• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 1995.11a
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• pp.340-342
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• 1995

We prepared $LiCo_{1-x}Ni_{x}O_2$ by reacting stoichiometric mixture of LiOH.$H_2O$, $CoCO_3$.$xH_2O$ and $Ni(OH)_2$(mole ratio respectively) and heating at $850^{\circ}C$ for 5n. In the result of X-ray diffraction analysis, along fluctuation of the function of x in $LiCo_{1-x}Ni_{x}O_2$(003) peak and (104) peak indensities and ratio were varied. We awared through XRD that from 0 to 0.5 at x in $LiCo_{1-x}Ni_{x}O_2$ is well formed for hexagonal structure at one step heat treatment($850^{\circ}C$), but if Ni involve at $LiCo_{1-x}Ni_{x}O_2$ hexagonal structure is not well formed. In the result of charge/discharge tests charge/discharge capacity and effiency is different about various cathode. Therefore, the appropriate charge/discharge method must be selected for good characteristics.

• Journal of the Korean Ceramic Society
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• v.35 no.5
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• pp.451-457
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• 1998

$Li_2$$ZrO_3$ powder which is one of the candidates of breeding materials for the fusion reactor was syn-thesized by a precipitation-combustion process. Although precipitates from the reaction between zirconium nitrate and citric acid were existed in a precursor solution. $Li_2$$ZrO_3$ could easily be obtained by using the mixed fuel of urea and citric acid in stoichiometric composition. The phases of as-synthesized powder con-sisted of $Li_2$$ZrO_3$ and small amounts of $Li_6$$Zr_2O_3$ and $Li_2$$ZrO_3$ The latter phases disappeared after the cal-cination at $1100^{\circ}C$ for 2 h. The primary particle size and the specific surface area of as-synthesized powders were smaller than 20nm and 10-14 $M^2$/g, respectively. The primary particle size of the precipitation-combustion synthesized powders was affected by the size of precipitates present in a precursor solution.

• Journal of Electrochemical Science and Technology
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• v.1 no.1
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• pp.45-49
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• 2010

$Li_2PtO_3$ thin film electrodes, which might be possible candidate for the cathode materials for implantable batteries, were synthesized using an electrostatic spray deposition (ESD) technique onto a platinum foil substrate. Single phase $Li_2PtO_3$with a structure similar to layered $LiCoO_2$ structure were synthesized by spraying a precursor solution of $CH_3CO_2Li2H_2O$ in ethanol onto a Pt substrate at temperatures ranging from 200 to $400^{\circ}C$ followed by annealing at above $600^{\circ}C$. Lithium carbonate was the only major phase at temperatures up to $500^{\circ}C$. The X-ray diffraction (XRD) peaks of the Pt foil substrate and lithium carbonate disappeared at temperatures >$600^{\circ}C$. The volumetric capacity of the $Li_2PtO_3$ thin film synthesized using the ESD technique was approximately 817 mAh/$cm^3$, which exceeded that of $LiCoO_2$ (711 mAh/$cm^3$).

• Proceedings of the Materials Research Society of Korea Conference
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• 1996.11a
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• pp.185-185
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• 1996

• Proceedings of the Korean Nuclear Society Conference
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• 2002.10a
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• pp.338.1-338
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• 2002

• Journal of the Korean Ceramic Society
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• v.48 no.5
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• pp.379-383
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• 2011

This paper presents the synthesis of one-dimensional spinel $LiMn_2O_4$ nanostructures using a facile and scalable two-step process. $LiMn_2O_4$ nanorods with average diameter of 100 nm and length of 1.5 ${\mu}m$ have been prepared by solid-state lithiation of hydrothermally synthesized ${\beta}$-$MnO_2$ nanorods. $LiMn_2O_4$ nanowires with diameter of 10 nm and length of several micrometers have been fabricated via solid-state lithiation of ${\beta}$-$MnO_2$ nanowires. The precursors have been lithiated with LiOH and reaction temperature and pressure have been controlled. The complete structural transformation to cubic phase and the maintenance of 1-D nanostructure morphology have been evaluated by XRD, SEM, and TEM analysis. The size distribution of the spinel $LiMn_2O_4$ nanorods/wires has been similar to the $MnO_2$ precursors. By control of reaction pressure, cubic 1-D spinel $LiMn_2O_4$ nanostructures have been fabricated from tetragonal $MnO_2$ precursors even below $500^{\circ}C$.

