• 한국세라믹학회지
• /
• 제36권10호
• /
• pp.1056-1061
• /
• 1999

Phase formation and oxygen ion conduction of La(Ba)Ga(Mg)O3-$\delta$ system was studied, BaLaGa3O7 and BaLaGaO4 formed as a secondary phase above the solubility limit of Ba2+ in La3+ sites. The oxygen ionic conductivity of La(Ba)Ga(Mg)O3-$\delta$ was 0.1 S/cm 80$0^{\circ}C$ The activation energy of the oxygen ion conduction was dependent on temperature. This value was higher at low temperature than at high temperature.

• Journal of Electrochemical Science and Technology
• /
• 제9권3호
• /
• pp.212-219
• /
• 2018

Perovskite type ceramic membranes which exhibit dual ion conduction (proton and oxygen ion conduction) can permeate water and can aid solving operational problems such as temperature gradient and carbon deposition associated with a working solid oxide fuel cell. From this point of view, it is crucial to reveal water transport mechanism and especially the nature of the surface sites that is necessary for water incorporation and evolution. $BaCe_{0.8}Y_{0.2}O_{3-{\alpha}}$ (BCY20) was used as a model proton and oxygen ion conducting membrane in this work. Four different catalytically modified membrane configurations were used for the investigations and water flux was measured as a function of temperature. In addition, CO was introduced to the permeate side in order to test the stability of membrane against water and $CO/CO_2$ and post operation analysis of used membranes were carried out. The results revealed that water incorporation occurs on any exposed electrolyte surface. However, the magnitude of water permeation changes depending on which membrane surface is catalytically modified. The platinum increases the water flux on the feed side whilst it decreases the flux on the permeate side. Water flux measurements suggest that platinum can block water permeation on the permeate side by reducing the access to the lattice oxygen in the surface layer.

• 한국세라믹학회지
• /
• 제32권3호
• /
• pp.359-365
• /
• 1995

The grain boundary effect on the ionic conductivity was investigated using a.c. admittance analysis in (Bi2O3)0.715(CaO)0.285 oxygen-ion conducting solid electrolyte. As a separated arc representing grain boundary polarization was not observed in the admittance plane, bulk conductivity was measrued for samples with various grain sizes in the temperature range from 48$0^{\circ}C$ to 72$0^{\circ}C$ and the conductivity distribution between grain interior and grain boundary was determined by the reported analytical methods. In the above temperature range, grain boundary worked as a high conductive path instead of blocking layer and ionic conduction through grain boundary was significant. The activation energy for conduction through grain and grain boundary was 78 and 106 kJ/mol, respectively.

• 한국신재생에너지학회:학술대회논문집
• /
• 한국신재생에너지학회 2011년도 추계학술대회 초록집
• /
• pp.97.2-97.2
• /
• 2011

Pt-Ru and Pt-Ni bimetallic catalysts were prepared and tested for heavy hydrocarbon reforming. Metals were supported on CGO($Ce_{0.8}Gd_{0.2}O_{2.0-x}$) by incipient wetness method. The prepared catalysts were characterized by Temperature programmed reduction(TPR). Oxidative steam reforming of n-dodecane was conducted to compare the activity of the catalysts. The reforming temperature was varied from $500^{\circ}C$ to $800^{\circ}C$ at fixed $O_2$/C of 0.3, $H_2O$/C of 3.0 and GHSV of 5,000/h.Reduction peaks of metal oxide, surface CGO and bulk CGO were detected. Reduction temperature of metal oxide decreased over the bi-metallic catalysts. It is considered that interaction between metals leads to decrease interaction between metal and oxygen. On the other hands, reduction temperatures of surface CGO were dectected in the order of Pt-Ru > Pt-Ni > Pt. low reduction temperatures of surface CGO indicates the low activation energy for oxygen ion conduction to metal. Oxygen ion conduction is known as de-coking mechanism of ionic conducting supports such as CGO. In activity test, fuel conversion was in the same order of Pt-Ru > Pt-Ni > Pt. Especially, 100% of fuel conversion was obtained over Pt-Ru catalysts at $500^{\circ}C$.

• 한국세라믹학회지
• /
• 제41권8호
• /
• pp.623-627
• /
• 2004

Ba가 첨가된 LaBaGa $O_4$ 층상 perovskite의 생성상과 전도거동에 대해 고찰하였다. LaBaGa $O_4$의 La-site에 20at% 이하의 $Ba^{2＋}$ 이온을 첨가한 조성은 $K_2$Ni $F_4$구조 사방정 단일상을 형성하였다. 건조분위기에서 L $a_{0.8}$B $a_{1.2}$G $a_{3.9}$는 높은 산소분압영역에서 산소이온전도와 hole(p-type)전도의 혼합전도를 나타내었다. 수증기분위기에서는 수증기가 산소빈자리로 유입되어 proton전도가 발생되었으며, 온도가 낮아질수록 총전도에 대한 proton 전도도의 기여가 증가하여 35$0^{\circ}C$ 이하의 온도에서는 proton 전도가 지배적인 전도를 나타내었다. Proton 전도에 대한 활성화 에너지는 0.72 eV였다.

