• Title/Summary/Keyword: Li reduction

검색결과 738건 처리시간 0.024초

리툼 이차 전지용 Co3O4 및 Ni-Co3O4 복합물의 전기화학적 특성 및 표면 형상의 관계 (A Relation between the Electrochemical Behaviors and Morphology of Co3O4 and Ni-Co3O4 Composites as Anode Materials for Li Ion Secondary Batteries)

  • 강용묵;이용주;송민상;박민식;이재영
    • 한국수소및신에너지학회논문집
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    • 제14권3호
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    • pp.217-228
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    • 2003
  • Li 이차 전지 음극용 활물질인 $Co_3O_4$의 초기 충방전 효율을 향상시키기 위해 chemical reduction method나 mechanical milling법을 이용하여 $Co_3O_4$에 Ni을 첨가하여 $Ni-Co_3O_4$, 복합물을 제조하였다. 그 결과 초기 충방전 효율이 약 69%에 불과한 $Co_3O_4$에 비해 mechanical milling법을 이용하여 제조된 $Ni-Co_3O_4$ 복합물은 약 79%이상의 대폭 향상된 초기 충방전 효율 특성을 나타내었다. 하지만 chemical reduction method를 이용하여 제조된 $Ni-Co_3O_4$ 복합물은 약 71%의 초기 충방전 효율 특성만을 나타내었다. SEM 분석을 통해 각 물질의 표면 형상을 관찰한 결과 mechanical milling법과 chemical reduction method를 통해 제조된 $Ni-Co_3O_4$ 복합물에서는 $Co_3O_4$ 표면에 분포된 Ni의 균일성의 차이가 존재하였다. $Co_3O_4$$Li_2O$의 분해, 형성에 의해 충방전되고 Ni이 $Li_2O$의 분해를 촉진시키는 효과를 가지고 있음을 고려할 때 이러한 균일성의 차이는 결국 Ni 과 $Co_3O_4$ 사이의 접촉면적의 차이로 이어져 $Ni-Co_3O_4$ 복합물의 초기 충방전 효율 특성이 그 제조 방법에 따라 달라지는 것으로 보인다.

Admittance Spectroscopic Analysis of Organic Light Emitting Diodes with a LiF Buffer Layer

  • Kim, Hyun-Min;Park, Hyung-June;Yi, Jun-Sin;Oh, Se-Myoung;Jung, Dong-Geun
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2006년도 6th International Meeting on Information Display
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    • pp.1014-1017
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    • 2006
  • Admittance Spectroscopic analysis was applied to study the effect of LiF buffer layer and to model the equivalent circuit for $ITO/Alq_3/LiF/Al$ device structure. The admittance spectroscopic analysis of the devices with LiF layer shows reduction in contact resistance $(R_C)$, parallel resistance $(R_P)$ and increment in parallel capacitance $(C_P)$.

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Generalization of Fisher′s linear discriminant analysis via the approach of sliced inverse regression

  • Chen, Chun-Houh;Li, Ker-Chau
    • Journal of the Korean Statistical Society
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    • 제30권2호
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    • pp.193-217
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    • 2001
  • Despite of the rich literature in discriminant analysis, this complicated subject remains much to be explored. In this article, we study the theoretical foundation that supports Fisher's linear discriminant analysis (LDA) by setting up the classification problem under the dimension reduction framework as in Li(1991) for introducing sliced inverse regression(SIR). Through the connection between SIR and LDA, our theory helps identify sources of strength and weakness in using CRIMCOORDS(Gnanadesikan 1977) as a graphical tool for displaying group separation patterns. This connection also leads to several ways of generalizing LDA for better exploration and exploitation of nonlinear data patterns.

