4.7 Article

Effect of the Pd/MWCNTs anode catalysts preparation methods on their morphology and activity in a direct formic acid fuel cell

期刊

APPLIED SURFACE SCIENCE
卷 387, 期 -, 页码 929-937

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2016.06.152

关键词

Electro-oxidation; DFAFC; Pd/MWCNTs; Preparation conditions; Reducing agents; Microwave conditions

资金

  1. Polish Academy of Sciences and Academy of Sciences of the Czech Republic
  2. National Centre for Research and Development [PBS1/A5/15/2012, Pl-TW/1/2013/08]
  3. European Union by the European Social Fund
  4. Academy of Sciences of the Czech Republic [M100101202]

向作者/读者索取更多资源

Impact of Pd/MWCNTs catalysts preparation method on the catalysts morphology and activity in a formic acid electrooxidation reaction was investigated. Three reduction methods of Pd precursor involving reduction in a high pressure microwave reactor (Pdl), reduction with NaBH4 (Pd2) and microwave assisted polyol method (Pd3) were used in this paper. Crystallites size and morphology were studied using the scanning transmission electron microscopy (STEM), X-ray diffraction (XRD), whereas elemental composition, Pd chemical state and functional groups content by the X-ray photoelectron spectroscopy (XPS). The prepared catalysts were tested in a direct formic acid fuel cell (DFAFC) as an anode material. The catalytic activity was correlated with a mean fraction of the total Pd atoms exposed at the surface (FE). The value of FE was calculated from the crystallites size distribution determined by the STEM measurements. Non-linear dependence of a current density versus FE, approaching the maximum at FE approximate to 0.25 suggests that the catalytic process proceeded at Pd nanocrystallites faces, with inactive edges and corners. Pd2 catalyst exhibited highest activity due to its smallest Pd crystallites (3.2 nm), however the absence of Pd crystallites aggregation and low content of carbon in PdCx phase, i.e. x = 4 at.% may also affect the observed. (C) 2016 Elsevier B.V. All rights reserved.

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