• 제목/요약/키워드: Cathode reduction

검색결과 244건 처리시간 0.029초

비정질 IZO 애노드를 이용한 형광 유기발광소자의 특성 (Characteristics of Fluorescent Organic Light Emitting Diodes using Amorphous IZO Anode Film)

  • 문종민;배정혁;정순욱;강재욱;김한기
    • 한국전기전자재료학회논문지
    • /
    • 제19권11호
    • /
    • pp.1044-1049
    • /
    • 2006
  • We reported on characteristics of the fluorescent OLED fabricated on commercial ITO/glass and BCS grown IZO/glass substrate, respectively. The amorphous IZO anode film grown by box cathode sputtering(BCS) exhibited similar electrical and optical characteristics to commercial ITO anode even though it was deposited at room temperature. In addition, the amorphous IZO anode showed higher workfunction (5.2 eV) than that of the commercial ITO anode (5.0 eV) after ozone treatment for 10 min. Furthermore, fluorescent OLED fabricated on amorphous IZO anode film showed improved current-voltage-luminance characteristics, external quantum efficiency and power efficiency en contrast with fluorescent OLED fabricated on commercial ITO anode film. It was thought that smooth surface and high workfunction of amorphous IZO anode lead to more efficient hole injection by reduction of interface barrier height between anode and organic layers.

전기화학적 반응을 이용한 질산성 질소의 암모니아성 질소로 전환 (Transformation of Nitrogen in the Form of Nitrate into Ammonia by Electrochemical Reaction)

  • 이재광;김도연;탁용석
    • Korean Chemical Engineering Research
    • /
    • 제46권5호
    • /
    • pp.1013-1016
    • /
    • 2008
  • 본 연구에서는 폐수 내 존재하는 질산성 질소를 제거하기 위해 캐소드물질로 철(Fe), 구리(Cu), 니켈(Ni), 아연(Zn)을 선택하여 전기화학적 환원반응 특성을 조사하였다. $NO_3^-$로부터 $NH_3$로의 변환반응에 있어서 Zn이 가장 우수한 촉매 특성을 가지고있으며, pH 8.5에서 가장 높은 질산성 질소 제거 효율을 나타내었다. 전극표면에서 질산성 질소는 아질산성 질소로 환원된 후, 암모니아성 질소로 전환되는 것을 확인하였으며 암모니아성 질소는 HOCl과의 화학반응을 통하여 질소 형태로 완전히 제거할 수 있었다.

연료전지 자동차용 TMS 히터 개발 (Development of Thermal Management System Heater for Fuel Cell Vehicles)

  • 한수동;김성균;김치명;박용선;안병기
    • 한국수소및신에너지학회논문집
    • /
    • 제23권5호
    • /
    • pp.484-492
    • /
    • 2012
  • The TMS(Thermal Management System) heater in a fuel cell vehicle has been developed to prevent a decline of fuel cell durability and cold start durability. Main functions of the COD(Cathode Oxygen Depletion) heater are depletion of oxygen in a cathode as heat energy and consumption of electric power for rapid warming up of a fuel cell stack. This paper covers subjects including the design specification of a heater, heater controller for detection of overheat and reliability assessment including coolant pressure cycle test of a heater. To verify the design concept, burst pressure and deformation analysis of plastic housing were carried out. Also, temperature distribution analysis of heater surface and coolant inside of housing were carried out to verify the design concept. By designing the plastic housing instead of a steel housing, the 30% weight lightening and 50% cost reduction were attained. A module-based design of a TMS system including a heater or reducing the watt density of a heater is a problem to be solved in the near future work.

EUV 세정에서 정전기 제어를 위한 전해이온수 거동의 분자궤도 이해 (Understanding Behaviors of Electrolyzed Water in Terms of Its Molecular Orbitals for Controlling Electrostatic Phenomenon in EUV Cleaning)

  • 김형원;정윤원;최인식;최병선;김재영;유근걸
    • 반도체디스플레이기술학회지
    • /
    • 제21권4호
    • /
    • pp.6-13
    • /
    • 2022
  • The electrostatic phenomenon seriously issued in extreme ultraviolet semiconductor cleaning was studied in junction with molecular dynamic aspect. It was understood that two lone pairs of electrons in water molecule were subtly different each other in molecular orbital symmetry, existed as two states of large energy difference, and became basis for water clustering through hydron bonds. It was deduced that when hydrogen bond formed by lone pair of higher energy state was broken, two types of [H2O]+ and [H2O]- ions would be instantaneously generated, or that lone pair of higher energy state experiencing reactions such as friction with Teflon surface could cause electrostatic generation. It was specifically observed that, in case of electrolyzed cathode water, negative electrostatic charges by electrons were overlapped with negative oxidation reduction potentials without mutual reaction. Therefore, it seemed that negative electrostatic development could be minimized in cathode water by mutual repulsion of electrons and [OH]- ions, which would be providing excellences on extreme ultraviolet cleaning and electrostatic control as well.