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Direct Transformation of Carboxylic Acids into Aldehydes through Acyloxy-9-borabicyclo[3.3.1]nonane$^1$

  • 차진순;오세연;이광우;윤말숙;이재철
    • Bulletin of the Korean Chemical Society
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    • 제9권1호
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    • pp.48-52
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    • 1988
  • New methods for the direct reduction of carboxylic acids to aldehydes through the treatments of B-acyloxy-9-borabicyclo[3.3.1]nonane (acyloxy-9-BBN) with tert-butyllithium and 9-borabicyclo[3.3.1]nonane or with lithium 9-boratabicyclo[3.3.1]nonane (Li 9-BBNH) are described. Both these systems provide the corresponding aldehydes from various carboxylic acids in high yields. A mechanism for the recuction through stepwise treatment of acyloxy-9-BBN with tert-butylithium and 9-BBN, which seems to involve the hydride migration through 9-BBN, is proposed and discussed in connection with the reduction through treatment of acyloxy-9-BBN with Li 9-BBNH.

금속전환체 조성의 전해정련 전해조 UCl3 농도변화에 대한 영향 (Effect of the Composition of a Reduced Fuel on the Concentration Change of UCl3 in the Electrorefiner)

  • 백승우;이창화;이성재
    • 방사성폐기물학회지
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    • 제17권3호
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    • pp.347-353
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    • 2019
  • 파이로프로세싱의 전해환원공정에서 생산된 금속전환체의 조성은 전해정련공정 운전의 중요한 운전변수인 용융염 중 $UCl_3$의 농도변화에 영향을 미친다. 따라서, 본 연구에서는 금속전환체에 함유된 TRU와 RE 원소의 함량 및 금속전환체에 동반되어 전해정련 전해조에 유입될 수 있는 $Li_2O$ 농도가 전해정련 전해조의 $UCl_3$ 농도 변화에 미치는 영향을 검토하였다. 금속전환체의 TRU 원소와 RE 원소의 농도만을 고려하였을 때 전해정련 운전 batch 수 증가에 따라 $UCl_3$ 농도가 감소하였다. 전해정련 1 campaign(20 batch)를 운전하기 위해서는 $UCl_3$를 3회 이상 추가 보충해야 함을 알 수 있었다. 한편, 금속전환체에 동반되어 전해정련 전해조에 유입되는 $Li_2O$의 유입량 증가에 따라 $UCl_3$ 농도 감소의 영향이 크게 나타났으며, 이에 따라 운전 가능 batch 수가 급격히 감소하게 되어 전해정련 운전에 중요한 운전 변수임을 보여주었다. 이러한 결과는 전해정련 운전 중 $UCl_3$ 농도 유지를 위해 금속전환체에 포함된 TRU 및 RE 원소뿐만 아니라 금속전환체에 동반되어 유입될 가능성이 있는 $Li_2O$의 영향도 고려하여 전해정련 운전모드를 설정하여야 함을 보여주었다.

차량 속도 기반 정확도 제어를 통한 차량용 LiDAR 센서의 효율적 전력 절감 기법 (Efficient Power Reduction Technique of LiDAR Sensor for Controlling Detection Accuracy Based on Vehicle Speed)

  • 이상훈;이동규;최평;박대진
    • 대한임베디드공학회논문지
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    • 제15권5호
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    • pp.215-225
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    • 2020
  • Light detection and ranging (LiDAR) sensors detect the distance of the surrounding environment and objects. Conventional LiDAR sensors require a certain amount of a power because they detect objects by transmitting lasers at a regular interval depending on a constant resolution. The constant power consumption from operating multiple LiDAR sensors is detrimental to autonomous and electric vehicles using battery power. In this paper, we propose two algorithms that improve the inefficient power consumption during the constant operation of LiDAR sensors. LiDAR sensors with algorithms efficiently reduce the power consumption in two ways: (a) controlling the resolution to vary the laser transmission period (TP) of a laser diode (LD) depending on the vehicle's speed and (b) reducing the static power consumption using a sleep mode depending on the surrounding environment. A proposed LiDAR sensor with a resolution control algorithm reduces the power consumption of the LD by 6.92% to 32.43% depending on the vehicle's speed, compared to the maximum number of laser transmissions (Nx·max). The sleep mode with a surrounding environment-sensing algorithm reduces the power consumption by 61.09%. The proposed LiDAR sensor has a risk factor for 4-cycles that does not detect objects in the sleep mode, but we consider it to be negligible because it immediately switches to an active mode when a change in surrounding conditions occurs. The proposed LiDAR sensor was tested on a commercial processor chip with the algorithm controlling the resolution according to the vehicle's speed and the surrounding environment.

