Anion Exchange Membranes Based on Polystyrene-Block-Poly(ethylene-ran-butylene)-Block-Polystyrene Triblock Copolymers: Cation Stability and Fuel Cell Performance
Source abstract
Abstract
A series of polystyrene- block -poly(ethylene- ran -butylene)- block -polystyrene (SEBS)-based anion exchange membranes (AEMs) were synthesized via chloromethylation of SEBS followed by quaternization with trimethylamine (TMA). SEBS-based AEMs functionalized with TMA + cations exhibited a hydroxide ion conductivity of 136 mS/cm at 70°C. This membrane exhibited a phase-separated morphology with wide and interconnected ionic channels as observed by atomic force microscopy. Poly (phenylene oxide) (PPO)-based AEMs with quaternary benzyl-trimethylammonium (TMA + ) and quaternary benzyl-tris(2,4,6-trimethoxyphenyl) phosphonium (TTMPP + ) and PPO-based AEMs with hexyl pendant chains were also synthesized and evaluated as binders in AMFC electrodes. PPO-based AEMs functionalized with TTMPP + demonstrated the best ex situ alkaline stability, losing only 9% of their ion-exchange-capacity after 30 days in 1M KOH (at 60°C). The best in situ stability was achieved by SEBS-based MEAs (as membrane and as binder in the electrodes); The peak power density dropped approx. 35% after holding the cell at a constant voltage of 0.55V for 12 hours. Fuel cell performance with SEBS-based AEMs resulted in peak power densities of 300 mW/cm 2 at 70°C. The optimum performance was obtained with MEAs made with SEBS-based AEMs and PPO-based ionomers containing a hexyl pendant chain.
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.
References (76)
Show source-provided references
1. 10.1016/j.elecom.2012.03.03710.1016/j.elecom.2012.03.037 ↗
2. 10.1039/C4EE01303D10.1039/C4EE01303D ↗
3. 10.1149/2.0551608jes10.1149/2.0551608jes ↗
4. 10.1149/1.348468210.1149/1.3484682 ↗
5. 10.1149/05002.2183ecst10.1149/05002.2183ecst ↗
6. 10.1039/C4RA13101K10.1039/C4RA13101K ↗
7. 10.1002/cplu.20140209610.1002/cplu.201402096 ↗
8. 10.1021/ma802613k10.1021/ma802613k ↗
9. 10.1021/ja307466s10.1021/ja307466s ↗
10. 10.1149/2.1301704jes10.1149/2.1301704jes ↗
11. 10.1039/C4EE00165F10.1039/C4EE00165F ↗
12. 10.1039/c1jm10320b10.1039/c1jm10320b ↗
13. 10.1039/c3ta11459g10.1039/c3ta11459g ↗
14. 10.1149/2.0601410jes10.1149/2.0601410jes ↗
15. 10.1021/ma401568f10.1021/ma401568f ↗
16. 10.1039/c3ra46630b10.1039/c3ra46630b ↗
17. 10.1039/c1ee01913a10.1039/c1ee01913a ↗
18. 10.1016/j.memsci.2014.02.02710.1016/j.memsci.2014.02.027 ↗
19. 10.1002/polb.2317010.1002/polb.23170 ↗
20. 10.1149/2.049311jes10.1149/2.049311jes ↗
21. 10.1021/ja302439z10.1021/ja302439z ↗
22. 10.1016/j.jpowsour.2009.11.11810.1016/j.jpowsour.2009.11.118 ↗
