| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 10154656 | 1666309 | 2018 | 14 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Fabrication and characterization of Ca2+, Sr2+, Ba2+, Sm3+, and La3+ co-doped ceria-based electrolyte powders for low-temperature anode-supported solid oxide fuel cells
												
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																																												کلمات کلیدی
												
											موضوعات مرتبط
												
													مهندسی و علوم پایه
													شیمی
													 الکتروشیمی
												
											پیش نمایش صفحه اول مقاله
												 
												چکیده انگلیسی
												In this study, CeO2-based electrolytes are synthesized by a sol-gel method. Ce0.8Sm0.2O1.9, Ce0.8Sm0.15Ca0.05O1.875, Ce0.8Sm0.15Ca0.025Sr0.025O1.875 (S15CS05DC), Ce0.8Sm0.15La0.05O1.9, (La0.77Sr0.2Ba0.03)0.15Ce0.85O1.908, and (La0.77Sr0.2Ba0.03)0.2Ce0.8O1.877 specimens are prepared at sintering temperature 1300 °C for either 2 h or 4 h. The microstructures and electrical properties of the electrolytes are analyzed using X-ray diffraction, scanning electron microscopy, and alternating current (AC) impedance spectroscopy. All samples are cubic fluorite structure. It is found that while Ca2+ and Sr2+ contribute to grain growth, Sm3+ and La2+ inhibit it. The conductivity increases with temperature in a linear manner and reaches approximately 0.16 S·cmâ1 at 800 °C for the 4 h-sintered S15CS05DC sample. Six anode-supported cells are fabricated and tested at 600 °C-800 °C. Cell-C has the highest maximum power density (0.96 W·cmâ2) at 800 °C. It is also found that ohmic resistance predominantly determines the total cell resistance at temperatures above 700 °C.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Hydrogen Energy - Volume 43, Issue 39, 27 September 2018, Pages 18463-18476
											Journal: International Journal of Hydrogen Energy - Volume 43, Issue 39, 27 September 2018, Pages 18463-18476
نویسندگان
												Yu-Chuan Wu, Wan-Yu Chen,