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Abstract:
Protonic ceramic fuel cells (PCFCs) are promising for efficient, clean energy conversion at low to intermediate temperatures, but the widely used BaZr0.1Ce0.7Y0.1Yb0.1O3−δ (BZCYYb) electrolyte has poor chemical stability in humid environments. Herein, we show that under oxygen reduction reaction (ORR) conditions, water accumulates at the BaGd0.8La0.2Co2O6−δ (BGLC) cathode–BZCYYb electrolyte interface, causing selective loss of Ba cations and decomposition of BZCYYb electrolyte. The introduction of triply ion–electron conducting La2Ce2O7−δ (LCeO) into the BGLC cathode expands its active reaction area, accelerates ORR kinetics, and suppresses water accumulation at the cathode–electrolyte interface and electrolyte decomposition. A single cell with the BGLC-LCeO composite cathode achieves a peak power density of 1.07 W cm−2 at 700 °C, with no profound degradation at 0.5 A cm−2 over 100 h. These findings provide guidance for the development of high-performance, durable PCFCs. © Youke Publishing Co.,Ltd 2025.
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Rare Metals
ISSN: 1001-0521
Year: 2025
9 . 6 0 0
JCR@2023
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ESI Highly Cited Papers on the List: 0 Unfold All
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