• 제목/요약/키워드: Lithium oxide

검색결과 353건 처리시간 0.029초

가수된 산화 망간(Ⅳ)에 의한 리튬 동위원소의 크로마토그래피적 분리 (Chromatographic Separation of Lithum Isotopes by Hydrous Managanese(Ⅳ) Oxide)

  • 김동원
    • 대한화학회지
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    • 제45권3호
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    • pp.219-222
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    • 2001
  • 용리 크로마토그래피를 사용하여 가수된 산화 망간(Ⅳ)이온교환체로 화학적 이온교환을 통하여, 리튬 동위원소를 분리하는 연구를 하였다. 산화 망간(Ⅳ)이온교환체의 이온교환 용량은 0.5meq/g이었다. 무거운 리튬 동위원소는 용액상에, 그리고 가벼운 동위원소는 이온교환 수지상에 농축되었다. 분리인자는, Glueckauf의 방법으로 용리곡선과 동위원서 분석 값들로부터 구하였다. $^6Li^+$-$^7Li^+$ 동위원소쌍의 분별로부터 얻은 분리인자의 값은 1.018이었다.

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리튬이차전지용 리튬과잉계 양극 산화물의 충방전 과정 중 원자 구조 열화 과정과 전기화학 특성에 대한 분석 (Analysis for Atomic Structural Deterioration and Electrochemical Properties of Li-rich Cathode Materials for Lithium Ion Batteries)

  • 박서현;오필건
    • 공업화학
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    • 제31권1호
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    • pp.97-102
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    • 2020
  • 최근 리튬이차전지 양극 소재의 다양한 열화 메커니즘들이 밝혀지면서 이것을 제어하여 새로운 전기화학적 특성을 구현하고 기존 소재의 한계점을 극복하고자 하는 연구결과들이 많이 보고되고 있다. 특히, 리튬과잉산화물은 250 mA h g-1 이상의 고 용량 차세대 리튬이차전지 양극 물질로 주목받고 있으나, 충방전 과정 중에 소재 특유의 원자 구조 열화로 인해 활용이 제한되고 있다. 본 연구는 0.4Li2MnO3_0.6LiNi1/3Co1/3Mn1/3O2 리튬과잉소재의 충방전 과정 중에서 겪는 원자 구조 변화 과정을 분석하여 소재의 열화 과정을 밝히고 이를 개선하기 위한 연구 방향을 제시하고자 한다. 이를 위해, 원자 단위의 분해능을 갖는 전자투과현미경을 활용하여 충방전 중 원자 구조의 변화 과정을 분석하고 이러한 구조 변화가 소재의 전기화학적 특성에 어떠한 영향을 미치는지 밝히고자 하였다. 충전 과정 중에 발생한 다량의 리튬 빈자리로 인해 구조 불안정성이 일어났고, 이로 인해 전이 금속이 리튬 빈 자리로 이동하면서 구조 열화가 확인되었다. 결과적으로 이러한 구조 변이는 리튬과잉소재의 가장 큰 문제점인 방전 전압 강하 특성을 야기한다는 것을 알아내었다.

리튬-공기전지용 탄소/망간산화물 복합구조 공기극의 전기화학적 특성 (Electrochemical Properties of Carbon/Manganese Oxide Composite Air Cathode for Lithium-Air Batteries)

  • 이선영;차은희;모선일;주재백;조원일
    • 전기화학회지
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    • 제15권3호
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    • pp.198-205
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    • 2012
  • 리튬-공기전지 공기극으로서 탄소 상에 직접 수열합성법으로 망간산화물을 생성한 탄소지지 망간산화물 촉매를 합성하였다. 각 수열합성 조건에 따라서 만들어진 복합체에 대한 XRD, FE-SEM 분석을 통하여, 복합체의 결정구조, 형태, 크기 등을 확인하였는데 특히, 수열합성 온도 및 시간이 각각 $170^{\circ}C$, 12시간인 조건에서 만들어진 산화망간은 길이가 40-50 nm인 막대 모양을 갖는 것으로 나타났다. 합성된 복합체를 사용하여 만든 공기극과 리튬금속을 음극으로 하는 코인셀 형태의 리튬-공기전지를 만들어 전기화학적 특성을 조사한 결과 초기 방전 용량이 3,852 mAh/g으로 높았고 충 방전 횟수가 4회 정도 발현되었다.

