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Pt-Ir and Pt-Cu binary alloys as the electrocatalyst for ammonia oxidation

机译:Pt-Ir和Pt-Cu二元合金作为氨氧化的电催化剂

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The electrocatalytic activities of Pt{sub}0.8Ir{sub}0.2, Pt{sub}0.5Cu{sub}0.5, Pt{sub}0.67Cu{sub}0.33, Pt, and Ir for ammonia oxidation have been studied comparatively in KOH solutions by cyclic voltammetry and potentiostatic polarization. The anodic oxidation began on Ir at a lower potential than on Pt by about 0.1 V, whereas the oxidation peak current density on Ir was much lower than that on Pt. On the binary alloy of Pt{sub}0.8Ir{sub}0.2, the oxidation started at slightly lower potential than on Pt, and the peak current density was slightly higher than that on Pt. In contrast, Pt{sub}0.5Cu{sub}0.5 and Pt{sub}0.67Cu{sub}0.33 alloys showed almost the compatible activity inferior to Pt. These facts suggested that alloying in the Pt-Ir binary system may lead to the enhancement of ammonia oxidation activity due to a kind of cooperative interaction between Pt and Ir.
机译:在KOH中比较研究了Pt {sub} 0.8Ir {sub} 0.2,Pt {sub} 0.5Cu {sub} 0.5,Pt {sub} 0.67Cu {sub} 0.33,Pt和Ir对氨氧化的电催化活性循环伏安法和恒电位极化法制备溶液。 Ir的阳极氧化开始时的电位比Pt低约0.1 V,而Ir的氧化峰值电流密度远低于Pt。在Pt {sub} 0.8Ir {sub} 0.2的二元合金上,氧化开始时的电位略低于Pt,并且峰值电流密度略高于Pt。相反,Pt {sub} 0.5Cu {sub} 0.5和Pt {sub} 0.67Cu {sub} 0.33合金的相容性几乎不如Pt。这些事实表明,Pt-Ir二元体系中的合金化可能会由于Pt和Ir之间的一种协作相互作用而导致氨氧化活性的增强。

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