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首页> 外文期刊>Journal of power sources >Electrocatalysis of the Ethylene glycol oxidation reaction and in situ Fourier-transform infared study on PtMo/C electrocatalysts in alkaline and acid media
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Electrocatalysis of the Ethylene glycol oxidation reaction and in situ Fourier-transform infared study on PtMo/C electrocatalysts in alkaline and acid media

机译:碱性和酸性介质中PtMo / C电催化剂对乙二醇氧化反应的电催化和原位傅里叶变换红外光谱研究

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摘要

PtMo/C (Pt:Mo atomic ratios of 1:1, 2:1 and 3:1) and Pt/C electrocatalysts synthesized by the formic acid method are investigated for the ethylene glycol oxidation reaction (EGOR) in alkaline and acid media. From XRD measurements, the crystallite sizes are between 2.5 and 4.3 nm. Electrochemical characterization of the EGOR on the electrocatalysts shows that the PtMo/C series exhibit higher electrocatalytic activity. When comparing the two electrolytes, the mass current densities obtained in alkaline media are significantly higher than in the acid counterpart. Among the bimetallic anodes, PtiMoi/C delivered a high performance in both media. In situ FTIR spectroscopy analysis has been performed to study the pathway of the EGOR. In alkaline media, the PtMo/C electrocatalysts have a higher selectivity for the C2 pathway resulting in the formation of species such as glycolate, glyoxal and glyoxylate. On the other hand, in acid electrolyte, the PtMo/C anodes show a preferential C1 pathway at high potentials and the main intermediate is identified as glycolic acid. The results indicate that the higher catalytic activity of PtMo/C electrocatalysts towards the EGOR may be attributed to the bifunctional mechanism and also to an electronic effect because of the incorporation of Mo atoms into the catalysts structure. (C) 2017 Elsevier B.V. All rights reserved.
机译:研究了用甲酸法合成的PtMo / C(Pt:Mo原子比为1:1、2:1和3:1)和Pt / C电催化剂在碱性和酸性介质中的乙二醇氧化反应(EGOR)。根据XRD测量,微晶尺寸在2.5至4.3nm之间。 EGOR在电催化剂上的电化学表征表明PtMo / C系列具有较高的电催化活性。当比较两种电解质时,在碱性介质中获得的质量电流密度显着高于在酸性介质中获得的质量电流密度。在双金属阳极中,PtiMoi / C在两种介质中均具有高性能。已经进行了原位FTIR光谱分析以研究EGOR的途径。在碱性介质中,PtMo / C电催化剂对C2途径具有更高的选择性,从而导致形成乙醇酸,乙二醛和乙醛酸等物质。另一方面,在酸性电解质中,PtMo / C阳极在高电势下显示出优先的C1途径,主要中间体被鉴定为乙醇酸。结果表明,由于Mo原子掺入催化剂结构,PtMo / C电催化剂对EGOR的较高催化活性可能归因于双功能机理以及电子效应。 (C)2017 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《Journal of power sources》 |2018年第31期|335-344|共10页
  • 作者单位

    Univ Politecn Victoria, Av Nuevas Tecnol 5902, Ciudad Victoria 87138, Tamaulipas, Mexico;

    Univ Politecn Victoria, Av Nuevas Tecnol 5902, Ciudad Victoria 87138, Tamaulipas, Mexico;

    CINVESTAV, Unidad Saltillo, Av Ind Met 1062,Parque Ind Ramos, Arizpe Ramos Arizpe 25900, Coahuila, Mexico;

    CINVESTAV, Unidad Saltillo, Av Ind Met 1062,Parque Ind Ramos, Arizpe Ramos Arizpe 25900, Coahuila, Mexico;

    Univ Poitiers, UMR CNRS 7285, Equipe SAMCat, 4 Rue Michel Brunet,B27,TSA 51106, F-86073 Poitiers 09, France;

    Univ Poitiers, UMR CNRS 7285, Equipe SAMCat, 4 Rue Michel Brunet,B27,TSA 51106, F-86073 Poitiers 09, France;

    CINVESTAV, Unidad Saltillo, Av Ind Met 1062,Parque Ind Ramos, Arizpe Ramos Arizpe 25900, Coahuila, Mexico;

  • 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

    Ethylene glycol oxidation reaction; PtMo/C electrocatalysts; Alkaline and acid media; In situ FTIR analysis;

    机译:乙二醇氧化反应;PtMo / C电催化剂;碱性和酸性介质;原位FTIR分析;

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