical tube. Adsorption isotherms were applied Langmuir and Freundlich models for adsorption equilibrium test of INTs. Pseudo first order and pseudo second order models were applied for interpretation of adsorption rate by reaction time. The determination coefficient (R2) values of Langmuir and Freundlich models were 0.9157 and 0.8876 respectively.

In this study, we demonstrate the photoelectrochromic devices composed of TiO2 and WO3 nanostructuresprepared by anodization method. The morphology and the crystal structure of anodized TiO2 nanotubes and WO3 nan-oporous layers are investigated by SEM and XRD. To fabricate a transparent photoelectrode on FTO substrate, a TiO2nanotube membrane, which has been detached from Ti substrate, is transferred to FTO substrate and annealed at 450°Cfor 1 hr. The photoelectrode of TiO2 nanotube and the counter electrode of WO3 nanoporous layer are assembled andthe inner space is filled with a liquid electrolyte containing 0.5 M LiI and 5 mM I2 as a redox mediator. The propertiesof the photoelectrochromic devices is investigated and Pt-WO3 electrode system shows better electrochromic perform-ance compared toWO3 electrode.

Anodic aluminum oxide (AAO) has been widely used for the development and fabrication of nano-powder with various morphologies such as particle, wire, rod, and tube. So far, many researchers have reported about shape control and fabrication of AAO films. However, they have reported on the shape control with different diameter and length of anodic aluminum oxide mainly. We present a combined mild-hard (or hard-mild) anodization to prepare shape-controlled AAO films. Two main parameters which are combination mild-hard (or hard-mild) anodization and run-time of voltage control are applied in this work. The voltages of mild and hard anodization are respectively 40 and 80 V. Anodization was conducted on the aluminum sheet in 0.3 mole oxalic acid at 4oC. AAO films with morphologies of varying interpore distance, branch-shaped pore, diameter-modulated pore and long funnel-shaped pore were fabricated. Those shapes will be able to apply to fabricate novel nano-materials with potential application which is especially a support to prevent volume expansion of inserted active materials, such as metal silicon or tin powder, in lithium ion battery. The silicon powder electrode using an AAO as a support shows outstanding cycle performance as 1003 mAh/g up to 200 cycles.

Vertically oriented nickel nanowire arrays with a different diameter and length are synthesized in porous anodic aluminium oxide templates by an electrodeposition method. The pore diameters of the templates are adjusted by controlling the anodization conditions and then they are utilized as templates to grow nickel nanowire arrays. The nickel nanowires have the average diameters of approximately 25 and 260 nm and the crystal structure, morphology and microstructure of the nanowires are systematically investigated using XRD, FE-SEM and TEM analysis. The nickel nanowire arrays show a magnetic anisotropy with the easy axis parallel to the nanowires and the coercivity and remanence enhance with decreasing a wire diameter and increasing a wire length.

In this study, in order to increase surface ability of hardness and corrosion of magnesium alloy, anodizingand sealing with nano-diamond powder was conducted. A porous oxide layer on the magnesium alloy was successfullymade at 85℃ through anodizing. It was found to be significantly more difficult to make a porous oxide layer in themagnesium alloy compared to an aluminum alloy. The oxide layer made below 73℃ by anodizing had no porous layer.The electrolyte used in this study is DOW 17 solution. The surface morphology of the magnesium oxide layer wasinvestigated by a scanning electron microscope. The pores made by anodizing were sealed by water and aqueous nano-diamond powder respectively. The hardness and corrosion resistance of the magnesium alloy was increased by the anod-izing and sealing treatment with nano-diamond powder.

