• Bulletin of the Korean Chemical Society
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• 제25권6호
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• pp.913-916
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• 2004

• 전기화학회지
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• 제7권1호
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• pp.32-37
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• 2004

리튬 이차전지의 음극재료로서 천연흑연의 충방전 속도에 따른 용량특성을 조사하였다 정전류 조건에서 $0.0-2.0V(vs. Li/Li^+)$의 범위에서 충방전 하였을 때, 충전전류가 증가할수록 충전반응의 과전압이 증가하여 $Li^+$이온이 충분히 삽입되지 못한 상태에서 컷오프 전압(0.0 V)에 도달하기 때문에 충전용량은 충전전류의 크기가 클수록 감소하였다. 한편, 방전전류가 증가함에 따라 방전반응의 과전압도 증가하여 0.0-0.3V범위에서 방전반응이 일어나나 방전 컷오프 전압(2.0 V)과는 격차가 커서 $Li^+$이온이 탈리되지 못한 상태에서 방전 컷오프에 도달하는 현상은 없기 때문에 방전용량이 방전전류의 크기에 영향을 받지 않았다. 충전전류가 증가함에 따라 부반응인 리튬 전착반응의 과전압도 증가하므로 충전 컷오프 전압을 0.0V 이하로 낮출 수 있었다. 그러나 $Li^+$이온의 삽입반응에 비해 전착반응의 저항이 적어 충전전류에 따른 전착반응의 과전압 증가에는 한계가 있었다. 1C조건에서 -0.04V까지 충전 z컷오프 전압을 낮추었을 때 리튬의 전착반응은 없었고, 이로부터 약 $11\%$의 방전용량을 증가시킬 수 있었다.

• 전기화학회지
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• 제7권3호
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• pp.143-147
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• 2004

Vapor grown carbon fiber(VGCF)가 각기 달리 첨가된 부극으로 제조된 LPB의 특성을 조사하였다. MCMB를 활물질로, VGCF를 도전재로 사용하였을 경우, 전지의 내부저항과 1차 Ah효율은 VGCF첨가량이 많아질수록 감소하였고 방전 용량과 이용률은 증가하였다. $6wt\%$의 VGCF가 첨가된 부극으로 제조된 전지가 최저 임피던스를 나타내었고, $8wt\%$의 VGCF첨가한 경우는 VGCF를 첨가하지 않은 것과 유사한 임피던스를 나타내었다. $6wt\%$의 VGCF가 첨가된 부극으로 제조된 전지가 최고의 전지 특성을 나타내었다. 이 전지의 내부저항은 실온에서 $0.918\Omega$이였고, 2C에서의 고율 방전 시의 용량은 $93\%$였다. 율 특성과 수명 특성은 $4wt\%$와 $6wt\%$운의 VGCF가 첨가된 부극으로 제조된 전지가 타 전지에 비해 우수하였고 두 경우는 매우 유사한 결과를 나타내었다. $6wt\%$의 VGCF가 첨가된 부극으로 제조된 전지의 경우, 방전 용량은 충방전 사이클링을 진행함에 따라 서서히 감소하여 100회에서 178mAh/g의 비용량을 나타내었으며 이후에는 완만한 감소경향을 나타내었다. $6wt\%$의 VGCF첨가의 경우 이용률은 100회에서 $90\%$ 이상으로 $4wt\%$의 VGCF가 첨가된 부극으로 제조된 전지 보다 우수하였다.

