Multication Cross-Linked Poly(p-terphenyl isatin) Anion Exchange Membranes for Fuel Cells: Effect of Cross-Linker Length on Membrane Performance
Source abstract
Abstract
As a key component of anion exchange membrane fuel cells (AEMFCs), anion exchange membranes (AEMs) have been investigated in the last decades. Herein, a series of multication cross-linkers were introduced into side-chain-type poly(p-terphenyl isatin) to develop high-performance and long-term stable AEMs. Additionally, the effects of the hydrophilic cross-linker length on the membrane performance were systematically investigated. The resulting cross-linked membranes possess a low swelling ratio (<18% at 80 °C) and high tensile strength (51.1–58.3 MPa). Notably, the cross-linker length influences the AEM internal morphology. With hexyl as the spacer between backbones and cation groups in the cross-linker, 0.9q-PTI-6C exhibits the highest hydroxide ion conductivity of 118.5 mS/cm at 80 °C, which is ascribed to well-developed ion channels. Furthermore, alkyl spacer chains and cross-linked networks contribute to the excellent alkali stability of membranes. After immersion in 2 M NaOH for 1200 h at 80 °C, 0.9q-PTI-8C only shows 11 and 12.7% losses in ion conductivity and ion exchange capacity (IEC), respectively. The fuel cell fabricated using 0.9q-PTI-6C can achieve the maximum power density of 310 mW/cm2 at 80 °C.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Fuel Cells and Related Materials · Membrane-based Ion Separation Techniques · Advanced battery technologies research
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
National Natural Science Foundation of China · National Key Research and Development Program of China
References (54)
Show source-provided references
1. 10.1016/j.progpolymsci.2019.10117710.1016/j.progpolymsci.2019.101177 ↗
2. 10.1016/j.progpolymsci.2020.10134510.1016/j.progpolymsci.2020.101345 ↗
3. 10.1016/j.memsci.2011.04.04310.1016/j.memsci.2011.04.043 ↗
4. 10.1149/1.149123710.1149/1.1491237 ↗
5. 10.1016/j.jiec.2018.10.02610.1016/j.jiec.2018.10.026 ↗
6. 10.1016/j.jpowsour.2017.07.11710.1016/j.jpowsour.2017.07.117 ↗
7. 10.1016/j.jpowsour.2017.08.01010.1016/j.jpowsour.2017.08.010 ↗
8. 10.1039/C7EE02468A10.1039/C7EE02468A ↗
9. 10.1016/j.memsci.2021.11908810.1016/j.memsci.2021.119088 ↗
10. 10.1039/C8TA05785K10.1039/C8TA05785K ↗
11. 10.1039/C6EE03079C10.1039/C6EE03079C ↗
12. 10.1021/acs.macromol.6b0040810.1021/acs.macromol.6b00408 ↗
13. 10.1021/acs.macromol.5b0255010.1021/acs.macromol.5b02550 ↗
14. 10.1016/j.memsci.2019.11765010.1016/j.memsci.2019.117650 ↗
15. 10.1021/acs.accounts.9b0035510.1021/acs.accounts.9b00355 ↗
16. 10.1021/acsenergylett.9b0090810.1021/acsenergylett.9b00908 ↗
17. 10.1021/acsmacrolett.5b0014510.1021/acsmacrolett.5b00145 ↗
18. 10.1039/D0PY01291B10.1039/D0PY01291B ↗
19. 10.1016/j.memsci.2021.11933510.1016/j.memsci.2021.119335 ↗
20. 10.1021/acs.iecr.9b0265610.1021/acs.iecr.9b02656 ↗
21. 10.1002/adfm.20170275810.1002/adfm.201702758 ↗
22. 10.1021/jo990454i10.1021/jo990454i ↗
23. 10.1038/s41560-019-0372-810.1038/s41560-019-0372-8 ↗
24. 10.1039/C8TA11291F10.1039/C8TA11291F ↗
25. 10.1016/j.jpowsour.2017.08.01010.1016/j.jpowsour.2017.08.010 ↗
26. 10.1016/j.ijhydene.2021.02.20310.1016/j.ijhydene.2021.02.203 ↗
27. 10.1039/C9RA07775H10.1039/C9RA07775H ↗
28. 10.1021/acs.jpcb.8b0862210.1021/acs.jpcb.8b08622 ↗
29. 10.1021/acs.chemrev.6b0058610.1021/acs.chemrev.6b00586 ↗
30. 10.1016/j.memsci.2021.11933510.1016/j.memsci.2021.119335 ↗
31. 10.1016/j.memsci.2020.11782910.1016/j.memsci.2020.117829 ↗
32. 10.1016/j.jpowsour.2020.22942910.1016/j.jpowsour.2020.229429 ↗
33. 10.3389/fmats.2020.0000410.3389/fmats.2020.00004 ↗
34. 10.1016/j.memsci.2019.04.06610.1016/j.memsci.2019.04.066 ↗
35. 10.1002/cssc.20140302210.1002/cssc.201403022 ↗
36. 10.1021/jacs.8b0397910.1021/jacs.8b03979 ↗
37. 10.1021/acs.macromol.8b0235510.1021/acs.macromol.8b02355 ↗
38. 10.1016/j.jpowsour.2018.04.06410.1016/j.jpowsour.2018.04.064 ↗
39. 10.1016/j.memsci.2021.11916710.1016/j.memsci.2021.119167 ↗
40. 10.1039/C5TA06209H10.1039/C5TA06209H ↗
41. 10.1016/j.jpowsour.2019.22685610.1016/j.jpowsour.2019.226856 ↗
42. 10.1021/acs.macromol.6b0114010.1021/acs.macromol.6b01140 ↗
43. 10.1016/j.memsci.2018.12.04910.1016/j.memsci.2018.12.049 ↗
44. 10.1016/j.memsci.2020.11877410.1016/j.memsci.2020.118774 ↗
45. 10.1016/j.memsci.2019.05.04410.1016/j.memsci.2019.05.044 ↗
46. 10.1016/j.memsci.2019.11752110.1016/j.memsci.2019.117521 ↗
47. 10.1016/j.ijhydene.2021.02.20910.1016/j.ijhydene.2021.02.209 ↗
48. 10.1039/C9TA09213G10.1039/C9TA09213G ↗
49. 10.1021/acs.macromol.6b0138110.1021/acs.macromol.6b01381 ↗
50. 10.1016/j.radphyschem.2018.06.03310.1016/j.radphyschem.2018.06.033 ↗
51. 10.1016/j.jpowsour.2017.07.10610.1016/j.jpowsour.2017.07.106 ↗
52. 10.1016/j.ijhydene.2015.04.04010.1016/j.ijhydene.2015.04.040 ↗
53. 10.1039/C8TA05428B10.1039/C8TA05428B ↗
54. 10.1002/aenm.20200198610.1002/aenm.202001986 ↗