Development of a Mass Transfer Model and Its Application to the Behavior of the Cs, Sr, Ba, and Oxygen ions in an Electrolytic Reduction Process for SF

  • 박병흥;강대승;서중석;박성원
    • 방사성폐기물학회지
    • /
    • 제3권2호
    • /
    • pp.85-93
    • /
    • 2005
  • Isotopes of alkali and alkaline earth metals (AM and AEM) are the main contributors to the heat load and the radiotoxicity of spent fuel (SF) . These components are separated from the SF and dissolved in a molten LiCl in an electrolytic reduction process. A mass transfer model is developed to describe the diffusion behavior of Cs, Sr, and Ba in the SF into the molten salt. The model is an analytical solution of Fick's second law of diffusion for a cylinder which is the shape of a cathode in the electrolytic reduction process. And the model is also applied to depict the concentration profile of the oxygen ion which is produced by the electrolysis of Li$_{2}$O. The regressed diffusion coefficients of the model correlating the experimentally measured data are evaluated to be greater in the order of Ba, Cs, and Sr for the metal ions and the diffusion of the oxygen ion is slower than the metal ions which implies that different mechanisms govern the diffusion of the metal ions and the oxygen ions in a molten LiCl.

  • PDF

AC Impedance Study of Hydrogen Oxidation and Reduction at Pd/Nafion Interface

  • Song, Seong-Min;Koo, Il-Gyo;Lee, Woong-Moo
    • 한국수소및신에너지학회논문집
    • /
    • 제12권3호
    • /
    • pp.231-238
    • /
    • 2001
  • Electrocatalytic activity of palladium for hydrogen oxidation and reduction was studied using AC impedance method. The system under study was arranged in electrolytic mode consisting of Pd electrode under study, Pt counter electrode and Nafion electrolyte between them. Two types of Pd electrodes were used - carbon-supported Pd (Pd/C) and Pd foil electrode. Pd/C anode contacting pure hydrogen showed a steady decrease of charge transfer resistance with the increase of anodic overpotential, which is an opposite trend to that found with Pd foil anode. But Pd foil cathode also exhibited a decrease of the resistance with the increase of cathodic overpotential. The relationship between imposition of overpotential and subsequent change of the charge transfer resistance is determined by the ratio of the rate of faradaic process to the rate of mass transportation; if mass transfer limitation holds, increase of overpotential accompanies the increase of charge transfer resistance. Regardless of the physical type of Pd electrode, the anode contacting hydrogen/oxygen gas mixture did not reveal any independent arc originated from local anodic oxygen reduction.

  • PDF

Fabrication and Characterization of High-activity Pt/C Electrocatalysts for Oxygen Reduction

  • Lim, Bo-Rami;Kim, Joung-Woon;Hwang, Seung-Jun;Yoo, Sung-Jong;Cho, Eun-Ae;Lim, Tae-Hoon;Kim, Soo-Kil
    • Bulletin of the Korean Chemical Society
    • /
    • 제31권6호
    • /
    • pp.1577-1582
    • /
    • 2010
  • A 20 wt % Pt/C is fabricated and characterized for use as the cathode catalyst in a polymer electrolyte membrane fuel cell (PEMFC). By using the polyol method, the fabrication process is optimized by modifying the carbon addition sequence and precursor mixing conditions. The crystallographic structure, particle size, dispersion, and activity toward oxygen reduction of the as-prepared catalysts are compared with those of commercial Pt/C catalysts. The most effective catalyst is obtained by ultrasonic treatment of ethylene glycol-carbon mixture and immediate mixing of this mixture with a Pt precursor at the beginning of the synthesis. The catalyst exhibits very uniform particle size distribution without agglomeration. The mass activities of the as-prepared catalyst are 13.4 mA/$mg_{Pt}$ and 51.0 mA/$mg_{Pt}$ at 0.9 V and 0.85 V, respectively, which are about 1.7 times higher than those of commercial catalysts.

