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Synthesis of flower-like molybdenum sulfide/graphene hybrid as an efficient oxygen reduction electrocatalyst for anion exchange membrane fuel cells

机译:花状硫化钼/石墨烯杂化物的合成作为阴离子交换膜燃料电池的高效氧还原电催化剂

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摘要

Nanostructured transition metal chalcogenides (TMCs) have significant interest towards electrochemical devices such as fuel cells, metal-ion batteries, due to their unique physical and electrochemical properties. Herein, we report a facile hydrothermal synthesis of flower-like nanostructured molybdenum sulphide and its incorporation on to graphene as a potential oxygen reduction reaction catalyst in alkaline medium. The phase purity and morphological evolution of MoS2 is systematically studied through X-ray diffraction and scanning electron microscopic techniques. The electronic states of metal and non-metallic species are deeply studied by X-ray photoelectron spectroscopy. The effect of annealing temperatures and TMC concentrations are also investigated by electrochemical techniques such as cyclic and linear sweep voltammograms. The optimised electrocatalyst (MoS2/G-500) delivers significant ORR activity with onset and half-wave potentials of 0.91 and 0.80 V (vs. RHE), respectively. Superior durability compared to state-of-art Pt/C catalyst is ascertained by repeating potential cycles for about 5000 times and also by chronoamperometric technique. Finally, the hybrid catalyst is evaluated in AEMFC as cathode catalyst which delivers peak power density of about 29 mW cm(-2) under ambient temperature and pressure. The present findings emphasis that MoS2/G catalyst is promising as cost-effective and alternative to noble metal-based catalysts for fuel cell applications. (C) 2017 Elsevier B.V. All rights reserved.
机译:纳米结构的过渡金属硫族化物(TMC)由于其独特的物理和电化学特性,对电化学装置(例如燃料电池,金属离子电池)具有极大的兴趣。在此,我们报道了一种花状纳米结构硫化钼的简便水热合成方法,并将其掺入到石墨烯中作为碱性介质中潜在的氧还原反应催化剂。通过X射线衍射和扫描电子显微镜技术系统地研究了MoS2的相纯度和形貌演化。 X射线光电子能谱对金属和非金属物种的电子态进行了深入研究。还通过电化学技术,例如循环和线性扫描伏安图,研究了退火温度和TMC浓度的影响。经过优化的电催化剂(MoS2 / G-500)具有显着的ORR活性,起始和半波电势分别为0.91和0.80 V(相对于RHE)。与现有技术的Pt / C催化剂相比,通过重复潜在的循环约5000次并通过计时电流法技术可以确定其优越的耐久性。最后,杂化催化剂在AEMFC中作为阴极催化剂进行评估,该阴极催化剂在环境温度和压力下可提供约29 mW cm(-2)的峰值功率密度。本研究结果强调,MoS2 / G催化剂有望成为具有成本效益的燃料电池替代贵金属基催化剂。 (C)2017 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《Journal of power sources》 |2017年第15期|104-114|共11页
  • 作者单位

    CSIR, Cent Electrochem Res Inst, Madras Unit, CSIR Madras Complex, Chennai 600113, Tamil Nadu, India;

    CSIR, Cent Electrochem Res Inst, Madras Unit, CSIR Madras Complex, Chennai 600113, Tamil Nadu, India;

    CSIR, Cent Electrochem Res Inst, Madras Unit, CSIR Madras Complex, Chennai 600113, Tamil Nadu, India;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Molybdenum sulfide; Graphene; Oxygen reduction reaction; Alkaline medium; Durability; Fuel cells;

    机译:硫化钼;石墨烯;氧还原反应;碱性介质;耐久性;燃料电池;

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