Trobec Francesca, Thangadurai Venkataraman
Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, Alberta, T2N 1N4 Canada.
Inorg Chem. 2008 Oct 6;47(19):8972-84. doi: 10.1021/ic8010025. Epub 2008 Aug 16.
Fast oxide ion conducting Ce 1- x M x O 2-delta (M = In, Sm; x = 0.1, 0.2) and Ce 0.8Sm 0.05Ca 0.15O 1.825 were prepared from the corresponding perovskite-like structured materials with nominal chemical composition of BaCe 1- x M x O 3-delta and BaCe 0.8Sm 0.05Ca 0.15O 2.825, respectively, by reacting with CO 2 at 800 degrees C for 12 h. Powder X-ray diffraction (PXRD) analysis showed the formation of fluorite-type CeO 2 and BaCO 3 just after reaction with CO 2. The amount of CO 2 gained per ceramic gram was found to be consistent with the Ba content. The CO 2 reacted samples were washed with dilute HCl and water, and the resultant solid product was characterized structurally and electrically employing various solid-state characterization methods, including PXRD, and alternating current (ac) impedance spectroscopy. The lattice constant of presently prepared Ce 1- x M x O 2-delta and Ce 0.8Sm 0.05Ca 0. 15O 1.825 by a CO 2 capture technique follows the expected ionic radii trend. For example, In-doped Ce 0.9In 0.1O 1.95 (In (3+) (VIII) = 0.92 A) sample showed a fluorite-type cell constant of 5.398(1) A, which is lower than the parent CeO 2 (5.411 A, Ce (4+) (VIII) = 0.97 A). Our attempt to prepare single-phase In-doped CeO 2 samples at 800, 1000, and 1500 degrees C using the ceramic method was unsuccessful. However, we were able to prepare single-phase Ce 0.9In 0.1O 1.95 and Ce 0.8In 0.2O 1.9 by the CO 2 capture method from the corresponding barium perovskites. The PXRD studies showed that the In-doped samples are thermodynamically unstable above 800 degrees C. The ac electrical conductivity studies using Pt electrodes showed the presence of bulk, grain-boundary, and electrode contributions over the investigated temperature range in the frequency range of 10 (-2)-10 (7) Hz. The bulk ionic conductivity and activation energy for the electrical conductivity of presently prepared Sm- and (Sm + Ca)-doped CeO 2 samples shows conductivities similar to those of materials prepared by the ceramic method reported in the literature. For instance, the conductivity of Ce 0.8Sm 0.2O 1.9 using the CO 2 capture technique was determined to be 4.1 x 10 (-3) S/cm, and the conductivity of the same sample prepared using the ceramic method was 3.9 x 10 (-3) S/cm at 500 degrees C. The apparent activation energy of the area-specific polarization resistance for the symmetric cell (Sm,Sr)CoO 3- x |Ce 0.8Sm 0.2O 1.9|(Sm,Sr)CoO 3- x was determined to be 1 eV in air.
通过在800℃下与CO₂反应12小时,分别由名义化学组成为BaCe₁₋ₓMₓO₃₋δ和BaCe₀.₈Sm₀.₀₅Ca₀.₁₅O₂.₈₂₅的相应类钙钛矿结构材料制备了快速氧离子传导的Ce₁₋ₓMₓO₂₋δ(M = In,Sm;x = 0.1,0.2)和Ce₀.₈Sm₀.₀₅Ca₀.₁₅O₁.₈₂₅。粉末X射线衍射(PXRD)分析表明,与CO₂反应后立即形成了萤石型CeO₂和BaCO₃。发现每克陶瓷获得的CO₂量与Ba含量一致。将与CO₂反应的样品用稀盐酸和水洗涤,并用包括PXRD和交流(ac)阻抗谱在内的各种固态表征方法对所得固体产物进行结构和电学表征。通过CO₂捕获技术制备的当前Ce₁₋ₓMₓO₂₋δ和Ce₀.₈Sm₀.₀₅Ca₀.₁₅O₁.₈₂₅的晶格常数遵循预期的离子半径趋势。例如,In掺杂的Ce₀.₉In₀.₁O₁.₉₅(In³⁺(VIII)= 0.92 Å)样品显示出萤石型晶胞常数为5.398(1) Å,低于母体CeO₂(5.411 Å,Ce⁴⁺(VIII)= 0.97 Å)。我们尝试使用陶瓷方法在800、1000和1500℃下制备单相In掺杂CeO₂样品未成功。然而,我们能够通过CO₂捕获方法从相应的钡钙钛矿制备单相Ce₀.₉In₀.₁O₁.₉₅和Ce₀.₈In₀.₂O₁.₉。PXRD研究表明,In掺杂样品在800℃以上热力学不稳定。使用Pt电极的交流电导率研究表明,在10⁻² - 10⁷Hz频率范围内,在所研究的温度范围内存在体相、晶界和电极贡献。当前制备的Sm和(Sm + Ca)掺杂CeO₂样品的体相离子电导率和电导率活化能显示出与文献中报道的通过陶瓷方法制备的材料相似的电导率。例如,使用CO₂捕获技术制备的Ce₀.₈Sm₀.₂O₁.₉的电导率在500℃下测定为4.1×10⁻³S/cm,使用陶瓷方法制备的相同样品的电导率为3.9×10⁻³S/cm。对称电池(Sm,Sr)CoO₃₋ₓ|Ce₀.₈Sm₀.₂O₁.₉|(Sm,Sr)CoO₃₋ₓ的面积比极化电阻的表观活化能在空气中测定为1 eV。