• 대한화학회지
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• 제22권1호
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• pp.37-44
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• 1978

$BH_3$-THF 용액에 염화리튬을 가한 새로운 환원계의 환원특성에 대한 연구가 대표적인 작용기를 가진 유기화합물을 가지고 표준조건($0^{\circ}$, THF)에서 이루어졌다. 조사 연구된 화합물중 벤조페논, 4가지 에스테르 및 시클로헥센은 $BH_3$ 환원과 별 차이를 보이지 않았으나, 2-헵탄온, 아세토페논, 염화벤조일, 프탈산무수물, 그리고 3가지 에폭시화물은 소량의 염화리튬에 의해 빠른 속도로 환원이 완결 되었다. 특히 에폭시화시클로헥센의 환원에 있어서는 소량의 염화리튬 존재하에서는 정량적으로 시클로헥산올을 생성하였으나 염화리튬의 양이 증가하면 2-클로로시클로헥산올이 시클로헥산올과 함께 생성됨을 알았다. 또한, 에폭시화시클로헥센과의 반응에 있어서 질산리튬은 염화리튬과는 달리 별로 효과가 없었다. 따라서 보란-염화리튬용액에 클로로수소화붕소리튬의 생성가능성을 논의하였다.

• 전기화학회지
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• 제3권2호
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• pp.96-99
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• 2000

리튬 망간 산화물 박막의 고율 방전 특성을 향상시키기 위하여 사진 식각 법을 이용하여 미세 패턴된 양극 박막을 제조하였다. 방전 전류 밀도를 달리하여 측정한 결과, 리튬 이온의 intercalations kinetic레 관계하는 전하 전달 저항 값이 감소하게 되어 고율 방전 특성이 향상되었다.

• Carbon letters
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• 제19권
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• pp.40-46
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• 2016

Nitrogen-atom doped graphene oxide was considered to prevent the dissolution of polysulfide and to guarantee the enhanced redox reaction of sulfur for good cycle performance of lithium sulfur cells. In this study, we used urea as a nitrogen source due to its low cost and easy preparation. To find the optimum urea content, we tested three different ratios of urea to graphene oxide. The morphology of the composites was examined by field emission scanning electron microscope. Functional groups and bonding characterization were measured by X-ray photoelectron spectroscopy. Electrochemical properties were characterized by cyclic voltammetry in an organic electrolyte solution. Compared with thermally reduced graphene/sulfur (S) composite, nitrogen-doped graphene/S composites showed higher electroactivity and more stable capacity retention.

• Macromolecular Research
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• 제12권5호
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• pp.431-436
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• 2004

Cross-linked network solid polymer electrolytes were prepared by means of in situ hydrosilylation between poly[hydromethylslioxane-g-oligo(ethylene oxide)] and diallyl or triallyl group-containing poly(ethylene glycols). The conductivities of the resulting polymer electrolytes were greatly enhanced upon the addition of poly(ethylene glycol) dimethyl ether (PEGDME) as an ion-conducting plasticizer. Conductivities of the cross-linked polymer electrolytes were more dependent on the molecular weight of PEGDME than on the cross-linkers. The maximum conductivity was found to be 5.6${\times}$10$\^$-4/ S/cm at 30$^{\circ}C$ for the sample containing 75 wt% of PEGDME (M$\_$n/ =400). These electrolytes exhibited electrochemical stability up to 4.5 V against the lithium reference electrode. We observed reversible electrochemical plating/stripping of lithium on the nickel electrode.

• Journal of Electrochemical Science and Technology
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• 제10권2호
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• pp.250-255
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• 2019

Poly(ethylene oxide) (PEO)-based solid polymer electrolytes (SPEs) show promise for improving the lithium ion battery safety. However, due to oxidation of the PEO group and corrosion of the Al current collector, PEO-based SPEs have not previously been effective for use in $LiCoO_2$ (LCO) cathode materials at room temperature. In this paper, a semi-interpenetrating polymer network (semi-IPN) PEO-based SPE was applied to examine the performance of a LCO/SPE/Li metal cell at different voltage ranges. The results indicate that the SPE can be applied to LCO-based lithium polymer batteries with high electrochemical performance. By using a carbon-coated aluminum current collector, the Al corrosion was mostly suppressed during cycling, resulting in improvement of the cell cycle stability.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1999년도 추계학술대회 논문집
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• pp.159-162
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• 1999

All solid state thin film micro-batteries consisting of lithium metal anode, an amorphous LiPON electrolyte and cathode of vanadium oxide have been fabricated and characterized, which were fabricated with cell structure of Li/LiPON/V$_2$O$\sub$5/Pt. The vanadium oxide thin films were formed by d.c. reactive sputtering on Pt current collector. After deposition of vanadium oxide films, in-situ growths of lithium phosphorus oxynitride film were conducted by r.f. sputtering of Li$_3$PO$_4$ target in mixture gas of N$_2$ and O$_2$. The pure metal lithium film was deposited by thermal evaporation on thin film LiPON electrolyte. The cell capacity was about 45${\mu}$Ah/$\textrm{cm}^2$ $\mu\textrm{m}$ after 200 cycle. No appreciable degradation of the cell capacity could be observed after 50 cycles .

