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Copolymer electrolytes based on 5‐(methacrylamido)tetrazole (MTet) and vinyl phosphonic acid (VPA) are prepared. The obtained copolymers are analyzed by FTIR, 1H NMR, 13C NMR, and 31P NMR spectroscopy, thermogravimetric analysis (TGA), differantial scanning calorimetry (DSC), energy dispersive X‐ray spectrometry (EDS), elemental analysis (EA), cyclic voltammetry (CV), and impedance spectroscopy. The morphology of the copolymers is characterized by X‐ray diffraction (XRD), atomic force microscopy (AFM) and scanning electron microscopy (SEM). The highest proton conductivity is obtained as 0.01 S/cm at 150 °C and in anhydrous conditions.

Heterocyclic molecules are generally used in the proton conducting membranes as dopant or polymer side group due to their high proton transfer ability. Composite proton conducting membranes based on poly(vinylphosphonic acid) (PVPA) and poly(5-(methacrylamido)tetrazole) (PMTet) were produced. The homopolymers, prepared from their corresponding monomers, were blended at several mol ratios to obtain the polymer electrolyte membranes. All samples were characterized by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA), differantial scanning calorimetry (DSC), cyclic voltammetry (CV), and impedance analysis. Besides, the morphology of the membranes was studied by X-ray diffraction (XRD), atomic force microscopy (AFM) and scanning electron microscopy (SEM). FTIR spectra confirmed the formation of hydrogen bonding network between PVPA and PMTet units. TGA showed that the polymer electrolyte membranes were thermally stable up to 210 C. CV curves demonstrated the oxidative stability of the samples in 3 V region. In anhydrous conditions, the maximum proton conductivity was determined as 0.06 Scm 21 at 150 C for PMTetP(VPA) 4 . POLYM. ENG. SCI.,