Jin Li, Guoliang Liu, Fangfang Zhang, Jun Liao, Haolin Tang, Haining Zhang
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引用次数: 0
摘要
掺杂磷酸的聚苯并咪唑膜中巧妙的交联网络结构可以缓解质子传导性和机械性能之间的相互限制。然而,定制大分子交联剂的复杂合成和耗时的后处理阻碍了其作为高温质子交换膜的实际应用。本文采用一步交联策略,使用含有亲酸性季铵基团的小分子交联剂合成了交联聚苯并咪唑膜。在掺入磷酸后,季铵-二磷酸离子对配位和交联结构使形成的膜与无交联结构的样品相比,在无水质子传导性、氧化稳定性和机械强度方面都得到了改善。具有优化交联度的膜在 160 °C 时的无水电导率为 72.27 mS cm-1,抗拉强度为 12.14 MPa。得益于交联结构和高质子传导性,相应形成的膜电极组件具有 1.01 V 的高开路电压和改进的欧姆极化,使用氢气作为燃料和空气作为氧化剂可提供 0.66 W cm-2 的峰值功率密度。
Improving the Ohmic polarization of high temperature proton exchange membrane fuel cells using crosslinked polybenzimidazole membranes containing acidophilic quaternary ammonium groups synthesized by one-step strategy
Ingenious crosslinked network structure in phosphoric acid doped polybenzimidazole membranes can mitigate the mutual restriction of proton conductivity and mechanical properties. However, the complicated synthesis of tailored macromolecular crosslinker and the time-consuming post-treatment hinder their practical application as high temperature proton exchange membranes. Herein, crosslinked polybenzimidazole membranes are synthesized using small molecular crosslinker containing acidophilic quaternary ammonium groups through a one-step crosslinking strategy. After doping with phosphoric acid, the quaternary ammonium-biphosphate ion-pair coordination and the crosslinked structure result in the improved anhydrous proton conductivity, oxidation stability, and mechanical strength of the formed membranes compared to sample without crosslinking structure. Membrane with the optimized degree of crosslinking exhibits an anhydrous conductivity of 72.27 mS cm-1 at 160 °C with a tensile strength of 12.14 MPa. Benefiting from the crosslinked structure and high proton conductivity, the accordingly formed membrane electrode assembly possesses a high open circuit voltage of 1.01 V and the improved Ohmic polarization, delivering a peak power density of 0.66 W cm-2 using hydrogen as fuel and air as oxidant.
期刊介绍:
Materials Today Energy is a multi-disciplinary, rapid-publication journal focused on all aspects of materials for energy.
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