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Mitigating the decomposition phenomenon at the cathode-electrolyte interface of protonic ceramic fuel cells
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作者 xin-rong huang Jia-Qi Qian +7 位作者 Hai-Peng Zhang Zhi-Yi Chen Chang-Gen Lin Jiong-Yuan huang Na Ai Cheng-Zhi Guan San Ping Jiang Kong-Fa Chen 《Rare Metals》 2025年第8期5393-5403,共11页
Protonic ceramic fuel cells(PCFCs) are promising for efficient,clean energy conversion at low to intermediate temperatures,but the widely used BaZr_(0.1)-Ce_(0.7)Y_(0.1)Yb_(0.1)O_(3-δ)(BZCYYb) electrolyte has poor ch... Protonic ceramic fuel cells(PCFCs) are promising for efficient,clean energy conversion at low to intermediate temperatures,but the widely used BaZr_(0.1)-Ce_(0.7)Y_(0.1)Yb_(0.1)O_(3-δ)(BZCYYb) electrolyte has poor chemical stability in humid environments.Herein,we show that under oxygen reduction reaction(ORR) conditions,water accumulates at the BaGd_(0.8)La_(0.2)Co_(2)O_(6-δ)(BGLC)cathode-BZCYYb electrolyte interface,causing selective loss of B a cations and decomposition of BZCYYb electrolyte.The introduction of triply ion-electron conducting La_(2)Ce_(2)O_(7-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℃,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. 展开更多
关键词 Chemical stability Nanocomposite cathode Direct assembly Water accumulation
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