纳米复合材料
膜
聚合物
高分子化学
材料科学
共聚物
化学工程
电解质
电导率
侧链
乙醚
极限抗拉强度
化学
复合材料
电极
纳米技术
有机化学
物理化学
生物化学
工程类
作者
Gang Wang,Jialin Li,Haibin Li,Hu He,Liang Zhai,Xiang Li,Tingting Li,Chengji Zhao,Lixin Wu,Haolong Li
标识
DOI:10.1016/j.cclet.2022.05.011
摘要
The most practical high-temperature proton exchange membranes (PEMs) are phosphoric acid (PA)-doped polymer electrolytes. However, due to the plasticizing effect of PA, it is a challenge to address the trade-off between the proton conductivity and the mechanical performance of these materials. Here, we report an effective strategy to fabricate robust high-temperature PEMs based on the in situ electrostatic crosslinking of polyoxometalates and polymers. A comb copolymer poly(ether-ether-ketone)-grafted-poly(2-ethyl-2-oxazoline) (PGE) with transformable side chains was synthesized and complexed with H3PW12O40 (PW) by electrostatic self-assembly, forming PGE/PW nanocomposite membranes with bicontinuous nanostructures. After a subsequent PA-treatment of these membranes, high-temperature PEMs of PGE/PW/PA ternary nanocomposites were obtained, in which the in situ electrostatic crosslinking effect between PW and PGE side chains was generated in the hydrophilic domains of the bicontinuous structures. The microphase separation structure and the electrostatic crosslinking feature endow the PGE/PW/PA membranes with excellent anhydrous proton conductive ability while retaining high mechanical performance. The membranes show a high proton conductivity of 42.5 mS/cm at 150 °C and a high tensile strength of 13 MPa. Our strategy can pave a new route based on electrostatic control to design nanostructured polymer electrolytes.
科研通智能强力驱动
Strongly Powered by AbleSci AI