Improved polypyrrole/silicon junctions by surfacial modification of hydrogen-terminated silicon using organolithium reagents [7]

Journal of the American Chemical Society

Volumn 121, Issue 30, 1999, Pages 7162-7163

  Kim, Namyong Y ^a   Laibinis, Paul E ^b  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^b Massachusetts Institute of Technology Cambridge   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGEN; ORGANOLITHIUM COMPOUND; POLYPYRROLE; SILICON DERIVATIVE;

CHEMICAL ANALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; LETTER; POLYMERIZATION; STRUCTURE ANALYSIS;

EID: 0033523275     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja990260k     Document Type: Letter

References (18)

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7. The improved formation of conducting polymers on gold using monomer-terminated thiol-based monolayers has been reported by: (a) Willicut, R. J.; McCarley, R. L. Langmuir 1995, 11, 296-301. (b) Sayre, C. N.; Collard, D. M. Langmuir 1995, 11, 302-306. (c) Rubinstein, I.; Rishpon, J.; Sabatani, E.; Redondo, A.; Gottesfeld, S. J. Am. Chem. Soc. 1990, 112, 6135-6136. (d) Kowalik, J.; Tolbert, L.; Ding, Y.; Bottomley, L. A. Synth. Met. 1993, 55-57, 1171-1175.
8. The improved formation of conducting polymers on gold using monomer-terminated thiol-based monolayers has been reported by: (a) Willicut, R. J.; McCarley, R. L. Langmuir 1995, 11, 296-301. (b) Sayre, C. N.; Collard, D. M. Langmuir 1995, 11, 302-306. (c) Rubinstein, I.; Rishpon, J.; Sabatani, E.; Redondo, A.; Gottesfeld, S. J. Am. Chem. Soc. 1990, 112, 6135-6136. (d) Kowalik, J.; Tolbert, L.; Ding, Y.; Bottomley, L. A. Synth. Met. 1993, 55-57, 1171-1175.
9. The improved formation of conducting polymers on gold using monomer-terminated thiol-based monolayers has been reported by: (a) Willicut, R. J.; McCarley, R. L. Langmuir 1995, 11, 296-301. (b) Sayre, C. N.; Collard, D. M. Langmuir 1995, 11, 302-306. (c) Rubinstein, I.; Rishpon, J.; Sabatani, E.; Redondo, A.; Gottesfeld, S. J. Am. Chem. Soc. 1990, 112, 6135-6136. (d) Kowalik, J.; Tolbert, L.; Ding, Y.; Bottomley, L. A. Synth. Met. 1993, 55-57, 1171-1175.
10. The improved formation of conducting polymers on gold using monomer-terminated thiol-based monolayers has been reported by: (a) Willicut, R. J.; McCarley, R. L. Langmuir 1995, 11, 296-301. (b) Sayre, C. N.; Collard, D. M. Langmuir 1995, 11, 302-306. (c) Rubinstein, I.; Rishpon, J.; Sabatani, E.; Redondo, A.; Gottesfeld, S. J. Am. Chem. Soc. 1990, 112, 6135-6136. (d) Kowalik, J.; Tolbert, L.; Ding, Y.; Bottomley, L. A. Synth. Met. 1993, 55-57, 1171-1175.
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12. Kim, N. Y.; Laibinis, P. E. J. Am. Chem. Soc. 1998, 120, 4516-4517.
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14. IR spectra for crystalline silicon were obtained by attenuated total reflection.
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16. 2, and the resulting polymers were ∼2.5 μm thick based on coulometry. The rms roughnesses in Figure 2c and 2d were 25 and 219 nm, respectively.
17. A similar result was reported for polypyrrole films on gold. Polypyrrole deposited on gold modified with an n-alkanethiol exhibited similar characteristics to that formed on bare gold. See refs 7a and 7b.
18. Vermeir, I. E.; Kim, N. Y.; Laibinis, P. E. Appl. Phys. Lett., 1999, 74, 3860-3862.