journal article·2022-08-31

Cross-Linked Anion-Exchange Membranes with Dipole-Containing Cross-Linkers Based on Poly(terphenyl isatin piperidinium) Copolymers

Lin Tian, Junmin Li, Qiao Liu, Wenli Ma, Fanghui Wang, Hong Zhu, Zhongming Wang

ACS Applied Materials & Interfaces· Volume 14· Issue 34
Publisher page

Abstract

To balance the ionic conductivity and dimensional stability of anion-exchange membranes (AEMs), several cross-linked ether-free poly(terphenyl isatin piperidinium) copolymers were synthesized using 1,2-bis(2-aminoethoxy)ethane as a cross-linker. By introducing an alkyl diamine-based hydrophobic cross-linker as a control, the effects of the dipolar-molecule-containing cross-linker on the comprehensive performance of the membranes were investigated. Cation–dipole interactions between the cations and the hydrophilic ethylene oxide cross-linker enhance the self-assembly capability of the cationic groups. The introduction of the rotatable ethylene oxide cross-linker facilitates the flexibility of the cross-linked networks, thereby promoting hydrophilic/hydrophobic phase separation and inhibiting excessive swelling of the corresponding AEMs simultaneously. The resulting PTPBHIN-O19 membrane showed a high hydroxide conductivity (151.69 mS cm–1) and low swelling ratio (10.53%) at 80 °C. Furthermore, owing to the cross-linked structure and ether-free polymer backbone with high alkali resistance, the membranes treated in 3 M NaOH at 80 °C for 1600 h maintained ≥85% of their hydroxide conductivity, indicating excellent alkaline stability. A H2/O2 fuel cell based on the PTPBHIN-O19 AEM exhibited a maximum power density of 398 mW cm–2 at 515 mA cm–2.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Fuel Cells and Related Materials · Membrane-based Ion Separation Techniques · Electrocatalysts for Energy Conversion

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Chemical Resource Engineering, Institute of Modern Catalysis, Department of Organic Chemistry, College of Chemistry, Beijing University of Chemical Technology, Beijing 100029, P. R. China

Funding

Ministry of Science and Technology of the People's Republic of China · Central University Basic Research Fund of China · Beijing University of Chemical Technology · National Natural Science Foundation of China

References (57)

Show source-provided references
1. 10.1016/j.jpowsour.2017.08.01010.1016/j.jpowsour.2017.08.010 ↗
2. 10.1039/c3cs60053j10.1039/c3cs60053j ↗
3. 10.1016/j.jpowsour.2017.07.06810.1016/j.jpowsour.2017.07.068 ↗
4. 10.3390/membranes1106043610.3390/membranes11060436 ↗
5. 10.1016/j.memsci.2021.11996610.1016/j.memsci.2021.119966 ↗
6. 10.1016/j.ijhydene.2021.09.01410.1016/j.ijhydene.2021.09.014 ↗
7. 10.1016/j.jpowsour.2021.22954410.1016/j.jpowsour.2021.229544 ↗
8. 10.1016/j.memsci.2021.11956910.1016/j.memsci.2021.119569 ↗
9. 10.1016/j.polymer.2020.12308510.1016/j.polymer.2020.123085 ↗
10. 10.1016/j.memsci.2020.11877410.1016/j.memsci.2020.118774 ↗
11. 10.1016/j.memsci.2019.11770010.1016/j.memsci.2019.117700 ↗
12. 10.1002/admt.20200122010.1002/admt.202001220 ↗
13. 10.1016/j.jpowsour.2017.07.07410.1016/j.jpowsour.2017.07.074 ↗
14. 10.1021/acsmacrolett.5b0037510.1021/acsmacrolett.5b00375 ↗
15. 10.1021/ma901538c10.1021/ma901538c ↗
16. 10.1021/acs.macromol.7b0040110.1021/acs.macromol.7b00401 ↗
17. 10.1016/j.memsci.2021.11933510.1016/j.memsci.2021.119335 ↗
18. 10.1016/j.jcis.2021.10.12210.1016/j.jcis.2021.10.122 ↗
19. 10.1016/j.memsci.2021.11998610.1016/j.memsci.2021.119986 ↗
20. 10.1016/j.polymertesting.2021.10709210.1016/j.polymertesting.2021.107092 ↗
21. 10.1016/j.memsci.2019.11721610.1016/j.memsci.2019.117216 ↗
22. 10.1016/j.memsci.2019.11732010.1016/j.memsci.2019.117320 ↗
23. 10.1016/j.memsci.2019.11752110.1016/j.memsci.2019.117521 ↗
24. 10.1021/ja307466s10.1021/ja307466s ↗
25. 10.1016/j.memsci.2021.12000810.1016/j.memsci.2021.120008 ↗
26. 10.1039/D0TA11011F10.1039/D0TA11011F ↗
27. 10.1021/ja211365r10.1021/ja211365r ↗
28. 10.1016/j.memsci.2017.05.06310.1016/j.memsci.2017.05.063 ↗
29. 10.1016/j.ijhydene.2021.11.20910.1016/j.ijhydene.2021.11.209 ↗
30. 10.1016/j.memsci.2021.11916710.1016/j.memsci.2021.119167 ↗
31. 10.1021/acsaem.1c0315310.1021/acsaem.1c03153 ↗
32. 10.1021/acs.chemmater.7b0149410.1021/acs.chemmater.7b01494 ↗
33. 10.1021/acs.macromol.5b0267110.1021/acs.macromol.5b02671 ↗
34. 10.1021/ja403671u10.1021/ja403671u ↗
35. 10.1039/C5TA01123J10.1039/C5TA01123J ↗
36. 10.1038/nature1299310.1038/nature12993 ↗
37. 10.1002/adma.20140557910.1002/adma.201405579 ↗
38. 10.1002/aic.1713310.1002/aic.17133 ↗
39. 10.1016/j.memsci.2021.11940410.1016/j.memsci.2021.119404 ↗
40. 10.1016/j.memsci.2010.01.00310.1016/j.memsci.2010.01.003 ↗
41. 10.1016/j.memsci.2022.12030310.1016/j.memsci.2022.120303 ↗
42. 10.1021/acs.macromol.8b0028410.1021/acs.macromol.8b00284 ↗
43. 10.1039/C7TA03967K10.1039/C7TA03967K ↗
44. 10.1039/C8TA04699A10.1039/C8TA04699A ↗
45. 10.1039/C9SE00106A10.1039/C9SE00106A ↗
46. 10.1039/C8TA11291F10.1039/C8TA11291F ↗
47. 10.1016/j.memsci.2019.11730710.1016/j.memsci.2019.117307 ↗
48. 10.1002/adfm.20170275810.1002/adfm.201702758 ↗
49. 10.1016/j.memsci.2019.01.03610.1016/j.memsci.2019.01.036 ↗
50. 10.1021/acs.chemmater.7b0095810.1021/acs.chemmater.7b00958 ↗
51. 10.1016/j.colcom.2022.10058410.1016/j.colcom.2022.100584 ↗
52. 10.1021/acsapm.1c0192610.1021/acsapm.1c01926 ↗
53. 10.1016/j.memsci.2019.05.04410.1016/j.memsci.2019.05.044 ↗
54. 10.1016/j.coelec.2018.03.01910.1016/j.coelec.2018.03.019 ↗
55. 10.1021/acsaem.1c0103710.1021/acsaem.1c01037 ↗
56. 10.1021/acsaem.1c0094210.1021/acsaem.1c00942 ↗
57. 10.1039/D0EE01133A10.1039/D0EE01133A ↗