• 한국산학기술학회논문지
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• 제15권7호
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• pp.4692-4697
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• 2014

태양광 전원은 태양광 패널이 설치된 지역의 위치와 날씨 그리고 기후 등에 매우 큰 영향을 받으며, 전원으로서의 사용시간의 제한과 출력의 불확실성이라는 특성을 갖는다. 이러한 태양광 전원의 불확실성을 가능한 줄이기 위해, 태양광 전원의 출력에 대한 오랜 기간 동안의 데이터를 분석하여 출력의 평균값을 산출해 내었다. 태양광 전원의 출력의 평균값은 태양광 전원에 직접 연결되어 그리드에 안정적인 전력을 공급하기 위한 Li 에너지 저장장치의 적정 용량산정과 운용방식에 꼭 필요한 데이터이며, 이로부터 Li 배터리의 충방전모드에 의해 그리드에 일정한 출력의 전력을 공급하는 것이 가능하도록 하였다. 태양광 전원과 Li 배터리를 포함하는 시스템이 악조건의 그리드 운전상태에서의 동작특성을 관찰하기 위해 Li 배터리의 충전율이 100%에서 10%로 단시간에 감소될 정도의 과부하 상태에 대해 태양광 전원과 Li 배터리의 운용특성을 분석하고 Li 배터리 셀 단위의 출력 및 온도특성을 해석하였다.

• 분석과학
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• 제16권6호
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• pp.443-449
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• 2003

붕산수에 대한 열중성자 (thermal neutron) 조사실험을 하나로를 이용하여 다음과 같은 세가지 조건에서 수행하였다: (A) $^{10}B$ 농도 = $203.0{\mu}g/mL$, 조사시간 = 1 시간; (B) $^{10}B$ 농도 = $381.4{\mu}g/mL$, 조사시간 = 1 시간; (C) $^{10}B$ 농도 = $381.4{\mu}g/mL$, 조사시간 = 0.5 시간. 열중성자 조사 시 발생하는 핵반응 [$^{10}B(n{\cdot}{\alpha})^7Li$]으로부터 생성된 $^7Li$의 양은 불꽃 없는 원자흡수분광분석법 (flameless atomic absorption spectroscopy)으로 측정하였다. (A), (B), (C) 실험에서 측정된 $^7Li$의 농도는 각각 0.18 (이론치 = 0.23), 0.31 (이론치 = 0.44), 0.16 (이론치 = 0.22) ${\mu}g/mL$로 이 값들은 각각 이론치의 78.3, 70.5, 71.6%에 해당한다 중성자 조사 후 붕산수의 pH는 조사 전의 값에 비하여 상당히 낮은 값을 보였다. 이는 물의 방사분해물의 영향으로 붕산수가 해리도가 큰 polyborate 형태로 전이되기 때문으로 판단된다.

• 센서학회지
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• 제8권5호
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• pp.359-367
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• 1999

CsI에 lithium을 활성제로 0.02, 0.1, 0.2 및 0.3 mole% 첨가한 CsI(Li) 단결정을 Czochralski 방법으로 육성하였다. 육성한 CsI(Li) 단결정의 격자구조는 bcc구조였으며, 격자상수 $a_o$ 값은 $4.568\;{\AA}$이었다. CsI(Li) 단결정의 흡수단은 245 nm이였으며, 흡수단으로 여기 시킨 발광스펙트럼의 파장범위는 $300{\sim}600\;nm$이었고 중심파장은 425 nm이었다. Li 농도를 0.2 mole% 첨가한 경우 에너지 분해능은 $^{137}Cs$(662 keV)에 대해서는 14.5%, $^{54}Mn$(835 keV)에 대해서는 11.4%이었고 $^{22}Na$의 511 keV와 1275 keV에 대한 에너지 분해능은 각각 17.7%와 7.9% 이었다. 그리고, $\gamma$선 에너지와 에너지 분해능 사이의 관계식은 ln (FWHM%) = -0.893lnE + 8.456이였으며, 에너지 교정곡선은 ${\log}E_r=1.455\;{\log}(ch.)-1.277$이었다. Li를 0.2 mole% 첨가한 CsI(Li) 단결정의 인광감쇠시간은 실온에서 0.51 s이었고, 일정비율 시간분석법(CFT:constant-fraction timing method)으로 측정한 시간분해능은 9.0 ns 이었다.