23. 10.1021/ma200836d10.1021/ma200836d ↗
24. 10.1149/2.0361507jes10.1149/2.0361507jes ↗
25. 10.1039/C4CP05755D10.1039/C4CP05755D ↗
26. 10.1039/C4TA00558A10.1039/C4TA00558A ↗
27. 10.1021/ma500125t10.1021/ma500125t ↗
28. 10.1016/j.ijhydene.2014.04.09910.1016/j.ijhydene.2014.04.099 ↗
29. 10.1016/j.memsci.2015.04.04610.1016/j.memsci.2015.04.046 ↗
30. 10.1016/j.electacta.2014.06.05810.1016/j.electacta.2014.06.058 ↗
31. 10.1039/c2ta01178f10.1039/c2ta01178f ↗
32. 10.1149/2.056309jes10.1149/2.056309jes ↗
33. 10.1021/ma902430y10.1021/ma902430y ↗
34. 10.1021/ja403671u10.1021/ja403671u ↗
35. 10.1002/polb.2339510.1002/polb.23395 ↗
36. 10.1021/am401858r10.1021/am401858r ↗
37. 10.1149/2.044405jes10.1149/2.044405jes ↗
38. 10.1016/j.ijhydene.2014.03.05310.1016/j.ijhydene.2014.03.053 ↗
39. 10.1016/j.memsci.2015.04.05210.1016/j.memsci.2015.04.052 ↗
40. 10.1039/C4RA07616H10.1039/C4RA07616H ↗
41. 10.1021/ma201864u10.1021/ma201864u ↗
42. 10.1021/jp711557710.1021/jp7115577 ↗
43. 10.1007/s10973-007-8930-x10.1007/s10973-007-8930-x ↗
44. 10.1021/cm400468u10.1021/cm400468u ↗
45. 10.1021/ma402334t10.1021/ma402334t ↗
46. 10.1016/j.memsci.2013.04.05910.1016/j.memsci.2013.04.059 ↗
47. 10.1016/j.jpowsour.2015.08.00210.1016/j.jpowsour.2015.08.002 ↗
48. 10.1016/j.memsci.2013.10.05410.1016/j.memsci.2013.10.054 ↗
49. 10.1149/1.363570910.1149/1.3635709 ↗
50. 10.1021/ja211365r10.1021/ja211365r ↗
51. 10.1038/srep1166810.1038/srep11668 ↗
52. 10.1002/anie.20080629910.1002/anie.200806299 ↗
53. 10.1002/polb.2314910.1002/polb.23149 ↗
54. 10.1149/2.0891510jes10.1149/2.0891510jes ↗
55. 10.1021/ma101247c10.1021/ma101247c ↗
56. 10.1016/j.jpowsour.2011.11.02310.1016/j.jpowsour.2011.11.023 ↗
57. 10.1021/acs.chemmater.5b0445210.1021/acs.chemmater.5b04452 ↗
58. 10.1039/C6TA10838E10.1039/C6TA10838E ↗
59. 10.1021/acs.macromol.5b0138210.1021/acs.macromol.5b01382 ↗
60. 10.1016/j.jpowsour.2010.12.03210.1016/j.jpowsour.2010.12.032 ↗
61. 10.1021/ma021107510.1021/ma0211075 ↗
62. 10.1039/c3ta10308k10.1039/c3ta10308k ↗
63. 10.1039/c2jm14898f10.1039/c2jm14898f ↗
64. 10.1039/c2ra21402d10.1039/c2ra21402d ↗
65. 10.1080/1060132970801003610.1080/10601329708010036 ↗
66. Badertscher M. Bühlmann P. Pretsch E. , Structure Determination of Organic Compounds, Springer Berlin (2009).
67. 10.1039/C3EE43275K10.1039/C3EE43275K ↗
68. 10.1002/cssc.20140266410.1002/cssc.201402664 ↗
69. 10.1039/C6EE01958G10.1039/C6EE01958G ↗
70. 10.1021/acsami.6b0771110.1021/acsami.6b07711 ↗
71. 10.1039/C4PY01588F10.1039/C4PY01588F ↗
72. 10.1039/C6TA06653D10.1039/C6TA06653D ↗
73. 10.1039/C4EE02564D10.1039/C4EE02564D ↗
74. 10.1039/C5TA09438K10.1039/C5TA09438K ↗
75. 10.1149/2.0131506jes10.1149/2.0131506jes ↗
76. 10.1073/pnas.131966311110.1073/pnas.1319663111 ↗