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首页> 外文期刊>Journal of power sources >Enhanced hydrogen oxidation activity and H_2S tolerance of Ni-infiltrated ceria solid oxide fuel cell anodes
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Enhanced hydrogen oxidation activity and H_2S tolerance of Ni-infiltrated ceria solid oxide fuel cell anodes

机译:渗镍二氧化铈固体氧化物燃料电池阳极增强的氢氧化活性和H_2S耐受性

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摘要

The effect of Ni infiltration into porous Gd-doped ceria (GDC) anodes on their H_2 oxidation performance, with and without added 10 ppm H_2S, is reported here. Porous GDC anodes (ca. 10 μm thick) were deposited on yttria stabilized zirconia (YSZ) supports and then infiltrated with catalytic amounts of a Ni nitrate solution, followed by electrochemical testing in a 3-electrode half-cell setup at 500-800 ℃. Infiltration of 3 wt.% Ni into the porous GDC anode lowered the polarization resistance by up to 85%, affecting mainly the low frequency impedance arc. When exposed to 10 ppm H_2S, the Ni-infiltrated anodes exhibited a ca. 5 times higher tolerance toward sulfur poisoning compared to GDC anodes alone, also showing excellent long-term stability in 10 ppm H_2S. In the presence of H_2S, it is proposed that Ni, likely distributed as a nanophase, helps to maintain a clean GDC surface at the Ni/GDC interface at which the H_2 oxidation reaction takes place. In turn, the GDC will readily supply oxygen anions to the adjacent Ni surfaces, thus helping to remove adsorbed sulfur.
机译:此处报道了在有和没有添加10 ppm H_2S的情况下,Ni渗入多孔掺Gd的二氧化铈(GDC)阳极中对其H_2氧化性能的影响。将多孔GDC阳极(约10μm厚)沉积在氧化钇稳定的氧化锆(YSZ)载体上,然后用催化量的硝酸镍溶液渗透,然后在500-800℃的三电极半电池装置中进行电化学测试。 3%(重量)的Ni渗入多孔GDC阳极,使极化电阻降低了多达85%,主要影响了低频阻抗电弧。当暴露于10 ppm H_2S时,渗入镍的阳极显示出约1。与单独的GDC阳极相比,其对硫中毒的耐受性高5倍,在10 ppm H_2S中也显示出出色的长期稳定性。在存在H_2S的情况下,提出了可能以纳米相分布的Ni有助于在发生H_2氧化反应的Ni / GDC界面上保持清洁的GDC表面。反过来,GDC将很容易将氧阴离子提供给相邻的Ni表面,从而帮助除去吸附的硫。

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