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Journal of Chemistry
Volume 2014, Article ID 963131, 11 pages
Research Article

An Investigation of Proton Conductivity of Vinyltriazole-Grafted PVDF Proton Exchange Membranes Prepared via Photoinduced Grafting

1Department of Chemistry, Faculty of Arts and Science, Fatih University, Büyükçekmece, 34500 Istanbul, Turkey
2Department of Chemical Engineering, Faculty of Chemical and Metallurgical Engineering, Yildiz Technical University, Davutpaşa Campus, Esenler, 34220 Istanbul, Turkey

Received 12 April 2014; Accepted 5 June 2014; Published 2 July 2014

Academic Editor: Barbara Gawdzik

Copyright © 2014 Sinan Sezgin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Proton exchange membrane fuel cells (PEMFCs) are considered to be a promising technology for clean and efficient power generation in the twenty-first century. In this study, high performance of poly(vinylidene fluoride) (PVDF) and proton conductivity of poly(1-vinyl-1,2,4-triazole) (PVTri) were combined in a graft copolymer, PVDF-g-PVTri, by the polymerization of 1-vinyl-1,2,4-triazole on a PVDF based matrix under UV light in one step. The polymers were doped with triflic acid (TA) at different stoichiometric ratios with respect to triazole units and the anhydrous polymer electrolyte membranes were prepared. All samples were characterized by FTIR and 1H-NMR spectroscopies. Their thermal properties were examined by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). TGA demonstrated that the PVDF-g-PVTri and PVDF-g-PVTri-(TA)x membranes were thermally stable up to 390°C and 330°C, respectively. NMR and energy dispersive X-ray spectroscopy (EDS) results demonstrated that PVDF-g-PVTri was successfully synthesized with a degree of grafting of 21%. PVDF-g-PVTri-(TA)3 showed a maximum proton conductivity of  Scm−1 at 150°C and anhydrous conditions. CV study illustrated that electrochemical stability domain for PVDF-g-PVTri-(TA)3 extended over 4.0 V.