• Journal of Electrochemical Science and Technology
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• v.10 no.3
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• pp.294-301
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• 2019

The quasi-solid-state hybrid electrolytes were synthesized by chemical cross-linking reaction of methacrylate-functionalized $SiO_2$ ($MA-SiO_2$) and tetra (ethylene glycol) diacrylate in aqueous electrolyte. A quasi-solid-state electrolyte synthesized by 6 wt.% $MA-SiO_2$ exhibited a high ionic conductivity of $177mS\;cm^{-1}$ at room temperature. The electrochemical $H_2$ sensor assembled with quasi-solid-state electrolyte showed relatively fast response and high sensitivity for hydrogen gas at ambient temperature, and exhibited better durability and stability than the liquid electrolyte-based sensor. The simple construction of the sensor and its sensing characteristics make the quasi-solid-state hydrogen sensor promising for practical application.

• Journal of Electrochemical Science and Technology
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• v.10 no.2
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• pp.206-213
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• 2019

The development of simple methods for As detection has received great attention because As is a toxic chemical element causing environmental and health-related issues. In this work, the effect of nanostructures of Au electrodes on their electroanalytical performance during As detection was investigated. Different Au nanostructures with various surface morphologies such as nanoplate Au, nanospike Au, and dendritic Au structures were prepared, and their electrochemical behaviors toward square-wave anodic stripping voltammetric As detection were examined. The difference in intrinsic efficiency for As detection between nanostructured and flat Au electrodes was explained based on the crystallographic orientations of Au surfaces, as examined by the underpotential deposition of Pb. The most efficient As detection performance was obtained with nanoplate Au electrodes, and the effects of the pre-deposition time and interference on As detection of the nanoplate Au electrodes were also investigated.

• Transactions of the Korean hydrogen and new energy society
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• v.31 no.6
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• pp.578-586
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• 2020

There is growing interest worldwide in a hydrogen economy that uses hydrogen as an energy medium instead of hydrocarbon-based fossil fuels as a way to combat climate change. Since hydrogen has a very low energy density per unit volume at room temperature, hydrogen must be compressed and stored in order to use as an energy carrier. There are mechanical and non-mechanical methods for compressing hydrogen. The mechanical method has disadvantages such as high energy consumption, durability problems of moving parts, hydrogen contamination by lubricants, and noise. Among the non-mechanical compression methods, electrochemical compression consumes less energy and can compress hydrogen with high purity. In this paper, research trends are reviewed, focusing on research papers on electrochemical hydrogen compression technology, and future research directions are suggested.

• Journal of Electrochemical Science and Technology
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• v.12 no.2
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• pp.266-271
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• 2021

A commercial PbO₂ electrode was adopted as the anode for the electrochemical degradation of the real textile effluent with the initial COD of 56.0 mg L^-1 and the stainless steel plate as the cathode. The effect of the initial pH, the electrolyte flow rate and the cell voltage on the COD, the current efficiency and the energy consumption were investigated without the addition of NaCl or Na₂SO₄. The experimental results illustrated that the PbO₂ electrode can reduce the COD of the textile effluent from 56.0 mg L^-1 to 26.0 mg L^-1 with the current efficiency of 86.1% and the energy consumption of 17.5 kWh kg^-1 (per kilogram of degraded COD) under the optimal operating conditions. Therefore PbO₂ electrode as the anode was promising to further electrochemically degrade the real textile effluent.

• Journal of Electrochemical Science and Technology
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• v.13 no.4
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• pp.486-496
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• 2022

The effect of solution-treated on the self-corrosion performance and discharge performance of AZ91 magnesium alloy as anode material was analyzed by microscopic characterization, immersion tests, electrochemical measurements, and discharge performance tests. The study shows that the β-phase in the AZ91 magnesium alloy gradually dissolved in the matrix with the increase of the solution temperature, and the electrochemical activity of the magnesium alloy anode was significantly improved. Through the comparison of three different solution-treated processes, it is found that the AZ91 magnesium alloy has the most vigorous activity and better discharge performance after solution-treated of 415℃+12 h. In addition, the proportion and distribution of β-phase AZ91 magnesium alloy have a direct impact on its discharge performance as an anode material.

