Zuoqing Liu, Minghao Tao, Ming Xiao, Junbiao Li, Ruijia Xu, Bin Chen, Tao Li, Guangming Yang, Yuan Zhang, Nai Shi, Ran Ran, Wei Wang, Wei Zhou, Zongping Shao
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引用次数: 0
Abstract
Ammonia, as an ideal carbon-free hydrogen carrier, enables direct application in protonic ceramic fuel cells while bypassing energy-intensive hydrogen regeneration. However, conventional Ni-based anodes for direct ammonia protonic ceramic fuel cells (DA-PCFCs) suffer from weak interfacial coupling and structural instability. Herein, we report a strategy of anodic heterogeneous engineering to build a strongly coupled Ni-BaZr0.1Ce0.7Y0.1Yb0.1O3-δ interface combined with a Cs2O-decorated Ru catalyst for surface modification. This design enhances ammonia decomposition by providing a highly interconnected network that facilitates efficient proton conduction and electron transfer, while the Ru catalyst introduces abundant active sites with superior ammonia adsorption capacity. The cell delivers a peak power density of 1.01 W cm−2 at 650°C and maintains 98.1% of its initial ammonia decomposition activity after 200 h at 500°C of operation. By overcoming the bottlenecks of DA-PCFCs, this study paves the way for their practical application in carbon-neutral energy systems.
期刊介绍:
Chem Catalysis is a monthly journal that publishes innovative research on fundamental and applied catalysis, providing a platform for researchers across chemistry, chemical engineering, and related fields. It serves as a premier resource for scientists and engineers in academia and industry, covering heterogeneous, homogeneous, and biocatalysis. Emphasizing transformative methods and technologies, the journal aims to advance understanding, introduce novel catalysts, and connect fundamental insights to real-world applications for societal benefit.