Hydroxide Ion Conducting Membranes Dually Functionalized with Cationic and Zwitterionic Groups
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide A series of ether-free poly( p -terphenyl piperidinium)s carrying both cationic and zwitterionic groups were prepared and evaluated as anion-exchange membranes (AEMs). First, a zwitterionic monomer (zwPip) was synthesized by sulfoalkylation of N -methyl-4-piperidone (Pip) using 1,4-butane sultone. Pip and zwPip were then employed in superacid-mediated polyhydroxyalkylations with p -terphenyl to prepare precursor copolymers containing 20, 30, and 40 mol % of zwPip units. Next, the Pip units were fully quaternized in a Menshutkin reaction with iodomethane. AEMs cast from these copolymers with ion-exchange capacities between 1.8 and 2.2 m equiv g –1 displayed excellent hydroxide ion conductivities, reaching up to 171 mS cm –1 at 80 °C. At lower temperatures, 20 and 40 °C, the water uptake decreased with increasing zwitterionic content, most probably because of the increased ionic cross-linking through piperidinium–sulfonate complexes. AEMs containing 30 and 40% zwPip units showed only a minor ionic loss (<10%) when stored in 1 M aq NaOH solution at 80 °C over a period of 720 h. The overall results show that the co-introduction of zwitterionic and cationic groups is an efficient strategy to initiate ionic cross-linking and improve the performance of hydroxide-conducting AEMs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Fuel Cells and Related Materials · Advanced battery technologies research · Membrane-based Ion Separation Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Polymer & Materials Chemistry, Department of Chemistry, Lund University, P.O. Box 124, 22100 Lund, Sweden
Funding
Vetenskapsrådet · Energimyndigheten · Stiftelsen för Strategisk Forskning · Kungliga Fysiografiska Sällskapet i Lund
References (51)
Show source-provided references
1. 10.1016/j.rser.2013.09.02510.1016/j.rser.2013.09.025 ↗
2. 10.1039/c8ee01157e10.1039/c8ee01157e ↗
3. 10.1016/j.rser.2014.01.01210.1016/j.rser.2014.01.012 ↗
4. 10.1021/cr500720t10.1021/cr500720t ↗
5. 10.1021/cr100290v10.1021/cr100290v ↗
6. 10.1016/j.rser.2007.01.02310.1016/j.rser.2007.01.023 ↗
7. 10.1039/c5ra05914c10.1039/c5ra05914c ↗
8. 10.1039/c0ee00770f10.1039/c0ee00770f ↗
9. 10.1002/cssc.20110006810.1002/cssc.201100068 ↗
10. 10.1016/j.progpolymsci.2011.01.00310.1016/j.progpolymsci.2011.01.003 ↗
11. 10.1016/j.apenergy.2010.09.03010.1016/j.apenergy.2010.09.030 ↗
12. 10.1016/j.ijhydene.2019.09.09610.1016/j.ijhydene.2019.09.096 ↗
13. 10.1016/j.cherd.2011.10.01510.1016/j.cherd.2011.10.015 ↗
14. 10.1016/j.memsci.2011.04.04310.1016/j.memsci.2011.04.043 ↗
15. 10.1039/d0se01373k10.1039/d0se01373k ↗
16. 10.1039/c5ra04741b10.1039/c5ra04741b ↗
17. 10.1002/aenm.20220093410.1002/aenm.202200934 ↗
18. 10.1039/c8ta05428b10.1039/c8ta05428b ↗
19. 10.1016/j.memsci.2012.08.04510.1016/j.memsci.2012.08.045 ↗
20. 10.1002/adfm.20170275810.1002/adfm.201702758 ↗
21. 10.1021/acs.macromol.0c0020110.1021/acs.macromol.0c00201 ↗
22. 10.1021/acs.chemmater.8b0035810.1021/acs.chemmater.8b00358 ↗
23. 10.1016/j.memsci.2020.11802510.1016/j.memsci.2020.118025 ↗
24. 10.1021/acs.macromol.7b0016810.1021/acs.macromol.7b00168 ↗
25. 10.1021/ma901538c10.1021/ma901538c ↗
26. 10.1021/acs.macromol.8b0020910.1021/acs.macromol.8b00209 ↗
27. 10.1021/acsmacrolett.1c0050610.1021/acsmacrolett.1c00506 ↗
28. 10.1021/ma102267f10.1021/ma102267f ↗
29. 10.1002/ange.20210523110.1002/ange.202105231 ↗
30. 10.1039/c8ta04699a10.1039/c8ta04699a ↗
31. 10.1016/j.memsci.2019.11768010.1016/j.memsci.2019.117680 ↗
32. 10.1016/j.memsci.2022.12113510.1016/j.memsci.2022.121135 ↗
33. 10.1016/j.jmst.2020.08.03210.1016/j.jmst.2020.08.032 ↗
34. 10.1021/acsami.9b1587210.1021/acsami.9b15872 ↗
35. 10.1016/j.electacta.2020.13687910.1016/j.electacta.2020.136879 ↗
36. 10.1021/acsami.8b1861710.1021/acsami.8b18617 ↗
37. 10.1021/acsami.8b1199310.1021/acsami.8b11993 ↗
38. 10.1016/j.memsci.2021.11911810.1016/j.memsci.2021.119118 ↗
39. 10.1016/j.progpolymsci.2019.10117710.1016/j.progpolymsci.2019.101177 ↗
40. 10.1016/j.ijhydene.2021.02.20910.1016/j.ijhydene.2021.02.209 ↗
41. 10.1021/acs.accounts.9b0035510.1021/acs.accounts.9b00355 ↗
42. 10.1016/j.jcis.2022.08.18310.1016/j.jcis.2022.08.183 ↗
43. 10.1016/j.memsci.2021.11933510.1016/j.memsci.2021.119335 ↗
44. 10.1016/j.memsci.2019.11779710.1016/j.memsci.2019.117797 ↗
45. 10.1016/j.memsci.2022.12090310.1016/j.memsci.2022.120903 ↗
46. 10.1016/j.jpowsour.2020.22880510.1016/j.jpowsour.2020.228805 ↗
47. 10.1021/acssuschemeng.1c0197810.1021/acssuschemeng.1c01978 ↗
48. 10.1016/j.memsci.2015.02.01410.1016/j.memsci.2015.02.014 ↗
49. 10.1039/c9ta05531b10.1039/c9ta05531b ↗
50. 10.1016/j.cej.2021.12877610.1016/j.cej.2021.128776 ↗
51. 10.1039/d0ee01842b10.1039/d0ee01842b ↗