用于直接氨质子陶瓷燃料电池的活性持久氨裂解层

Liyan Chen, Hua Zhang, Kang Xu, Yangsen Xu, Xirui Zhang, Feng Zhu, Fan He, Yu Chen
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引用次数: 0

摘要

氨质子陶瓷燃料电池(NH3-PCFCs)因其高效率、环保责任和良性安全特性而成为极具吸引力的能源转换技术。然而,氨裂解用标准镍金属陶瓷阳极性能有限、寿命不足,尤其是在 550 °C 或更低的温度下,这明显阻碍了 NH3-PCFCs 的发展。在此,我们报告了一种配方为 xCo3O4/100-xBaZr0.8Y0.2O3-δ (Co/BZY) (x=10, 20, 30) 的高效氨裂解层,该层沉积在 Ni-BaZr0.1Ce0.7Y0.1Yb0.1O3-δ (BZCYYb) 阳极,可显著提高 NH3 分解催化活性,从而改善 NH3-PCFCs 在低温下的性能和耐用性。添加了 20Co/80BZY 阳极催化层 (ACL) 的电池在 NH3 条件下表现出较低的特定区域电阻 (ASR),并有望获得较长的运行寿命。在 550°C 的温度下,带有 20Co/80BZY ACL 的 NH3-PCFC 电池的峰值功率密度高达 0.626 W cm-2,并且具有良好的运行耐久性。这项研究为构建高性能、耐用的 NH3-PCFCs 提供了重要指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An active and durable ammonia cracking layer for direct ammonia protonic ceramic fuel cells
Ammonia protonic ceramic fuel cells (NH3-PCFCs) are highly appealing energy conversion technologies due to their high efficiency, environmental responsibility, and benign safety features. Nonetheless, progress in NH3-PCFCs is notably impeded by the restricted performance and insufficient lifespan of standard Ni-cermet anodes for ammonia cracking, especially at 550 °C or below. Herein, we report an efficient ammonia cracking layer with a formula of xCo3O4/100-xBaZr0.8Y0.2O3-δ (Co/BZY) (x=10, 20, 30), which is deposited onto the Ni-BaZr0.1Ce0.7Y0.1Yb0.1O3−δ (BZCYYb) anode to significantly enhance the NH3 decomposition catalytic activity, thereby improving the performance and durability of NH3-PCFCs at low temperatures. The cells with the addition of a 20Co/80BZY anode catalytic layer (ACL) exhibit low area-specific resistance (ASR) and promising operational longevity under NH3 conditions. At 550°C, the NH3-PCFCs with a 20Co/80BZY ACL exhibit a high peak power density of 0.626 W cm−2 and promising operation durability. This study provides important guidance for constructing high-performance and durable NH3-PCFCs.
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