• 제목/요약/키워드: $(La_{1-x}Sr_x)Mn_{1+y}O_{3-\delta}$

검색결과 10건 처리시간 0.023초

${La_{1-x}}{Sr_x}{MnO_{3-{\delta}}}$(0.19$\leq$x$\leq$0.31) 박막의 결정구조 및 전기전도 특성 (Crystal Structure and Electrical Transport Characteristics of ${La_{1-x}}{Sr_x}{MnO_{3-{\delta}}}$(0.19$\leq$x$\leq$0.31) Thin Films)

  • 허현;임세주;조남희
    • 한국재료학회지
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    • 제10권6호
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    • pp.437-444
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    • 2000
  • 기판온도, 박막조성 및 증착후 열처리 등의 조건에 따른 ${La_{1-x}}{Sr_x}{MnO_{3-{\delta}}}$(0.19$\leq$x$\leq$0.31) 박막의 결절구조와 전기전도 특성을 조사하였다. 스퍼터법을 이용하여 $500^{\circ}C$에서 증착된 박막은 강한 <001> 우선배향성과 유사정방정(pseudo-tetrag-onal, a/c-=0.97) 결정체를 나타냈다. 이러한 박막의 단위포는 산소분위기 내에서 증착후 열처리에 의하여 입장정 결정계로 변하였다. $La_{0.67}Sr_{0.33}MnO_3$ 조성의 주타겟과 $La_{0.3}Sr_{0.7}MnO_3$조성의 보조타겟을 동시에 이용하여 박막의 조성을 조절하였다. 보조타겟의 개수에 따라 박막내의 Sr 함량(x)은 0.19-0.31 범위의 값을 나타내었으며, x값이 0.19로부터 0.31로 증가시 금소-반도체의 전이 온도가 상승하였고, 전지비저항이 대체로 감소하였다. 0.18 T의 자기장 하에서, $La_{0.69}Sr_{0.31}MnO_3$조성의 박막의 자기저항변화 MR((%) = (${\rho}_o-{\rho}_H/{\rho}_H$)는 약 390% 이었다.

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GNP법에 의한 $(La_{1-x}Sr_x)MnO_{3+\delta}$ 분말의 환원특성 (Reduction Properties of $(La_{1-x}Sr_x)MnO_{3+\delta}$ Powder by GNP)

  • 이미재;백종후;김세기;박상선;최병현;이경희
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2005년도 추계학술대회 논문집 Vol.18
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    • pp.242-243
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    • 2005
  • In this study, (La,Sr)$MnO_{3+\delta}$ powder used cathode material for SOFC was synthesized with precursor by GNP and the properties of powder, crystal phase, electric properties and deoxidization properties with precursor were investigated. The synthesis powder was prepared when oxidant/fuel mole and pH were 1 and 1, respectively and the synthesis powder was synthesized by GNP method using nitrate solution or oxide solution as precursor. Deoxidization peak of the nitrate solution was appeared lower temperature than the oxide solution, at $450^{\circ}C$. In this result, synthesis (La,Sr)$MnO_{3+\delta}$ powder using nitrate solution with Mn excess was suitable cathode material for SOFC due to had higher deoxidization properties. Also synthesis (La,Sr)$MnO_{3+\delta}$ powder according to precursor had difference electrical conductivity according to influence sintering density and crystal phase with precursor. Specially, the synthesis method and starting material had effect on deoxidization properties for SOFC.

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LSGM 전해질과 LSM 양극의 합성분말을 이용한 SOFC 단위전지의 특성 (Cell Properties for SOFC Using Synthesized Powder of Electrolyte LSGM System and Cathode LSM System)

