• Title/Summary/Keyword: Solid-electrolyte

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Properties of Capacity on Carbon Electrode in EC:MA Electrolytes - I. Effect of Mixing Ratio on the Electrochemical Properties - (EC:MA 혼합전해질에서 카본 전극의 용량 특성 - I. 전기화학적 특성에 대한 혼합비의 영향 -)

  • Park, Dong-Won;Kim, Woo-Seong;Son, Dong-Un;Kim, Sung-Phil;Choi, Yong-Kook
    • Applied Chemistry for Engineering
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    • v.17 no.2
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    • pp.183-187
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    • 2006
  • The choice of solvents for electrolytes solutions is very important to improve the characteristics of charge/discharge in the Li-ion battery system. Such solvent systems have been widely investigated as electrolytes for Li-ion batteries. In this paper, the electrochemical properties of the solid electrolyte interphase film formed on carbon anode surface and the solvent decomposition voltage in 1 M LiPF6/EC:MA(x:y) electrolyte solutions prepared from the various mixing volume ratios are investigated by chronopotentiometry, cyclic voltammetry, and impedance spectroscopy. As a result, the solvent decomposition voltages are varied with the ionic conductivity of the electrolyte. Electrochemical properties of the passivation film were different, which are dependent on the mixture ratio of the solvents. Therefore, the most appropriate mixing ratio of EC and MA as a solvent in 1 M $LiPF_6/(EC+MA)$ system for Li-ion battery is approximately 1:3 (EC:MA, volume ratio).

Effect of Plasticizer on Electrolyte Membranes for Dye Sensitized Solar Cells (염료감응형 태양전지를 위한 고분자 전해질막에서의 가소제의 효과)

  • Cho, Doo-Hyun;Jung, Yoo-Young;Yun, Mi-Hye;Kwon, So-Young;Koo, Ja-Kyung
    • Membrane Journal
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    • v.20 no.1
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    • pp.13-20
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    • 2010
  • Using poly(ethylene oxide) (PEO) as a polymer host, poly(ethylene glycol) (PEG) as a plasticizer, potassium iodide and iodine as sources of $I^-/{I_3}^-$ PEO-PEG-KI/$I_2$ polymer gel electrolytes were prepared. Based on the polymer gel electrolytes, solid-state dye-sensitized solar cell(DSSC)s were fabricated. The content of PEG in the electrolyte was changed from 0 to 85%. The electrolyte showed self-supporting form through whole range of the PEG content. As the PEG content increased, the ionic conductivity and ${I_3}^-$ diffusivity increased and the light-to electrical energy conversion efficiency increased under irradiation of 100 $mWcm^{-2}$ simulated sunlight.

Power Densities According to Anode Functional Layers on the Manufactured SOFC Unit Cells Using Decalcomania Method (전사지를 이용 적층한 셀 구조 및 연료극 기능층 형성에 따른 출력 특성)

  • An, Yong-Tae;Ji, Mi-Jung;Gu, Ja-Bin;Choi, Jin-Hoon;Hwang, Hae-Jin;Choi, Byung-Hyun
    • Korean Journal of Materials Research
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    • v.22 no.11
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    • pp.626-630
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    • 2012
  • The properties of SOFC unit cells manufactured using the decalcomania method were investigated. SOFC unit cell manufacturing using the decalcomania method is a very simple process. In order to minimize the ohmic loss of flattened tube type anode supports of solid oxide fuel cells(SOFC), the cells were fabricated by producing an anode function layer, YSZ electrolyte, LSM electrode, etc., on the supports and laminating them. The influence of these materials on the power output characteristics was studied when laminating the components and laminating the anode function layer between the anode and the electrolyte to improve the output characteristics. Regarding the performance of the SOFC unit cell, the output was 246 $mW/cm^2$ at a temperature of $800^{\circ}C$ in the case of not laminating the anode function layer; however, this value was improved by a factor of two to 574 $mW/cm^2$ due to the decrease of the ohmic resistance and polarization resistance of the cell in the case of laminating the anode function layer. The outputs appeared to be as high as 574 and 246 $mW/cm^2$ at a temperature of $800^{\circ}C$ in the case of using decalcomania paper when laminating the electrolyte layer using the in dip-coating method; however, the reason for this is that interfacial adhesion was improved due to the dense structure, which leads to a thin thickness of the electrolyte layer.

The Effect of Electrolyte Concentration for Colloid Adsorption toward a Fluid-Fluid Interface (유체 계면에서 콜로이드 흡착에 대한 전해질 농도의 영향)

  • Park, Bum Jun
    • Korean Chemical Engineering Research
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    • v.51 no.4
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    • pp.527-530
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    • 2013
  • I present the behavior of colloidal adsorption to an oil-water interface in the presence of electrolyte in an aqueous subphase. The optical laser tweezers and the piezo controller are used to trap an individual polystyrene microsphere in water and forcibly transfer it to the interface in the vertical direction. Addition of an electrolyte (i.e., NaCl) in the aqueous subphase enables the particle to attach to the interface, whereas the particle escapes from the trap without the adsorption in the absence of the electrolyte. Based on the analytical calculations of the optical trapping force and the electrostatic disjoining pressure between the particle and the oil-water interface, it is found that a critical energy barrier between them should exist. This study will provide a fundamental understanding for applications of colloidal particles as solid surfactants that can stabilize the immiscible fluid-fluid interfaces, such as emulsions (i.e., Pickering emulsions) and foams.

