Poly(oxyalkylene)diamine-Functionalized Carbon Nanotube/Perfluorosulfonated Polymer Composites: Synthesis, Water State, and Conductivity
Source abstract
Abstract
A new class of organic−inorganic composite membranes has been constructed, as proton exchange electrolytes, in which the structures of the composites have been designed at the molecular scale to possess fast proton conduction. Polysiloxane-functionalized multiwall carbon nanotubes (CNTs) were synthesized by covalently grafting hydrophilic layers composed of poly(oxyalkylene)diamines and tetraethyl orthosilicate-reinforced polysiloxane in a layer-by-layer manner onto the tube walls. The modified carbon nanotubes were blended with Nafion to form a proton-conducting membrane. Scanning electron microscopy images showed that the functionalized nanotubes had a better dispersion than the unfunctionalized nanotubes on the composite fracture surfaces. The incorporation of the inorganic polysiloxane layer onto the CNT sidewalls forms a resistance, which effectively prohibits electron conduction between the nanotubes. The incorporation of the amino-containing polymer onto the CNTs promotes Nafion coalescence on the CNTs through ionic interactions between amines and sulfonate groups, as evidenced by the shift of the −SO 3 − symmetric stretching peak in the FTIR, the N 1s region in X-ray photoelectron spectroscopy, and the increase of the decomposition temperature of sulfonate groups in thermogravimetric analysis. This approach provides continuous paths suitable for fast proton conduction (σ = 2.8 × 10 −2 S/cm at 30 °C) and also maintains the proton conduction at high temperatures (σ = 6.3 × 10 −2 S/cm at 130 °C).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Fuel Cells and Related Materials · Conducting polymers and applications · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering, National Cheng Kung University, Tainan, Taiwan 70101
References (42)
Show source-provided references
1. Andrews R. · Acc. Chem. Res. · 2002 · 35 · 100810.1021/ar010151m ↗
2. Sun Y.-P. · Acc. Chem. Res. · 2002 · 35 · 109610.1021/ar010160v ↗
3. Ajayan P. M. · Chem. Rev. · 1999 · 99 · 178710.1021/cr970102g ↗
4. Thess A. · Science · 1996 · 273 · 48310.1126/science.273.5274.483 ↗
5. Holzinger M. · Angew. Chem., Int. Ed. · 2001 · 40 · 400210.1002/1521-3773(20011105)40:21<4002::AID-ANIE4002>3.0.CO;2-8 ↗
6. Riggs J. E. · J. Am. Chem. Soc. · 2000 · 122 · 587910.1021/ja9942282 ↗
7. Zhu J. · Nano Lett. · 2003 · 3 · 123910.1021/nl034459d ↗
8. Tasis D. · Chem. Rev. · 2006 · 106 · 110510.1021/cr050569o ↗
9. Moore V. C. · Nano Lett. · 2003 · 3 · 137910.1021/nl034524j ↗
10. Matarredona O. · J. Phys. Chem. B · 2003 · 107 · 1335710.1021/jp0365099 ↗
11. Yurekli K. · J. Am. Chem. Soc. · 2004 · 126 · 990210.1021/ja047451u ↗
12. Bachilo S. M. · Science · 2002 · 298 · 236110.1126/science.1078727 ↗
13. O’Connell M. J. · Science · 2002 · 297 · 59310.1126/science.1072631 ↗
14. Ladewig B. P. · Chem. Mater. · 2007 · 19 · 237210.1021/cm0628698 ↗
15. Rhee C. H. · Chem. Mater. · 2005 · 17 · 169110.1021/cm048058q ↗
16. Truffier-Bountry D. · Macromolecules · 2007 · 40 · 825910.1021/ma0706576 ↗
17. Chen W.-F. · Macromolecules · 2007 · 40 · 198710.1021/ma062512p ↗
18. Jiang S. P. · Adv. Mater. · 2006 · 18 · 106810.1002/adma.200502462 ↗
19. Deng W. Q. · J. Am. Chem. Soc. · 2004 · 126 · 1564410.1021/ja046999y ↗
20. Landi B. J. · Nano Lett. · 2002 · 2 · 132910.1021/nl025800h ↗
21. Wang J. · J. Am. Chem. Soc. · 2003 · 125 · 240810.1021/ja028951v ↗
22. Olek M. · Langmuir · 2005 · 21 · 314610.1021/la0470784 ↗
23. Liu J. · Science · 1998 · 280 · 125310.1126/science.280.5367.1253 ↗
24. Karlsson L. E. · Electrochim. Acta · 2002 · 47 · 326910.1016/S0013-4686(02)00244-X ↗
25. Nakamura K. · Polymer · 1983 · 24 · 87110.1016/0032-3861(83)90206-9 ↗
26. Hull R. V. · Chem. Mater. · 2006 · 18 · 178010.1021/cm0518978 ↗
27. Liang W.-J. · J. Phys. Chem. B · 2005 · 109 · 2431110.1021/jp051026l ↗
28. Kuo P.-L. · J. Polym. Sci., Part A: Polym. Chem. · 2005 · 43 · 335910.1002/pola.20754 ↗
29. Moulder J. F. · 1992
30. Sharma J. · J. Phys. Chem. B · 2004 · 108 · 1328010.1021/jp0482013 ↗
31. Haimov A. · J. Am. Chem. Soc. · 2004 · 126 · 1176210.1021/ja046349u ↗
32. Iwamoto R. · J. Phys. Chem. B · 2002 · 106 · 697310.1021/jp013709g ↗
33. Lowry S. R. · J. Am. Chem. Soc. · 1980 · 102 · 466510.1021/ja00534a017 ↗
34. Lage L. G. · Eur. Polym. J. · 2004 · 40 · 130910.1016/j.eurpolymj.2004.02.021 ↗
35. Park H. S. · Macromolecules · 2005 · 38 · 228910.1021/ma047650y ↗
36. Tannenbaum R. · J. Polym. Sci., Part B: Polym. Phys. · 2003 · 41 · 181410.1002/polb.10557 ↗
37. Bae B. · J. Phys. Chem. B · 2006 · 110 · 424010.1021/jp055159i ↗
38. Wróbel A. M. · Chem. Mater. · 2003 · 15 · 174910.1021/cm021250c ↗
39. Miyatake K. · Macromolecules · 2001 · 34 · 206510.1021/ma0019959 ↗
40. Almeida S. H. · J. Therm. Anal. Calorim. · 1999 · 58 · 56910.1023/A:1010196226309 ↗
41. Park H. S. · J. Membr. Sci. · 2006 · 272 · 2810.1016/j.memsci.2005.07.019 ↗
42. Moore El B. R. · Macromolecules · 1989 · 22 · 3549