• Journal of Electrochemical Science and Technology
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• v.13 no.2
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• pp.167-176
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• 2022

Electrochemical impedance spectroscopy (EIS) is a unique non-destructive technique employed to analyze various devices in different energy storage applications. It characterizes materials and interfaces for their properties in heterogeneous systems employing equivalent circuits as models. So far, it has been used to analyze the performance of various photovoltaic cells, fuel cells, batteries, and other energy storage devices, through equivalent circuit designing. This review highlights the diverse applications of EIS in fuel cells and specific parameters affecting its performance. A particular emphasis has been laid on the challenges faced by this technique and their possible solutions.

• Transactions of the Korean hydrogen and new energy society
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• v.35 no.2
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• pp.168-174
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• 2024

The electrochemical hydrogen compressor was run under diverse operating conditions in order to probe its capabilities and limitations. It was found that, unlike single-cell operations, the electrochemical hydrogen compressor stack performance improved with a rise in temperature. This improvement in performance was attributed to the gradual weakening of the electro-osmotic drag over time, impacting membrane resistance. As a result of these experiments, compression levels, up to an impressive 120 bar, using the electrochemical hydrogen serial stack were achieved.

• Journal of Electrochemical Science and Technology
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• v.15 no.1
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• pp.152-160
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• 2024

In this study, ZnCo₂O₄ nanoparticles were synthesized via the coprecipitation method using different annealing temperatures from 200℃ to 800℃. By varying the treatment temperature, the morphology changed from amorphous to tetragonal, and finally to polygonal particles. As temperature increased, the sizes of the nanoparticles also changed from 5 nm at 200℃ to approximately 500 nm at 800℃. The fabricated material was used to modify the working electrode of a screen-printed carbon electrode (SPE), which was subsequently used to survey the detection performance of the antibiotic, chloramphenicol (CAP). The electrochemical results revealed that the material exhibits a good response to CAP. Further, the sample that annealed at 600℃ displayed the best performance, with a linear range of 1-300 μM, and a limit of detection (LOD) of 0.15 μM. The sensor modified with ZnCo₂O₄ also exhibited the potential for utilitarian application when the recovery in a real sample was above 97%.

• Nuclear Engineering and Technology
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• v.56 no.1
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• pp.42-47
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• 2024

The electrochemical extraction of uranium in ternary low melting LiCl-KCl-CsCl eutectic on inert and reactive electrodes via different electrochemical techniques was investigated. It was established that the electrochemical reduction process of U(III) ions on the inert W electrode was irreversible and proceeded in one stage. On reactive liquid Ga and liquid Cd electrodes the reduction of uranium ions took place with the considerable depolarization with the formation of UGa₂, UGa₃ and UCd₁₁ intermetallic compounds. Thermodynamic characteristics of uranium compounds and alloys were calculated. The conditions for the extraction of uranium from the electrolyte in the form of alloys on both liquid reactive electrodes via potentiostatic electrolysis were found.

• Journal of Korean Society of Water and Wastewater
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• v.21 no.4
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• pp.375-383
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• 2007

Treatment efficiency research was performed using Fenton process and the electrochemical process in the presence of ferrous ion and hydrogen peroxide for the industrial wastewater including 1,4-Dioxane produced during polymerization of polyester. The Fenton process and the electrochemical Iron Redox Reaction (IRR) process were applied for this research to use hydroxyl radical as the powerful oxidant which is continuously produced during the redox reaction with iron ion and hydrogen peroxide. The results of $COD_{Cr}$ and the concentration of 1,4-Dioxane were compared with time interval during the both processes. The rapid removal efficiency was obtained for Fenton process whereas the slow removal efficiency was occurred for the electrochemical IRR process. The removal efficiency of $COD_{Cr}$ for 310 minutes was 84% in the electrochemical IRR process with 1,000 mg/L of iron ion concentration, whereas it was 91% with 2,000 mg/L of iron ion concentration. The lap time to remove all of 1,4-Dioxane, 330 mg/L in the wastewater took 150 minutes with 1,000 mg/L of iron ion concentration, however it took 120 minutes with 2,000 mg/L of iron ion concentration in the electrochemical IRR process.