• 한국세라믹학회지
• /
• 제38권11호
• /
• pp.993-999
• /
• 2001

Bao를 첨가한 perovskite 구조 LaSc $O_3$의 생성상과 proton 전도에 대해 연구하였다. La자리에 $Ba^{2+}$를 40 at% 첨가한 조성에서는 입방정 단일상이 생성된 반면, $Ba^{2+}$를 30 at% 이하로 첨가한 조성은 입방정과 사방정이 생성되었다. $N_2$분위기에서 $650^{\circ}C$ 이상의 온도에서는 주로 산소이온에 의한 전도를 나타내었고, 그 이하의 온도에서는 wet 분위기에서 proton 전도가 관찰되었다. 모든 조성의 물질은 30$0^{\circ}C$ 이하에서는 순수한 proton 전도체의 거동을 보였으며, proton에 의한 bulk(grain)의 전도도는 L $a_{0.6}$B $a_{0.4}$Sc $O_{2.8}$의 경우에 가장 높았다.높았다.다.

• Bulletin of the Korean Chemical Society
• /
• 제11권4호
• /
• pp.339-342
• /
• 1990

$Gd_2O_3-ThO_2$ solid solutions containing 8,10 and 12 mol % $ThO_2$ were synthesized with spectroscopically pure $Gd_2O_3,$ and $ThO_2$ polycrystalline powders. X-ray diffraction revealed that all synthesized specimens have the modified fluorite structure, and the lattice parameter of $Gd_2O_3$ is nearly unchanged with increasing $ThO_2$ mol %. Both ac and dc conductivities were measured in the temperature range $500-1100^{\circ}C$ under $Po_2's$ from $10^{-6}$ to $10^{-1}$ atm. The dc conductivities are nearly independent of $Po_2,$ and agree with the ac values. This implies that the solid solutions are ionic conductors. The conductivity increases with increasing $ThO_2$ mol % with an average activation energy of 1.23 eV. An oxygen interstitial defect and ionic hopping conduction are suggested.

• 대한화학회지
• /
• 제31권4호
• /
• pp.301-307
• /
• 1987

600~$1050^{\circ}C$와 $1{\times}10^{-6}\~\1{\times}10^2\;torr$에서 고순도의 $La_2O_3$의 전기전도도가 연구되었다. 결합구조 및 반도체형이 온도 및 산소분압의 함수로 연구되었으며 위의 온도 및 산소압력의 영역에서 $La_2O_3$의 전도도값은 $1{\times}10^{-9}\~\1{\times}10^{-3}\(ohm{-}cm)^{-1}$ 로 나타났다. 전기전도도의 산소압력의존성은 $700^{\circ}C$에서 5.7, $1,000^{\circ}C$에서 5.3이며 $700^{\circ}C$이하의 낮은 오도영역에서는 9~14의 값은 나타내었다. 온도 감소에 따른 n값의 증가는 ${\alpha}-La_2O_3$의 전기전도가 단순한 전도메카니즘을 나타내지 않는다는 사실을 보여준다. 낮은 산소압력에서 전기운반체는 금속공위가 아니라 산소이온이다. 또한 낮은 온도영역에서 전기전도는 이온성을 띄며 높은 온도영역에서는 전자전도성을 나타낸다.

• 한국세라믹학회지
• /
• 제52권5호
• /
• pp.299-303
• /
• 2015

The electrolyte is an important component in determining the performance of Fuel Cells. Especially, investigation of the conduction properties of electrolytes plays a key role in determining the performance of the electrolyte. The electrochemical properties of Yttrium stabilized zirconia (YSZ) were measured to allow the use of this material as an electrolyte for solid oxide fuel cells (SOFC) in the temperature range of $700-1000^{\circ}C$ and in $0.21{\leq}pO_2/atm{\leq}10^{-23}$. A Hebb-Wagner polarization experimental cell was optimally manufactured; here we discuss typical problems associated with making cells. The partial conductivities due to electrons and holes for 8YSZ, which is known as a superior oxygen conductor, were obtained using I-V characteristics based on the Hebb-Wagner polarization method. Activation energies for holes and electrons are $3.99{\pm}0.17eV$ and $1.70{\pm}0.06eV$ respectively. Further, we calculated the oxygen ion conductivity with electron, hole, and total conductivity, which was obtained by DC four probe conductivity measurements. The oxygen ion conductivity was dependent on the temperature; the activation energy was $0.80{\pm}0.10eV$. The electrolyte domain was determined from the top limit, bottom limit, and boundary (p=n) of the oxygen partial pressure. As a result, the electrolyte domain was widely presented in an extensive range of oxygen partial pressures and temperatures.

• 한국세라믹학회지
• /
• 제35권12호
• /
• pp.1323-1328
• /
• 1998

The electrical conductivities of the yttria (8mol%) stabilizedzirconia-ceria solid solutions were measured as a function of oxygen partial between 80$0^{\circ}C$ and 100$0^{\circ}C$ using 4-probe d.c. method Under pure oxygen atmosphere the oxygen ionic conductivity of CeO2-ZrO2 decreased with the concentration of CeO2 Under reducing condition electronic conduction due to the redox equilibrium of Ce ion was observed. Total ionic and electronic conductivities fitted by a defect model enabled to determine the electronic transference number(tei) which increased with the concentration of CeO2 and with the degree of reduction.