4.7 Article

Polyaniline-metal organic framework nanocomposite as an efficient electrocatalyst for hydrogen evolution reaction

Journal

COMPOSITES PART B-ENGINEERING
Volume 137, Issue -, Pages 129-139

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.compositesb.2017.11.016

Keywords

Polyaniline; Metal organic frameworks; Polymer-matrix composites (PMCs); Hydrogen evolution reaction

Funding

  1. National Research Foundation (NRF) [99166, 99278]
  2. University of Limpopo, South Africa [R202, R232]

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Polyaniline-metal organic framework (PANI/MOF) composite was prepared by chemical oxidation of aniline monomer in the presence of 3.6 wt% MOF content for hydrogen evolution reaction (HER). The structure, morphology and properties of the fabricated composite were investigated. There was a clear interaction of MOF on the backbone of the PANI matrix through electrostatic interaction as investigated by both Raman and Fourier transform infrared analyses. The MOF exhibited irregular crystals with further wrapping of MOF by PANI matrix as evidenced by both scanning electron microscopy and transmission electron microscopy studies. The PANI composite showed some nanorods and microporous structure. The energy band gap values of PANI and its composite were found to be 1.50 and 1.35 eV, respectively. The thermal stability of the neat PANI increased upon composite formation, which was due to a stabilizing effect of MOF and a change in morphology of the composite. The catalytic effect of MOF, PANI and PANI/MOF composite on HER was studied using exchange current density (to) and charge transfer coefficient determined by the Tafel slope method. A drastic increase in catalytic H-2 evolution was observed in the composite. In addition, the Tafel slope values of PANI and the composite decreased with increasing the concentration of the acid, suggesting the Volmer reaction coupled with either Heyrovsky or Tafel reaction. The i(o) increased with increasing the acid concentration and in an order of PANI/MOF > MOF > PANI at various concentrations.

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