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Microstructure and electrochemical properties of gadolinia-doped ceria cathodes for SOEC application

机译:氧化g掺杂二氧化铈阴极的微观结构和电化学性能

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High temperature co-electrolysis (HTCE) technology has become a new research focus in world' s energy field, which can produce synthesis gas by dissociation of CO_2 and H_2O using a solid oxide electrolysis cell (SOEC) .The polarization loss, operational stability and interfacial behavior of SOEC cathode are the key issues for the development of HTCE technology1. In this paper, several high performance CeO_2 based catalysts were introduced into the cathode/electrolyte interface of the SOECs ' and their catalytic performance for high temperature reverse water-gas shift (RWGS) reaction were investigated in detail. By material selection and interfacial structure control, the composite cathode materials with higher performance for HTCE were developed successfully. The X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to determine the crystallinities and structure of the samples. Cathode supported cells with different CeO2 based cathodes were studied by electrochemical impedance spectroscopy (EIS).The results showed that the electrode polarization loss in the HTCE process were smaller than that of the conventional Ni-YSZ cathode. Based on the above results, the mechanisms of HTCE's electrochemical reaction were investigated by the material characterization coupled with electrochemical measurements..
机译:高温共电解(HTCE)技术已成为世界能源领域的一个新研究热点,高温共电解技术可以通过使用固体氧化物电解池(SOEC)分解CO_2和H_2O来产生合成气。 SOEC阴极的界面行为是HTCE技术发展的关键问题1。本文将几种高性能的基于CeO_2的催化剂引入SOEC的阴极/电解质界面,并详细研究了它们对高温反向水煤气变换(RWGS)反应的催化性能。通过材料的选择和界面结构的控制,成功开发了高性能的HTCE复合阴极材料。使用X射线衍射(XRD)和扫描电子显微镜(SEM)来确定样品的结晶度和结构。通过电化学阻抗谱(EIS)研究了带有不同CeO2基阴极的阴极支撑电池,结果表明,HTCE工艺中电极极化损失小于常规的Ni-YSZ阴极。基于以上结果,通过材料表征和电化学测量研究了HTCE的电化学反应机理。

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