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Exploring mixed proton/electron conducting air electrode materials in protonic electrolysis cell

机译:探索质子电解槽中的混合质子/电子传导空气电极材料

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摘要

In this work, we investigate and compare the performance and cell polarization resistance of Ba0.5La0.5CoO3-delta (BLC) and double perovskite oxide BaGd0.8La0.2Co2O6-delta (BGLC) anode on cathode supported protonic steam electrolysis cells using a 20 mu m SrZr0.5Ce0.4Y0.1O3-delta electrolyte with Ni-SZCY541 composite as the cathode. The kinetics of protons through the bulk and across the gas electrolyte interfaces of both anode materials were also studied by direct measurement of their tracer diffusions using time-of-flight secondary ion mass spectrometry depth profiling (TOF-SIMS). Cell terminal voltages of 1.74 and 1.93 V, were observed at a current density of 0.5 A cm(-2) for both BLC and BGLC whereas a hydrogen evolution rate of 121.85 and 111.15 mu mol cm(-2) every minute was also obtained at the same current density, translating to a current efficiency of 78 and 72% respectively. Hydrogen tracer diffusion studies confirm BGLC can incorporate protons into the bulk relative to BLC even though the present steam electrolysis results show a better performance for BLC at 600 degrees C.
机译:在这项工作中,我们研究并比较BA0.5LA0.5COO3-DELTA(BLC)和双钙钛矿氧化物BAG0.8LA0.2CO2O6-DELTA(BGLC)阳极在阴极上使用20的验证蒸汽电解细胞的性能和细胞偏振电阻。 MU M SRZR0.5CE0.4Y0.1O3-DELTA电解质与Ni-SZCY541复合材料作为阴极。通过直接测量它们使用飞行时间二次离子质谱深度分析(TOF-SIM),通过直接测量其示踪剂扩散,通过直接测量它们的阳极材料的质子和跨越气体电解质界面的动力学。对于BLC和BGL的电流密度为0.5Acm(-2)的电池末端电压,而BGLC的电流密度也可以每分钟获得121.85和111.15μmmolcm(-2)的氢进化率。电流密度相同,分别转化为78和72%的电流效率。氢示踪剂扩散研究证实BGLC可以将质子掺入体积相对于BLC中的块状,即使本蒸汽电解结果为600摄氏度的BLC表现出更好的性能。

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