• 제목/요약/키워드: $CoMnO_2$

검색결과 745건 처리시간 0.028초

Nickel Substitution Effects on Nano-sized Co, Mn and MnZn Ferrites Synthesized by Sol-gel Method

  • Choi, Won-Ok;Kwon, Woo Hyun;Chae, Kwang Pyo;Lee, Young Bae
    • Journal of Magnetics
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    • 제21권1호
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    • pp.40-45
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    • 2016
  • Nickel substituted nano-sized ferrite powders, $Co_{1-x}Ni_xFe_2O_4$, $Mn_{1-x}Ni_xFe_2O_4$ and $Mn_{1-2x}Zn_xNi_xFe_2O_4$ ($0.0{\leq}x{\leq}0.2$), were fabricated using a sol-gel method, and their crystallographic and magnetic properties were subsequently compared. The lattice constants decreased as quantity of nickel substitution increased, while the particle size decreased in $Co_{1-x}Ni_xFe_2O_4$ ferrite but increased for the $Mn_{1-x}Ni_xFe_2O_4$ and $Mn_{1-2x}Zn_xNi_xFe_2O_4$ ferrites. For the $Co_{1-x}Ni_xFe_2O_4$ and $Mn_{1-x}Ni_xFe_2O_4$ ($0.0{\leq}x{\leq}0.2$) ferrite powders, the $M{\ddot{o}}ssbauer$ spectra could be fitted as the superposition of two Zeeman sextets due to the tetrahedral and octahedral sites of the $Fe^{3+}$ ions. However, the $M{\ddot{o}}ssbauer$ spectrum of $Mn_{0.8}Zn_{0.1}Ni_{0.1}Fe_2O_4$ consisted of two Zeeman sextets and one single quadrupole doublet due to the ferrimagnetic and paramagnetic behavior. The area ratio of the $M{\ddot{o}}ssbauer$ spectra could be used to determine the cation distribution equation, and we also explain the variation in the $M{\ddot{o}}ssbauer$ parameters by using this cation distribution equation, the superexchange interaction and the particle size. The saturation magnetization decreased in the $Co_{1-x}Ni_xFe_2O_4$ and $Mn_{1-2x}Zn_xNi_xFe_2O_4$ ferrites but increased in the $Mn_{1-x}Ni_xFe_2O_4$ ferrite with nickel substitution. The coercivity decreased in the $Co_{1-x}Ni_xFe_2O_4$ and $Mn_{1-2x}Zn_xNi_xFe_2O_4$ ferrites but increased in the $Mn_{1-x}Ni_xFe_2O_4$ ferrite with nickel substitution. These variations could thus be explained by using the site distribution equations, particle sizes and spin magnetic moments of the substituted ions.

ZnO계 바리스터의 입계포획준위 (Grain Boundary Trap Levels in ZnO-based Varistor)

  • 김명철;박순자
    • 한국재료학회지
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    • 제2권1호
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    • pp.12-18
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    • 1992
  • 등온용량과도분광법(Isothermal Capacitance Transient spectroscopy)을 이용하여 ZnO 바리스터의 포획준위를 결정하였다. 여기서 등온용량과도분광기는 YHP 4192A 임피던스 Analyzer와 데이터해석을 위한 개인용 컴퓨터로 구성된다. 이 실험에서 우리는 $ZnO-Bi_2O_3$에 MnO 및 CoO를 첨가한계에서 $-40^{\circ}C~60^{\circ}C$ 온도범위에서 0.28, 0.48, 0.50, 0.94eV 등의 입계포획준위가 존재함을 볼 수 있었다. 또한, $ZnO-Bi_2O_3$계는 CoO를 첨가하면 hole에 의한 emission특성을 나타내고, MnO를 첨가하면 전자에 의한 emission특성을 나타냄을 알 수 있었다. 그리고 비 직선저항계수 $\alpha$는 도너농도의 감소에 직접적으로 비례하였으나, 포획준위의 밀도와는 별다른 비례관계를 발견할 수 없었다. 결론적으로 $ZnO-Bi_2O_3-MnO$계에 CoO를 첨가함에 따라 $\alpha$값이 증가하는 한편, 포획준위밀도는 CoO의 첨가로 감소함을 알 수 있었다.