• Journal of Electrochemical Science and Technology
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• 제8권2호
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• pp.101-106
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• 2017

$Li_2SiO_3$ was used as a coating material to improve the electrochemical performance of $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$. $Li_2SiO_3$ is not only a stable oxide but also an ionic conductor and can, therefore, facilitate the movement of lithium ions at the cathode/electrolyte interface. The surface of the $Li_2SiO_3$-coated $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$ was covered with island-type $Li_2SiO_3$ particles, and the coating process did not affect the structural integrity of the $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$ powder. The $Li_2SiO_3$ coating improved the discharge capacity and rate capability; moreover, the $Li_2SiO_3$-coated electrodes showed reduced impedance values. The surface of the lithium-ion battery cathode is typically attacked by the HF-containing electrolyte, which forms an undesired surface layer that hinders the movement of lithium ions and electrons. However, the $Li_2SiO_3$ coating layer can prevent the undesired side reactions between the cathode surface and the electrolyte, thus enhancing the rate capability and discharge capacity. The thermal stability of $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$ was also improved by the $Li_2SiO_3$ coating.

• 한국수소및신에너지학회논문집
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• 제8권3호
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• pp.137-141
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• 1997

The effects of Ag addition to Zr-based hydrogen storage alloys ($Zr_{0.7}Ti_{0.3}V_{0.4}Ni_{1.2}Mn_{0.4}$, $Zr_{0.7}Ti_{0.3}V_{0.4}Ni_{1.2}Mn_{0.3}Cr_{0.1}$ and $Zr_{0.6}Ti_{0.4}V_{0.4}Ni_{1.2}Mn_{0.3}Fe_{0.1}$) on the electrode properties were examined. Ag-free and Ag-added Ze-based alloys were prepared by arc melting, crushed mechanically, and subjected to the electrochemical measurement. In $Zr_{0.7}Ti_{0.3}V_{0.4}Ni_{1.2}Mn_{0.4}$ alloy, 0.08 wt% Ag addition to the alloy improved the activation rate. Also Ag addition improved both activation property and discharge capacity in $Zr_{0.7}Ti_{0.3}V_{0.4}Ni_{1.2}Mn_{0.3}Cr_{0.1}$. For these Ag-added alloys, discharge capacities with the change of charge-discharge current density(10mA, 15mA and 30mA) are almost constant. Showing very high rate capability, discharge capacity of $Zr_{0.6}Ti_{0.4}V_{0.4}Ni_{1.2}Mn_{0.3}Fe_{0.1}$ alloy increased by Ag addition to the alloy. When the amount of Ag addition in $Zr_{0.7}Ti_{0.3}V_{0.4}Ni_{1.2}Mn_{0.4}$ alloy increased too much, the electrode properties became worse. Unveiling mechanism of effect of Ag addition is now progressing in our laboratory.

• 한국수자원학회논문집
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• 제41권5호
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• pp.455-462
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• 2008

본 연구에서는 격자강우량과 격자기반의 수문정보와 연계하여 홍수기 유출량의 시공간적 분포를 파악할 수 있도록 물리적인 운동파(kinematic wave)이론에 근거한 분포형 강우-유출모형을 개발하였다. 이 모형은 홍수기동안의 지표흐름과 지표하 흐름의 시간적 변화와 공간적 분포를 모의할 수 있으며, 전처리과정으로서 ArcGIS 혹은 ArcView등의 GIS 프로그램을 이용하여 모형에 필요한 ASCII형태의 입력 매개변수 자료들을 가공하였다. 또한 후처리과정으로서 모형의 수행결과인 유역내의 유출량 분포 등을 GIS상에서 나타낼 수 있도록 ASCII형태로 출력하도록 구성하였다. 개발된 모형의 적용가능성을 검토하기 위하여 남강댐유역을 대상으로 유역을 500m의 정방형 격자로 분할하고 수계망을 통하여 유역 출구까지 운동파이론에 의해 추적 계산하였으며, 수문곡선 비교결과 재현성 높은 결과를 보여주었다.

