• Transactions of the Korean hydrogen and new energy society
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• v.25 no.3
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• pp.305-310
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• 2014

This study examined the morphological changes in lithium surface immersed in 1mol $dm^{-3}$ (M) $LiPF_6 $ dissolved in propylene carbonate (PC) containing different 1,2-dimethoxyethane (DME) concentrations as a co-solvent. A passivation film was formed on the surface of lithium metal by electrolyte decomposition. The passivation film formation reactions were significantly affected by the amount of co-solvent, DME, in electrolyte solution. A stable film was obtained from the 1 M $LiPF_6 $ / PC:DME (67:33) solution in which lithium electrode showed good electrochemical performances. Atomic force microscope (AFM) and electrochemical impedance spectroscopy (EIS) results revealed that there were no direct correlations between changes in the surface morphology of lithium metal and the resistance behavior of its passivation film.

• Proceedings of the KIEE Conference
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• 2001.07c
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• pp.1537-1539
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• 2001

The radiation degradation of five insulating materials such as silicone rubber, ethylene-propylene rubber polybutylene terephthalte, poly carbonate, nylon 66 were evaluated by using thermogravimetry analysis (TGA) and tensile properties as a function of radiation doses. The results of temperature at 5% weight loss and activation energy from TGA showed linearly decreasing and increasing tendency as radiation doses comparing with tensile properties. Consequently, the assessment of TGA for the radiation degradation of materials was effective.

• Proceedings of the Korean Vacuum Society Conference
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• 1999.07a
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• pp.157-157
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• 1999

Electrochromic tungsten oxide films were prepared by the electron beam deposition, and the dependence of the electrochemical stability and the optical properties on the titanium concentration, and on the annealing temperature, that was investigated. coloring and bleaching experiments were repeated by cyclic voltammetry in a propylene carbonate solution of LiClO4. Spectrometry was used to assess the stability of the transmittance in the degraded films. Tungsten oxide films with titanium contents of about 10~15 mol% were found to be most stable, undergoing the least degradation during the repeated for coloring and bleaching cycles. The reason for this small amount of degradation was the reduction of lithium ion trapping sites in the films, which results in an increased durability. Tungsten oxide films with titanium contents of about 20 mol% were annealed at 20$0^{\circ}C$ for 1 hour, and this results showed that durability of films were increased.

• Journal of Pharmaceutical Investigation
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• v.40 no.5
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• pp.263-267
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• 2010

Nanoemulsions have been widely investigated for many years because of their attractive and unique characteristics. Nanoemulsions are composed of oil, surfactant, co-surfactant and water. Especially, cosurfactant plays a critical role in formation of nanoemulsions. In pharmaceutical area, a pre-concentrate form of nanoemulsions which is known as self-nanoemulsifying drug delivery systems (SNEDDS) was available for some water-insoluble drugs. In this study, we investigated the functional behaviors of cosurfactant in design of SNEDDS and nanoemulsions. Cremophor RH 40$^{(R)}$, Propylene carbonate and medium chain triglyceride were selected for surfactant, cosurfactant and oil, respectively. Cyclosporine was employed as a drug. Phase diagrams showed the area of isotropic o/w region which forms o/w nanoemulsions was not significantly affected by the compositional ratio of cosurfactant. But, drug solubilization capacity, droplet size of nanoemulsions and drug release rate were greatly affected by the cosurfactant.

• Journal of the Korean Electrochemical Society
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• v.5 no.4
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• pp.192-196
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• 2002

Ionic liquids based on l-ethyl-3-methylimidazolium cation $(EMI^+)$ and inorganic or organic anions containing fluorine atoms were applied to electrolyte materials for double-layer capacitors. The double-layer capacitors composed of a pair of activated carbon electrodes and an ionic liquid selected from $EMIBF_4,\; EMINbF_6,\;EMITaF_6,\;EMICF_3SO_3,\;EMI(CF_3SO_2)_2N,\;and\;EMI(C_2F_5SO_2)_2N$ showed inferior low-temperature characteristics to those of a conventional nonaqueous electrolyte based on propylene carbonate (PC) solvent. On the other hand, the capacitor using $EMIF{\cdot}2.3HF$ showed excellent low-temperature characteristics due to its high conductivity at low temperatures, however, it had a lower working voltage $(\~2V)$ than the conventional nonaqueous counterpart $(\~3V)$.

