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High‐Efficiency Direct Ammonia Fuel Cells Based on BaZr0.1Ce0.7Y0.2O3−δ/Pd Oxide‐Metal Junctions

机译:基于BaZr0.1Ce0.7Y0.2O3-的高效直接氨燃料电池δ/ Pd氧化物-金属结

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摘要

A direct ammonia‐type intermediate temperature fuel cell is examined by means of a hydrogen membrane fuel cell (HMFC) comprising 1‐µm‐thick BaZr0.1Ce0.7Y0.2O3− δ (BZCY) thin‐film electrolyte and Pd solid anode. It generates the maximum power density of 0.58 W cm−2 at 600 °C with ammonia fuels, and this value is found to be three times larger than the champion data of the recently reported direct ammonia‐type proton‐conducting ceramic fuel cells (PCFCs). AC impedance spectroscopy is performed to determine the interfacial polarization resistances, disclosing that the anodic overpotentials of HMFCs are at least one order of magnitude smaller than those of anode‐supported PCFC under relatively high DC outputs. The anode reactions are driven by the oxidation of monoatomic hydrogen dissolving at the BZCY/Pd solid–solid interface, mediated via proton transfer from Pd to BZCY. The electrochemical analysis reveals that the BZCY/Pd junction forms Ohmic contact without growth of wide depletion layer and thus facilitates the proton transfer reactions because the interfacial region beneath Pd electrode can accommodate amounts of protonic defects as well as the bulk of BZCY due to the small depletion of holes under hole–proton thermodynamic equilibrium.
机译:通过氢膜燃料电池(HMFC)对直接氨型中温燃料电池进行了检查,该电池包括厚度为1 µm的BaZr0.1Ce0.7Y0.2O3-δ(BZCY)薄膜电解质和Pd固体阳极。在使用氨燃料的情况下,它在600°C时产生的最大功率密度为0.58 W cm −2 ,发现该值是最近报道的直接氨型质子的冠军数据的三倍。导电陶瓷燃料电池(PCFC)。进行交流阻抗谱分析以确定界面极化电阻,结果表明在相对较高的直流输出下,HMFC的阳极超电势至少比阳极支撑的PCFC的阳极超电势小一个数量级。阳极反应是由在BZCY / Pd固-固界面处溶解的单原子氢氧化所驱动,这是由质子从Pd转移到BZCY介导的。电化学分析表明,BZCY / Pd结形成欧姆接触而没有宽耗尽层的生长,因此促进了质子转移反应,因为Pd电极下方的界面区域可以容纳大量的质子缺陷以及由于体积小而引起的BZCY的大量存在空穴-质子热力学平衡下的空穴耗竭。

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