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Sodium Borohydride 하에서 산소에 의한 포화- 및 불포화-질소주게 거대고리 착물 $(M=Co^{3+},\;Fe^{3+}$$Mn^{3+})$을 촉매로 한 Hindered Phenols의 산화반응 (Saturated- and Unsaturated-Azamacrocyclic Complexes $(M = Co^{3+}, Fe^{3+}$ or $Mn^{3+})$ Catalyzed Oxidation of Hindered Phenols by Molecular Oxygen under Sodium Borohydride)

  • 박유철;김성수;나훈길
    • 대한화학회지
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    • 제37권7호
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    • pp.648-654
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    • 1993
  • $[M(cyclam)X_2]Y(M=Co^{3+},\;Fe^{3+},\;Mn^{3+}\;:\;X=Cl-^,\;Br^-,\;NCS^-\;:\;Y=Cl^-,\;Br^-,\;NCS^-),\;[Co(trans-14-diene)X_2]Y(X=Cl^-,\;Br^-\;:\;Y= ClO_4^-)$$[Co(trans-14-diene)](ClO_4)_2$ 착이온은 sodium borohydride 하에서 산소를 활성화시킬 수 있었다. 활성화된 산소에 의한 2,4-di-tert-butylphenol 과 2,6-di-tert-butylphenol 산화반응의 생성물질을 각각 2,4-tert-butyl-1,6-benzoquinone(BQ) 와 3,5,3',5'-tetra-tert-butyldiphenoquinone(DPQ) 이었다. BQ와 DPQ 생성반응에서 포화 거대고리 리간드 착물인 $[Co(cyclam)X_2]Y$은 불포화 거대고리착물 $[Co(trans-14-diene)X_2]Y$에 비하여 더 효과적인 촉매제이었다. 촉매로 작용한 Co(III)-거대고리착물과 산소간의 몰 결합비$(O_2/M)$는 1/1이었고, $[M(cyclam)Cl_2]Cl(M=Fe(III)$, Mn(III))에서는 이들 비가 1/2이었다. 반응(10)과 (2)에서 산소분자의 활성종은 Co(III) 거대고리착물이온과 $[M(cyclam)Cl_2]Cl(M=Fe(III)$, Mn(III))에서 각각 superoxolike$({O_2}^-)$와 peroxolike$({O_2}^{2-})$로 가정하였다.

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Crystallographic and Magnetic Properties of Co, Zn, Ni-Zn Substituted Nano-size Manganese Ferrites Synthesized by Sol-gel Method

  • Noh, Kwang Mo;Lee, Young Bae;Kwon, Woo Hyun;Kang, Jeoung Yun;Choi, Won-Ok;Chae, Kwang Pyo
    • Journal of Magnetics
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    • 제21권3호
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    • pp.308-314
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    • 2016
  • Cobalt-, zinc-, and nickel-zinc-substituted nano-size manganese ferrite powders, $MnFe_2O_4$, $Mn_{0.8}Co_{0.2}Fe_2O_4$, $Mn_{0.8}Zn_{0.2}Fe_2O_4$ and $Mn_{0.8}Ni_{0.1}Zn_{0.1}Fe_2O_4$, were fabricated using a sol-gel method, and their crystallographic and magnetic properties were subsequently studied. The $MnFe_2O_4$ ferrite powder annealed at temperatures above 523 K exhibited a spinel structure, and the particle size increased as the annealing temperature increased. All ferrites annealed at 773 K showed a single spinel structure, and the lattice constants and particle size decreased with the substitution of Co, Zn, and Ni-Zn. The $M{\ddot{o}}ssbauer$ spectrum of the $MnFe_2O_4$ ferrite powder annealed at 523 K only showed a doublet due to its superparamagnetic phase, and the $M{\ddot{o}}ssbauer$ spectra of the $MnFe_2O_4$, $Mn_{0.8}Co_{0.2}Fe_2O_4$, and $Mn_{0.8}Zn_{0.2}Fe_2O_4$ ferrite powders annealed at 773 K could be fitted as the superposition of two Zeeman sextets due to the tetrahedral and octahedral sites of the $Fe^{3+}$ ions. However, the $M{\ddot{o}}ssbauer$ spectrum of the $Mn_{0.8}Ni_{0.1}Zn_{0.1}Fe_2O_4$ ferrite powder annealed at 773 K consisted of two Zeeman sextets and one quadrupole doublet due to its ferrimagnetic and paramagnetic behavior. The area ratio of the $M{\ddot{o}}ssbauer$ spectra could be used to determine the cation distribution equation, and we also explained the variation in the $M{\ddot{o}}ssbauer$ parameters by using this cation distribution equation, the superexchange interaction and the particle size. Relative to pure $MnFe_2O_4$, the saturation magnetizations and coercivities were larger in $Mn_{0.8}Co_{0.2}Fe_2O_4$ and smaller in $Mn_{0.8}Zn_{0.2}Fe_2O_4$, and $Mn_{0.8}Ni_{0.1}Zn_{0.1}Fe_2O_4$. These variations could be explained using the site distribution equations, particle sizes and magnetic moments of the substituted ions.

리튬2차전지용 층상계 $LiNi_{1/3}Mn_{1/3}Co_{1/3}O_2$의 표면개질에 따른 전지특성 변화 (Battery Performances of with Surface Treatment of Layered $LiNi_{1/3}Mn_{1/3}Co_{1/3}O_2$ Materials in Lithium Secondary Batteries)

  • 김현수;공명철;김기택;문성인;윤문수;김우성
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2006년도 하계학술대회 논문집 Vol.7
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    • pp.348-349
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    • 2006
  • $LiNi_{1/3}Mn_{1/3}Co_{1/3}O_2$ cathode material was synthesized by a mixed hydroxide methode. The surface of the $LiNi_{1/3}Mn_{1/3}Co_{1/3}O_2$ was coated with a carbon by using a sol-gel method to improve further its electrochemical properties. Electrochemical studies were performed by assembling 2032 coin cells with lithium metal as an anode. OSC (differential scanning calorimetry) data showed that exothermic reactions of charged to 4.3V vs. Li was suppressed in the carbon-coated materials. The carbon-coated $LiNi_{1/3}Mn_{1/3}Co_{1/3}O_2$ showed the improved rate capability and thermal stability.

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$BaTiO_3$ 세라믹의 유전손실에 미치는 Mn 첨가의 영향 (Effect of Mn Addition on the Dielectric Loss characteristics of $BaTiO_3$ Ceramics)

  • 김태중;한주환;이재열;이희영
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2000년도 하계학술대회 논문집
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    • pp.436-439
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    • 2000
  • Change of dielectric loss of use in high relative permitivity capacitor BaTiO$_3$ ceramic depends on Mn doping have been investigated. The powders used in this study were commercial BaTiO$_3$, TiO$_2$and, MnCO$_3$. Sample was fabricated by conventional ceramic process. The quantity of Mn was changed gradually from 0.lmol% to 10mo1%. The sintering densities were reduced with increasing amount of MnCO$_3$. This result is because of increase of low density second phase BaMnO$_3$. When the samples were doped by over 0.2mol% of MnCO$_3$, average grain sizes were enlarge to several tens ${\mu}{\textrm}{m}$. The dielectric losses were reduced by Mn doping to lmol% but, increased from lmol% to 10mo1% gradually.

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리튬 이차전지용 LiMn1.92Co0.08O4, LiNi1-yCoyO2 의 합성과 그들의 혼합물의 전기화학적 특성 (Syntheses of LiMn1.92Co0.08O4 and LiNi1-yCoyO2 and Electrochemical Properties of their Mixtures for Lithium Secondary Battery)

  • 권익현;김훈욱;송명엽
    • 한국수소및신에너지학회논문집
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    • 제15권1호
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    • pp.62-71
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    • 2004
  • $LiMn_{1.92}Co_{0.08}O_4-x\;wt.%LiNi_{0.7}Co_{0.3}O_2$를 단순화한 연소법에 의하여 합성하고, 그것들의 전기화학적 특성을 조사하였다. 또한 30분동안 밀링하여 준비한 $LiMn_{1.92}Co_{0.08}O_4-x\;wt.%LiNi_{0.7}Co_{0.3}O_2$ (x=9, 23, 33, 41 and 47) 혼합물 전극의 전기화학적 특성을 조사하였다. x=33 조성의 전극이 가장 큰 초기방전용량(132.0mAh/g at 0.1C)을 나타내었다. x=9조성의 전극은 비교적 큰 초기방전용량(109.9mAh/g at 0.1C)과 우수한 싸이클 특성을 나타내었다. 싸이클링에 따른 혼합물 전극의 방전용량의 감소는 주로 $LiNi_{0.7}Co_{0.3}O_2$의 퇴화에 기인한다고 생각된다. 그런데 $LiNi_{0.7}Co_{0.3}O_2$의 퇴화는 $LiMn_{1.92}Co_{0.08}O_4$로부터 용해된 Mn이 $LiNi_{0.7}Co_{0.3}O_2$를 둘러쌈(coating)으로써 야기되는 것으로 생각된다.

