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PdCo supported on multiwalled carbon nanotubes as an anode catalyst in a microfluidic formic acid fuel cell

机译:载于多壁碳纳米管上的PdCo作为微流甲酸燃料电池中的阳极催化剂

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摘要

This work reports the synthesis of Pd-based alloys of Co and their evaluation as anode materials in a microfluidic formic acid fuel cell (μFAFC). The catalysts were prepared using the impregnation method followed by thermal treatment. The synthesized catalysts contain 22wt.% Pd on multiwalled carbon nanotubes (Pd/MWCNT) and its alloys with two Co atomic percent in the sample with 4 at.% Co (PdCol/MWCNT) and 10 at.% Co (PdCo2/MWCNT). The role of the alloying element was determined by XRD and XPS techniques. Both catalysts were evaluated as anode materials in a U.FAFC operating with different concentrations of HCOOH (0.1 and 0.5 M), and the results were compared to those obtained with Pd/MWCNT. A better performance was obtained for the cell using PdCol/MWCNT (1.75 mWcm~(-2)) compared to Pd/MWCNT (0.85 mWcm~(-2)) in the presence of 0.5 M HCOOH. By means of external electrode measurements, it was also possible to observe shifts in the formic acid oxidation potential due to a fuel concentration increment (ca. 0.05 V for both PdCol/MWCNT and PdCo2/MWCNT catalysts and 0.23 V for Pd/MWCNT) that was attributed to deactivation of the catalyst material. The maximum current densities obtained were 8 mA cm~2 and 5.2 mA cm~(-2) for PdCo2/MWCNT and Pd/MWCNT, respectively. In this way, the addition of Co to the Pd catalyst was shown to improve the tolerance of intermediates produced during formic acid oxidation that tend to poison Pd, thus improving the catalytic activity and stability of the cell.
机译:这项工作报告了Co的Pd基合金的合成及其在微流体甲酸燃料电池(μFAFC)中作为阳极材料的评估。使用浸渍方法,然后进行热处理来制备催化剂。合成的催化剂在多壁碳纳米管(Pd / MWCNT)上含22wt。%的Pd及其合金,样品中的Co含量为2%,Co含量为4 at。%(PdCol / MWCNT),Co含量为10 at。%(PdCo2 / MWCNT) 。合金元素的作用是通过XRD和XPS技术确定的。在使用不同浓度的HCOOH(0.1和0.5 M)的U.FAFC中,两种催化剂均作为阳极材料进行了评估,并将结果与​​Pd / MWCNT获得的结果进行了比较。与存在0.5 M HCOOH的Pd / MWCNT(0.85 mWcm〜(-2))相比,使用PdCol / MWCNT(1.75 mWcm〜(-2))获得的电池性能更好。通过外部电极测量,还可以观察到由于燃料浓度增加而引起的甲酸氧化电位的变化(PdCol / MWCNT和PdCo2 / MWCNT催化剂均为0.05 V,Pd / MWCNT为0.23 V)这归因于催化剂材料的失活。 PdCo2 / MWCNT和Pd / MWCNT的最大电流密度分别为8 mA cm〜2和5.2 mA cm〜(-2)。以这种方式,显示出向Pd催化剂中添加Co可以提高在甲酸氧化过程中产生的中间产物的耐受性,该中间产物往往会毒化Pd,从而提高了催化活性和电池的稳定性。

著录项

  • 来源
    《Journal of power sources》 |2011年第22期|p.9270-9275|共6页
  • 作者单位

    Centra de Investigation y Desarrollo Tecnologico en Electroquimica, 76703 Queretaro, Mexico;

    Centra de Investigation y de Estudios Avanzados del IPN., Unidad Queretaro, 76001 Queretaro, Mexico;

    Centra de Investigation y Desarrollo Tecnologico en Electroquimica, 76703 Queretaro, Mexico;

    Centro de Investigation en Materials Avanzados, Laboratorio National de Nanotecnologia, 31109 Chihuahua, Mexico;

    Unidad Academica de Ciencias Quimicas-Siglo XXI, Universidad Autonoma deZacatecas, 98160 Zacatecas, Mexico;

    Centra de Investigation y Desarrollo Tecnologico en Electroquimica, 76703 Queretaro, Mexico;

    Centra de Investigation y Desarrollo Tecnologico en Electroquimica, 76703 Queretaro, 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

    microfluidic fuel cell; formic acid; pdco anode catalyst; mwcnts;

    机译:微流体燃料电池甲酸pdco阳极催化剂;多媒体;
  • 入库时间 2022-08-18 00:24:35

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