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Promoting the ambient-condition stability of Zr-doped barium cerate: Toward robust solid oxide fuel cells and hydrogen separation in syngas

机译:促进Zr掺杂的铈钡的环境稳定性:建立坚固的固体氧化物燃料电池和合成气中的氢分离

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Increasing the stability of perovskite proton conductor against atmospheric CO2 and moisture attack at ambient conditions might be equally important as that at the elevated service temperatures. It can ease the transportation and storage of materials, potentially reducing the maintenance cost of the integral devices. In this work, we initially examined the surface degradation behaviors of various Zr-doped barium cerates (BaCe0.7Zr0.1Me0.1O3) using XRD, SEM, STEM and electron energy loss spectroscopy. Though that the typical lanthanide (Y, Yb and Gd) and In incorporated Zr-doped cerates well resisted CO2-induced carbonation in air at elevated temperatures, they were unfortunately vulnerable at ambient conditions, suffering slow decompositions at the surface. Conversely, Sn doped samples (BCZYSn) were robust at both conditions yet showed high protonic conductivity. Thanks to that, the anode supported solid oxide fuel cells equipped with BCZYSn electrolyte delivered a maximum power density of 387 mW cm(-2) at 600 degrees C in simulated coal-derived syngas. In the hydrogen permeation test using BCZYSn based membrane, the H-2 flux reached 0.11 mL cm(-2) min(-1) at 850 degrees C when syngas was the feedstock. Both devices demonstrated excellent stability in the presence of CO2 in the syngas.
机译:在环境条件下,增加钙钛矿质子导体对大气中CO2和水分侵蚀的稳定性可能与在高温下使用同样重要。它可以简化材料的运输和存储,潜在地减少了集成设备的维护成本。在这项工作中,我们最初使用XRD,SEM,STEM和电子能量损耗光谱法研究了各种掺Zr的钡铈酸盐(BaCe0.7Zr0.1Me0.1O3)的表面降解行为。尽管典型的镧系元素(Y,Yb和Gd)和掺入Zr的铈酸盐在高温下都能很好地抵抗空气中的CO2诱导的碳化,但不幸的是,它们在环境条件下易受腐蚀,在表面缓慢分解。相反,Sn掺杂样品(BCZYSn)在两种条件下均很坚固,但质子传导率很高。因此,配备有BCZYSn电解质的阳极支撑固体氧化物燃料电池在模拟的煤衍生合成气中于600摄氏度下提供了387 mW cm(-2)的最大功率密度。在使用BCZYSn基膜的氢渗透测试中,当以合成气为原料时,H-2通量在850摄氏度下达到0.11 mL cm(-2)min(-1)。两种设备在合成气中存在CO2时均表现出出色的稳定性。

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