journal article·2011-03-23

Water-Processable Polyaniline with Covalently Bonded Single-Walled Carbon Nanotubes: Enhanced Electrochromic Properties and Impedance Analysis

Shanxin Xiong, Jia Wei, Pengtao Jia, Liping Yang, Jan Ma, Xuehong Lu

Publisher page

Abstract

Hybrid electrochromic materials were readily synthesized via copolymerization of aniline with p-phenylenediamine-functionalized single-walled carbon nanotubes (SWCNTs) in the presence of poly(styrene sulfonate) (PSS) dopant in an aqueous medium. Polyaniline (PANI)-grafted SWCNTs are formed, and they are uniformly dispersed in the PANI/PSS matrix. Impedance analysis shows that the charge-transfer resistances of the hybrids at all states are reduced drastically with increasing SWCNT loading. With 0.8 wt % SWCNTs, the charge-transfer resistances of the hybrid at +1.5 and -1.5 V are only about 20% and 12% of those of PANI/PSS, respectively, which is due to the greatly increased redox reactivity given by the enhanced electron transport in the hybrid and further doping function of the SWCNTs. The remarkable increase in redox reactivity leads to much enhanced electrochromic contrast from 0.34 for PANI to 0.47 for PANI-SWCNT-0.8%.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Engineering and Technology Innovations · Decision Support System Applications · Management and Optimization Techniques

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

Affiliations

Temasek Laboratories, Nanyang Technological University, 50 Nanyang Drive, Singapore 637553

School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798

References (28)

Show source-provided references
1. Pichler T. · Phys. Rev. Lett. · 1998 · 80 · 472910.1103/PhysRevLett.80.4729 ↗
2. Yosida Y. · J. Appl. Phys. · 1999 · 86 · 99910.1063/1.370838 ↗
3. Zahab A. · Phys. Rev. B · 2000 · 62 · 1000010.1103/PhysRevB.62.10000 ↗
4. Jouguelet E. · Chem. Phys. Lett. · 2000 · 318 · 56110.1016/S0009-2614(00)00089-0 ↗
5. Hong K. · ACS Appl. Mater. Interfaces · 2009 · 1 · 233210.1021/am900483y ↗
6. Curran S. A. · Adv. Mater. · 1998 · 10 · 109110.1002/(SICI)1521-4095(199810)10:14<1091::AID-ADMA1091>3.0.CO;2-L ↗
7. Nurmawati M. H. · Adv. Funct. Mater. · 2006 · 16 · 234010.1002/adfm.200600362 ↗
9. Chen G. Z. · Adv. Mater. · 2000 · 12 · 52210.1002/(SICI)1521-4095(200004)12:7<522::AID-ADMA522>3.0.CO;2-S ↗
10. An K. H. · Adv. Mater. · 2004 · 16 · 100510.1002/adma.200306176 ↗
11. Kaempgen M. · J. Electroanal. Chem. · 2006 · 586 · 7210.1016/j.jelechem.2005.09.009 ↗
12. Zengin H. · Adv. Mater. · 2002 · 14 · 148010.1002/1521-4095(20021016)14:20<1480::AID-ADMA1480>3.0.CO;2-O ↗
13. Qiao Y. · J. Power Sources · 2007 · 170 · 7910.1016/j.jpowsour.2007.03.048 ↗
14. Bhandari S. · Macromol. Rapid Commun. · 2008 · 29 · 195910.1002/marc.200800550 ↗
15. Topart P. · Thin Solid Films · 1999 · 352 · 24310.1016/S0040-6090(99)00401-0 ↗
16. Lippe J. · J. Electroanal. Chem. · 1992 · 339 · 41110.1016/0022-0728(92)80465-G ↗
17. Xiong S. · Electrochim. Acta · 2008 · 53 · 352310.1016/j.electacta.2007.12.034 ↗
18. Kumar N. A. · Surf. Rev. Lett. · 2009 · 16 · 48710.1142/S0218625X09012895 ↗
19. Philip B. · Polym. Bull. · 2005 · 53 · 12710.1007/s00289-004-0321-x ↗
20. Xiong S. · Macromol. Rapid Commun. · 2007 · 28 · 28110.1002/marc.200600717 ↗
21. Hirsch A. · Angew Chem., Int. Ed. · 2002 · 41 · 185310.1002/1521-3773(20020603)41:11<1853::AID-ANIE1853>3.0.CO;2-N ↗
22. Neelgund G. M. · Polym. Int. · 2008 · 57 · 108310.1002/pi.2445 ↗
23. Wu M. · J. Mater. Chem. · 2005 · 15 · 229710.1039/b418835g ↗
24. Wang J. · Langmuir · 2005 · 21 · 910.1021/la0475977 ↗
25. Xiong S. · Chem. Mater. · 2010 · 22 · 25510.1021/cm903058c ↗
26. Moon H. · Solid State Ionics · 1999 · 120 · 110.1016/S0167-2738(99)00003-X ↗
27. Ferloni P. · Electrochim. Acta · 1996 · 41 · 2710.1016/0013-4686(95)00290-U ↗
28. Pelster R. · Phys. Rev. B · 1994 · 49 · 1271810.1103/PhysRevB.49.12718 ↗