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Catalytic performance of non-platinum-based hybrid carbon hetero-structure for oxygen reduction and hydrogen oxidation reactions in proton exchange membrane fuel cell

机译:非铂基杂化碳杂结构对质子交换膜燃料电池中氧还原和氢氧化反应的催化性能

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The present work describes the potential of a hybrid carbon hetero-structure having the unique properties of one-dimensional carbon nanotubes and two-dimensional graphene as a catalyst support material for platinum-free electrocatalysts in polymer electrolyte membrane fuel cell (PEMFC) for hydrogen oxidation reaction (HOR) or oxygen reduction reaction (ORR). Partially exfoliated carbon nanotubes (PCNT), which have the synergistic effect of good electrical conductivity and high surface area, have been used as the support material for Pd3Co alloy catalysts. This provides more active sites for the dispersion of catalyst particles along with quick electron transport through the carbon structure. This unique characteristic increases the catalytic activity of the electrocatalysts. The electrochemical half-cell studies confirm that, ORR on Pd3Co/PCNT proceeds via a four-electron process. The single cell measurements were carried out by preparing a membrane electrode assembly (MEA) using Pd3Co/PCNT at the anode, cathode separately as well as simultaneously at both the anode and cathode. A maximum power density of 327 mW cm(-2), 240 mW cm(-2) and 96 mW cm(-2) is attained from the use of Pd3Co/PCNT nanocomposite at anode, cathode and at both electrodes simultaneously in a PEMFC at 60 degrees C, respectively. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:本工作描述了具有一维碳纳米管和二维石墨烯独特性质的杂化碳杂结构的潜力,该杂化碳杂结构作为聚合物电解质膜燃料电池(PEMFC)中用于氢氧化的无铂电催化剂的催化剂载体材料反应(HOR)或氧还原反应(ORR)。具有良好导电性和高表面积的协同作用的部分剥离碳纳米管(PCNT)已用作Pd3Co合金催化剂的载体材料。这为催化剂颗粒的分散以及通过碳结构的快速电子传输提供了更多的活性位点。这种独特的特性提高了电催化剂的催化活性。电化学半电池研究证实,Pd3Co / PCNT上的ORR通过四电子过程进行。通过在阳极,阴极以及同时在阳极和阴极同时使用Pd3Co / PCNT制备膜电极组件(MEA)来进行单电池测量。通过在PEMFC中同时在阳极,阴极和两个电极上使用Pd3Co / PCNT纳米复合材料,可实现327 mW cm(-2),240 mW cm(-2)和96 mW cm(-2)的最大功率密度分别在60摄氏度。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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