• Journal of the Korean Vacuum Society
• /
• v.9 no.1
• /
• pp.48-59
• /
• 2000

Electrochromic NiO films were prepared by using an electron-beam deposition method. The influence of the preparation conditions, especially the substrate temperature, on the electrochemical stability of film was investigated. The optical properties and stability of as-deposited films strongly depended on the substrate temperature during deposition. The NiO film prepared at a substrate temperature of 150~$200^{\circ}C$ was found to be the stabel when subjected to 5000cycles in a 0.5M solution of KOH between -6.0 and +0.8V. The best electrochromic parameters after 5000cycles were obtained for samples with substrate temperature of $150^{\circ}C$. The obtained electrochromic parameters are CE=-0.049($\lambda$=550nm), $\Delta$OD=0.88($\lambda$=550nm)$\textrm{cm}^2$/mC, Qin=-18.11mC/$\textrm{cm}^2$ and Qleft= 14.8mC/$\textrm{cm}^2$.

• Journal of the Korean Electrochemical Society
• /
• v.4 no.2
• /
• pp.47-52
• /
• 2001

AAO template having nano scale pores of high aspect ratio has been prepared through anodizing of aluminum foil in sulfuric acid electrolyte. The effect of anodizing parameters on the pore size and distribution was also examined to obtain the proper AAO as a template material of nanowire. The surface of AAO template prepared was observed by SEM to examine the mean size and distribution of pores generated by the anodizing and Fe nanowires obtained by AC electroforming using AAO template were also observed with TEM to determine the length and shape of them. From the results of work, it was found that the mean size or distribution of pores was influenced significantly by the anodizing parameters such as voltage and temperature of electrolyte. Mean length and aspect ratio of Fe nanowires prepared in the work were found to be $10{\mu}m\;and\;300\;to\;1,000$, respectively.

• Journal of Electrochemical Science and Technology
• /
• v.1 no.1
• /
• pp.31-38
• /
• 2010

In this study, we have demonstrated the fine structure effect of PdCo electrocatalyst on oxygen reduction reaction activity with different alloy composition and heat-treatment time. In order to identify the intrinsic factors for the electrocatalytic activity, various X-ray analyses were used, including inductively coupled plasma-atomic emission spectrometer, transmission electron microscopy, X-ray diffractometer, and X-ray Absorption Spectroscopy technique. In particular, extended X-ray absorption fine structure was employed to extract the structural parameters required for understanding the atomic distribution and alloying extent, and to identify the corresponding simulated structures by using FEFF8 code and IFEFFIT software. The electrocatalytic activity of PdCo alloy nanoparticles for the oxygen reduction reaction was evaluated by using rotating disk electrode technique and correlated to the change in structural parameters. We have found that Pd-rich surface was formed on the Co core with increasing heating time over 5 hours. Such core shell structure of PdCo/C showed that a superior oxygen reduction reaction activity than pure Pd/C or alloy phase of PdCo/C electrocatalysts, because the adsorption energy of adsorbates was apparently reduced by lowering the dband center of the Pd skin due to a combination of the compressive strain effect and ligand effect.

• Journal of Electrochemical Science and Technology
• /
• v.13 no.4
• /
• pp.438-452
• /
• 2022

For cuboid and ellipsoid crystallites of LiFePO₄ powders, by X-ray diffraction (XRD) and microscopic (TEM) studies, it is possible to determine the anisotropic parameters of the crystallite size distribution functions. These parameters were used to describe the cathode rate capability within the model of averaging the diffusion coefficient D over the length of the crystallite columns along the [010] direction. A LiFePO₄ powder was chosen for testing the developed model, consisting of big cuboid and small ellipsoid crystallites (close to them). When analyzing the parts of big and small rate capabilities, the fitting values D = 2.1 and 0.3 nm²/s were obtained for cuboids and ellipsoids, respectively. When analyzing the results of cyclic voltammetry using the Randles-Sevcik equation and the total area of projections of electrode crystallites on their (010) plane, slightly different values were obtained, D = 0.9 ± 0.15 and 0.5 ± 0.15 nm²/s, respectively. We believe that these inconsistencies can be considered quite acceptable, since both methods of determining D have obvious sources of error. However, the developed method has a clearly lower systematic error due to the ability to actually take into account the shape and statistics of crystallites, and it is also useful for improving the accuracy of the Randles-Sevcik equation. It has also been demonstrated that the shape engineering of crystallites, among other tasks, can increase the cathode capacity by 15% by increasing their size correlation coefficients.

• Journal of Internet of Things and Convergence
• /
• v.9 no.3
• /
• pp.93-98
• /
• 2023

In this paper, an artificial neural network based on simulated annealing was constructed. The mapping relationship between the parameters of micro-scaled flow channels electrochemical machining and the channel shape was established by training the samples. The depth and width of micro-scaled flow channels electrochemical machining on stainless steel surface were predicted, and the flow channels experiment was carried out with pulse power supply in NaNO3 solution to verify the established network model. The results show that the depth and width of the channel predicted by the simulated annealing artificial neural network with "4-7-2" structure are very close to the experimental values, and the error is less than 5.3%. The predicted and experimental data show that the etching degree in the process of channels electrochemical machining is closely related to voltage and current density. When the voltage is less than 5V, a "small island" is formed in the channel; When the voltage is greater than 40V, the lateral etching of the channel is relatively large, and the "dam" between the channels disappears. When the voltage is 25V, the machining morphology of the channel is the best.

