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Impact of Sintering Mechanism Evolution on Electrochemical Performance of Cathode Support Tubular Solid Oxide Fuel Cells

机译:烧结机理演变对阴极支撑管状固体氧化物燃料电池电化学性能的影响

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Cathode-supported tubular solid oxide fuel cells (CS-T-SOFCs) are regarded as promising energy conversion devices; however, their commercialization is blocked by high manufacturing cost. We have been researching dip-coating and co-sintering techniques for fabricating CS-T-SOFCs in order to reduce e cost. In this paper, we improved the sintering process and found that the degree of co-sintering has significant effects on the microstructure of electrodes and the electrolyte. The co-sintering temperature is limited by the reaction between (La_(0.8)Sr_(0.2))_(0.95)MnO_(3+δ) (LSM95) cathode and Zr_(0.89)Sc_(0.1)Ce_(0.01)O_(2+δ) ( SSZ ) electrolyte; however, by changing the co-firing temperature of the cathode-supported electrolyte tube, the relative density of electrolyte and the connection of anode particles to CS-T-SOFC could be improved. As a result, the maximum power density of a CS-T-SOFC reached 740, 635and 489 rnWcm~(-2) at 850, 800 and 750°C, respectively, with hydrogen as fuel. The long-term stability of the improved CS-T-SOFC was also investigated.
机译:阴极支撑的管状固体氧化物燃料电池(CS-T-SOFC)被认为是很有前途的能量转换装置;然而,它们的商业化受到高制造成本的阻碍。为了降低电子成本,我们一直在研究用于制造CS-T-SOFC的浸涂和共烧结技术。在本文中,我们改进了烧结工艺,发现共烧结程度对电极和电解质的微观结构有重要影响。共烧结温度受(La_(0.8)Sr_(0.2))_(0.95)MnO_(3 +δ)(LSM95)阴极与Zr_(0.89)Sc_(0.1)Ce_(0.01)O_( 2 +δ)(SSZ)电解质;然而,通过改变阴极支撑的电解质管的共烧温度,可以提高电解质的相对密度以及阳极颗粒与CS-T-SOFC的连接。结果,以氢气为燃料,CS-T-SOFC的最大功率密度分别在850、800和750°C达到740、635和489 rnWcm〜(-2)。还研究了改进的CS-T-SOFC的长期稳定性。

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