ZrO2 films were coated on aluminum etching foil by the sol-gel method to apply ZrO2 as a dielectric material in an aluminum(Al) electrolytic capacitor. ZrO2 films annealed above 450˚C appeared to have a tetragonal structure. The withdrawal speed during dip-coating, and the annealing temperature, influenced crack-growth in the films. The ZrO2 films annealed at 500˚C exhibited a dielectric constant of 33 at 1 kHz. Also, uniform ZrO2 tunnels formed in Al etch-pits 1μm in diameter. However, ZrO2 film of 100-200 nm thickness showed the withstanding voltage of 15 V, which was unsuitable for a high-voltage capacitor. In order to improve the withstanding voltage, ZrO2-coated Al etching foils were anodized at 300 V. After being anodized, the Al2O3 film grew in the directions of both the Al-metal matrix and the ZrO2 film, and the ZrO2-coated Al foil showed a withstanding voltage of 300 V. However, the capacitance of the ZrO2-coated Al foil exhibited only a small increase because the thickness of the Al2O3 film was 4-5 times thicker than that of ZrO2 film.

In this study, an aluminum oxide layer for sealing treatment of nano-diamond powder was synthesized byanodizing under constant current. The produced pore size and oxide thickness were investigated using scanning electronmicroscopy. The pore size increased as the treatment time increased, current density increased, sulfuric acid concentra-tion decreased, which is different from the results under constant voltage, due to a dissolution of the oxide layers. Theoxide layer thickness by the anodizing increased as temperature, time, and current density increased. The results of thisstudy can be applied to optimize the sealing treatment process of nano-diamond particles of 4-10 nm to enhance theresistances of corrosion and wear of the matrix.

Electrochemical surface treatment is commonly used to form a thin, rough, and porous oxidation layer on the surface of titanium. The purpose of this study was to investigate the formation of nanotubular titanium oxide arrays during short anodization processing. The specimen used in this study was 99.9% pure cp-Ti (ASTM Grade II) in the form of a disc with diameter of 15 mm and a thickness of 1 mm. A DC power supplier was used with the anodizing apparatus, and the titanium specimen and the platinum plate (3mm×4mm×0.1mm) were connected to an anode and cathode, respectively. The progressive formation of TiO2 nanotubes was observed with FE-SEM (Field Emission Scanning Electron Microscopy). Highly ordered TiO2 nanotubes were formed at a potential of 20 V in a solution of 1M H3PO4 + 1.5 wt.% HF for 10 minutes, corresponding with steady state processing. The diameters and the closed ends of TiO2 nanotubes measured at a value of 50 cumulative percent were 100 nm and 120 nm, respectively. The TiO2 nanotubes had lengths of 500 nm. As the anodization processing reached 10 minutes, the frequency distribution for the diameters and the closed ends of the TiO2 nanotubes was gradually reduced. Short anodization processing for TiO2 nanotubes of within 10 minutes was established.

Single crystalline Cu nanowires with controlled diameters and aspect ratios have been synthesized using electrochemical deposition within confined nanochannels of a porous anodic aluminium oxide(AAO) template. The diameters of nano-sized cylindrical pores in AAO template were adjusted by controlling the anodization conditions. Cu nanowires with diameters of approximately 38, 99, 274 nm were synthesized by the electrodeposition using the AAO templates. The crystal structure, morphology and microstructure of the Cu nanowires were systematically investigated using XRD, FE-SEM, TEM and SAED. Investigation results revealed that the Cu nanowires had the controlled diameter, high aspect ratio and single crystalline nature.

To compare the photocatalytic performances of titania for purification of waste water according to applied voltages and doping, TiO2 films were prepared in a 1.0 M H2SO4 solution containing NH4F at different anodic voltages. Chemical bonding states of F-N-codoped TiO2 were analyzed using surface X-ray photoelectron spectroscopy (XPS). The photocatalytic activity of the co-doped TiO2 films was analyzed by the degradation of aniline blue solution. Nanotubes were formed with thicknesses of 200-300 nm for the films anodized at 30 V, but porous morphology was generated with pores of 1-2 μm for the TiO2 anodized at 180 V. The phenomenon of spark discharge was initiated at about 98 V due to the breakdown of the oxide films in both solutions. XPS analysis revealed the spectra of F1s at 684.3 eV and N1s at 399.8 eV for the TiO2 anodized in the H2SO4-NH4F solution at 180 V, suggesting the incorporation of F and N species during anodization. Dye removal rates for the pure TiO2 anodized at 30 V and 180 V were found to be 14.0% and 38.9%, respectively, in the photocatalytic degradation test of the aniline blue solution for 200 min irradiation; the rates for the F-N-codoped TiO2 anodized at 30 V and 180 V were found to be 21.2% and 65.6%, respectively. From the results of diffuse reflectance absorption spectroscopy (DRS), it was found that the absorption edge of the F-N-codoped TiO2 films shifted toward the visible light region up to 412 nm, indicating that the photocatalytic activity of TiO2 is improved by appropriate doping of F and N by the addition of NH4F.