• Bulletin of the Korean Chemical Society
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• 제28권3호
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• pp.451-456
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• 2007

Tetraazamacrocyclic ion exchangers tethered to Merrifield peptide resin (DTDM, TTTM) were prepared and the ion exchange capacity of these was characterized. The isotope separation of lithium was determined using breakthrough method of column chromatography. The isotope separation coefficient was strongly dependent on the ligand structure by Glueckauf's theory. We found that the isotope separation coefficients were increased as the values of distribution coefficients were increased. In this experiment the lighter isotope, 6Li was enriched in the resin phase, while the heavier isotope, 7Li in the solution phase. The ion radius of lighter isotope, 6Li was shorter than the heavier isotope, 7Li. The hydration number of lithium ion with the same charge became small as mass number was decreased. Because 6Li was more strongly retained in the resin than 7Li, the isotopes of lithium were separated with subsequent enrichment in the resin phase.

• Journal of Electrochemical Science and Technology
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• 제12권4호
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• pp.424-430
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• 2021

The element iron (Fe) is affordable and abundantly available, and thus, it finds use in a wide range of applications. As regards its application in rechargeable lithium-ion batteries (LIBs), the electrochemical reactions of Fe must be clearly understood during battery charging and discharging with the LIB electrolyte. In this study, we conducted systematic electrochemical analyses under various voltage conditions to determine the voltage at which Fe corrosion begins in general lithium salts and organic solvents used in LIBs. During cyclic voltammetry (CV) experiments, we observed a large corrosion current above 4.0 V (vs. Li/Li⁺). When a constant voltage of 3.7 V (vs. Li/Li⁺), was applied, the current did not increase significantly at the beginning, similar to the CV scenario; on the other hand, at a voltage of 3.8 V (vs. Li/Li⁺), the current increased rapidly. The impact of this difference was visually confirmed via scanning electron microscopy and optical microscopy. Our X-ray photoelectron spectroscopy measurements showed that at 3.7 V, a thick organic solid electrolyte interphase (SEI) was formed atop a thin fluoride SEI, which means that at ≥3.8 V, the SEI cannot prevent Fe corrosion. This result confirms that Fe corrosion begins at 3.7 V, beyond which Fe is easily corrodible.

• 동의생리병리학회지
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• 제24권5호
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• pp.814-821
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• 2010

The purpose of this study was to investigate effects of moxibustion at combined acupoints on sex and age in rats. This study measured the effects of moxibustion on small intestinal motility in rats. Cauterizing with moxa was applied 5 times to the acupoints on SI8, LI11 SP9 and ST36 under enflurane anesthesia in the groups divided with sex and age. In single acupoint groups, cauterizing with moxa on ST36 increased in all of sex and age groups. The SP9 group with 5, 6 weeks in female and 5, 8 weeks in male, the SI8 group with 5, 7 weeks in female and only 7 weeks in male, the LI11 group with only 5, 6, 7 weeks in female and only 7 weeks in male showed increasing on small intestinal motility. In combined acupoints groups, the SI8+SP9 group with 7 weeks in female and 5, 6, 8 weeks in male, the SI8+ST36 group with 5, 6 weeks in female and 8 weeks in male, the LI11+SP9 group with 5, 6 weeks in female and 6 weeks in male, the LI11+ST36 group with 5 weeks in female and 5, 6, 7 weeks in male showed increasing respectively. Although these different according to the sex and age in rats do not have a established tendency, the results suggested that the effects of combined acupoints of cauterizing with moxa have relation with individuality.

• 한국세라믹학회지
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• 제42권5호
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• pp.319-325
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• 2005

[ $LiNiO_2$ ] was synthesized by the solid-state method after mixing $LiOH{\cdot}H_2O$ and $Ni(OH)_2$ with SPEX mill. The optimum condition for the synthesis of $LiNiO_2$ was the calcination at $750^{\circ}C$ for 30h in $O_2$ stream after milling for 1 h. The $LiNiO_2$ synthesized under this condition showed relatively large value of $I_{003}/I_{104}$ and relatively small value of R-factor. When $LiNiO_2$ was cycled in 2.7$\~$4.15 V at 0.1C-rate, the first discharge capacity was not very large (145.8 mAh/g) but it showed good cycling performance. When $LiNiO_2$ was cycled in 2.7$\~$4.2 V at 0.1C-rate, the first discharge capacity was large but ,it showed poor cycling performance probably because of the transition of H2 hexagonal structure to H3 hexagonal structure. In addition, when $LiNiO_2$ was cycled in 1.0$\~$4.8 V at 1/24C- rate, the first discharge capacity was very large (257.7 mAh/g) and the discharge capacity increased with the number of cycles.

