journal article·2003-07

Electrochemical deposition of polypyrrole films on organosilane-modified ITO substrates

D. Cossement, F. Plumier, J. Delhalle, L. Hevesi, Z. Mekhalif

Synthetic Metals· Volume 138· Issue 3
Publisher page

Abstract

Abstract We report in this work the organosilane modification of ITO substrates and subsequent electrodeposition of polypyrrole films. First, n -hexyltrichlorosilane (HTCS) and 6-(1′-pyrrolyl)- n -hexyltrichlorosilane (PyHTCS) were grafted on ITO substrates. The resulting monolayers were qualified by X-ray photoelectron spectroscopy, contact angle measurements and cyclovoltammetry, and they were found to be dense and well-covering. Second, pyrrole was electrochemically polymerized on modified ITO substrates in acetonitrile and aqueous solutions. Chronoamperometry was used to study the effect of the monolayers on polypyrrole growth kinetics. PyHTCS monolayers, compared to bare substrates, accelerate the polymer growth while HTCS monolayers delay and slow down the polymer growth. Qualitative peel tests and scanning electron microscopy (SEM) further evidenced the beneficial effect of PyHTCS monolayers. Polypyrrole grown from PyHTCS monolayers were found to be more uniform and more adherent, compared to bare and HTCS-modified ITO substrates. Cyclic voltamograms gave some additional indications in this sense. UV spectroscopy revealed differences in polymer quality arising from growth solutions: acetonitrile leads to better quality polymer films than aqueous solutions.
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Research context

OpenAlex topics: Conducting polymers and applications · Molecular Junctions and Nanostructures · Organic Electronics and Photovoltaics

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References (42)

Show source-provided references
1. Diaz · J. Electroanal. Chem. · 1981 · 129 · 11510.1016/S0022-0728(81)80008-3 ↗
2. Posdorfer
3. Burroughes · Nature · 1990 · 347 · 53910.1038/347539a0 ↗
4. Dodabalapur · Science · 1995 · 268 · 27010.1126/science.268.5208.270 ↗
5. Guiseppi-Elie · Langmuir · 1995 · 11 · 176810.1021/la00005a055 ↗
6. Simon · J. Am. Chem. Soc. · 1982 · 104 · 203110.1021/ja00371a045 ↗
7. T. Komori, T. Nonaka, Chem. Lett. (1984) 509–512.10.1246/cl.1984.509 ↗
8. E.P. Plueddemann, Silane Coupling Agents, Plenum Press, New York, 1991.10.1007/978-1-4899-2070-6 ↗
9. Luzinov · Langmuir · 2000 · 16 · 50410.1021/la990500+ ↗
10. Prucker · Langmuir · 1998 · 14 · 689310.1021/la971035o ↗
11. Willicut · J. Am. Chem. Soc. · 1994 · 116 · 1082310.1021/ja00102a073 ↗
12. Sayre · Langmuir · 1997 · 13 · 71410.1021/la960420v ↗
13. Kowalik · Synth. Met. · 1993 · 55–57 · 117110.1016/0379-6779(93)90219-M ↗
14. Sabatani · J. Phys. Chem. · 1995 · 99 · 1230510.1021/j100032a039 ↗
15. Mekhalif · Synth. Met. · 1998 · 96 · 16510.1016/S0379-6779(98)00068-X ↗
16. Rozsnyai · Chem. Mater. · 1996 · 8 · 30910.1021/cm9502838 ↗
17. Wu · J. Mater. Chem. · 1997 · 7 · 140910.1039/a608365j ↗
18. Faverolle · Chem. Mater. · 1998 · 10 · 74010.1021/cm970466p ↗
19. Xia · Chem. Mater. · 2001 · 13 · 168210.1021/cm000918p ↗
20. Huang · Langmuir · 1997 · 13 · 648010.1021/la970537z ↗
21. D. Cossement, C. Pierard, J. Delhalle, J.-J. Pireaux, L. Hevesi, Z. Mekhalif, Surf. Interface Anal. 31 (2001) 18–22.10.1002/sia.947 ↗
22. Markovich · J. Electroanal. Chem. · 2000 · 484 · 19410.1016/S0022-0728(00)00084-X ↗
23. G. Beamson, D. Briggs, HRXPS of Organic Polymers, The Scienta ESCA A300 Database, Wiley, Chichester, 1992.
24. Chiu · J. Appl. Electrochem. · 1992 · 22 · 52210.1007/BF01024092 ↗
25. Kaplin · Electrochim. Acta · 1995 · 40 · 114910.1016/0013-4686(95)00011-3 ↗
26. Sabatani · Langmuir · 1993 · 9 · 297410.1021/la00035a040 ↗
27. Sullivan · Langmuir · 2000 · 16 · 979710.1021/la000225n ↗
28. Sagiv · J. Am. Chem. Soc. · 1980 · 102 · 9210.1021/ja00521a016 ↗
29. Wasserman · Langmuir · 1989 · 5 · 107410.1021/la00088a035 ↗
30. Cossement · Surf. Interf. Anal. · 2000 · 30 · 5610.1002/1096-9918(200008)30:1<56::AID-SIA833>3.0.CO;2-O ↗
31. Clark · J. Chem. Phys. Lett. · 1971 · 9 · 25410.1016/0009-2614(71)85038-8 ↗
32. Barr · J. Phys. Chem. · 1978 · 82 · 180110.1021/j100505a006 ↗
33. More accurately, the Si-O and SnO2 lines have been set with a binding energy difference of 1.9eV, in agreement with published values in the literature (see Ref. [23] and [32]).
34. Porter · J. Am. Chem. Soc. · 1987 · 109 · 355910.1021/ja00246a011 ↗
35. Miller · J. Phys. Chem. · 1991 · 95 · 87710.1021/j100155a072 ↗
36. Weidemann · Langmuir · 1998 · 14 · 648510.1021/la980188o ↗
37. Tillman · J. Am. Chem. Soc. · 1988 · 110 · 613610.1021/ja00226a031 ↗
38. Willicut · Langmuir · 1995 · 11 · 29610.1021/la00001a050 ↗
39. Mekhalif · J. Chim. Phys. · 1995 · 92 · 83110.1051/jcp/1995920831 ↗
40. Lo · J. Am. Chem. Soc. · 1996 · 118 · 1129510.1021/ja9610343 ↗
41. Collard · Synth. Met. · 1997 · 84 · 32910.1016/S0379-6779(97)80768-0 ↗
42. Rubinstein · J. Am. Chem. Soc. · 1990 · 112 · 613510.1021/ja00172a043 ↗