• 전기화학회지
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• 제15권2호
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• pp.67-73
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• 2012

본 연구에서는 습식분쇄, 구형화 분무건조 및 열처리 공정을 통해 구형의 $LiMn_{2-x}M_xO_4$(M = Al, Mg, B) 스피넬계 양극소재를 합성하고, 이의 전기화학적 성능을 평가하였다. $MnO_2$ (Tosoh, 91.94%), $Li_2CO_3$ (SQM, 97%), $MgCO_3$ (Aldrich, 99%), $Al(OH)_3$ (Aldrich, 99%) 및 $B_2O_3$ (Aldrich, 99%)를 원료로 사용하였으며, 분무건조공정에서 전구체의 구형화도 증가를 위해 PAAH 바인더를 첨가하였다. 200~500 nm 크기로 분쇄된 혼합 슬러리 용액으로부터 분무건조법을 통해 구형의 전구체를 제조하고, 이를 다양한 조건에서 열처리하여 최종 스피넬계 $LiMn_{2-x}M_xO_4$ (M = Al, Mg, B) 양극소재를 제조하였다. 제조된 구형의 $LiMn_{2-x}M_xO_4$ (M = Al, Mg, B) 양극재료는 이종원소 치환량, 특히 Boron 치환량에 따라 입자 표면 및 내부의 치밀도가 변화하는 것을 확인할 수 있었으며, 치밀도가 증가함에 따라 소재의 출력특성이 향상되었으며, 최적 조성의 양극소재는 상온 5 C 용량이 0.2 C 용량 대비 90% 이상이 됨을 확인하였다. 또한 표면의 치밀도도 증가함에 따라 $60^{\circ}C$ 고온 충방전 조건에서 수명특성이 향상되어 500회 사이클 이후에도 초기용량의 80% 이상을 유지하였다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2007년도 하계학술대회 논문집 Vol.8
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• pp.46-46
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• 2007

There has been rapid progress in the portable electronics industry. which has led to a great increase for a demand of portable, lightweight power sources. Lithium 2'nd batteries have met these demand. and many studies on the cahtod materials for the lithium 2,nd batteries have been reported during the last decade. Possible candidates for the cathode materials for lithium 2,nd batteries are $LiCoO_2$, $LiNiO_2$, and $LiMn_2O_4$. Currently $LiCoO_2$ is widely used. but $LiMn_2O_4$ is an excellent alternative material in view of its several advantages such a low cost as well as the wasy availability of raw materials and environmental benignity. In this study, find the most suitable synthesis method that satisfied high capacitor and stability cycle character, etc in Li-Mn oxide for 2'nd batteries. And also made an experiment on doping the $LiMn_2O_4$ spinel with a small amount of metal ions has a remarkable effect on the electrochemical properties and characterics of powder, BET, PSA, Porosity, etc.

• The Korean Journal of Ceramics
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• 제5권3호
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• pp.250-254
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• 1999

Synthesis of the spinel $LiMn_2O_4$ by emulsion method was investigated. $LiOH.H_2O \;and \;Mn(NO_3)_2.6H_2O$ were used as starting materials to prepare mixed aqueous solution (0.5 mol/$\ell$ for the $LiMn_2O_4$). Kerosene, paraffin oil and span 80 were used for organic phase. The aqueous solutioin and organic phase were mixed in the ratio of 2:1 and emulsified at the speed of 4000 rpm for 5 min. The prepared emulsions were dropped into the petroleum heated at $170^{\circ}C$ to evaporate water in the silicon oil bath, dried at $120^{\circ}C$ in the oven the remove petroleum and calcined at temperature ranges from 600 to $900^{\circ}C$ for 48 hrs. The characteristics of powders were investigated by XRD, SEM, BET and electrochemical properties of synthesized cathode materials were measured with Galvanostatic system. $Li_{1.05}Mn_2O_4$ calcined at $800^{\circ}C$ for 48 hrs showed initial discharge capacity of 125.9mAH/g.

• 한국전기전자재료학회논문지
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• 제14권8호
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• pp.663-669
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• 2001

Spinel LiM $n_2$ $O_4$ and LiM $n_{1.9}$M $g_{0.1}$ $O_4$ power was synthesized with solid-state method by calcining the mixture of LiOH.$H_2O$, Mn $O_2$ and MgO at 80$0^{\circ}C$ for 36 h in an air atmosphere. To investigate the effect of temperature on he cycle performance of cathode material during cycling, charge-discharge experiments and ac impedance measurement were performed. Initial discharge capacity was gradually increased with the increase of charge-discharge temperature. Discharge capacity at high temperature was suddenly decreased during cycling. On the other hand, discharge capacity at low temperature was almost constant during cycling. It confirmed that Mn dissolution is serious at high temperature than at low temperature. LiM $n_2$ $O_4$ and LiM $n_{1.9}$M $g_{0.1}$ $O_4$ showed the best capacity and stability at room temperature.ure.ure.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1998년도 추계학술대회 논문집
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• pp.175-178
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• 1998

LiMn$_2$O$_4$-based spinels has been studied extensively as positive electrode materials for rechargeable lithium and lithium ion batteries. We describe here that LiMn$_2$O$_4$ cathode active materials is preparated by sol-gel process using water as solvent, which often yields inorganic oxides of excellent phase purity and well-controlled stoichiometry. Using this process, it has been possible to synthesize phase-pure crystalline spinel LiMn$_2$O$_4$ by calcining the appropriate precursors in air at 80$0^{\circ}C$ for several hours. The influence of different time have also been explored. LiMn$_2$O$_4$ preparated in the present study exhibit the single phase of cubic and active reaction at 400 ~ $600^{\circ}C$. Electrochemical studies show that the this method- synthesized materials appear to present reversible oxidation and reduction reactions at 3.0V ~ 4.5V and cycle stability during 50 cycle.