• Journal of Electrochemical Science and Technology
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• 제5권4호
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• pp.109-114
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• 2014

The $Li_3V_2(PO_4)_3$/graphene nano-particles composite was successfully synthesized by a facile sol-gel method. The addition of a graphene in $Li_3V_2(PO_4)_3(LVP)$(LVP) showed the high crystallinity and influenced the morphology of the $Li_3V_2(PO_4)_3$ particles observed in X-ray diffraction (XRD) and scanning electron microscopy (SEM). The LVP/graphene samples were well connected, resulting in fast charge transfer. The effect of the addition graphene nano-particles on electrochemical performance of the materials was investigated. Compared with the pristine LVP, the LVP/graphene composite delivered a higher discharge capacity of $122mAh\;g^{-1}$ at 0.1 C-rate, better rate capability and cyclability in the potential range of 3.0-4.3 V. The electrochemical impedance spectra (EIS) measurement showed the improved electronic conductivity for the LVP/graphene composite, which can ensure the high specific capacity and rate capability.

• 한국분말재료학회지
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• 제24권2호
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• pp.87-95
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• 2017

Lithium silicate, a lithium-ion conducting ceramic, is coated on a layer-structured lithium nickel manganese oxide ($LiNi_{0.7}Mn_{0.3}O_2$). Residual lithium compounds ($Li_2CO_3$ and LiOH) on the surface of the cathode material and $SiO_2$ derived from tetraethylorthosilicate are used as lithium and silicon sources, respectively. Powder X-ray diffraction and scanning electron microscopy with energy-dispersive spectroscopy analyses show that lithium silicate is coated uniformly on the cathode particles. Charge and discharge tests of the samples show that the coating can enhance the rate capability and cycle life performance. The improvements are attributed to the reduced interfacial resistance originating from suppression of solid-electrolyte interface (SEI) formation and dissolution of Ni and Mn due to the coating. An X-ray photoelectron spectroscopy study of the cycled electrodes shows that nickel oxide and manganese oxide particles are formed on the surface of the electrode and that greater decomposition of the electrolyte occurs for the bare sample, which confirms the assumption that SEI formation and Ni and Mn dissolution can be reduced using the coating process.

• Bulletin of the Korean Chemical Society
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• 제31권11호
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• pp.3233-3237
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• 2010

A $Li[Ni_{0.3}Co_{0.4}Mn_{0.3}]O_2$ cathode was modified by coating with Li-La-Ti-O, and the effect of the coating thickness on their electrochemical properties was studied. The thickness of the coating on the surface of $Li[Ni_{0.3}Co_{0.4}Mn_{0.3}]O_2$ was increased by increasing the wt % of the coating material. The rate capability of the Li-La-Ti-O-coated electrode was superior to that of the pristine sample. 1- and 2-wt %-coated samples showed considerable improvement in capacity retention at high C rates. However, the rate capability of a 5-wt %-coated sample decreased. All the coated samples showed a high discharge capacity and slightly improved cyclic performance under a high cut-off voltage (4.8 V) condition. Results of a storage test confirmed that the Li-La-Ti-O coating layer was effective in suppressing the dissolution of the transition metals as it offered protection from the attack of the acidic electrolyte. In particular, the 2- and 5-wt %-coated samples showed a better protection effect than the 1-wt %-coated sample.

• 전기화학회지
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• 제10권4호
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• pp.252-256
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• 2007

A series of spherical porous carbons were prepared via resorcinol-formaldehyde (RF) sol-gel polymerization in the presence of cationic surfactant (CTAB, cetyltrimethylammonium bromide), wherein the carbon sphere size was controlled by varying the CTAB introduction time after a pre-determined period of addition reaction (termed as "pre-curing"). The sphere size gradually decreases with an increase in the pre-curing time within the range of 30-150 nm. The carbons possess two types of pores; one inside carbon spheres (intra-particle pores) and the other at the interstitial sites made by carbon spheres (inter-particle pores). Of the two, the surface exposed on the former was dominant to determine the electric double-layer capacitor (EDLC) performance of porous carbons. As the intra-particle pores were generated inside RF gel spheres by gasification, the pore diameter was similar for all these carbons, thereby the pore length turned out to be a decisive factor controlling the EDLC performance. The charge-discharge voltage profiles and complex capacitance analysis consistently illustrate that the smaller-sized RF carbons deliver a better rate capability, which must be the direct result of facilitated ion penetration into shorter pores.