材料科学
金属陶瓷
电解质
阳极
钙钛矿(结构)
烧结
催化作用
电导率
氨
质子导体
化学工程
氧化物
镍
无机化学
陶瓷
冶金
电极
物理化学
化学
有机化学
工程类
作者
Fan He,Qinning Gao,Zuoqing Liu,Jing Wang,Ran Ran,Guangming Yang,Wei Wang,Wei Zhou,Zongping Shao
标识
DOI:10.1002/aenm.202003916
摘要
Abstract The combination of ammonia fuel and proton‐conducting fuel cells (PCFCs) technology may provide an ideal clean energy system for the future, considering matured NH 3 synthesis technology and transportation and storage infrastructure, the high energy density of NH 3 , and the high efficiency of fuel cells. However, poor catalytic activity of the anode for NH 3 decomposition, quick performance degradation due to the ammonia induced nickel coarsening, difficult sintering, and insufficient proton conductivity of electrolytes are the main challenges for stable and high‐power generation from ammonia‐fueled PCFCs. Herein, a new Ba(Zr 0.1 Ce 0.7 Y 0.1 Yb 0.1 ) 0.95 Pd 0.05 O 3− δ perovskite is reported as a key anode component and electrolyte, which demonstrates multifunctionalities and tackles most challenges of conventional PCFCs. The incorporation of a small amount of Pd boosts catalytic activity of the nickel‐perovskite cermet anode for NH 3 decomposition and increases proton conductivity from the creation of B‐site cation deficiency and electrolyte sintering. The corresponding thin‐film electrolyte PCFC delivers a maximum power density of 724 mW cm –2 at 650 °C operated on NH 3 , much higher than the similar cell without Pd incorporation (450 mW cm –2 ). Furthermore, no apparent performance decay is observed for the cell operated at 550 °C in H 2 and NH 3 for 350 h, making it highly promising for practical applications.
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