  • 이미재;남중희;최병현
    • 한국세라믹학회지
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    • 제39권4호
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    • pp.359-366
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    • 2002
  • 고체산화물 연료전지의 운전온도를 낮추기 위해 구성재 중 LSGM 전해질과 LSM 양극을 합성하고, 그 특성을 조사한 후 최적 조성과 공정으로 단위전지를 제작하고 출력을 측정하였다. 전해질 조성인 $(La_{0.85}Sr_{0.15})(Ga_{0.8}Mg_{0.2})O_{3-\delta}와 (La_{0.8}Sr_{0.2})(Ga_{0.8}Mg_{0.2})O_{3-\delta}$$1500^{\circ}$에서 6시간 소결한 경우 두 조성 모두 $LaGaO_3$의 단일상을 형성하였고, $10∼3{\mu}m$의 결정 크기를 갖는 치밀한 미세구조를 얻었으며, 저기전도도는 $800^{\circ}$에서 0.13S/cm를 나타내었다. 양극의 경우 GNP법으로 $(La1-xSrx)MnO_3$를 합성한 경우 Sr의 양이 0.2mole일 때까지는 $LaMnO_3$ perovskite 단일상이 생성되었으며, 입자의 크기는 약 40nm였다. 단위전지는 $(La_{0.8}Sr_{0.2})(Ga_{0.8}Mg_{0.2})O_{3-\delta}$ 조성으로 소결한 전해질 양면에 $(La_{0.9}Sr_{0.1})MnO_3$ 양극과 음극의 입자크기는 $1{\mu}m$ 정도였고 다공성을 나타내었다. 이때 단위전지의 출력은 $800^{\circ}$에서 약 $0.3W/cm^2$를 나타내었다

GNP법에 의해 합성한 (La1-xSrx)Mn1+yO3−δ 분말의 출발물질에 따른 특성 (Effect of Starting Materials on the Characteristics of (La1-xSrx)Mn1+yO3−δ Powder Synthesized by GNP)

  • 이미재;김세기;지미정;최병현;박상선;이경희
    • 한국세라믹학회지
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    • 제44권1호
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    • pp.52-57
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    • 2007
  • We synthesized $(La_{1-x}Sr_x)MnO_3$ as a cathode for SOFC by glycine nitrate process (GNP) and knew the different properties of $(La_{1-x}Sr_x)MnO_3$ by using nitrate solution and oxide solution as a starting material. In case of using nitrate solution as a starting material, main crystal phase peak of $LaMnO_3$ increased as Sr content added up and a peak of $Sr_2MnO_4\;and\;La_2O_3$ was showed as a secondary phase. We added Mn excess to control a crystal phase. In this case, the electrical conductivity had a high value 210.3 S/cm at $700^{\circ}C$. On the other side, when we used oxide solution as a starting material, we found main crystal phase of $LaMnO_3$ to increase as Sr content added up and a peak of $La_2O_3$ as a secondary phase. Similary, we added Mn excess to control a crystal phase in this case. We knew $(La,Sr)MnO_3$ powder to sinter well and the electrical conductivity of the sintered body at $1200^{\circ}C$ for 4 h was 152.7 S/cm at $700^{\circ}C$. The sintered $(La,Sr)MnO_3$ powder at $1000^{\circ}C$ for 4 h got the deoxidization peak, depending on the temperature and in case of using nitrate solution as a starting material, the deoxidization peak was showed at $450^{\circ}C$ which is lower than used a oxide solution as a starting material. As a result, when $(La,Sr)MnO_3$ powder was synthesized to add Mn excess and to use nitrate solution as a starting material, we found it to have the higher deoxidization property and considered it as a cathode for SOFC properly. And we found it to have different electrical conductivity the synthesized $(La,Sr)MnO_3$ powder by using different starting materials like nitrate solution and oxide solution which influence a sintering density and crystal phase.

$(La,\;Sr)MnO_{3+{\delta}$ 합성에 있어서 출발물질에 따른 양극특성 (Cathode Characteristics in the Synthesis of $(La,\;Sr)MnO_{3+{\delta}$ of Precursor)