DEVELOPMENT OF PYROPROCESSING AND ITS FUTURE DIRECTION

  • Inoue, Tadashi;Koch, Lothar
    • Nuclear Engineering and Technology
    • /
    • 제40권3호
    • /
    • pp.183-190
    • /
    • 2008
  • Pyroprocessing is the optimal means of treating spent metal fuels from metal fast fuel reactors and is proposed as a potential option for GNEP in order to meet the requirements of the next generation fuel cycle. Currently, efforts for research and development are being made not only in the U.S., but also in Asian countries. Electrorefining, cathode processing by distillation, injection casting for fuel fabrication, and waste treatment must be verified by the use of genuine materials, and the engineering scale model of each device must be developed for commercial deployment. Pyroprocessing can be effectively extended to treat oxide fuels by applying an electrochemical reduction, for which various kinds of oxides are examined. A typical morphology change was observed following the electrochemical reduction, while the product composition was estimated through the process flow diagram. The products include much stronger radiation emitter than pure typical LWR Pu or weapon-grade Pu. Nevertheless, institutional measures are unavoidable to ensure proliferation-proof plant operations. The safeguard concept of a pyroprocessing plant was compared with that of a PUREX plant. The pyroprocessing is better adapted for a collocation system positioned with some reactors and a single processing facility rather than for a centralized reprocessing unit with a large scale throughput.

화학환원법(化學還元法)을 이용(利用)해 제조(製造)한 20% Pt/C 캐소드 촉매(觸媒)의 열처리(熱處理)에 따른 산소환원반응(酸素還元反應) 평가(評價) (Oxygen Reduction Reaction Evaluation of Synthesized 20% Pt/C with Beat Treatment by Chemical Reduction Method)

  • 김진환;강석민;;류호진
    • 자원리싸이클링
    • /
    • 제18권5호
    • /
    • pp.12-18
    • /
    • 2009
  • 고분자전해질 연료전지용 캐소드 촉매로서 화학환원법을 이용하여 20% Pt/C 제조하고 다양한 온도($300-600^{\circ}C$)열처리하여 산소환원반응을 평가하였다 $300-400^{\circ}C$에서 열처리한 20% Pt/C가 높은 산소환원반응 활성을 나타냈으며, 특히 $300^{\circ}C$에서 열처리한 촉매를 0.6V에서의 정전위를 측정한결과, 열처리하지 않은 촉매에 비해서 산소환원 반응 활성정도가 2배 높게 나타났다. TEM 및 XRD 분석을 이용하여 조사한 결과, 열처리 온도가 높아짐에 따라서 백금 입자 크기가 커지고 결정화도가 증가하는 것을 확인하였다. 이러한 결과에서 산소환원반응 활성을 위한 백금의 입자 크기와 결정화도가 $300^{\circ}C$에서 최적화되는 것으로 판단된다.

LiCl-Li$_2$O 용융염계에서 우라늄 산화물의 전기화학적 금속전환 반응 메카니즘에 관한 연구 (A Study on the Electrolytic Reduction Mechanism of Uranium Oxide in a LiCl-Li$_2$O Molten Salt)

  • 오승철;허진목;서중석;박성원
    • 방사성폐기물학회지
    • /
    • 제1권1호
    • /
    • pp.25-39
    • /
    • 2003
  • 본 연구에서는 고온의 LiCl-Ll$_2$O 용융염계에서 우라늄 산화물의 금속전환과 Li$_2$O의 전해반응이 동시에 진행되는 통합 반응 메카니즘을 기초로 한 전기화학적 금속전환기술을 제안하였다. 본 실험에서는 전기화학적 환원반응에 의해 생성된 Li 금속이온이 음극에 전착과 동시에 우라늄 산화물과 반응하여 금속전환율 99 % 이상의 우라늄 감속을 생성하는 통합 반응 메카니즘을 확인할 수 있었다. 또한 전기화학적 금속전환기술의 공정 적용성 평가 일환으로 우라늄 산화물의 금속전환성, 반응 메카니즘 규명, Li$_2$O의 closed recycle rate 및 물질전달 특성 등의 기초 데이터를 확보하였다 향후 전기화학적 금속전환기술은 LiCl-Li 용융염계의 금속전환공정의 반응조건 제한성 해소, 금속전환율 향상 및 공정의 단순화 등의 기술성과 경제성 향상 측면에서 획기적인 방안으로 고려될 수 있을 것으로 판단된다.

  • PDF