Title Side-chain-type imidazolium-functionalized anion exchange membranes: The effects of additional hydrophobic side chains and their hydrophobicity
Authors Wei, Haibing
Li, Yan
Wang, Sheng
Tao, Guoqing
Wang, Tie
Cheng, Sheng
Yang, Shanzhong
Ding, Yunsheng
Affiliation Hefei Univ Technol, Sch Chem & Chem Engn, Anhui Key Lab Adv Funct Mat & Devices, Anhui Key Lab Adv Catalyt Mat & React Engn, Hefei 230009, Anhui, Peoples R China
Peking Univ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci, Key Lab Polymer Chem & Phys,Minist Educ, Beijing 100871, Peoples R China
Keywords Anion exchange membrane
Phase separation
Perfluorinated side chain
Issue Date 2019
Publisher JOURNAL OF MEMBRANE SCIENCE
Abstract Ionic-conducive polymers with highly ordered, phase-separated structure are the promising materials used as anion exchange membranes (AEMs), thanks to their pronounced ion mobility. In this study, apart from imidazolium-functionalized hydrophilic pendants, additional octyl and perfluorooctyl-containing grafts were tethered to the polymer backbone and the resultant structure-morphology relationships were systemically investigated. The results revealed that the introduction of hydrophobic side chains as well as the corresponding hydrophobicity plays an important role in the formation of a phase-separated morphology in the membrane. AEMs containing perfluorooctyl-containing pendants (PPO-x-Im(y)8F(z)) exhibited a pronounced microphase-separated morphology with ion clusters of about 2-5 nm size and a spacing of similar to 6 nm, while the membranes with octyl pendants (PPO-x-Im(y)8C(z)) or no additional hydrophobic side chains (PPO-x-Im) only showed indistinct or no phase separation. In addition, PPO-x-Im(y)8F(z) AEMs showed better ion conductivity and suppressed water absorption, thereby exhibiting a good balance between water uptake and ion conductivity. The results of this study provide an efficient strategy to guide the architectural design of high-performance AEMs.
URI http://hdl.handle.net/20.500.11897/548079
ISSN 0376-7388
DOI 10.1016/j.memsci.2019.02.058
Indexed SCI(E)
EI
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