• 제목/요약/키워드: Ru$O_{2}$/Ti

검색결과 147건 처리시간 0.035초

전도성 세라믹인 티타늄 아산화물 TiO와 $Ti_4O_{7}$의 산화전극으로서의 전기화학적 특성

  • 박소영;김철;모선일;지은옥;권영옥
    • 한국에너지공학회:학술대회논문집
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    • 한국에너지공학회 1994년도 춘계학술발표회 초록집
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    • pp.121-125
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    • 1994
  • 전극물질 및 전극촉매로서의 세라믹물질의 중요성은 상당히 크다. magneli phase를 갖는 $Ti_4O_{7}$과 rock salt구조를 갖는 TiO등의 티타늄 아산화물들은 전도성 세라믹으로서 전기전도도는 탄소보다도 좋으며, 높은 산화전위에서도 산화되지 않을 뿐만아니라, 강산용액에서도 내식성이 강하여 $SO_2$$O_2$의 산화전극 물질로 사용할 수 있다. $SO_2$$O_2$의 산화에 뛰어난 활동도를 보이는 촉매인 Pt나 Ru를 전기화학적으로 $Ti_4O_{7}$이나 TiO에 입혀서 그 전기화학적인 특성을 조사하였다.

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MMO(Ti/Ru) 코팅된 타이타늄의 고분자 전해질 연료전지 양극환경에서의 전기화학적 거동 (Electrochemical Characteristics of MMO(Ti/Ru)-Coated Titanium in a Cathode Environment of Polymer Electrolyte Membrane Fuel Cell)

  • 허호성;김성종
    • Corrosion Science and Technology
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    • 제21권5호
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    • pp.340-347
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    • 2022
  • In this research, mixed metal oxide (TiO2, RuO2) coating was applied to grade 1 titanium as a bipolar plate for polymer electrolyte membrane fuel cell (PEMFC). Electrochemical experiments were carried out in an aqueous solution of pH 3 (H2SO4 + 0.1 ppm HF, 80 ℃) determined by DoE. The air was bubbled to simulate a cathode environment. Potentiodynamic polarization test revealed that corrosion current densities of the titanium substrate and MMO-coated specimen were 0.180 µA/cm2 and 4.381 µA/cm2, respectively. There was no active peak. After potentiostatic experiment, current densities of the titanium substrate and the MMO-coated specimen were 0.19 µA/cm2 and 1.05 µA/cm2, respectively. As a result of observing the surface before and after the potentiostatic experiment, cracked dried clay structures were observed without corrosion damage. Both the titanium substrate and the MMO-coated specimen could not satisfy the interfacial contact resistance suggested by the DoE. Thus, further research is needed before they could be applied as bipolar plates.

Interaction between RuO2 and Carbon Nanotubes - Photoemission and X-ray Absorption Study

  • Lee, Seung-Youb;Kim, Yoo-Seok;Jeon, Chel-Ho;Ihm, Kyu-Wook;Kang, Tai-Hee;Park, Chong-Yun
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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    • pp.567-567
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    • 2012
  • Since the carbon nanotubes (CNTs) have extraordinary material properties, many researchers are trying to make a practical application in various fields [1]. In particular, the high surface area of CNTs was fascinated for nano-template on the catalytic system. $RuO_2$ coated CNTs are useful functional nano-composites in many applications, including super capacitors, fuel cells, biosensors, and field emitters. However, the research of interaction between CNTs and $RuO_2$ was not satisfied with various fields [2]. In this study, we will introduce the change of chemical and electrical state of $RuO_2$/CNTs at different temperatures by synchrotron radiation photoemission spectroscopy (SRPES). The t-MWCNTs used in this experiment were grown on the Ni/TiN/Si substrates by chemical vapor deposition. $RuO_2$ of 4-20 nm in thickness was deposited on the t-MWNTs by sputter. The SRPES measurements were carried out at the 4B1 beamline of the Pohang Accelerator Laboratory in Korea. The result of XPS measurement indicates that the deposited $RuO_2$ on the CNTs was reduced into pure Ru at above $300^{\circ}C$. And we confirmed that the effective work function of $RuO_2$/CNTs was decreased with increasing temperature.

