材料科学
复合数
电导率
燃料电池
耐久性
磷酸
质子交换膜燃料电池
微型多孔材料
膜
氢
复合材料
化学工程
化学稳定性
膜电极组件
质子输运
质子
氢键
作者
Shijie Ge,Ying Yang,Tao Zhang,Hanyu Wu,Shizhe Wang
标识
DOI:10.1007/s42114-025-01598-2
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI