• 한국결정성장학회지
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• 제6권4호
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• pp.600-608
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• 1996

리튬 이온이 intercalation되어 스핀넬 구조를 이루고 있는 $Li_{x}Mn_{2}O_{4}(0.2{\leq}x{\leq}2.0)$의 구조적 특성을 X-선 회절분석과 Li/1M $LiClO_{4}$-propylene carbonate solution/$Li_{x}Mn_{2}O_{4}$ 전지에서 이들의 구조적 특징에 의한 전기화학적 특성을 연구하였다. $Li_{x}Mn_{2}O_{4}$의 전기화학적 특성에 대한 조성과 반응온도의 영향은 상전이 현상과, 결정 상수 측정과 열분석에 의하여 연구하였다. 산처리 후 $Li_{x}Mn_{2}O_{4}$는 거의 순수한 ${\lambda}-MnO_{2}$구조로 상전이 되었으며 이때 격자상수 $a_{c}$가 8.255에서 $8.031\;{\AA}$으로 수축되었다. $Li_{x}Mn_{2}O_{4}$의 조성 범위가 $0.2{\leq}x{\leq}0.6$일 때 격자상수 $8.255\;{\AA}$의 단일상을 나타내며 3.9~3.7 V의 전위 평탄 영역을 나타낸다.

• 한국진공학회지
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• 제20권3호
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• pp.205-210
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• 2011

졸-겔(sol-gel) 방법을 이용하여 스피넬(spinel) 구조의 산화물 $LiMn_2O_4$ 박막을 Pt/Ti/$SiO_2$/Si 기판 위에 제작하여 그 구조적 성질 및 이차 전지 전기화학적 특성을 조사하였다. 박막에서의 Li/Mn 몰비(molar ratio)가 0.5 미만일 경우 박막에 $LiMn_2O_4$ 상뿐만 아니라 $Mn_2O_3$ 상이 존재함이 관측되었다. $LiMn_2O_4$ 박막을 이용한 반전극(half cell) 전지를 제작하여 충전-방전 순환과정을 반복수행 하였고, 과정 시작 전후에 X-ray diffraction 및 Raman spectroscopy 측정을 통하여 과정 중 발생하는 박막의 구조적 성질 변화를 조사하였다. 순수한 $LiMn_2O_4$ 박막 전지의 경우 충전-방전 횟수가 증가함에 따라 방전 용량은 서서히 감소하여 300회에 이르러서는 초기 용량의 72%로 줄어들었다. 이와 같은 결과는 충전-방전 과정 중 스피넬 구조의 사면체 자리로부터 탈리되었다가 다시 삽입되는 $Li^+$ 이온 수의 감소 및 이에 따르는 $Mn^{4+}$ 이온 수 증가와 관련이 있는 것으로 해석된다. 또한, 순환 횟수가 증가함에 따라 박막 내에 $Mn_2O_3$ 상의 밀도가 점차 증가함이 관측되었다.

• 한국전기전자재료학회논문지
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• 제25권5호
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• pp.398-402
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• 2012

Synthesis of $Li_2MnSiO_4$ was attempted by the conventional solid-state reaction method, and the phase formation behavior according to the change of the calcination condition was investigated. When the mixture of the three source materials, $Li_2O$, MnO and $SiO_2$ powders, were used for calcination in air, it was difficult to develop the $Li_2MnSiO_4$ phase because the oxidation number of $Mn^{2+}$ could not be maintained. Therefore, two-step calcination was applied: $Li_2SiO_3$ was made from $Li_2O$ and $SiO_2$ at the first step, and $Li_2MnSiO_4$ was synthesized from $Li_2SiO_3$ and MnO at the second step. It was easy to make $Li_2MnSiO_3$ from $Li_2O$ and $SiO_2$. $Li_2MnSiO_4$ single phase was developed by the calcination at $900^{\circ}C$ for 24 hr in Ar atmosphere as the oxidation of $Mn^{2+}$ was prevented. However, the $Li_2MnSiO_4$ was ${\gamma}-Li_2MnSiO_4$, one of the polymorph of $Li_2MnSiO_4$, which could not be used as the cathode materials in Li-ion batteries. By applying the additional low temperature annealing at $400^{\circ}C$, the single phase ${\beta}-Li_2MnSiO_4$ powder was synthesized successfully through the phase transition from ${\gamma}$ to ${\beta}$ phase.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2009년도 하계학술대회 논문집
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• pp.452-452
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• 2009

HEV용 리튬 이차전지의 양극물질로서 $LiMn_2O_4$는 일반적으로 사용되고 있는 $LiCoO_2$에 비해 값이 저렴하고 독성이 낮으며, 높은 전압과 좋은 율 특성을 갖는 물질이다. 하지만 고온에서 전이금속인 Mn이 전해액으로 용출되어 급격한 용량감소로 인한 짧은 수명의 단점을 가지고 있다. 흔히 전구체로 쓰이는 $MnO_2$, $Mn_3O_4$, MnOOH등은 전기 분해법을 이용한 EMD가 주로 이용된다. 본 연구에서는 출발 물질로 $KMnO_4$와 $Mn(NO_3)_2$를 수용액 반응을 시켜서 농도, 온도변화에 따른 입자 형상 및 크기와 결정상의 변화를 관찰하고, 화학적 방법으로 얻어진 $MnO_2$와 LiOH를 합성하여 각각의 $LiMn_2O_4$를 비교 분석하고자한다.

• 한국재료학회지
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• 제11권6호
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• pp.498-501
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• 2001

0.9Pb($Mg_{1/3}Nb_{2/3}$)$O_3$-0.1Pb$TiO_3$계 완화형 강유전체에서 MnO$_2$ 첨가가 압전물성에 미치는 영향을 강유전성이 우세한 온도영역인 -40~3$0^{\circ}C$의 온도범위에 걸쳐 조사하였다. MnO$_2$ 첨가에 의한 효과를 유전특성, 압전특성, 전계유기 변형특성 등의 영역에서 고찰하였다 MnO$_2$ 첨가량이 증가할수록 유전성 및 압전성은 hard piezoelectric의 경향을 나타내었다. 이러한 실험적 고찰로부터 첨가된 Mn은 강유전 도메인 분역을 고정하는 역할을 하는 것으로 제안되었다.

• Transactions on Electrical and Electronic Materials
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• 제7권2호
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• pp.76-80
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• 2006

Well-defined orthorhombic $LiMnO_2\;and\;LiCo_{0.1}Mn_{0.9}O_2$ were synthesized by a solid-state reaction and quenching process. X-ray diffraction (XRD) results revealed that the as-synthesized powders showed an orthorhombic phase of a space group with Pmnm. The $Li/LiMnO_2\;and\;Li/LiCo_{0.1}Mn_{0.9}O_2$ cells were constituted and cycled galvanostatically in the voltage range of 2.0-4.3 V vs. $Li/Li^+$ at a current density of $0.5\;mA\;cm^{-2}$ at room temperature and $50^{\circ}C$, respectively. The results demonstrated that the highest specific capacity of $Li/LiMnO_2$ cells at room temperature and $50^{\circ}C$ was 95 and $155\;mAh\;g^{-1}$, respectively. As for $Li/LiCo_{0.1}Mn_{0.9}O_2$ cells, the highest specific capacity at room temperature and $50^{\circ}C$ was 160 and $250\;mAh\;g^{-l}$, respectively. It could be seen that the performance of $Li/LiCo_{0.1}Mn_{0.9}O_2$ cells was better than that of $Li/LiMnO_2$ cells.

• 한국결정성장학회지
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• 제13권2호
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• pp.63-67
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• 2003

Synthesis of $PbLaTiO_{3}$ : Mn powders containing La and Mn was carried out using $PbO,\;TiO_{2},\;La_{2}O_{3}\;and\;MnO_{2}$ as starting materials by hydrothermal method. In the synthesis of single phase $PbLaTiO_{3}$ : Mn powder containing La and Mn, the optimal x value corresponding to La substitution was 0.01 which corresponds to $0.99(Pb_{1-x}La_{2x/3}TiO_{3})+0.01MnO_{2}$. The optimal conditions for the preparation of the powder synthesis were 8 M-KOH solvent of hydrothermal solvent, $270^{\circ}C$ of reaction temperature and 24 hrs of run time. It was found that the synthesized powders had spherical morphology with average particle size of 70 nm and specific surface area of $5.5\;m^{2}/g$.

• 한국세라믹학회지
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• 제30권1호
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• pp.25-33
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• 1993

Formation reaction of Mn-Zn ferrite depending on various synthetic conditions of wet process was investigated using FeCl2.nH2O(n≒4), MnCl2.4H2O, ZnCl2 as starting materials. A stable intermediate precipitate was formed by the addition of H2O2. And the precipitate was hard to transform to spinel phase of Mn-Zn Fe2O4. Single phase of Mn-Zn Fe2O4 spinel was obtained above 8$0^{\circ}C$ reaction temperature. The powder had spherical particle shape and 0.02~0.05${\mu}{\textrm}{m}$ particle size. Fe(OH)2 solid solution, -FeO(OH) solid solution, -FeOOH, Mn-Zn Fe2O4 spinel were formed with air flow rate 180$\ell$/hr. However, single phase of Mn-Zn Fe2O4 spinel with cubic particle shape and 0.1~0.2${\mu}{\textrm}{m}$ particle size was formed with synthetic conditions of 8$0^{\circ}C$ and 90 munutes. The particle shape of the -FeOOH was needle-like.

• 한국재료학회지
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• 제22권8호
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• pp.385-389
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• 2012

Significant improvements in the switching voltage distribution are required for the development of unipolar resistive memory devices using $MnO_x$ thin films. The $V_{set}$ of the as-grown $MnO_x$ film ranged from 1 to 6.2 V, whereas the $V_{set}$ of the oxygen-annealed film ranged from 2.3 to 3 V. An excess of oxygen in an $MnO_x$ film leads to an increase in $Mn^{4+}$ content at the $MnO_x$ film surface with a subsequent change in the $Mn^{4+}/Mn^{3+}$ ratio at the surface. This was attributed to the change in $Mn^{4+}/Mn^{3+}$ ratios at the $MnO_x$ surface and to grain growth. Oxygen annealing is a possible solution for improving the switching voltage distribution of $MnO_x$ thin films. In addition, crystalline $MnO_x$ can help stabilize the $V_{set}$ and $V_{reset}$ distribution in memory switching in a Ti/$MnO_x$/Pt structure. The improved uniformity was attributed not only to the change of the crystallinity but also to the redox reaction at the interface between Ti and $MnO_x$.

• 한국분말재료학회지
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• 제25권4호
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• pp.296-301
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• 2018

In this study, an experiment is performed to recover the Li in $Li_2CO_3$ phase from the cathode active material NMC ($LiNiCoMnO_2$) in waste lithium ion batteries. Firstly, carbonation is performed to convert the LiNiO, LiCoO, and $Li_2MnO_3$ phases within the powder to $Li_2CO_3$ and NiO, CoO, and MnO. The carbonation for phase separation proceeds at a temperature range of $600^{\circ}C{\sim}800^{\circ}C$ in a $CO_2$ gas (300 cc/min) atmosphere. At $600{\sim}700^{\circ}C$, $Li_2CO_3$ and NiO, CoO, and MnO are not completely separated, while Li and other metallic compounds remain. At $800^{\circ}C$, we can confirm that LiNiO, LiCoO, and $Li_2MnO_3$ phases are separated into $Li_2CO_3$ and NiO, CoO, and MnO phases. After completing the phase separation, by using the solubility difference of $Li_2CO_3$ and NiO, CoO, and MnO, we set the ratio of solution (distilled water) to powder after carbonation as 30:1. Subsequently, water leaching is carried out. Then, the $Li_2CO_3$ within the solution melts and concentrates, while NiO, MnO, and CoO phases remain after filtering. Thus, $Li_2CO_3$ can be recovered.