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Ru-Co가 치환된 M-형 육방정 페라이트(BaFe12-2xRuxCoxO19)의 자기적 성질 및 전파흡수 특성 (Magnetic and Microwave Absorbing Properties of M-type Hexagonal Ferrites Substituted by Ru-Co(BaFe12-2xRuxCoxO19))

  • 조한신;김성수
    • 한국자기학회지
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    • 제18권4호
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    • pp.136-141
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    • 2008
  • Ru-Co가 복합 치환된 M-type Ba-ferrite($BaFe_{12-2x}Ru_xCo_xO_{19}$)의 치환량 x의 변화에 따른 자기적 특성과 전파흡수 특성에 관해 조사하였다. 기존의 Ti-Co를 치환시킨 경우보다 적은 양의 치환(x=0.3)으로 면내 자기이방성을 보이는 낮은 보자력($H_c$)과 높은 포화자화($M_s$) 값을 얻을 수 있었다. 따라서 Ru-Co 치환량 조절에 의해 GHz 대역에서 자연공명주파수의 조절이 가능하였다. 소결체 및 복합체에서 흡수 주파수 대역은 보자력이 증가할수록 고주파 대역으로 이동한다. 복합체에서 페라이트 혼합량이 증가함에 따라 복소투자율과 복소유전율의 값이 증가하기 때문에 정합주파수는 저주파 대역으로 이동한다. 이러한 특성들을 이용하여 순수한 M-형 육방정 페라이트에 Ru-Co의 치환량, 복합체에서 페라이트 분말의 혼합량, 그리고 흡수체의 두께의 제어를 통하여 GHz 주파수 대역에서 양호한 전자파 흡수체, 노이즈 감쇠재의 제조가 가능함을 제시할 수 있다.

Influences of Coating Cycles and Composition on the Properties of Dimensionally Stable Anode for Cathodic Protection

  • Yoo, Y.R.;Chang, H.Y.;Take, S.;Kim, Y.S.
    • Corrosion Science and Technology
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    • 제5권2호
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    • pp.45-51
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    • 2006
  • Properties of the anode for cathodic protection need low overvoltage for oxygen evolution and high corrosion resistance. It is well known that DSA (Dimensionally Stable Anode) has been the best anode ever since. DSA is mainly composed of $RuO_2$, $IrO_2$, $ZrO_2$, $Co_2O_3$, and also $Ta_2O_5$, $TiO_2$, $MnO_2$ are added to DSA for better corrosion resistance. The lifetime of DSA for cathodic protection is also one of the very important factors. $RuO_2$, $IrO_2$, $RhO_2$, $ZrO_2$ are well used for life extension, and many researches are focused on life extension by lowering oxygen evolution potential and minimizing dissolution of oxide coatings. This work aims to evaluate the influence of constituents of MMO and coating cycles and $ZrO_2$ coating on the electrochemical properties and lifetime of DSA electrodes. From the results of lifetime assessment in the anodes coated with single component, $RuO_2$ coating was more effective and showed longer lifetime than $IrO_2$ coating. Also, an increased coating cycle and an electrochemically coated $ZrO_2$ could enhance the lifetime of a DSA.

전기용융 분말로부터 합성된 $Al_2$TiO$_5$ Ceramics의 열충격 저항성 (Thermal Shock Resistance of $Al_2$TiO$_5$ Ceramics Prepared from Electrofused Powders)

  • 김익진
    • 한국세라믹학회지
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    • 제35권10호
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    • pp.1061-1069
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    • 1998
  • The thermal instability of Al2TiO5 Ceramics was contrlled by solid solution with MgO SiO2 and ZrO2 through electrofusion in an arc furnace. The thermal expansion properties of Al2TiO5 composites show the hysteresis due to the strong anisotropy of The crystal axes of these material. These phenomena are ex-plained by the opening and closing of microcracks. The difference in microcracking temperatures e.g 587.6(ATG2), 405.9(ATG3) and 519.7$^{\circ}C$(ATG4) is caused by the difference in grain size and stabilizer type. The thermal shock behaviour under cyclic conditions between 750-1400-75$0^{\circ}C$ show no change in mi-crostructure and phase assemblage for all three stabilized specimens. After the thermal loading test at 110$0^{\circ}C$ for 100hrs. ATG1 and ATG2 materials decomposes completely to its components corundum and ru-tile in both cases. However with approximatelly 20% retention of the Al2TiO5 Thus in order to prevent decomposition of the stabilized material in the critical temperature range 800-130$0^{\circ}C$ it must be traversed within a short period of time.