층상계 하이니켈 양극재의 잔류 리튬 생성 및 저감 메커니즘 연구 (A Mechanism Study on Formation and Reduction of Residual Li of High Nickel Cathode for Lithium-ion Batteries)

  • 빈민욱;나범탁;홍태은;김영진
    • 산업기술연구
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    • 제42권1호
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    • pp.7-12
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    • 2022
  • High nickel layered oxide cathodes are gaining increasing attention for lithium-ion batteries due to their higher energy density and lower cost compared to LiCoO2. However, they suffer from the formation of residual lithium on the surface in the form of LiOH and Li2CO3 on exposure to ambient air. The residual lithium causes notorious issues, such as slurry gelation during electrode preparation and gas evolution during cell cycling. In this review, we investigate the residual lithium issues through its impact on cathode slurry instability based on deformed polyvinylidene fluoride (PVdF) as well as its formation and reduction mechanism in terms of inherently off-stoichiometric synthesis of high nickel cathodes. Additionally, new analysis method with anhydrous methanol was introduced to exclude Li+/H+ exchange effect during sample preparation with distilled water. We hope that this review would contribute to encouraging the academic efforts to consider practical aspects and mitigation in global high-energy-density lithium-ion battery manufacturers.

지르코니아 강화 리튬 실리케이트 세라믹의 특성과 임상적용 (Material properties and clinical application of zirconia-reinforced lithium silicate ceramics)

  • 김종은;김지환;심준성;박영범
    • 대한치과의사협회지
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    • 제56권3호
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    • pp.159-166
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    • 2018
  • 지르코니아 강화 리튬 실리케이트 세라믹 재료는, 현재 널리 사용되고 있는 e.max(리튬디실리케이트 세라믹) 재료에 비하여 더 개선된 강도를 지니고 있다. 단일 크라운의 수복에 사용될 수 있으며, 1.5mm 의 두께를 확보하는 것이 예지성 있는 치료를 위해 매우 중요하다. Celtra Duo의 경우 열처리를 수행하는 것이 강도나 마모 저항성 측면에서 도움이 될 것이다. 접착을 위해서는 불산의 처리가 도움이 되며, 너무 짧은 시간의 불산은 접착 강도의 개선에 도움을 주지 못할 수 있으므로 충분한 시간의 불산 처리가 필요하다. 지르코니아 강화 리튬 실리케이트 세라믹 재료는 실험실 연구가 지속적으로 수행되고 출판되고 있지만, 아직 신뢰할만한 임상연구는 매우 부족한 실정이다. 추가적인 임상연구를 통해 과학적인 근거를 마련하는 것이 매우 중요한 부분이 될 것이다.

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Electrochemical properties of all solid state Li/LiPON/Sn-substituted LiMn2O4 thin film batteries

  • Kong, Woo-Yeon;Yim, Hae-Na;Yoon, Seok-Jin;Nahm, Sahn;Choi, Ji-Won
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2011년도 제40회 동계학술대회 초록집
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    • pp.409-409
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    • 2011
  • All solid-state thin film lithium batteries have many applications in miniaturized devices because of lightweight, long-life, low self-discharge and high energy density. The research of cathode materials for thin film lithium batteries that provide high energy density at fast discharge rates is important to meet the demands for high-power applications. Among cathode materials, lithium manganese oxide materials as spinel-based compounds have been reported to possess specific advantages of high electrochemical potential, high abundant, low cost, and low toxicity. However, the lithium manganese oxide has problem of capacity fade which caused by dissolution of Mn ions during intercalation reaction and phase instability. For this problem, many studies on effect of various transition metals have been reported. In the preliminary study, the Sn-substituted LiMn2O4 thin films prepared by pulsed laser deposition have shown the improvement in discharge capacity and cycleability. In this study, the thin films of LiMn2O4 and LiSn0.0125Mn1.975O4 prepared by RF magnetron sputtering were studied with effect of deposition parameters on the phase, surface morphology and electrochemical property. And, all solid-state thin film batteries comprised of a lithium anode, lithium phosphorus oxy-nitride (LiPON) solid electrolyte and LiMn2O4-based cathode were fabricated, and the electrochemical property was investigated.