• Proceedings of the Korean Vacuum Society Conference
• /
• 2012.08a
• /
• pp.86-86
• /
• 2012

The new approaches for silicon solar cell of new concept have been actively conducted. Especially, solar cells with wire array structured radial p-n junctions has attracted considerable attention due to the unique advantages of orthogonalizing the direction of light absorption and charge separation while allowing for improved light scattering and trapping. One-dimenstional semiconductor nano/micro structures should be fabricated for radial p-n junction solar cell. Most of silicon wire and/or pillar arrays have been fabricated by vapour-liquid-solid (VLS) growth because of its simple and cheap process. In the case of the VLS method has some weak points, that is, the incorporation of heavy metal catalysts into the growing silicon wire, the high temperature procedure. We have tried new approaches; one is electrochemical etching, the other is noble metal catalytic etching method to overcome those problems. In this talk, the silicon pillar formation will be characterized by investigating the parameters of the electrochemical etching process such as HF concentration ratio of electrolyte, current density, back contact material, temperature of the solution, and large pre-pattern size and pitch. In the noble metal catalytic etching processes, the effect of solution composition and thickness of metal catalyst on the etching rate and morphologies of silicon was investigated. Finally, radial p-n junction wire arrays were fabricated by spin on doping (phosphor), starting from chemical etched p-Si wire arrays. In/Ga eutectic metal was used for contact metal. The energy conversion efficiency of radial p-n junction solar cell is discussed.

• Transactions of the Korean Society of Mechanical Engineers B
• /
• v.40 no.11
• /
• pp.697-704
• /
• 2016

Coal modified by acid treatment was investigated to analyze the correlation between the cell performance and electrochemical parameters in a direct carbon fuel cell (DCFC). The fuels were subjected to thermogravimetry analysis, gas adsorption test, and X-ray photoelectron spectroscopy to investigate the fuel properties and surface characteristics. After the treatment of raw coal, the thermal reactivity of the treated fuels increased, and the specific surface area decreased, though the mean pore diameters of three fuels were similar. The coal treated by $HNO_3$ showed the highest ratio of oxygen to carbon, and also an increase in the surface oxygen groups on the fuel surface. Through comparison between the fuel surface properties and electrochemical performance, it was confirmed that the surface oxygen groups have an influence on the improvement in the DCFC performance.

• Carbon letters
• /
• v.26
• /
• pp.18-24
• /
• 2018

Pollution of chloride ion-reinforced concrete can trigger active corrosion processes that reduce the useful life of structures. Multifunctional materials used as a counter-electrode by electrochemical techniques have been used to rehabilitate contaminated concrete. Cement-based pastes added to carbonaceous material, fibers or dust, have been used as an anode in the non-destructive Electrochemical Chloride Extraction (ECE) technique. We studied the performance of the addition of Carbon Fiber (CF) in a cement-graphite powder base paste used as an anode in ECE of concretes contaminated with chlorides from the preparation of the mixture. The experimental parameters were: 2.3% of free chlorides, 21 days of ECE application, a Carbon Fiber Volume Fraction (CFVF) of 0.1, 0.3, 0.6, 0.9%, a lithium borate alkaline electrolyte, a current density of $4.0A/m^2$ and a cement/graphite ratio of 1.0 for the paste. The efficiency of the ECE in the traditional technique using metal mesh as an anode was 77.6% and for CFVF of 0.9% it was 90.4%, with a tendency to increase to higher percentages of the CFVF in the conductive cement-graphite paste, keeping the pH stable and achieving a homogeneous ECE in the mass of the concrete contaminated with chlorides.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
• /
• v.16 no.3
• /
• pp.291-299
• /
• 2018

Under a pyro-processing concept, an electrolytic reduction process has been developed to reduce uranium oxide in molten salt by electrochemical means as a part of spent fuel treatment process development. Accordingly, a model based on electrochemical theory is required to design a reactor for the electrolytic reduction process. In this study, a 1D model based on the phase-field theory, which explains phase separation behaviors was developed to simulate electrolytic reduction of uranium oxide. By adopting parameters for diffusion of oxygen elements in a pellet and electrochemical reaction rate at the surface of the pellet, the model described the behavior of inward reduction well and revealed that the current depends on the internal diffusion of the oxygen element. The model for the electrolytic reduction is expected to be used to determine the optimum conditions for large scale reactor design. It is also expected that the model will be applied to simulate the integration of pyro-processing.

• The Transactions of The Korean Institute of Electrical Engineers
• /
• v.65 no.4
• /
• pp.622-627
• /
• 2016

This paper describes the development of a portable potentiostat which can perform square wave voltammetry on electrochemical sensors and wireless transmission of the measured data to a smartphone using Bluetooth. The potentiostat consists of a square wave potential pulse generation circuit for applying the potential pulse to the electrochemical sensor, a reduction/oxidation (or redox) current measurement circuit, and Bluetooth for wireless data transmission to an Android-based smartphone. The measured data are then processed to show the output graph on the smart phone screen in real time. This data transformation into a graph is carried out by developing and installing a simple transformation application software in the Android-based smartphone. This application software also enables the user to set and change the measurement parameters such as the applied voltage range and measured current range at user's convenience. The square voltammetry output data measured with the developed portable potentiostat were almost same as the data of the commercial potentiostat. The measured oxidation peak current with the commercial potentiostat was $11.35{\mu}A$ at 0.26 V and the measured oxidation peak current with the developed system was $12.38{\mu}A$ at 0.25 V. This proves that performance of the developed portable measurement system is comparable to the commercial one.