Effect of Salt Concentration on Electrolyte Membranes for Dye Sensitized Solar Cells (염료감응형 태양전지를 위한 고분자 전해질막에서의 이온농도의 효과)

  • Kwon, So-Young;Yun, Mi-Hye;Cho, Doo-Hyun;Jung, Yoo-Young;Koo, Ja-Kyung
    • Membrane Journal
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    • v.21 no.3
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    • pp.213-221
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    • 2011
  • Using poly(ethylene oxide) (PEO) as a polymer host, poly(ethylene glycol) (PEG) as a plasticizer, potassium iodide and iodine as sources of $I^-/I_3^-$, polymer electrolyte membranes were prepared. Based on the polymer electrolytes, solid-state dye-sensitized solar cell (DSSC)s were fabricated. The content of PEG in the electrolyte was controlled to be 95%. The mole number of KI per 1 mole of EO ([KI]/[EO] ratio) in the electrolyte was changed to be 0.022, 0.044, 0.066 and 0.088. The electrolyte membrane showed wax phase in ambient temperature. The ionic conductivity increased with increasing KI content to reach the maximum value at which [KI]/[EO] ratio is 0.066. After the maximum value, the ionic conductivity decreased with increasing KI content. In the case of DSSC, the Voc decreased continuously with increasing KI content in the polymeric electrolyte membrane. The $J_{SC}$ increased with increasing KI content to show maximum value at which [KI]/[EO] ratio is 0.044. In the higher KI content region, $J_{SC}$ value decreased with increasing KI content.

Analysis of the Phase Formation and the Sinterability of K+-β/β"-Al2O3 at High Temperatures (≥1600 ℃) (K+-β/β"-Al2O3의 고온 상관계와 소결성 분석)

  • Jang, Min-Ho;Kim, Seung-Gyun;Kim, Seok-Jun;Haw, Jung-Rim;Lim, Sung-Ki
    • Applied Chemistry for Engineering
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    • v.20 no.3
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    • pp.317-321
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    • 2009
  • In order to analyze the high temperature phase formation and the sinterability of super ionic conductor $K^+-{\beta}/{\beta}"-Al_2O_3$ which is commonly used as a solid oxide electrolyte, the pure $K^+-{\beta}/{\beta}"-Al_2O_3$ powder in the ternary system $K_2O-LiO_2-Al_2O_3$ was synthesized by solid state reaction and formed to tube and disk using slip casting method and cold isostatic pressing (CIP), respectively. The slip casting was conducted in an alumina mold with the slurry containing 40 wt% of solid contents and the CIP was carried out under 20 MPa. The samples were sintered at $1600^{\circ}C$, $1700^{\circ}C$ and $1750^{\circ}C$, respectively, and their phase formation and the sintering density were investigated according to the forming method. The samples produced by CIP showed far higher ${\beta}"-Al_2O_3$ fraction as compared with those by slip casting. On the other hand, the samples by slip casting showed slightly higher sintering density. The relative density reached to about 83% at $1750^{\circ}C$ and for 1 h, independent of the forming method. In the case of 90 min socking time, the density was decreased owing to the exaggerated grain growth and the pores by $K_2O$ evaporation.

Impedance measurements of solid electrolyte (고체 전해질의 임피던스 측정법)

  • 구할본;김현철
    • Electrical & Electronic Materials
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    • v.7 no.6
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    • pp.543-548
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    • 1994
  • 전기화학반응은 일반적으로 반응속도가 전류에, 반응의 구동력이 과전압에 대응하기 때문에 전류 또는 전위의 경시적 변화로 부터 적극 반응기구나 반응의 과정을 해석하는 법이 널리 이용되고 있다. cyclic voltammetry과 chrono-potentiometry을 비롯한 시간영역에서의 해석에 대해, 전극계의 동적인 특성을 주파수 영역에서 해석하는 것도 가능하며 교류임피던스법이 가장 잘 알려진 방법이다. 여기서는 교류임피던스법의 고찰법, 기본적인 측정법, 몇개의 계에 있어서 임피던스 특성 및 그 방법의 새로운 전개에 대해서 설명한다.

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Effect of Catalyst plated Titanium-mesh Electrodes in Water Electrolysis using Solid Polymer Electrolyte (Ti Mesh처리 촉매전극/SPE 가 전기분해에 미치는 영향)

  • 김연순;박기배;명광식;심규성;한상도
    • Proceedings of the Korea Society for Energy Engineering kosee Conference
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    • 1998.05a
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    • pp.167-171
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    • 1998
  • 수소는 2차 에너지원으로 그 자원이 풍부하며 청정에너지원으로 지구 환경문제를 해결할 수 있는 에너지로 주목을 받고 있다. 현재 무공해 수소를 제조하는 방법으로는 불을 전기 분해하는 방법 이외에 태양에너지 이용법, 바이오기술, 화학순환기술, 화석연료 분해법 등이 보고되고 있으며 모두 기초연구 단계에 있다. 이중에서 전기분해에 의한 수소의 제조기술은 경제성 및 효율향상을 위해 가장 많이 연구되고 있고 이미 우주선, 잠수함 등 특수용도로는 실용화되고 있는 기술이다. (중략)

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Electrochemical Promotion of Pt Catalyst for The Oxidation of Carbon Monoxide

  • Shin, Seock-Jae;Kang, An-Soo
    • Journal of the Korea Safety Management & Science
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    • v.2 no.4
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    • pp.187-195
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    • 2000
  • Electrochemical promotion of the reaction rate was investigated for CO oxidation in a solid electrolyte catalytic reactor where a thin film of Pt was deposited on the yttria stabilized zirconia as an electrode as well as a catalyst. It was shown under open circuit condition that potential was a mixed potential of $O_2$exchange reaction and electrochemical reaction induced by CO. The effect of electrochemical modification on the CO oxidation rate was studied at various overpotentials and $P_{CO}$$P_{O2}$.

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