کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7887065 | 1509789 | 2018 | 19 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Structures and electrical conductivities of Gd3+ and Fe3+ co-doped cerium oxide electrolytes sintered at low temperature for ILT-SOFCs
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی مواد
سرامیک و کامپوزیت
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Gd3+ and Fe3+ co-doped cerium oxide electrolytes, Ce0.9Gd0.1âxFexO2-δ (xâ¯=â¯0.00, 0.01, 0.03, 0.05, 0.07, 0.10), were prepared by co-precipitation for ultrafine precursor powders and sintering for densified ceramic pellets. The crystal and microscopic structures were characterized by XRD, FESEM and Raman spectroscopy and their electrical properties were studied by AC impedance spectroscopy and the measurement of single cell's outputs. In comparison with Ce0.9Gd0.1O1.95, the ceramic pellets of Ce0.9Gd0.1âxFexO2-δ with a relative density of 95% can be obtained after sintered at 1000â¯Â°C for 5â¯h, showing a remarkably enhanced sintering performance with a sintering temperature reduction of 500â¯Â°C, which might be ascribed to the highly activated migration of constituent species in the cerium oxide lattice doped with Gd3+ and Fe3+ions. Moreover, the electrical conductivity of Ce0.9Gd0.1âxFexO2-δ can be significantly enhanced depending on the mole fraction x, with Ce0.9Gd0.07Fe0.03O1.95 exhibiting the highest electrical conductivity of 38 mS/cm at 800â¯Â°C, about 36% higher than that of Ce0.9Gd0.1O1.95 electrolyte sintered at 1500â¯Â°C for 5â¯h. So, The Gd3+ and Fe3+ co-doped cerium oxide would be an excellent candidate electrolyte for ILT SOFCs due to its prominent sintering performance and enhanced electrical conductivity.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Ceramics International - Volume 44, Issue 9, 15 June 2018, Pages 10328-10334
Journal: Ceramics International - Volume 44, Issue 9, 15 June 2018, Pages 10328-10334
نویسندگان
Zhentao Wang, Yanwei Zeng, Chuanming Li, Zhupeng Ye, Liangliang Cao, Yuan Zhang,