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Anodic electrodeposition of iridium oxide particles on glassy carbon surfaces and their electrochemical/SEM/XPS characterization

机译:氧化铱颗粒在玻碳表面的阳极电沉积及其电化学/ SEM / XPS表征

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摘要

In this study an electrodeposition procedure of hydrated Ir(III) and Ir(IV) oxyhydroxide species operating under anodic conditions and directly from aged alkaline solution containing 6 mM IrCla(6)(3-) and 20 mM Cl- a ligand specie was defined for the surface modification of the glassy carbon electrode substrates. Optimum efficiency of iridium oxide deposition was obtained by cycling the potentials (100 mV s(-1)) between -0.7 V and 1.0 V vs. SCE. The SEM analysis reveals that the iridium oxide is uniformly distributed on the entire electrode surface with particles having a globular form. All particles, appear isolated or in aggregated structures with an average diameter comprised between 0.03 mu m and 0.4 mu m. The XPS curve fitting analysis reveals that the surface deposit is formed of hydrated Ir(III) and Ir(IV) oxyhydroxide species. The electrocatalytic activity of the GC/IrOx electrode toward the oxidation of semicarbazide under acidic condition (i.e., 50 mM HClO4) using cyclic voltammetry and chronoamperometry, was also investigated. (C) 2014 Elsevier B.V. All rights reserved.
机译:在这项研究中,定义了在阳极条件下直接从含有6 mM IrCla(6)(3-)和20 mM Cl-配体物种的老化碱溶液中直接操作的水合Ir(III)和Ir(IV)羟基氧化物的电沉积程序用于玻璃碳电极基材的表面改性。通过使电势(100 mV s(-1))在-0.7 V和1.0 V对SCE之间循环,可以获得最佳的氧化铱沉积效率。 SEM分析表明,氧化铱均匀地分布在整个电极表面上,具有球形的颗粒。所有颗粒均显示为孤立的或聚集的结构,平均直径为0.03μm至0.4μm。 XPS曲线拟合分析表明,表面沉积物是由水合的Ir(III)和Ir(IV)羟基氧化物形成的。还使用循环伏安法和计时电流法研究了GC / IrOx电极在酸性条件下(即50 mM HClO4)对氨基脲的氧化的电催化活性。 (C)2014 Elsevier B.V.保留所有权利。

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