Torrell M, García-Rodríguez S, Morata A, Penelas G, Tarancón A
Catalonia Institute for Energy Research (IREC), Jardins de les Dones de Negre, 1, 08930-Sant Adrià de Besòs, Barcelona, Spain.
REPSOL Technology Center, Ctra de Extremadura A-5, km 18, 28935 Móstoles, Madrid, Spain.
Faraday Discuss. 2015;182:241-55. doi: 10.1039/c5fd00018a.
The use of cermets as fuel electrodes for solid oxide electrolysis cells requires permanent circulation of reducing gas, e.g. H2 or CO, so called safe gas, in order to avoid oxidation of the metallic phase. Replacing metallic based electrodes by pure oxides is therefore proposed as an advantage for the industrial application of solid oxide electrolyzers. In this work, full-ceramic symmetrical solid oxide electrolysis cells have been investigated for steam/CO2 co-electrolysis. Electrolyte supported cells with La(0.75)Sr(0.25)Cr(0.5)Mn(0.5)O3-δ reversible electrodes have been fabricated and tested in co-electrolysis mode using different fuel compositions, from pure H2O to pure CO2, at temperatures between 850-900 °C. Electrochemical impedance spectroscopy and galvanostatic measurements have been carried out for the mechanistic understanding of the symmetrical cell performance. The content of H2 and CO in the product gas has been measured by in-line gas micro-chromatography. The effect of employing H2 as a safe gas has also been investigated. Maximum density currents of 750 mA cm(-2) and 620 mA cm(-2) have been applied at 1.7 V for pure H2O and for H2O : CO2 ratios of 1 : 1, respectively. Remarkable results were obtained for hydrogen-free fuel compositions, which confirmed the interest of using ceramic oxides as a fuel electrode candidate to reduce or completely avoid the use of safe gas in operation minimizing the contribution of the reverse water shift reaction (RWSR) in the process. H2 : CO ratios close to two were obtained for hydrogen-free tests fulfilling the basic requirements for synthetic fuel production. An important increase in the operation voltage was detected under continuous operation leading to a dramatic failure by delaminating of the oxygen electrode.
将金属陶瓷用作固体氧化物电解池的燃料电极时,需要还原性气体(例如H2或CO,即所谓的安全气体)持续循环,以避免金属相发生氧化。因此,提议用纯氧化物替代金属基电极,这对固体氧化物电解槽的工业应用而言是一个优势。在这项工作中,对全陶瓷对称固体氧化物电解池进行了蒸汽/CO2共电解研究。制备了具有La(0.75)Sr(0.25)Cr(0.5)Mn(0.5)O3-δ可逆电极的电解质支撑型电解池,并在850 - 900 °C的温度下,使用从纯H2O到纯CO2的不同燃料组成,以共电解模式进行了测试。进行了电化学阻抗谱和恒电流测量,以从机理上理解对称电池的性能。通过在线气体微色谱法测量了产物气体中H2和CO的含量。还研究了使用H2作为安全气体的效果。在1.7 V下,对于纯H2O和H2O : CO2比例为1 : 1的情况,分别施加了750 mA cm(-2)和620 mA cm(-2)的最大密度电流。对于无氢燃料组成获得了显著结果,这证实了使用陶瓷氧化物作为燃料电极候选材料以减少或完全避免在运行中使用安全气体的意义,从而使过程中逆水煤气变换反应(RWSR)的贡献最小化。对于无氢测试,获得了接近2的H2 : CO比例,满足了合成燃料生产的基本要求。在连续运行过程中检测到运行电压显著升高,导致氧电极分层而发生严重故障。