파이로프로세싱 발생 LiCl염폐기물의 열발생 (Thermal Release of LiCl Waste Salt from Pyroprocessing)

  • 김정국;김광락;김인태;안도희;이한수
    • 방사성폐기물학회지
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    • 제7권2호
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    • pp.73-78
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    • 2009
  • 사용후핵연료 파이로프로세싱의 전해환원 공정에서 발생하는 LiCl 염폐기물내 Cs과 Sr의 방사능 붕괴열을 계산하였다. 계산시 대부분의 LiCl염폐기물을 재생하여 재활용하고 나머지를 고화체로 만든다고 가정하였다. 계산결과 Cs 및 Sr의 붕괴로 생성되는 자핵종인 Ba와 Y에 의한 열발생량이 모핵종에 비해 최대 4.6배 더 많았다. LiCl염폐기물내 Cs 및 Sr에 의한 열발생은 초기 한달 정도에 최대이므로 일정 기간 초기 LiCl염폐기물의 온도 급상승을 제어할 냉각설비의 운영이 바람직할 것으로 보인다.

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물을 용매로 이용한 Sol-Ge1법에 의한 $LiMn_2O_4$ 정극 활물질의 제조와 전기화학적 특성 (Preparation and electrochemical property of $LiMn_2O_4$cathode active material by Sol-Gel method using water as solvent)

  • 정인성;구할본;박계춘
    • 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.

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Effect of the Calcination Temperature and Li(I) Doping on Ethanol Sensing Properties in p-Type CuO Thin Films

  • Choi, Yun-Hyuk
    • 한국재료학회지
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    • 제29권12호
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    • pp.764-773
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    • 2019
  • The gas response characteristic toward C2H5OH has been demonstrated in terms of copper-vacancy concentration, hole density, and microstructural factors for undoped/Li(I)-doped CuO thin films prepared by sol-gel method. For the films, both concentrations of intrinsic copper vacancies and electronic holes decrease with increasing calcination temperature from 400 to 500 to 600 ℃. Li(I) doping into CuO leads to the reduction of copper-vacancy concentration and the enhancement of hole density. The increase of calcination temperature or Li(I) doping concentration in the film increases both optical band gap energy and Cu2p binding energy, which are characterized by UV-vis-NIR and X-ray photoelectron spectroscopy, respectively. The overall hole density of the film is determined by the offset effect of intrinsic and extrinsic hole densities, which depend on the calcination temperature and the Li(I) doping amount, respectively. The apparent resistance of the film is determined by the concentration of the structural defects such as copper vacancies, Li(I) dopants, and grain boundaries, as well as by the hole density. As a result, it is found that the gas response value of the film sensor is directly proportional to the apparent sensor resistance.

Crystal Phase Changes of Zeolite in Immobilization of Waste LiCI Salt

  • KIM Jeong-Guk;LEE Jae-Hee;Lee Sung-Ho;KIM In-Tae;KIM Joon-Hyung;KIM Eung-Ho
    • 한국방사성폐기물학회:학술대회논문집
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    • 한국방사성폐기물학회 2005년도 Proceedings of The 6th korea-china joint workshop on nuclear waste management
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    • pp.176-181
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    • 2005
  • The electrolytic reduction process and the electrorefining process, which are being developed at the Korea Atomic Energy Research Institute (KAERI), are to generate molten waste salts such as LiCI salt and LiCI-KCI eutectic salt, respectively. Our goal in waste salt management is to minimize a total waste generation and fabricate a very low­leaching waste form such as a ceramic waste form. Zeolite has been known to one of the most desirable media to immobilize waste salt, which is water soluble and easily radiolyzed. Zeolite can be also used to the removal of fission products from the spent waste salt. Molten LiCI salt is mixed with zeolite A at $650^{\circ}C$ to form a salt-loaded zeolite, and then thermally treated in above $900^{\circ}C$ to become an immobilized product with crystal phase of $Li_{8}Cl_{2}$-Sodalite. In this work, a crystal phase changes of immobilization medium, zeolite, during immobilization of molten LiCI salt using zeolite A is introduced.

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