• 한국전기전자재료학회논문지
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• 제13권4호
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• pp.306-311
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• 2000

The purpose of this study is to research and develop solid polymer electrolyte(SPE) for Li polymer battery. The temperature dependence of conductivity impedance spectroscopy and electrochemical properties of PDF/PAN electrolytes as a function of a mixed ratio were reported for PVDF/PAN based polymer electrolyte films which were prepared by thermal gellification method of preweighed PVDF/PAN plasticizer and Li salt. The conductivity of PVDF/PAN electrolytes was 10$\^$-3/S/cm. 20PVDF5PEN LiCiO$\_$4//PC$\_$10//EC$\_$10/ electrolyte has the better conductivity compared to others. 20PVDF5PANLICIO$\_$4//PC$\_$10//EC$\_$10/ electroylte remains stable up to 5V vs. Li/Li$\^$+/. Steady state current method and ac impedance were used for the determination of transference numbers in PVDF/PAN electrolyte film. The transference number of 20PVDF5PANLiCO$\^$4//PC$\_$10//EC$\_$10/ electrolyte is 0.48.

• 한국세라믹학회지
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• 제54권5호
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• pp.406-412
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• 2017

$70V_2O_5-10Fe_2O_3-13P_2O_5-7B_2O_3$ glasses were prepared to study the electrical conductivity and catalytic properties of the structural change with crystallization. The structural changes were analyzed by determining the molecular volume from the sample density; using X-Ray Diffraction (XRD) analysis, which indicated that $V_2O_5$, $VO_2$ and $B_2O_3$ crystals in heat-treated more than 1h samples. Especially a new crystalline phase of non-stoichiometric $Fe_{0.12}V_2O_5$ was formed after 6 h heat treatment. The V-O bonding change after crystallization was analyzed by Fourier Transform Infrared Spectroscopy (FTIR); V ion change from $V^{5+}$ to $V^{4+}$ was shown by XPS. Conductivity and catalytic properties were examined based on the polaronic hopping of V and Fe ions, which exhibited different valence states with crystallization.

• 한국재료학회지
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• 제17권10호
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• pp.526-531
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• 2007

The sintering behavior and electrical property of $Ce_{0.8}Gd_{0.2}O_{1.9}$ ceramics were investigated with the iron oxide concentration ranging from 0 to 5 mol%. Both the sintered density and grain size were found to increase up to 2 mol% $Fe_2O_3$, and then to decrease with further additions. At a higher $Fe_2O_3$ content above 3 mol%, grain size decreased by a pinning effect induced by different shape grains. The electrical conductivity was also increased with increasing $Fe_2O_3$ content up to 2 mol%. Total conductivity of 2 mol% $Fe_2O_3-added$ specimen showed the maximum conductivity of $2{\times}10^{-2}{\Omega}{\cdot}cm^{-1}$ at $500^{\circ}C$. The addition of $Fe_2O_3$ was found to promote the sintering properties and electrical conductivities of $Gd_2O_3-dope\;CeO_2$.

• 한국결정성장학회지
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• 제20권3호
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• pp.141-146
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• 2010

크롬이 도핑된 $LiFePO_4$ 분말이 도핑되지 않은 것보다 이차전지용 양극활물질로서 우수한 전기화학적 특성을 나타내었다. 이러한 향상은 도핑에 의해서 양극활물질의 전자전도도가 높아지기 때문인 것으로 생각되고 있다. 크롬과 또 하나의 전형원소가 도핑된 $LiFe_{0.965}Cr_{0.03}B_{0.005}PO_4$와 $LiFe_{0.965}Cr_{0.03}Al_{0.005}PO_4$의 전기전도도를 30에서 $80^{\circ}C$ 범위에서 측정하였다. 도핑된 분말은 유성밀에 의한 기계화학적 혼합을 한 후 675~$750^{\circ}C$에서 5~10시간 열처리하여 합성하였다. 이러한 도핑은 분말의 전기전도도를 높이고 입자 성장을 촉진시켰다. 크롬과 알루미늄이 도핑된 $LiFe_{0.965}Cr_{0.03}Al_{0.005}PO_4$ 분말의 $30^{\circ}C$에서의 전기전도도는 $1{\times}10^{-8}S/cm$이었으며, 이 값은 도핑하지 않은 것보다 두 자릿수 높은 값 이었다.

• 폴리머
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• 제29권4호
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• pp.403-407
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• 2005

본 연구에서는 mobil crystalline material-41(MCM-41)의 함량 변화에 따른 고체 고분자 전해질(solid polymer electrolyte, SPE)의 이온전도도의 변화를 고찰하기 위하여, poly(ethylene oxide)(PEO), 메조포러스 기공 구조를 가지는 MCM-41 분자체, 그리고 리튬염을 이용하여 SPE를 제조하였다. SPE의 결정화도는 X-선 회절분석(XRD) 및 시차주사열량계(DSC)를 통하여 살펴보았으며, 주파수반응분석(FRA)으로 이온전도도를 측정하여 이온 전도거동을 고찰하였다. 그 결과, MCM-41을 고분자 혼합물에 첨가함에 따라 PEO의 견정성 영역의 성장을 억제할 수 있었으며, 이는 MCM-41이 메조포러스한 구조를 가지고 있기 때문이다. 또한, $P(EO)_{16}LiClO_4$/MCM-41 전해질 복합체의 이온 전도도는 8$wt\%$의 MCM-41을 첨가한 경우 가장 큰 이온전도도를 가지며, 8$wt\%$이상에서는 다소 감소된 이온전도도를 가짐을 관찰할 수 있었다. 이러한 이온전도도의 특성은 MCM-41의 첨가에 따른 고분자의 결정화도 변화와 밀접한 관계를 맺고 있다.

