• Electrical & Electronic Materials
• /
• v.8 no.1
• /
• pp.83-89
• /
• 1995

In this paper, the specimens-($Ba_{0.997}$ L $a_{0.003}$)Ti $O_{3}$ + xTi $O_{2}$, x=0.005, 0.01, 0.02, 0.03[mol]- were fabricated by a solid-state reaction method which is easy in microstructure control and good in mass production. Their crystalline structures and microstructures were analysed, and electrical properties were investigated. The perovskite-crystalline structure is confirmed by XRD, and it is exhibited by SEM that the grain grows with an addition of Ti $O_{2}$. Resistivity decreases with increasing sinteiing temperature, and the specimen of ($Ba_{0.997}$ L $a_{0.003}$)Ti $O_{3}$ + 0.02Ti $O_{2}$ sintered at 1350.deg. C shows the best PTC effects. The complex impedance plots exhibit the serial equivalent circuit of ( $R_{gb}$ / $C_{gb}$ ) and $R_{g}$ it is realized that PTC effect is attributed to the resistivity of grain boundary.ary.y.

• Journal of the Korean Ceramic Society
• /
• v.28 no.2
• /
• pp.101-108
• /
• 1991

0.2 mo1% La doped BaTiO3 samples were prepared by a wet chemical process (Pechini process) and electrical conductivity were measured from annealing temperatures(800-110$0^{\circ}C$) to room temperature continuously. 2 probe I-V characteristics showed that Pt electrodes were non-ohmic below about 80$0^{\circ}C$ for Ladoped sample. I-V curves showed varistor behavior and breakdown voltages showed PTC-like behavior. AC complex impedance of 0.2 La and 0.05 Mn mo1% doped BaTiO3 samples with three different electrodes (electroless Ni, Pt, Ag electrodes) were measured with temperature variation. Complex impedance plots showed that the samples with electroless Ni electrodes have negligible electrode resistance. Samples with Ag or Pt paste electrodes showed large electrode resistance. PTC effect, which is defined as the ratio of maximum resistance to minimum resistance, was found to be less than 10 for 0.2 mo1% La doped dense sample however greater than 105 with codoping of 0.05 mo1% Mn and 0.2 mol% La.

• Journal of the Korean Electrochemical Society
• /
• v.13 no.4
• /
• pp.223-234
• /
• 2010

In this review, the theory and applications of the complex capacitance analysis, which can be utilized in analyzing capacitor-like electrochemical systems, were summarized. Theoretically, it was suggested that the imaginary capacitance plots (Cim vs. log f) can provide a simple way to analyze electrochemical characteristics of capacitive systems, without complicated mathematical calculations. The usefulness of the complex capacitance analysis has been demonstrated by applying it to analyze EDLC characteristics of practical porous carbon electrodes, ionic conductivities inside small pores, and ionic resistances in the catalyst layers of polymer electrolyte membrane fuel cells.

• Journal of the Korean Ceramic Society
• /
• v.27 no.4
• /
• pp.529-535
• /
• 1990

This paper describes the factors which control the impedance-relative humidity characteristics of the TiO2-V2O5 humidity sensor. To obtain the quantitative relationships between impedance and many manufacturing parameters such as V2O5mol%, the sintering time and temperature, various sets of samples are preared and tested. With changing relative hymidity from 20% to 80%, it is measrued that the corresponding capacitance and impedance from the semicircles which complex impedance plots make. As a result we found that the impedance-relative humidity characteristics are mainly controlled by the doping amount of V2O5 total pore volume and bulk resistence of the elements. We can assume the equivalent circuits of each samples and finally control the sintering time to get a linear humidity impedance response curve which plays an important role in device making. 4mol% V2O5-TiO2 specimen sintered at 90$0^{\circ}C$ for 10min. show liear log(Z) vs. RH characteristics and 10mol% V2O5-TiO2 specimen sintered at the same temp. for 20min. show linear (Z) vs. RH.

• Korean Journal of Materials Research
• /
• v.29 no.12
• /
• pp.753-756
• /
• 2019

Orthorhombic dysprosium manganite DyMnO₃ with single phase is synthesized using solid-state reaction technique and the crystal structure and dielectric properties as functions of temperature and frequency are investigated. Thermally activated dielectric relaxations are shown in the temperature dependence of the complex permittivity, and the respective peaks are found to be shifted to higher temperatures as the measuring frequency increases. In Arrhenius plots, activation energies of 0.32 and 0.24 eV for the high- and low-temperature relaxations are observed, respectively. Analysis of the relationship between the real and imaginary parts of the permittivity and the frequencies allows us to explain the dielectric behavior of DyMnO₃ ceramics by the universal dielectric response model. A separation of the intrinsic grain and grain boundary properties is achieved using an equivalent circuit model. The dielectric responses of this circuit are discerned by impedance spectroscopy study. The determined grain and grain boundary effects in the orthorhombic DyMnO₃ ceramics are responsible for the observed high- and low-temperature relaxations in the dielectric properties.

• Journal of the Korean Electrochemical Society
• /
• v.6 no.4
• /
• pp.255-260
• /
• 2003

The complex capacitance analysis was performed in order to examine the potential-dependent EDLC characteristics of porous carbon electrodes. The imaginary capacitance profiles $(C_{im}\;vs.\;log\lf)$ were theoretically derived for a cylindrical pore and further extended to multiple pore systems. Two important electrochemical parameters in EDLC can be estimated from the peak-shaped imaginary capacitance plots: total capacitance from the peak area and $\alpha_0$ from the peak position. Using this method, the variation of capacitance and ion conductivity in pores can be traced as a function of electric potential. The electrochemical impedance spectroscopy was recorded on the mesoporous carbon electrode as a function of electric potential and analyzed by complex capacitance method. The capacitance values obtained from the peak area showed a maximum at 0.3V (vs. SCE), which was in accordance with cyclic voltammetry result. The ionic conductivity in pores calculated from the peak position showed a maximum at 0.2 V (vs. SCE), then decreased with an increase in potential. This behavior seems due to the enhanced electrostatic interaction between ion and surface charge that becomes enriched at more positive potentials.