• Journal of Electrochemical Science and Technology
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• 제15권1호
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• pp.51-66
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• 2024

Modern society is making numerous efforts to reduce reliance on carbon-based energy systems. A notable solution in this transition is the adoption of lithium-ion batteries (LIBs) as potent energy sources, owing to their high energy and power densities. Driven by growing environmental challenges, the application scope of LIBs has expanded from their initial prevalence in portable electronic devices to include electric vehicles (EVs) and energy storage systems (ESSs). Accordingly, LIBs must exhibit long-lasting cyclability and high energy storage capacities to facilitate prolonged device usage, thereby offering a potential alternative to conventional sources like fossil fuels. Enhancing the durability of LIBs hinges on a comprehensive understanding of the reasons behind their performance decline. Therefore, comprehending the degradation mechanism, which includes detrimental chemical and mechanical phenomena in the components of LIBs, is an essential step in resolving cycle life issues. The LIB systems presently being commercialized and developed predominantly employ graphite anode and layered oxide cathode materials. A significant portion of the degradation process in LIB systems takes place during the electrochemical reactions involving these electrodes. In this review, we explore and organize the aging mechanisms of LIBs, especially those with graphite anodes and layered oxide cathodes.

• Journal of Electrochemical Science and Technology
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• 제7권2호
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• pp.161-169
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• 2016

Porous tungsten oxide thin films were prepared by electrodeposition and tested as anodes of lithium secondary batteries. The synthesized films were composed of nanoparticles of 60-140 nm size, with porosities of 30-40 %. Increasing the temperature turned out to be a more effective approach to introduce porosity in the structure than increasing the electrolyte viscosity. The assessment of the synthesized films as anodes of lithium secondary batteries revealed a much higher initial discharge capacity for the porous than the dense samples. The discharge capacity retention significantly increased with increasing porosity and was further enhanced by heat treatment. In particular, a thin film composed of particles of about 140 nm in size and with a porosity of 40 % exhibited an initial discharge capacity higher than 600 mAh/g and a remaining capacity above 300 mAh/g after 30 cycles. Following heat treatment, the remaining capacity of this sample after 30 cycles increased to about 500 mA h/g.

• 전기화학회지
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• 제4권4호
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• pp.139-145
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• 2001

본 연구에서는 리튬전지내 양극 재료로서 리튬철계 산화물을 제조하여 전극재료의 다양한 조성에 따른 전기화학적 특성을 고찰하고자 하였다 출발 물질인 $FeCl_3-6H_2O,\; NaOH,\;LiOH$를 혼합하여 저온으로 가열하여 층상의 $LiFeO_2$를 합성하였으며 출발 물질의 조성비를 바꾸어 그 영향을 조사하였다. 그 결과 NaOH의 첨가량이 증가할수록 전극의 용량은 감소하나 효율 및 용량의 감소율은 작아짐을 알 수 있었다. $NaOH/FeCl_3/LiOH$의 중량비를 2/1/7로 조성하여 합성하였을 때 가장 큰 용량을 보였으나 효율은 30회 순환 후 급격히 감소하였다. 층상의 $LiFeO_2$ 양극을 사용한 리튬 전지의 충방전 실험을 수행한 결과 이 셀은 1.5-4.5V의 범위에서 가역적임을 알 수 있었다 CPR방법을 사용하여 1M $LiPF_6/EC/DEC$ 전해질에서 확산계수를 측정하였다. 확산계수는 0.5$10^{-11}cm^2/s$임을 알 수 있었다.

• 한국전기전자재료학회논문지
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• 제31권5호
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• pp.335-340
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• 2018

Transition metal oxide materials have attracted widespread attention as Li-ion battery electrode materials owing to their high theoretical capacity and good Li storage capability, in addition to various nanostructured materials. Here, we fabricated a CoO Li-ion battery in which Co nanoparticles (NPs) are deposited into a current collector through electrophoretic deposition (EPD) without binding and conductive agents, enabling us to focus on the intrinsic electrochemical properties of CoO during the conversion reaction. Through optimized Co NP synthesis and electrophoretic deposition (EPD), CoO Li-ion battery with 630 mAh/g was fabricated with high cycle stability, which can potentially be used as a test platform for a fundamental understanding of conversion reaction.