• Proceedings of the Korean Nuclear Society Conference
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• 2001.05a
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• pp.374.2-374
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• 2001

• Journal of the Korean Ceramic Society
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• v.34 no.3
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• pp.303-313
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• 1997

To enhance the strength and formability of MCFC matrixes, alumina/${\gamma}$-LiAlO2 fiber-reinforced ${\gamma}$-LiAlO2 ma-trixes have been investigated. The MCFC matrixes with the thickness of 500~600 ${\mu}{\textrm}{m}$ were prepared by tape-casting of the slurry containing 10~30wt% fibers, followed by heat-treating up to $650^{\circ}C$. The porosity of fi-ber-reinforced matrixes decreased with the content of fibers, while the appropriate porosity(50~60%) for MCFC matrixes could be attained by adding larger ${\gamma}$-LiAlO2 particles with the diameter of about 50${\mu}{\textrm}{m}$ up to 50 wt%. The optimum length and content of the alumina fiber, both in the alignment of fibers and the enhancement of the strength, were found to be below 250${\mu}{\textrm}{m}$ and 20 wt%, respectively. On the other hand, the strength(156 gf/$\textrm{mm}^2$) of the ${\gamma}$-LiAlO2 matrix reinforced with ${\gamma}$-LiAlO2 fibers prepared in this study was improved by 20~40% in comparison with the alumina-fiber-reinforced matrix. It was also found that the alu-mina-fiber-reinforced matrix was completely corroded in molten carbonates but the ${\gamma}$-LiAlO2 was not.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2007.06a
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• pp.497-497
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• 2007

활성탄소를 양쪽 전극에 사용하는 전기이중층 커패시터는 고출력 특성과 반영구적인 cycle 수명인 장점을 가지고 있는 반면, 단위 중랑 또는 부피 당 용량이 작아 메모리 백업용 보조전원으로서의 활용에 그치고 있다. 이를 보완하기 위하여 최근에는 앙쪽의 전극에 충방전 메카니즘을 달리하는 비대칭 전극 설계기술을 기반으로 하는 하이브리드 커패시터가 개발되었고, 에너지밀도로서는 유기계 전해액에서 약 15-20 Wh/kg를 가지는 것으로 보고되고 있다. 본 연구메서는 양극의 활성탄소에 비용량이 상대적으로 큰 LiCo02 분말을 혼합한 하이브리드 전극의 제조 및 전기화학적 특성을 조사하였다. 이때 $LiCoO_2$ 분말의 혼합 종량비의 영향에 의한 전극 부피 당 용량(mAh/cc)의 변화와 $LiCoO_2$ 분말의 입자 크기에 의한 하이브리드 전극의 출력 특성을 조사하였다. $LiCoO_2$ 분말은 불밀을 이용하여 입자크기를 조절하였고, 각각의 입자크기를 가지는 LiCoO2 분말을 활성탄소와 함께 혼합하여 혼합 활물질 : Carbon black : PTFE의 중량비가 90 : 5 : 5가 되도록 sheet 전극을 제조하였다. 제조한 전극을 양극에, Li foil을 음극에, 전해액을 LiPF6 in EC DMC를 사용하여 코인셀을 제조하고 전기화학적 특성은 MACCOR 충방전기를, AC 저항은 AC impedance를 각각 사용하여 평가하였다. 활성탄소에 $LiCoO_2$ 분말의 첨가 중량비가 증가할수록 전극 부피 당 용량은 증가하였으나, 원료 상태의 $LiCoO_2$ 분말의 첨가에서는 코인셀의 전극 저항은 첨가 중량에 따라 단순 증가하였다. 그러나 미세 $LiCoO_2$ 분말을 첨가할 경우, 20%의 첨가에서 전극 저항은 활성탄소 만을 사용한 전극과 동등한 전극저항을 나타내고 충방전 cycle 특성도 개선되는 것을 확인하였다.

• The Transactions of the Korean Institute of Electrical Engineers C
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• v.48 no.3
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• pp.179-184
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• 1999

In the past ten years, $LiMn_2O_4$-based spinels have been extensively studied as positive electrode materials for lithium-ion batteries. To improve the cycle performance of spinel $LiMn_2O_4$ as the cathode of 4V class lithium secondary batteries, spinel phases $LiMn_2O_4$ were prepared at various temperatures ranging form 600-900$^{\cire}C$ in air. The results showed that charge.dischare capacity of $LiMn_2O_4$ varied at 1st temperature from $200^{\circ}C to 600^{\circ}C$ increase with increasing temperature. $LiMn_2O_4$ synthesized at 2nd temperature $750^{\circ}C$excellent charge.discharge capacity, efficiency and cyclability compared to the samplesynthesized different temperatures. The value of lst charge.discharge capacity was 121mAh/g, 118mAh/g, Also, the efficiency value was about 97%.