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Electrocatalysis of oxygen reduction reaction on polyaniline-derived nitrogen-doped carbon nanoparticle surfaces in alkaline media

机译:碱性介质中聚苯胺衍生的氮掺杂碳纳米粒子表面的氧还原反应的电催化

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摘要

Nitrogen-doped carbon nanomaterials were synthesized by the carbonization of three different nanostructured polyaniline (PANI) salt precursors: PANI 3,5-dinitrosalicylate nanorods, PANI 5-sulfosalicylate nanorodsanotubes, and PANI hydrogen sulfate nanorodsanotubesanosheets. A comparative study of the electrocatalytic activity of these materials for oxygen reduction reaction (ORR) in alkaline solution was performed by using rotating disk electrode voltammetry. The electrochemical data were correlated to the structural and textural data obtained by Raman spectroscopy, X-ray diffractometry, X-ray photoelectron spectroscopy, elemental analysis and nitrogen sorption analysis. A fine interplay of textural characteristics, overall content of surface nitrogen and content of specific surface nitrogen functional groups were found to be responsible for a considerable variations in electrocatalytic properties toward ORR, involving variations in apparent number of electrons exchanged per O_2 molecule (from 2 to nearly 4) and variations in onset potential. The catalyst loading was found to influence remarkably the ORR kinetics. The excellent electrocatalytic activity was found for carbonized PANI 5-sulfosalicylate. Namely, it exhibited the most positive onset potential amounting to -0.05 V vs. SCE at a catalyst loading of 500 μg cm~(-2). The interrelation between the electrocatalytic activity and the electrical double layer charging/discharging characteristics of the investigated N-doped nanocarbon materials was revealed.
机译:通过碳化三种不同的纳米结构聚苯胺(PANI)盐前体:PANI 3,5-dinitrosalicylate纳米棒,PANI 5-磺基水杨酸酯纳米棒/纳米管和PANI硫酸氢纳米棒/纳米管/纳米片,来合成氮掺杂的碳纳米材料。使用旋转盘电极伏安法对这些材料在碱性溶液中对氧还原反应(ORR)的电催化活性进行了比较研究。电化学数据与通过拉曼光谱,X射线衍射法,X射线光电子能谱,元素分析和氮吸附分析获得的结构和纹理数据相关。发现结构特征,表面氮的总含量和特定表面氮官能团的含量之间的良好相互作用导致了对ORR的电催化性能的巨大变化,其中涉及每个O_2分子交换的表观电子数变化(从2到2)。近4)和发作电位的变化。发现催化剂负载显着影响ORR动力学。发现碳化的PANI 5-磺基水杨酸酯具有优异的电催化活性。即,在500μgcm 2-(-2)的催化剂负载量下,其相对于SCE表现出最正的起始电位,为-0.05V。揭示了所研究的N掺杂纳米碳材料的电催化活性与双电层充放电特性之间的相互关系。

著录项

  • 来源
    《Journal of power sources》 |2012年第15期|p.306-316|共11页
  • 作者单位

    University of Belgrade, Faculty of Physical Chemistry, Studentski trg 12-16, 11158 Belgrade, Serbia;

    University of Belgrade, Faculty of Physical Chemistry, Studentski trg 12-16, 11158 Belgrade, Serbia;

    University of Belgrade, Vinca Institute of Nuclear Sciences, P.O. Box 522, 11001 Belgrade, Serbia;

    Polymer Electronics Research Centre, School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland, New Zealand,MacDiarmid Institute for Advanced Materials and Nanotechnology, Victoria University of Wellington, P.O. Box 600, Wellington 6140, New Zealand;

    University of Belgrade, Faculty of Physical Chemistry, Studentski trg 12-16, 11158 Belgrade, Serbia;

    University of Belgrade, Faculty of Physical Chemistry, Studentski trg 12-16, 11158 Belgrade, Serbia,Serbian Academy of Sciences and Arts, Knez Mihailova 35, 11000 Belgrade, Serbia;

  • 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

    carbonized polyaniline; electrocatalyst; nitrogen-containing carbon nanostructures; oxygen reduction reaction; surface functional groups; textural properties;

    机译:碳化聚苯胺电催化剂含氮碳纳米结构;氧还原反应;表面官能团;质地特性;

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