• Korean Membrane Journal
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• 제9권1호
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• pp.52-56
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• 2007

A proton exchange membrane was prepared by ${\gamma}-irradiation-induced$ grafting of styrene into poly(tetrafluoro-ethylene-co-perfluoropropyl vinyl ether) (PFA) and subsequent sulfonation reaction. The degree of grafting (DOG) increased with an increase in the absorbed dose. The prepared membranes showed high ion exchange capacity reaching 3.0 meq/g, which exceeded the performance of commercially available perfluorosulfonic acid membranes such as Nafion. The proton conductivity of PFA-g-PSSA membrane increased with the DOG and reached 0.17 S/cm for the highest sample at room temperature. The DMFC performance of the prepared membranes with 50% DOG was comparable to that of Nafion membrane.

• Animal cells and systems
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• 제7권4호
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• pp.289-294
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• 2003

To quantify nutrient loading from emergent macrophytes through leaching in the littoral zones of Paldang Reservoir, we conducted incubation experiments using leaf litter of the emergent macrophyte, Zizaniz latifolia. To separate the leaching process from microbial decay, we used $HgCl_2$ to suppress microbial activity during the experiment. We measured electric conductivity, absorbance at 280nm, total nitrogen and dissolved inorganic nitrogen, total phosphorus and soluble reactive phosphorus, Na, K, Mg and Ca amounts in leaf litter and in water. In addition, we examined the effects of water temperature and ion concentrations of ambient water on the leaching process. A total of 6% of the initial ash-free dry mass of leaf litter was lost due to leaching during incubation (four days). Electric conductivity and A280 continued to increase and saturate during the incubation. To compare reaching rates of different nutrients, we fitted leaching dynamics with a hyperbolic saturation function [Y=AㆍX/(B+X)]. From these fittings, we found that ratios of leaching amounts to nutrient concentration in the litter were in the order of K > Na > Mg > P > Ca > N. Leaching from leaf litter of Z. latifolia was dependent on water temperature while it was not related with ion concentrations in the ambient water. Our results suggest that the leaching process of nutrients, especially phosphorus, from aquatic macrophytes provides considerable contribution to the eutrophication of the Paldang Reservoir ecosystem.

• 전기화학회지
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• 제14권2호
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• pp.92-97
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• 2011

In this study we have investigated the Li-ion coordination, thermal behavior and electrochemical stability of N-butyl-N-methyl-pyrrolidinium bis(trifluoromethanesulfonyl)imide ($Py_{14}TFSI$) with lithium bis(trifluoromethanesulfony)imide (LiTFSI) doping intended for use as electrolytes for lithium batteries. The ionic conductivity is reduced and glass transition temperature ($T_g$) increases with LiTFSI doping concentration. Also, the electrochemical stability increases with LiTFSI doping. A high LiTFSI doping could enhance the electrochemical stability of electrolytes for lithium batteries, whereas the decrease in the ionic conductivity limits the capacity of the battery.

• 한국세라믹학회지
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• 제33권4호
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• pp.385-390
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• 1996

The electrical resistivity of the ceramic glaze coated on ceramic substrate plays an important role on the characteristics of the thick and thin film electrical circuits. In this study the effects of the various modifiers on the electrical resistivity were examined in SiO2-Al2O3-B2O3-RO-Na2O (RO=CaO , SrO, BaO, PbO) glass system. In alkali free glasses where divalent cations are responsible for electrical conduction the electrical conductivity of th glasses increased with the ionic size of divalent cations due to the decrease in the bond strength between oxyben and divalent cation. In Na2O containing glasses however where Na+ ion is responsible for electrical conduction the ionic conductivity decreased with the ionic size of divalent cations because the blocking effect of the cations on Na+ ion movement increased with larger divalent cations. Na+ ionic conduction also depended on the glass structure relaxation due to the corrdination number changes of B2O3 and Al2O3 which varied with the NaO2 content in the glass.

• 한국결정성장학회지
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• 제20권6호
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• pp.249-253
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• 2010

A-자리 경함 perovskite $La_{1/3}NbO_3$ 단결정 시편을 제작하여 10~800 K 온도범위에서 유전특성을 조사하였다. 50 K와 650 K 부근에서 유전이상이 나타났으며, 고온영역(약 650 K)에서 유전상수의 thermal hysterisis가 크게 나타났다. 교류전도도 측정으로부터 560~690 K에서 입내 활성화 에너지는 0.43 eV로 가장 낮게 나타났다. 이들의 결과로부터 50 K 부근의 dielectric anomaly는 $Nb^{5+}$-이온의 antiparallel 변위에 기인한 것이며, 650 K 부근의 dielectric anomaly는 $La^{3+}$-이온의 재배열에 기인한 것으로 추측된다.