Recently, nanotubes have considerably researched because of their novel application about photocatalysis, dye-sensitized solar cells (DSSCs), lithium ion battery, etc. In this work, self-standing nanotube arrays were fabricated by anodic oxidation method using pure Ti foil as a working electrode in ethylene glycole with 0.3M + . Growth behavior of nanotube arrays was compared according to temperature, voltage and time. The morphology, structure and crystalline of anodized nanotube arrays were observed by FE-SEM (field emission scanning electron microscope) and XRD (X-ray diffraction).

Ni nanowires were fabricated using anodic aluminum oxide (AAO) membrane as a template by electrochemical deposition. The nanowires were formed within the walls of AAO template with 200 nm in pore diameter. After researching proper voltage and temperature for electrochemical deposition, the length of Ni nanowires was controlled by deposition time and the supply of electrolyte. The morphology and microstructure of Ni nanowires were investigated by field emission scanning electron microscope (FE-SE), X-ray diffraction (XRD) and transmission electron microscope (TEM).

Self-standing TiO2 nanotube arrays were fabricated by potentiostatic anodic oxidation method using pure Ti foil as a working electrode and ethylene glycol solution as electrolytes with small addition of NH4F and H2O. The influences of anodization temperature and time on the morphology and formation of TiO2 nanotube arrays were investigated. The fabricated TiO2 nanotube arrays were applied as a photoelectrode to dye-sensitized solar cells. Regardless of anodizing temperature and time, the average diameter and wall thickness of TiO2 nanotube show a similar value, whereas the thickness show a different trend with reaction temperature. The thickness of TiO2 nanotube arrays anodized at 20℃ and 30℃ was time-dependent, but on the other hand its at 10℃ are independent of anodization time. The conversion efficiency is low, which is due to a morphology breaking of the TiO2 nanotube arrays in manufacturing process of photoelectrode.

목적: 본 연구에서는 양극산화방법을 이용하여 착색된 티타늄 안경테의 산화막 두께에 따른 색상을 광 반사 스펙트럼을 통해서 규명하고자 한다. 방법: 양극산화 방법 제조 장치를 자체 제작하여 사용하였다. 연구에 사용한 티타늄 안경테원재료 조성은 EDS로 측정하였고, 구조분석은 XRD를 사용하여 X선 회절선으로부터 구하였다. 광 반사 측정은 UV-VIS-NIR spectrophotometer에 부착된 적분구를 사용했다. 결과 및 고찰: 조성 분석한 결과는 티타늄(Ti)이 97.09%와 탄소(C)2.91%로 합성된 합금으로 해석되었고, 구조는 Hexagonal이었다. 티타늄 안경테 재료에 인가 시간을 조정하여 산화막(TiO2) 두께를 변화시킴으로서 다양한 색상을 얻을 수 있었다. 광 반사 스펙트럼을 측정해 보면 양극산화 방법으로 착색한 티타늄 안경테는 양극산화 초기단계에서는 청색영역의 파장에서 하나의 넓은(broad)피크를 갖는 광 반사 스펙트럼이 관측되었고, 양극산화 시간이 진행되어 두께가 두꺼워 질수록 붉은색 영역에서 광 반사가 크게 일어나고, 피크도 분리되는 것을 알 수 있다. 결론: 티타늄 안경테의 색상은 양극산화에 의해 형성된 산화막의 굴절률과 두께에 의존한 광의 간섭효과에 의해서 변화는 것을 알 수 있다.