Li Wenjing, Li Yishan, Zhang Yanchao, Lu Jiahao, Wu Yuanlong, Song Jiaran, Li Jinsheng, Wang Zhe
School of Chemistry and Life Science, Key Laboratory of Advanced Functional Polymer Membrane Materials of Jilin Province, Changchun University of Technology, Changchun, Jilin 130012, P. R. China.
State Key Laboratory of Electroanalytic Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, P.R. China.
ACS Appl Mater Interfaces. 2024 Aug 28;16(34):45511-45522. doi: 10.1021/acsami.4c09126. Epub 2024 Aug 16.
In this work, a proton-conductive inorganic filler based on polyoxovanadate (NH)[MnVO] (AMV) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide (EMIM TFSI) was synthesized for hybridization with sulfonated poly(aryl ether ketone sulfone) (SPAEKS) to address the "trade-off" between high proton conductivity and mechanical strength. The novel inorganic filler AMV-EMIM TFSI (AI) was uniformly dispersed and stable within the polymer matrix due to the enhanced ionic interaction. AI provided additional proton transport sites, leading to an elevated ion exchange capacity (IEC) and improved proton conductivity, even at low swelling ratios. The optimized SPAEKS-50/AI-5 (50 for degree of sulfonation of SPAEKS and 5 for weight percentage of AI filler) membrane exhibited the highest proton conductivity of 0.188 S·cm at 80 °C with an IEC of 2.38 mmol·g. The enhancement of intermolecular forces improved the mechanical strength from 35 to 55 MPa and improved the elongation at break from 17 to 45%, indicating excellent mechanical properties. The hybrid membrane also demonstrated reinforced methanol resistance due to the hydrogen bonding network and blocking effect, making it suitable for direct methanol fuel cell (DMFC) applications, which exhibited a power density of 15.1 mW·cm at 80 °C. The possibility of further functionalizing these hybrid membranes to tailor their properties for specific applications presents exciting new avenues for research and development. By modification of the type and distribution of fillers or incorporation of additional functional groups, the membranes could be customized to meet the unique demands of various energy storage and conversion systems, enhancing their performance and broadening their application scope. This work provides new insights into the design of polymer electrolyte membranes through inorganic filler hybridization.
在这项工作中,合成了一种基于多氧钒酸盐(NH)[MnVO] (AMV)和1-乙基-3-甲基咪唑双(三氟甲基磺酰)亚胺(EMIM TFSI)的质子传导无机填料,用于与磺化聚(芳基醚酮砜)(SPAEKS)进行杂化,以解决高质子传导率和机械强度之间的“权衡”问题。由于离子相互作用增强,新型无机填料AMV-EMIM TFSI (AI)在聚合物基体中均匀分散且稳定。AI提供了额外的质子传输位点,即使在低溶胀率下也能提高离子交换容量(IEC)并改善质子传导率。优化后的SPAEKS-50/AI-5(SPAEKS的磺化度为50,AI填料的重量百分比为5)膜在80°C时表现出最高的质子传导率0.188 S·cm,IEC为2.38 mmol·g。分子间力的增强将机械强度从35 MPa提高到55 MPa,断裂伸长率从17%提高到45%,表明具有优异的机械性能。由于氢键网络和阻挡效应,杂化膜还表现出增强的耐甲醇性,使其适用于直接甲醇燃料电池(DMFC)应用,在80°C时功率密度为15.1 mW·cm。进一步功能化这些杂化膜以针对特定应用定制其性能的可能性为研究和开发提供了令人兴奋的新途径。通过改变填料的类型和分布或引入额外的官能团,可以定制膜以满足各种能量存储和转换系统的独特需求,提高其性能并拓宽其应用范围。这项工作为通过无机填料杂化设计聚合物电解质膜提供了新的见解。