  • 이미재;김세기;지미정;최병현;박상선
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2006년도 추계학술대회
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    • pp.360-363
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    • 2006
  • We synthesized $(La,\;Sr)MnO_{3+{\delta}$ as a cathode for SOFC by glycine nitrate process(GNP) and knew the different properties of $(La_{1-x}Sr_x)MnO_3$ by using nitrate solution and oxide solution as starting material. In case of using nitrate solution as a starting material, main crystal phase peak of $LaMnO_3$ increased as Sr content added up and a peak of $Sr_2MnO_4\;and\;La_2O_3$ was showed as a secondary phase. We added Mn excess to control a crystal phase. In this case, the electrical conductivity had a high value 210.3S/cm at $700^{\circ}C$ On the other side, when we used oxide solution as a starting material, we found main crystal phase of $LnMnO_3$ to increase as Sr content added up and a peak of $La_2O_3$ as a secondary phase. Similary, we added Mn excess to control a crystal phase in this case. We knew $(La,\;Sr)MnO_3$ powder to sinter well and the electrical conductivity of the sintered body at $1200^{\circ}C$ for 4hrs was 152.7s/cm at $700^{\circ}C$. The sintered $(La,\;Sr)MnO_3$ powder at $1000^{\circ}C$ for 4hrs got the deoxidization peak, depending on the temperature md in case of using nitrate solution as a start ing material the deoxidization peak was showed at $450^{\circ}C$ which is lower than used a oxide solution as a starting material. As a result, when $(La,\;Sr)MnO_3$ powder was synthesized to add Mn excess and to use nitrate solution as a starting material, we found it to have the higher deoxidization property and considered it as a cathode for m properly. And we found it to have different electrical conduct ivity the synthesized $(La,\;Sr)MnO_3$ powder by using different start ing materials like nitrate solution and oxide solution which influence a sintering density and crystal phase.

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Sr 함량이 Cu-doped LSM(La1-xSrxMn0.8Cu0.2O3)의 구조적변화와 전기전도도에 미치는 영향 (Structural change and electrical conductivity according to Sr content in Cu-doped LSM (La1-xSrxMn0.8Cu0.2O3))

  • 류지승;노태민;김진성;이희수
    • 한국결정성장학회지
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    • 제22권2호
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    • pp.78-83
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    • 2012
  • $La_{1-x}Sr_xMn_{0.8}Cu_{0.2}O_{3-{\delta}}$(LSMCu)에서 Sr 함량에 따른 구조적 변화와 전기전도도에 대해 연구, 고찰하였다. EDTA citric complexing process(ECCP)로 페로브스카이트 구조를 갖는 $La_{0.8}Sr_{0.2}MnO_3$(LSM)와 $La_{1-x}Sr_xMn_{0.8}Cu_{0.2}O_3$($0.1{\leq}x{\leq}0.4$)을 제조하였다. Sr 함량이 증가할수록 격자상수와 격자부피는 감소하는 경향을 나타내었으며, 이는 Sr 함량이 증가함에 따라 B-site에서 증가하는 $Mn^{4+}$ 이온과 $Cu^{3+}$ 이온의 영향인 것으로 판단하였다. $0.1{\leq}x{\leq}0.3$ 범위의 조성에서 Sr 함량이 증가할수록 $500{\sim}1000^{\circ}C$에서 측정된 전기전도도는 증가하였고, x = 0.3 조성에서는 $750^{\circ}C$$950^{\circ}C$에서 각각 172.6 S/cm와 177.7 S/cm (최고값)를 나타내었다. 반면, x = 0.4 조성에서는 전기전도도가 감소하였는데 이는 입계에 발생한 산화물에 의한 영향으로 판단하였다. Sr 함량이 증가함에 따라 B-site에 존재하는 $Mn^{4+}$ 이온과 $Cu^{3+}$ 이온의 증가로 인해 격자수축이 발생하고, hopping mechanism에 관여하는 charge carrier들이 늘어나 전기전도도가 증가한 것으로 판단하였다.

Effects of Sr Contents on Structural Change and Electrical Conductivity in Cu-doped LSM ($La_{1-x}Sr_xMn_{0.8}Cu_{0.2}O_{3{\pm}{\delta}}$)

