A review on materials, advantages, and challenges in thin film based solid oxide fuel cells

被引:38
作者
Chasta, Gaurav [1 ]
Himanshu [1 ]
Dhaka, Mahendra Singh [1 ]
机构
[1] Mohanlal Sukhadia Univ, Dept Phys, Udaipur 313001, Rajasthan, India
关键词
electrolytes; oxygen reduction reaction; solid oxide fuel cells; sputtering; thin films; YTTRIA-STABILIZED ZIRCONIA; PHYSICAL VAPOR-DEPOSITION; GADOLINIA-DOPED CERIA; INTERMEDIATE-TEMPERATURE SOFCS; PULSED-LASER DEPOSITION; PEROVSKITE-TYPE OXIDES; SCREEN-PRINTING INKS; ELECTROPHORETIC DEPOSITION; ELECTRICAL-PROPERTIES; OXYGEN REDUCTION;
D O I
10.1002/er.8238
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In accomplishment of massive energy demand, the solid oxide fuel cells (SOFCs) have proven as apotheosis candidates due to their high energy conversion efficiencies, low pollution exhaust, fuel flexibility, and environmental friendliness which make these the most promising alternatives to conventional electricity generators. Despite numerous advantages of SOFCs, large-scale industrial applications are yet to be realized owing to their high operating temperatures (800 degrees C-1000 degrees C). To lower the operating temperature, it is crucial to minimize ionic resistances which can be accomplished by reducing the electrolyte thickness to lesser than 5 mu m. Therefore, present article embraces a concise review on conventional materials, designs, and generations of SOFCs with their compatibility and drawbacks. The strengths and limitations of conventional and advanced tools for fabricating thin film based SOFCs (TF-SOFCs) as well as the associated properties of electrolytes and electrodes are thoroughly examined, and further route cast is provided to attain better performance. The present review encourages the development of TF-SOFCs using advanced techniques employing ultrathin single and bilayer electrolytes which can have potential to reduce the operating temperature of SOFCs from 450 degrees C to 600 degrees C region and pave the way for global commercialization.
引用
收藏
页码:14627 / 14658
页数:32
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