A step in the direction of the real-life
application of fuel cells
(FCs) has been realized through the fabrication of a promising proton
conductive membrane comprising a perfluorosulfonic-acid ionomer and
nitrogen-rich poly[2,2′-(4,4′-bipyridine)-5,5′-bibenzimidazole]
(BiPyPBI). The BiPyPBI-perfluorosulfonic acid membranes displayed
remarkable oxidative and mechanical stabilities with significant proton
conduction over wide ranges of temperatures (40 to 140 °C) and
humidities (30 to 90% RH). A 0.5 molar BiPyPBI feed ratio increased
the proton conduction of perfluorosulfonic acid by 2.6- and 1.5-fold
at 40 and 80 °C, respectively, due to the enhancement in the
ion-exchange capacity (1.9 mmol/g, which was twofold higher than that
of bare Nafion). The protonic conductivity reached 0.171 S/cm at 140
°C. Using a BiPyPBI feed increased the stability of the Nafion
membrane, corresponding to a 3.5-fold increase in the mechanical stress
(9.6 MPa) and a 2.2-fold decrease in the elongation at break. In addition,
the oxidation stability of the Nafion membrane increased by 26%. The
measured activation energy suggested that the presence of BiPyPBI
created an easier proton transport pathway (by the Grotthuss mechanism)
because of a stronger hydrogen-bonding network than in bare Nafion.
Compared to the power density of a perfluorosulfonic-based MEA, the
power density of the BiPyPBI-perfluorosulfonic-based membrane electrode
assembly (MEA) at 140 °C increased by approximately 20-fold to
175 mW cm–1 at 30% RH and by approximately 5-fold
to 201 mW cm–1 at 90% RH. Impedance spectra confirmed
the improvement of the FC performance of the BiPyPBI-perfluorosulfonic-based
MEA, indicating enhanced charge transfer. After 10,000 cycles of relative
humidity stress testing, the BiPyPBI-perfluorosulfonic-based MEA showed
a power density of 146 mW cm–1 (corresponding to
a 16% loss in the initial power density measured at 30% RH). The MEA
lost only 26% of its initial power density upon relative humidity
stress cycling.