  • 류지승;노태민;김진성;정철원;이희수
    • 한국재료학회:학술대회논문집
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    • 한국재료학회 2011년도 추계학술발표대회
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    • pp.33.1-33.1
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    • 2011
  • Strontium doped lanthanum manganite (LSM) with perovskite structure for SOFC cathode material shows high electrical conductivity and good chemical stability, whereas the electrical conductivity at intermediate temperature below $800^{\circ}C$ is not sufficient due to low oxygen ion conductivity. The approach to improve electrical conductivity is to make more oxygen vacancies by substituting alkaline earths (such as Ca, Sr and Ba) for La and/or a transition metal (such as Fe, Co and Cu) for Mn. Among various cathode materials, $LaSrMnCuO_3$ has recently been suggested as the potential cathode materials for solid oxide fuel cells (SOFCs). As for the Cu doping at the B-site, it has been reported that the valence change of Mn ions is occurred by substituting Cu ions and it leads to formation of oxygen vacancies. The electrical conductivity is also affected by doping element at the A-site and the co-doping effect between A-site and B-site should be described. In this study, the $La_{1-x}Sr_xMn_{0.8}Cu_{0.2}O_{3{\pm}{\delta}}$ ($0{\leq}x{\leq}0.4$) systems were synthesized by a combined EDTA-citrate complexing process. The crystal structure, morphology, thermal expansion and electrical conductivity with different Sr contents were studied and their co-doping effects were also investigated.

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Active Reaction Sites and Oxygen Reduction Kinetics on $La_1_{-x}Sr_xMnO_{3+\delta}$(x=0.1-0.4)/YSZ (Yttria-Stabilized Zirconia) Electrodes for Solid Oxide Fuel Cells

  • Lee, Hee Y.;Cho, Woo S.;오승모
    • Bulletin of the Korean Chemical Society
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    • 제19권6호
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    • pp.661-666
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    • 1998
  • Active reaction sites and electrochemical O2 reduction kinetics on La_{1-x}Sr_xMnO_{3+{\delta}} (x=0.1-0.4)/YSZ (yttria-stabilized zirconia) electrodes are investigated in the temperature range of 700-900 ℃ at $Po_2=10^{-3}$-0.21 atm. Results of the steady-state polarization measurements, which are formulated into the Butler-Volmer formalism to extract transfer coefficient values, lead us to conclude that the two-electron charge transfer step to atomically adsorbed oxygen is rate-limiting. The same conclusion is drawn from the $Po_2$-dependent ac impedance measurements, where the exponent m in the relationship of $I_o$ (exchange current density) ∝ $P_{o_{2}}^m$ is analyzed. Chemical analysis is performed on the quenched Mn perovskites to estimate their oxygen stoichiometry factors (δ) at the operating temperature (700-900 ℃). Here, the observed δ turns out to become smaller as both the Sr-doping contents (x) and the measured temperature increase. A comparison between the 8 values and cathodic activity of Mn perovskites reveals that the cathodic transfer coefficients $({\alpha}_c)$ for oxygen reduction reaction are inversely proportional to δ whereas the anodic ones $({\alpha}_a)$ show the opposite trend, reflecting that the surface oxygen vacancies on Mn perovskites actively participate in the $O_2$ reduction reaction. Among the samples of x= 0.1-0.4, the manganite with x=0.4 exhibits the smallest 8 value (even negative), and consistently this electrode shows the highest ${\alpha}_c$ and the best cathodic activity for the oxygen reduction reaction.

La$_{1-x}Ca_xMnO_3$ 박막에서 p파 초전도의 가능성 (Possible p-wave condensed conductor (or superconductor) for La$_{1-x}Ca_xMnO_3$ films)

  • 김현탁;강광용
    • 한국초전도학회:학술대회논문집
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    • 한국초전도학회 1999년도 High Temperature Superconductivity Vol.IX
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    • pp.200-205
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    • 1999
  • In the ferromagnetic phase with electrons for La$_{1-x}$(Ca or Sr)$_x$MnO$_3$, films, a remnant resistivity of the order of 10$^{-8}$ ${\omega}$m is observed up to 100 K and increases exponentially with temperature up to T$_c$ and above one Tesla as a function of magnetic field strength (a positive magnetoresistivity). The phase below T$_c$ is regarded as a polaronic state with a polaronic tunneling conduction. Possible p-wave condensation (or superconductor) with a parabolic density of states and the phase separation are discussed on the basis of the two-fold degeneracy of ${\varrho}_{\delta}$ orbitals.

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