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On the stability in alkaline conditions and electrochemical performance of A(2)BO(4)-type cathodes for liquid fuel cells

机译:关于碱性条件的稳定性和液体燃料电池(4)型型阴极的电化学性能及电化学性能

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Typical direct liquid fuel cells (DLFCs) use a liquid fuel and O-2 as the oxidant. However, for applications where O-2 is not available (e.g., space and underwater), the gas has been replaced by H2O2 as a liquid oxidant. This work presents a study of various ceramic disc electrodes with K2NiO4 structure and nominal compositions La2NiO4, La2CuO4, La1.9Pr0.1CuO4, La1.9Sr0.1CuO4, La1.8Ce0.2NiO4, La1.9Pr0.1NiO4, La1.8Pr0.2NiO4 and La1.9Sr0.1NiO4 to assess their stability and activity for the hydrogen peroxide reduction reaction (HPRR) in alkaline media. Stability tests conducted in 2 M NaOH show that Ni and Cu are readily dissolved, as occurs for substituting elements such as Sr, in agreement with calculated Pourbaix diagrams. Such degradation affects the surface of the materials, which is depleted of transition metals. This has consequences for the ORR and HPRR activity due to formation of a La-rich passivation layer on the surface. Only La2CuO4 and La1.8Ce0.2NiO4 display HPRR activity at around -0.25 V vs. RHE. An attempt is made to correlate the composition, chemical stability and electrochemical behaviour of these materials based on known molecular-orbital models proposed for the oxygen reduction reaction.
机译:典型的直接液体燃料电池(DLFC)使用液体燃料和O-2作为氧化剂。然而,对于应用,其中O-2不可用(例如,空间和水下),该气体已取代H 2 O 2作为液体氧化剂。这项工作提出与K2NiO4结构的各种陶瓷盘电极和标称组成La2NiO4,La2CuO4,La1.9Pr0.1CuO4,La1.9Sr0.1CuO4,La1.8Ce0.2NiO4,La1.9Pr0.1NiO4,La1.8Pr0.2NiO4的研究和LA1.9SR0.1NIO4评估其碱性介质中过氧化氢反应(HPRR)的稳定性和活性。在2M NaOH中进行的稳定性试验表明,对于代替诸如SR的元素,易于溶解Ni和Cu,与计算的PORBAIX图达成协议。这种降解影响了耗尽过渡金属的材料表面。由于在表面上形成La的钝化层,这对ORR和HPRR活性产生了后果。只有LA2CUO4和LA1.8CE0.2NIO4显示HPRR活性在-0.25 V与RHE左右。试图到组合物中,化学稳定性和基于提出了氧还原反应公知的分子轨道模型这些材料的电化学行为相关联。

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