4.7 Article

Tailoring of carbonized polypyrrole nanotubes core by different polypyrrole shells for oxygen reduction reaction selectivity modification

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 551, Issue -, Pages 184-194

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2019.04.064

Keywords

Polypyrrole; Nanotubes; Coating; Carbonization; Conductivity; Oxygen reduction reaction

Funding

  1. Czech Science Foundation [18-04669S]
  2. Austrian Federal Ministry of Science, Research and Economy (BMWFW) [DS-2016-0027, MULT_DR 06/2017]
  3. Ministry of Education, Youth and Sports of the Czech Republic [DS-2016-0027, 8X17027]
  4. Serbian Ministry of Education, Science and Technological Development [DS-2016-0027, DS-027]
  5. Ministry of Education, Science, Research and Sport of the Slovak Republic [DS-2016-0027, APW DS-2016-0027]
  6. European Regional Development Fund (EFRE)
  7. province of Upper Austria through the programme IWB 2014-2020

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By using methyl orange template, polypyrrole nanotubes were obtained by the oxidative polymerization of pyrrole. The nanotubes were carbonized in inert atmosphere to nitrogen-enriched carbon nanotubes. These were subsequently coated with 20 wt% of polypyrrole prepared in the absence or the presence of anionic dyes (methyl orange or Acid Blue 25). The morphology of all the samples was examined by the electron microscopies, FTIR and Raman spectroscopies. Moreover, X-ray photoelectron spectroscopy and elemental analysis were used to prove the chemical structure and the successful coating process. Electron paramagnetic resonance analysis was used to calculate the spin concentrations. Significant impact of coating method is evidenced with neat polypyrrole coating providing a two-fold capacitance increase compared to uncoated nanotubes, while coating in the presence of Acid Blue 25 decreasing it slightly. With respect to oxygen reduction reaction, coatings irreversibly transformed in the first few cycles in the presence of the products of O-2 reduction, presumably hydrogen peroxide, altering the oxygen reduction mechanism. This transformation allows the tailoring of the polymeric shell, over ORR active carbonaceous core, and tuning of the catalyst selectivity and optimization of materials performance for a given application - from alkaline fuel cells to hydrogen peroxide generation. (C) 2019 Elsevier Inc. All rights reserved.

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