• Journal of Electrochemical Science and Technology
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• 제1권2호
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• pp.97-101
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• 2010

In order to apply hybrid capacitor, $Li_2Mn_3O_7$ was synthesized by combustion method using $LiNO_3$, $Li(CH_3COO){\cdot}2H_2O$ and $Mn(CH_3COO){\cdot}4H_2O$. Spinel pattern was identified the samples calcined over $400^{\circ}C$ in XRD. Intensity of $Mn_2O_3$ peak increased as the calcination temperature increased. To decide n/p ratio and to investigate electrochemical properties, charge-discharge tests of Li/$Li_2Mn_3O_7$ and Li/AC half-cell were carried out. Applying to AC/$Li_2Mn_3O_7$ hybrid capacitor, it had high discharge capacitance of 32.8 F/cc at 100 mA/g.

• 공업화학
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• 제16권5호
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• pp.689-692
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• 2005

스피넬계 $LiMn_2O_4$를 양극 활물질로 사용하는 리튬이온전지의 전기화학적 성능을 향상시키기 위하여 서로 상이한 입자크기를 가지는 Super P Black 및 $Vulcan^{(R)}$ XC-72R을 사용한 이성분계 전도성물질을 제조하였다. 이렇게 이성분계 전도성물질을 사용하여 제조되어진 $LiMn_2O_4$ 전지 시스템은 충 방전 동안의 비용량 및 사이클 수명의 관점에서 특성 평가되었다. 결과적으로 Super P Black 및 $Vulcan^{(R)}$ XC-72R이 3:7의 비율로 구성되어진 이성분계 전도성물질을 사용하였을 때의 전지가 우수한 전기화학적 성능을 보여주었으며 이는 적절한 조합의 ionic diffusion rate와 electric contact에 의해 제어되어졌기 때문인 것으로 여겨진다.

• 한국응용과학기술학회지
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• 제18권3호
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• pp.167-173
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• 2001

The spinel $LiMn_{2}O_{4}$ powders were synthesized at $480^{\circ}C$ for 12 h in air by a sol-gel method using manganese acetate and lithium hydroxide as starting material and the $Fe_{3}O_{4}$ powders were synthesized by the precipitation method using $0.2M-FeSO_{4}{\cdot}H_{2}O$ and 0.5M-NaOH. The synthesized $Fe_{3}O_{4}$ powders were mixed at portion of 5, 10, 15 and 20 wt% about $LiMn_{2}O_{4}$ powders through ball-milling followed by drying at room temperature for 48 h in air. The mixed catalysts were reduced at $350^{\circ}C$ for 3 h by hydrogen and the decomposition rate of carbon dioxide was measured at $350^{\circ}C$ using the reduced catalysts. As the results of $CO_{2}$ decomposition experiments, the decomposition rates of carbon dioxide were 85% in all catalysts but the initial decomposition rates of $CO_{2}$ were slightly high in the case of the $5%-Fe_{3}O_{4}$ added catalyst.

• Bulletin of the Korean Chemical Society
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• 제23권5호
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• pp.679-682
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• 2002

Layered Na0.7[Ni0.05Mn0.95]O2 compounds have been synthesized by a sol-gel method, using glycolic acid as a chelating agent. Na0.7[Ni0.05Mn0.95]O2 precursors w ere used to prepare layered lithium manganese oxides by ion exchange for Na by Li, using LiBr in hexanol. Powder X-ray diffraction shows the layered Na0.7[Ni0.05Mn0.95]O2 has an O3 type structure, which exhibits a large reversible capacity of approximately 190 mA h g-1 in the 2.4-4.5 V range. Na0.7[Ni0.05Mn0.95]O2 powders undergo transformation to spinel during cycling.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2017년도 춘계학술대회 논문집
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• pp.169-169
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• 2017

Due to key roles for the electrochemical stability and charge capacity the solid-electrolyte interphase (SEI) has been extensively studied in anodes of a Li-ion battery cell. There is, however, few of investigation for cathodes. Using first-principles based calculations we describe atomic-level process of the SEI layer formation at the interface of a carbonate electrolyte and $LiMn_2O_4$ spinel cathode. Furthermore, using beyond the conventional density functional theory (DFT+U) calculations we examine the work function of the cathode and frontier orbitals of the electrolyte. Based on the results we propose that proton transfer at the interface is an essential mechanism initiating the SEI layer formation in the $LiMn_2O_4$. Our results can guide a design concept for stable and high capacity Li-ion battery cell through screening an optimum electrolyte fine-tuned energy band alignment for a given cathode.