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Strategic design for oxide-based anode materials and the dependence of their electrochemical properties on morphology and architecture

  • 강용묵
    • 한국재료학회:학술대회논문집
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    • 한국재료학회 2012년도 춘계학술발표대회
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    • pp.73-73
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    • 2012
  • Modern technology-driven society largely relies on hybrid electric vehicles or electric vehicles for eco-friendly transportation and the use of high technology devices. Lithium rechargeable batteries are the most promising power sources because of its high energy density but still have a challenge. Graphite is the most widely used anode material in the field of lithium rechargeable batteries due to its many advantages such as good cyclic performances, and high charge/discharge efficiency in the initial cycle. However, it has an important safety issue associated with the dendritic lithium growth on the anode surface at high charging current because the conventional graphite approaches almost 0 V vs $Li/Li^+$ at the end of lithium insertion. Therefore, a fundamental solution is to use an electrochemical redox couple with higher equilibrium potentials, which suppresses lithium metal formation on the anode surface. Among the candidates, $Li_4Ti_5O_{12}$ is a very interesting intercalation compound with safe operation, high rate capability, no volume change, and excellent cycleability. But the insulating character of $Li_4Ti_5O_{12}$ has raised concerns about its electrochemical performance. The initial insulating character associated with Ti4+ in $Li_4Ti_5O_{12}$ limits the electronic transfer between particles and to the external circuit, thereby worsening its high rate performance. In order to overcome these weak points, several alternative synthetic methods are highly required. Hence, in this presentation, novel ways using a synergetic strategy based on 1D architecture and surface coating will be introduced to enhance the kinetic property of Ti-based electrode. In addition, first-principle calculation will prove its significance to design Ti-based electrode for the most optimized electrochemical performance.

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용액공정으로 제작한 리튬 도핑된 N-ZTO/P-SiC 이종접합 구조의 전기적 특성 (The Effects of Lithium-Incorporated on N-ZTO/P-SiC Heterojunction Diodes by Using a Solution Process)

  • 이현수;박성준;안재인;조슬기;구상모
    • 한국전기전자재료학회논문지
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    • 제31권4호
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    • pp.203-207
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    • 2018
  • In this work, we investigate the effects of lithium doping on the electric performance of solution-processed n-type zinc tin oxide (ZTO)/p-type silicon carbide (SiC) heterojunction diode structures. The proper amount of lithium doping not only affects the carrier concentration and interface quality but also influences the temperature sensitivity of the series resistance and activation energy. We confirmed that the device characteristics vary with lithium doping at concentrations of 0, 10, and 20 wt%. In particular, the highest rectification ratio of $1.89{\times}107$ and the lowest trap density of $4.829{\times}1,022cm^{-2}$ were observed at 20 wt% of lithium doping. Devices at this doping level showed the best characteristics. As the temperature was increased, the series resistance value decreased. Additionally, the activation energy was observed to change with respect to the component acting on the trap. We have demonstrated that lithium doping is an effective way to obtain a higher performance ZTO-based diode.

리튬고분자 이차전지의 전기적 전기화학적 특성

  • 박수길;박종은;손원근;류부형;이주성
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 1998년도 춘계학술대회 논문집
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    • pp.159-162
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    • 1998
  • The new type polymer electrolyte composed of polyacrylonitrile(PAN) baed polymer electrolyte contain LiClO$_4$-EC/PC and LiPF$\sub$6/-EC/PC were developed for the weightless and long or life time of lithium polymer battery system with using polyaniline electrode. The gel type electrolytes were prepared by PAN at different lithium salts in the glove box. We prepared for polymer electrolyte with knife casting method. The minimum thickness of PAN gel electrolyte for the slim type is about <400∼500$\mu\textrm{m}$. These gel electrolytes showed good compatibility with lithium electrode. The test cell of Li/polymer electrolyte/Lithium cobalt oxide solid state cell which was prepared by different lithium salt was researched by electrochemical technique. Resistance of polymer electrolyte which consist of LiClO$_4$ is more less than that of LiPF$\sub$6/ and cycle life is more longer than that of LiPF$\sub$6/.

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Bulky carbon layer inlaid with nanoscale Fe2O3 as an excellent lithium-storage anode material

  • Nguyen, Thuy-An;Lee, Sang-Wha
    • Journal of Industrial and Engineering Chemistry
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    • 제68권
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    • pp.140-145
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    • 2018
  • Bulky carbon layer uniformly distributed with nanoscale $Fe_2O_3$ was prepared via a direct carbonation of $Fe^{3+}$-polyacrylonitrile complexes at $700^{\circ}C$ under $N_2$ flow. The iron oxide carbon composites exhibited an excellent cycling performance for lithium storage with a reversible capacity of ${\sim}810mAh\;g^{-1}$ after 250 cycles at a current rate of $100mA\;g^{-1}$. The enhancement was mainly attributed to dual functions of bulky carbon layer which facilitated the lithium-ion diffusion and accommodated the volume changes of active $Fe_2O_3$ during charge/discharge process. Our novel chemical strategy is quite effective for scalable fabrication of high capacity lithium-storage materials.