• 한국표면공학회지
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• 제27권2호
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• pp.65-73
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• 1994

Effects of deposition parameter on the ionic conductivity and structural change of the Lithium borosili-cate solid electrolyte films, prepared by rf sputtering using 7$LI_2O-3B_2O_3-1SiO_2$ single phase target and also a mosaic target enriched with $LI_2O$, were analyzed by measuring AC impedance and IR absorption spectra for the films. Thed solid electrolyte film deposited from the single phase target exhibited very low ionic conductivi-ty of $10^{-10}{\Omega}^{-1}cm{-1}$ at room temperature, a result of low $Li^+$ ion content(7.52 at%) in the film. The $Li^+$ con-ductivity for the films deposited from the mosaic target, however, significantly increased to $10^{-7}{\Omega}^{-1}cm{-1}$ due to both an increased $Li^+$content (14.75 at %) and a structural change of the films. The increased ionic conduc-tivity of the film appears to be associated with an easiness of ionic mobility by structural change of glassy film from a some close packed network structure to a open one. These structural changes of film were found to be closely related to the increase in the peak intensity at~$960cm^{-1}$ of IR absorption spectra for the glassy films. With increasing either argon pressure from 3 to 21 mtorr or rf power from 2 to 3 W/$cm^2$, the $Li^+$ conduc-tivity for the films significantly increased to an order of $10^{-6}{\Omega}^{-1}cm{-1}$ due to an increase in openness of film structure, as confirmed by both an increase in the IR absorption peak intensity at ~$960cm^{-1}$ and a resultant reduction of activation energy for mobility of $Li^+$ ion.

• 한국재료학회지
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• 제31권11호
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• pp.614-618
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• 2021

As the size of market for electric vehicles and energy storage systems grows, the demand for lithium-ion batteries (LIBs) is increasing. Currently, commercial LIBs are fabricated with liquid electrolytes, which have some safety issues such as low chemical stability, which can cause ignition of fire. As a substitute for liquid electrolytes, solid electrolytes are now being extensively studied. However, solid electrolytes have disadvantages of low ionic conductivity and high resistance at interface between electrode and electrolyte. In this study, Li₇La₃Zr₂O₁₂ (LLZO), one of the best ion conducting materials among oxide based solid electrolytes, is fabricated through RF-sputtering and various electrochemical properties are analyzed. Moreover, the electrochemical properties of LLZO are found to significantly improve with co-sputtered Li₂O. An all-solid thin film battery is fabricated by introducing a thin film solid electrolyte and an Li₄Ti₅O₁₂ (LTO) cathode; resulting electrochemical properties are also analyzed. The LLZO/Li₂O (60W) sample shows a very good performance in ionic conductivity of 7.3×10^-8 S/cm, with improvement in c-rate and stable cycle performance.

• 한국전기전자재료학회논문지
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• 제11권11호
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• pp.1049-1054
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• 1998

The LiCo$O_2$ powder was synthesized by a solution phase reaction. This shows a high (003) peak intensity and low (104) or (101) peak intensities in X-ray diffraction spectra. The LiCo$O_2$/Li cell shows an initial discharge capacity of 102.9mAh/g and an average discharge potential or 3.877V at a current density of 50mA/g between 3.0~4.2V. The peaks of dQ/dV plot are associated with Li ion intercalation/deintercalation reaction. To evaluate the cycleability of an actual battery system, cylindrical lithium ion cell was manufactured using graphitized MPCF anode and LiCoO$_2$ cathode. After 100th cycle, this cel maintains 80% capacity of 10th cycle value. The LiCoO$_2$/MPCF cell has a high discharge voltage of 3.6~3.7V and a good cycle life performance on cycling between 4.2~2.7V.