首页> 外文期刊>International journal of hydrogen energy >Fabrication of nanoporous gold-islands via hydrogen bubble template: An efficient electrocatalyst for oxygen reduction and hydrogen evolution reactions
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Fabrication of nanoporous gold-islands via hydrogen bubble template: An efficient electrocatalyst for oxygen reduction and hydrogen evolution reactions

机译:通过氢气泡模板制备纳米多孔金岛:一种用于氧还原和氢释放反应的高效电催化剂

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In this report, the fabrication of a high surface area nanoporous gold-island (NPG-islands) onto a glassy carbon (GC) surface by a simple one-step electrodeposition procedure based on a dynamic hydrogen bubble template method is described. The surface morphology, purity and crystalline structure of the porous NPG-islands were analyzed by field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray analysis (EDX), and X-ray diffraction (XRD) techniques. Cyclic voltammetry and linear sweep voltammetry methods were used for electrochemical studies and the electrocatalytic activity of the NPG-islands surface was investigated towards the oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER). Electrochemical results revealed exceptional ORR activity of the NPG-islands evaluated by the shift of the onset potential towards less negative values compared to bare GC (0.55 V) and Au (0.25 V) electrodes, respectively, with a 3-fold increased current density in neutral PBS solution (pH 7). Rotating-disk measurements indicate a direct conversion of oxygen to water via a four-electron reduction pathway. The electrocatalytic activity was also evaluated for HER in 0.5 mol L-1 H2SO4 solution and a benchmark current density of 10 mA cm(-2 )at a very low overpotential of -0.075 V was obtained, which is similar to bulk Pt performance. The plausible mechanism of the HER was realized from the Tafel plot and the obtained slope of 46 mV dec(-1) suggests the Volmer-Heyrovsky mechanism takes place in such electrochemical process. Furthermore, the durability of the catalyst was also studied and exceptional stability was observed in cyclic voltammetry (up to 2000 cycles) and chronopotentiometry (at 10 mA cm(-2) for 19 h). (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:在此报告中,描述了通过基于动态氢气泡模板法的简单一步电沉积程序在玻璃碳(GC)表面上制造高表面积纳米孔金岛(NPG-island)。通过场发射扫描电子显微镜(FE-SEM),能量色散X射线分析(EDX)和X射线衍射(XRD)技术分析了多孔NPG岛的表面形态,纯度和晶体结构。使用循环伏安法和线性扫描伏安法进行电化学研究,并研究了NPG岛表面对氧还原反应(ORR)和析氢反应(HER)的电催化活性。电化学结果显示,与裸GC(0.55 V)和Au(0.25 V)电极相比,NPG岛的异常ORR活性是通过将开始电势向较小的负值偏移进行评估的,其中电流密度增加了3倍。中性PBS溶液(pH 7)。圆盘测量表明氧气通过四电子还原途径直接转化为水。还对HER在0.5 mol L-1 H2SO4溶液中的电催化活性进行了评估,在-0.075 V的极低超电势下获得了10 mA cm(-2)的基准电流密度,这与Pt本体性能相似。 HER的合理机理是根据Tafel图实现的,获得的46 mV dec(-1)的斜率表明Volmer-Heyrovsky机理是在这种电化学过程中发生的。此外,还研究了催化剂的耐久性,并在循环伏安法(最多2000个循环)和计时电位法(在10 mA cm(-2)下持续19 h)中观察到了出色的稳定性。 (C)2019氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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