Abstract

Cathode materials are pivotal in advancing ceramic fuel cell (CFC) technology. However, they still suffer from insufficient oxygen reduction reaction (ORR) activity and a high thermal expansion coefficient (TEC). In this study, we develop a thermodynamically stable self-ordered nanocomposite cathode material with the unique composition, BaCo0.5Ce0.3Fe0.1Yb0.1O3-δ (BCCFYb). Upon calcination, the precursor material separates into a host cubic and ancillary rhombohedral phase. We compare the performance of the triple ionic and electronic (O2−/H+/e−) conducting BCCFYb to that of cobalt-rich oxide-ion and electron (O2−/e−) conducting BaCo0.833Yb0.167O3-δ (BCYb), cerium-rich proton and electronic (H+/e−) conducting BaCe0.75Fe0.25O3-δ (BCF), and Co–Ce-rich triple ionic and electronic (O2−/H+/e−) conducting BaCo0.833Yb0.167O3-δ - BaCe0.75Fe0.25O3-δ (BCYb-BCF) traditional composite materials. The BCCFYb demonstrates a low TEC, good operational stability, and superior cathodic performance in both oxygen ion- and proton-conducting CFC modes, making it a promising cathode material for ceramic fuel cells.

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