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Smart utilization of cobaltite-based double perovskite cathodes on barrier-layer-free zirconia electrolyte of solid oxide fuel cells

机译:固体氧化物燃料电池无阻挡层氧化锆电解质上钴基双钙钛矿阴极的智能利用

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摘要

Cobaltite-based double perovskite oxides with high electrocatalytic activity and conductivity have been developed as high-performance cathode alternatives for solid oxide fuel cells (SOFCs). However, the use of cobaltite-based double perovskites on YO stabilized ZrO (YSZ)-based SOFCs requires the application of a doped ceria barrier layer. This is due to their poor chemical and physical compatibility with the YSZ electrolyte during high-temperature sintering and fabrication processes. Here we report a viable approach to in operando assemble double perovskites such as PrBaSrCoFeO (PBSCF), on YSZ electrolyte and thus effectively form an electrode/electrolyte interface without high-temperature processing. The electrochemical performance of the in situ assembled PBSCF cathode is comparable to that of the cathode prepared by conventional methods. A single cell with an in situ assembled PBSCF–GDC (Gd-doped ceria) cathode achieved a peak power density (PPD) of 1.37 W cm at 750 °C and exhibited a high stability at 500 mA cm and 750 °C for 100 h. Surface and cross-sectional microstructure analysis offer solid evidence that the PBSCF–GDC cathode/YSZ electrolyte interface was formed by electrochemical polarization. This work offers new opportunities to effectively and effortlessly use high-performance double perovskite cathodes in commercial SOFCs.
机译:具有高电催化活性和导电性的钴基双钙钛矿氧化物已被开发为固体氧化物燃料电池(SOFC)的高性能阴极替代品。然而,在基于YO稳定的ZrO(YSZ)的SOFC上使用基于钴的双钙钛矿需要掺杂二氧化铈阻挡层。这是由于它们在高温烧结和制造过程中与YSZ电解质的化学和物理相容性差。在这里,我们报道了一种可行的方法,可在YSZ电解质上组装双钙钛矿,例如PrBaSrCoFeO(PBSCF),从而有效地形成电极/电解质界面,而无需高温处理。原位组装的PBSCF阴极的电化学性能与通过常规方法制备的阴极的电化学性能相当。具有原位组装的PBSCF–GDC(掺杂二氧化铈的)阴极的单个电池在750°C时达到1.37 W cm的峰值功率密度(PPD),并在500 mA cm和750°C下显示100 h的高稳定性。表面和横截面微观结构分析提供了可靠的证据,表明PBSCF–GDC阴极/ YSZ电解质界面是通过电化学极化形成的。这项工作为在商用SOFC中有效而轻松地使用高性能双钙钛矿阴极提供了新的机会。

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