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首页> 外文期刊>Electrochimica Acta >RuOx nanoparticles deposited on TiO2 nanotube arrays by ion-exchange method as electrocatalysts for the hydrogen evolution reaction in acid solution
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RuOx nanoparticles deposited on TiO2 nanotube arrays by ion-exchange method as electrocatalysts for the hydrogen evolution reaction in acid solution

机译:离子交换法在TiO2纳米管阵列上沉积的RuOx纳米颗粒作为在酸性溶液中析氢反应的电催化剂

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Nanocomposite cathodes for the hydrogen evolution reaction (HER) were prepared by deposition of RuOx catalyst particles on self-organized titania nanotube (TiNT) arrays of highly developed surface area, following a procedure that involved the initial cathodic intercalation of H+ into the TiNT walls and the subsequent two-step ion-exchange process. Transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS) analyses of obtained Ru-TiNT samples revealed that the concentration of RuOx particles in the size range of a few nanometers was the highest at the surface of the TiNT layer and steadily decreased to a minimum value at about 4.5 mu m inside the tubes. The capacitive behavior and electrocatalytic activity for the HER of Ru-TiNT nanocomposites, hydrogenated TiNT samples (H-TiNT) and compact TiO2 were investigated in 1.0 M HClO4 solution at room temperature by means of cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), Mott-Schottky analysis and steady-state polarization measurements. It was shown that cathodic hydrogenation treatment induced a four orders of magnitude higher concentration of electron donors in TiNT structures providing their quasimetallic behavior in the range of potentials corresponding to the HER. Ru-TiNT cathodes exhibited a more than 250 mV lower overpotential for the HER with respect to bare H-TiNT substrates at the current density of -50 mA cm (2). A decrease of the Tafel slope from about -120 mV/dec for H-TiNT samples to as low as -70 mV/dec for the Ru-TiNT sample with longer tubes was explained by the formal kinetics approach. (C) 2015 Elsevier Ltd. All rights reserved.
机译:通过将RuOx催化剂颗粒沉积在具有高度发达表面积的自组织二氧化钛纳米管(TiNT)阵列上,制备了用于氢释放反应(HER)的纳米复合阴极,该过程涉及将H +初始插入阴极和TiNT壁中。随后的两步离子交换过程。所获得的Ru-TiNT样品的透射电子显微镜(TEM)和能量色散X射线光谱(EDS)分析表明,在几纳米大小范围内,RuOx颗粒的浓度在TiNT层的表面最高且稳定。在管内约4.5μm处降低至最小值。在室温下通过循环伏安法(CV),电化学阻抗谱(EIS)研究了Ru-TiNT纳米复合材料,氢化TiNT样品(H-TiNT)和致密TiO2的HER的电容行为和电催化活性。 ),Mott-Schottky分析和稳态极化测量。结果表明,阴极加氢处理可以使TiNT结构中的电子供体浓度提高4个数量级,从而在与HER相对应的电位范围内提供准金属行为。相对于裸露的H-TiNT衬底,Ru-TiNT阴极在-50 mA cm的电流密度下相对于裸露的H-TiNT衬底而言,其过电位降低了250 mV以上(2)。形式动力学方法解释了塔菲尔斜率从H-TiNT样品的约-120 mV / dec降低到具有较长管的Ru-TiNT样品的低至-70 mV / dec。 (C)2015 Elsevier Ltd.保留所有权利。

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