• Journal of the Korean Electrochemical Society
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• v.1 no.1
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• pp.52-54
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• 1998

Polypyrrole (PPy), Poly(N-methyl Pyrrole) (PMPy) and Poly(N-phenyl Pyrrole) (PPhPy) films in acetonitrile (Af and propylene carbonate (PC) have been compared focusing on their different ion and solvent transport behaviors. During the redox reaction of PPy films, cation, anion, and solvent take part in mass transport. Whereas during the redox reaction of PMPy and PPhPy films, anion and solvent transport are dominant but cation transport is negligible. In addition, solvent transport occurs in the same direction with cation transport for PPy films. On the other hand, solvent transport occurs in the opposite direction to anion transport for PMPy films, and it changes its amount and direction with the kind of the dopant anion and the solvent used at electropolymerization for PPhPy films.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2008.06a
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• pp.146-147
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• 2008

Poly(3,4-ethylenedioxythiophene) (PEDOT) / poly(1-vinyl-3-ethylimidazolium bis(trifluoromethane sulfonyl)imide) (poly(ViEtIm $^+TFSI^-$) complex was prepared for organic solvent dispersible conductive nano particles. By molar ratio, PEDOT / poly(ViEtIm $^+TFSI^-$) complex was polymerized and dispersed in propylene carbonate by 1 wt%. The maximum conductivity of the complexes was $1.2\times10^{-1}$ S/cm.

• Solar Energy
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• v.19 no.1
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• pp.1-8
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• 1999

Electrochromic $WO_3$ thin films were prepared by electron beam deposition. The transmission and durability of films were investigated. Coloring and bleaching experiments were repeated in an electrolyte of propylene carbonate with 0.6M of $LiClO_4$ by cyclic voltammetry. Spectrophotometer was used to measure the transmission in the degraded films. The 5000 ${\AA}$ thick film was found to be the stable after repeated cycles. The durability of the annealed film also showed improvements over unannealed samples. Tungsten oxide films with titanium content of about $10{\sim}15$ mol% was found to be most stable, undergoing the least degradation during the repeated cycles.

• Bulletin of the Korean Chemical Society
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• v.18 no.1
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• pp.61-65
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• 1997

The electrochemical properties of LixCoyNi1-yO2 compounds (y=0.1, 0.3, 0.5, 0.7, 1.0) prepared by citrate sol-gel method have been investigated. The LixCoyNi1-yO2 compounds were annealed at 850 ℃ for 20 h after preheating at 650 ℃ for 6 h, in air. The x-ray diffraction (XRD) patterns for LixCoyNi1-yO2 have shown that these compounds have a well developed layered structure (R&bar{3} m). From the scanning electron microscopy of LixCoyNi1-yO2, particle size was estimated less than 5 μm. The Li//LixCoyNi1-yO2 electrochemical cell consists of Li metal anode and 1 M LiClO4-propylene carbonate (PC) solution as the electrolyte. The differences in intercalation rate of the LixCoyNi1-yO2 in the first charge/discharge cycle were less than 0.05 e-. The first discharge capacities of LixCoO2 and LixCo0.3Ni0.7O2 were ∼130 mAh/g and ∼160 mAh/g, respectively.

• Journal of the Korean Electrochemical Society
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• v.16 no.2
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• pp.91-97
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• 2013

Solid polymer electrolyte films are prepared by ultraviolet radiation in the mixtures of an ionic liquid salt (1-ethyl-3-methylimidazolium tetrafluoroborate, $EMIBF_4$) and solvent (acetonitrile (ACN) or propylene carbonate(PC)), and an oligomer (poly(ethylene glycol)diacrylate, PEGDA, 45-60 wt.%). Electrochemical properties of activated carbon supercapacitors adopting the solid polymer electrolyte films as a separator are also examined by cyclic voltammetry and impedance measurement techniques. As a result, the supercapacitor adopting the PEGDA as much as 45 wt.% exhibits a superior capacitance of $46Fg^{-1}$ at $20mVs^{-1}$. It seems that this is due to fast kinetics of ion conduction by sufficient film flexibility, which can be allowed by comparatively weak ultraviolet curing of small anount of the PEGDA.