$NiFe/Co/Al_2O_3/Co/IrMn$ 접합의 터널링 자기저항효과

  • 홍성민;이한춘;김택기
    • 한국자기학회지
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    • 제9권6호
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    • pp.291-295
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    • 1999
  • IrMn을 반강자성체로 사용하고 순수한 Al을 자연산화시켜서 제작한 Al203를 절연층으로 사용한 spin-valve 형태의 NiFe/Co/Al2O3/Co/IrMn 터널링 접합의 자기저항효과를 조사하였다. IrMn의 두께가 약 100$\AA$이상일 경우 강자성체와의 교환상호작용이 발생하기 때문에 NiFe(183$\AA$)/Co(17$\AA$)/Al-oxide(16$\AA$)IrMn(100$\AA$) 터널링 접합에서 자기저항효과가 관찰되며 TMR비(%)는 $\pm$20 Oe의 인가자장에서 10% 이상의 값을 갖는다. 하부 자성층인 NiFe/Co의 길이방향으로 수행한 자장 중 열처리에 의해 저항은 다소 감소하고 TMR비(%)는 열처리온도에 따라 증가하여 20$0^{\circ}C$에서 23%의 최대값을 갖는다. 자성층의 폭을 변호시켜 접합면적을 달리한 시료의 TMR비(%)는 접합면적이 증가할수록 증가하고 저항은 감소한다.

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La 개질을 통한 Ni-rich LiNi0.9Co0.05Mn0.05O2 양극재의 고도로 안정화된 미세구조 및 우수한 전기화학적 성능 (Highly stabilized microstructure and excellent electrochemical performances of Ni-rich LiNi0.9Co0.05Mn0.05O2 cathode via La modification)

  • 이승환
    • 산업기술연구
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    • 제42권1호
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    • pp.1-5
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    • 2022
  • Although the mileage of electric vehicles can be increased based on the excellent energy density of the LiNi0.9Co0.05Mn0.05O2, it is known that the reason for limiting its use is the low lifespan and poor surface stability due to the structural deformation of the LiNi0.9Co0.05Mn0.05O2. To improve the structural stability of LiNi0.9Co0.05Mn0.05O2, electrochemical performance is improved by La coating on the surface. La-modified LiNi0.9Co0.05Mn0.05O2 shows an initial capacity of 210.6 mAh/g, a capacity retention rate of 89.9 % after 50 cycles, and a retention rate of 52.5% at 6.0 C. These are superior performances than the pristine sample, because the structural stability of the LiNi0.9Co0.05Mn0.05O2 cathode is improved by the La coating.

${Li_2}{CO_3}-{Li_3}{PO_4}-{Al_2}{O_3}$계의 고체 전해질 및 ${LiMn_2}{O_4}$의 기준전극을 사용한 $CO_2$ 가스센서 (Solid-State $CO_2$ Sensor using ${Li_2}{CO_3}-{Li_3}{PO_4}-{Al_2}{O_3}$ Solid Electrolyte and ${LiMn_2}{O_4}$ as Reference Electrode)

  • 김동현;윤지영;박희찬;김광호
    • 한국세라믹학회지
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    • 제37권8호
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    • pp.817-823
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    • 2000
  • A solid-state electrochemicall cell for sensing CO2 gas was fabricated using a solid electrolyte of Li2CO3-Li3PO4-Al2O3 mixture and a reference electrode of LiMn2O4. The e.m.f. (electromotive force) of sensor showed a good accordance with theoretical Nernst slope (n=2) for CO2 gas concentration range of 100-10000 ppm above 35$0^{\circ}C$. The e.m.f. of sensor was constant regardless of oxygen partial pressure at the high temperature above 0.1 atm. It was, however, a little depended on oxygen partial pressure as the pressure decreased below 0.1 atm. The oxygen-dependency of our sensor gradually disappeared as the operating temperature increased. The sensing behavior of our CO2 sensor was affected by the presence of water vapor, but its effect was small comparing with other sensors.

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