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전이금속이 도핑된 ZnO의 전자구조와 자성에 대한 제일원리계산 (First Principles Calculations on Electronic Structure and Magnetism of Transition Metal Doped ZnO)

  • 윤선영;차기범;홍순철
    • 한국자기학회지
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    • 제15권1호
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    • pp.1-6
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    • 2005
  • 높은 큐리온도를 가질 수 것으로 예측된 전이금속이 도핑된 ZnO의 전자구조와 자성을 제일원리계산방법을 이용하여 연구하였다. 본 연구에서 전이금속은 Ti, Cr, Mn, Fe, Co, Ni, Ru, Pd, Ag 이고 도핑 수준은 25%로 두고 계산하였다. 자성연구에서 가장 적합한 방법으로 알려져 있는 Full-potential Linearized Augmented Plane Wave(FLAPW)방법을 사용하였으며 교환-상관 전위는 general gradient approximation(GGA)를 사용하였다. 도핑된 전이금속 (Ti, Cr, Mn, Fe, Co, Ni, Ru, Pd, Ag)은 각각 0.83, 3.03, 4.03, 3.48, 2.47, 1.56, 0.43, 0.75, 0.01 ${\mu}_B$의 자기모멘트를 가지며, 전이금속에 이웃한 O 원자도 가안 띠혼성으로 측정 가능한 자기모멘트를 가질 수도 있는 것으로 계산되었다. 3d 전이금속이 도핑된 ZnO는 (CoZnO를 제외하고) 절반금속 특성을 가지는 것으로 계산되었다. 또한 4d 전이금속이 도핑된 경우는 강자성 상태가 상자성 상태에 비해 에너지차이가 크지 않을 뿐 아니라 페르미 준위에 다수 스핀과 소수 스핀 상태 모두가 페르미 준위에 위치해 있어 스핀분극 정도가 낮았다.

Preparaton of ECR MOCVD $SrTiO_3$ thin films and their application to a Gbit-scale DRAM stacked capacitor structure

  • Lesaicherre, P-Y.
    • 한국진공학회지
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    • 제4권S1호
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    • pp.138-144
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    • 1995
  • It is commonly believed that high permittivity materials will be necessary for future high density Gbit DRAMs. In a first part, we explain the choice of SrTiO3 by ECR MOCVD for Gbit-scale DRAMs. In a second part, after describing the ECR MOCVD system and presenting the requirements SrTiO3 thin films should meet for use in Gbit-scale DRAMs, the physical and electrical properties of srTiO3 thi film prepared by ECR MOCVD are then studied. A stacked capacitor technology, suitable for use in 1 Gbit DRAM, and comprising high permittivity SrTiO3 thin films prepared by ECR MOCVD at $450^{\circ}C$ on electron beam and RIE patterned RuO2/TiN storage nodes is finally described.

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염료감응형 광전기화학 물분해 전지용 Tri-branched tri-anchoring organic dye 개발 (Tri-branched tri-anchoring organic dye for Visible light-responsive dye-sensitized photoelectrochemical water-splitting cells)

  • 박정현;김재홍;안광순
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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    • pp.87-87
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    • 2010
  • Photoelectrochemical (PEC) systems are promising methods of producing H2 gas using solar energy in an aqueous solution. The photoelectrochemical properties of numerous metal oxides have been studied. Among them, the PEC systems based on TiO2 have been extensively studied. However, the drawback of a PEC system with TiO2 is that only ultraviolet (UV) light can be absorbed because of its large band gap (3.2 - 3.4 eV). Two approaches have been introduced in order to use PEC cells in the visible light region. The first method includes doping impurities, such as nitrogen, into TiO2, and this technique has been extensively studied in an attempt to narrow the band gap. In comparison, research on the second method, which includes visible light water splitting in molecular photosystems, has been slow. Mallouk et al. recently developed electrochemical water-splitting cells using the Ru(II) complex as the visible light photosensitizer. the dye-sensitized PEC cell consisted of a dye-sensitized TiO2 layer, a Pt counter electrode, and an aqueous solution between them. Under a visible light (< 3 eV) illumination, only the dye molecule absorbed the light and became excited because TiO2 had the wide band gap. The light absorption of the dye was followed by the transfer of an electron from the excited state (S*) of the dye to the conduction band (CB) of TiO2 and its subsequent transfer to the transparent conducting oxide (TCO). The electrons moved through the wire to the Pt, where the water reduction (or H2 evolution) occurred. The oxidized dye molecules caused the water oxidation because their HOMO level was below the H2O/O2 level. Organic dyes have been developed as metal-free alternatives to the Ru(II) complexes because of their tunable optical and electronic properties and low-cost manufacturing. Recently, organic dye molecules containing multi-branched, multi-anchoring groups have received a great deal of interest. In this work, tri-branched tri-anchoring organic dyes (Dye 2) were designed and applied to visible light water-splitting cells based on dye-sensitized TiO2 electrodes. Dye 2 had a molecular structure containing one donor (D) and three acceptor (A) groups, and each ended with an anchoring functionality. In comparison, mono-anchoring dyes (Dye 1) were also synthesized. The PEC response of the Dye 2-sensitized TiO2 film was much better than the Dye 1-sensitized or unsensitized TiO2 films.

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