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The leaching of phosphoric acid (PA) from PA-doped polybenzimidazole (PBI) membrane caused by the weak interaction is the origin of its proton conductivity attenuation, which seriously hinders the performance and durability of high-temperature proton exchange membrane fuel cells (HT-PEMFCs). In this study, the Heptazine-COF (Hep-COF) featuring abundant basic C = N units and microporous structure was hybridized with the poly (2,5-benzimidazole) (ABPBI) to fabricate the composite membrane for HT-PEMFC applications. The introduced Hep-COF reinforced acid-base interaction with PA, enhanced the capacity to absorb PA, and simultaneously formed robust and continuous hydrogen bond networks among PA, ABPBI, and Hep-COF, resulting in the enhanced conductivity and PA retention ability of PA-Hep-ABPBI membrane under the HT-PEMFC operation. Furthermore, these hydrogen bond networks additionally contribute to enhanced mechanical properties and chemical stability of the composite membranes. Consequently, the optimized sample 20Hep-ABPBI composite membrane showed a considerable proton conductivity of 105 mS cm− 1 at 180 ℃, enabling a peak power density of 479 mW cm− 2 in single cell test- 2.3 times higher than that of pristine ABPBI membrane. In addition, the PA loss rate (26.95 ng h− 1 cm− 2) and voltage degradation rate (25 mV h− 1) of the single cell with PA-20Hep-ABPBI membrane were also lower than that of pristine ABPBI membrane after the continuous 120 h operation at 180 ℃. This work offered a valuable strategy for designing and developing a kind of high-performance proton exchange membranes.
Ge et al. (Wed,) studied this question.