-
1
-
-
0003586021
-
-
Cambridge University Press: Cambridge, UK
-
Nanofabrication and Biosystems: Integrating Materials Science, Engineering and Biology; Hoch, H. C., Jelinski, L. W., Craighead, H. G., Eds.; Cambridge University Press: Cambridge, UK, 1996.
-
(1996)
Nanofabrication and Biosystems: Integrating Materials Science, Engineering and Biology
-
-
Hoch, H.C.1
Jelinski, L.W.2
Craighead, H.G.3
-
3
-
-
0003515447
-
-
NATO ASI Ser. E: Applied Sciences - Kluwer: Dordrecht, The Netherlands
-
Microelectrodes: Theory and Applications NATO ASI Ser. E: Applied Sciences - Vol. 197; Montenegro, M. I., Queirós, Daschbach, J. L., Eds.; Kluwer: Dordrecht, The Netherlands, 1991.
-
(1991)
Microelectrodes: Theory and Applications
, vol.197
-
-
Montenegro, M.I.1
Queirós2
Daschbach, J.L.3
-
4
-
-
0003515447
-
-
NATO ASI Ser. E: Applied Sciences, Kluwer: Dordrecht, The Netherlands
-
Pletcher, D. In Microelectrodes: Theory and Applications NATO ASI Ser. E: Applied Sciences, Vol. 197; Montenegro, M. I., Queirós, Daschbach, J. L., Eds.; Kluwer: Dordrecht, The Netherlands, 1991; pp 3-16.
-
(1991)
Microelectrodes: Theory and Applications
, vol.197
, pp. 3-16
-
-
Pletcher, D.1
Montenegro, M.I.2
Queirós3
Daschbach, J.L.4
-
5
-
-
0002131660
-
-
Reller, H.; Kirowa-Eisner, E.; Gileadi, E. J. Electroanal. Chem. 1982, 138, 65.
-
(1982)
J. Electroanal. Chem.
, vol.138
, pp. 65
-
-
Reller, H.1
Kirowa-Eisner, E.2
Gileadi, E.3
-
9
-
-
0000382693
-
-
Bard, A. J., Ed.; Marcel Dekker: New York
-
Wightman, R. M.; Wipf, D. O. In Electroanalytical Chemistry: a Series of Advances; Bard, A. J., Ed.; Marcel Dekker: New York, 1989, Vol. 15, p 267.
-
(1989)
Electroanalytical Chemistry: A Series of Advances
, vol.15
, pp. 267
-
-
Wightman, R.M.1
Wipf, D.O.2
-
10
-
-
0004231373
-
-
Fleischmann, M., Pons, S., Rolison, D. R., Schmidt, P. P., Eds.; Datatech Systems: Morgantown, NC
-
Rolison, D. R. In Ultramicroelectrodes; Fleischmann, M., Pons, S., Rolison, D. R., Schmidt, P. P., Eds.; Datatech Systems: Morgantown, NC, 1987.
-
(1987)
Ultramicroelectrodes
-
-
Rolison, D.R.1
-
12
-
-
0001324126
-
Organized Monolayers on Electrodes
-
Bard, A. J., Rubinstein, I., Eds.; Marcel Dekker: New York, and references therein
-
Finklea, H. O. Organized Monolayers on Electrodes. Electroanalytical Chemistry-A series of advances; Bard, A. J., Rubinstein, I., Eds.; Marcel Dekker: New York, 1996; Vol. 19 and references therein.
-
(1996)
Electroanalytical Chemistry-A Series of Advances
, vol.19
-
-
Finklea, H.O.1
-
14
-
-
0027814402
-
-
Finklea, H. O.; Snider, D. A.; Fedyk, J.; Sabatani, E.; Gafni, Y.; Rubinstein, I. Langmuir 1993, 9, 3660-3667.
-
(1993)
Langmuir
, vol.9
, pp. 3660-3667
-
-
Finklea, H.O.1
Snider, D.A.2
Fedyk, J.3
Sabatani, E.4
Gafni, Y.5
Rubinstein, I.6
-
15
-
-
0023312655
-
-
Sabatani, E.; Rubinstein, I.; Maoz, R.; Sagiv, J. J. Electroanal. Chem. 1987, 219, 365.
-
(1987)
J. Electroanal. Chem.
, vol.219
, pp. 365
-
-
Sabatani, E.1
Rubinstein, I.2
Maoz, R.3
Sagiv, J.4
-
18
-
-
33644524447
-
-
Cheng, I. F.; Whiteley, L. D.; Martin, C. R. Anal. Chem. 1989, 61, 762.
-
(1989)
Anal. Chem.
, vol.61
, pp. 762
-
-
Cheng, I.F.1
Whiteley, L.D.2
Martin, C.R.3
-
22
-
-
11944257247
-
-
Chidsey, C. E. D.; Bertozzi, C. R.; Putvinski, T. M.; Mujsce, A. J. Am. Chem. Soc. 1990, 112, 4301.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 4301
-
-
Chidsey, C.E.D.1
Bertozzi, C.R.2
Putvinski, T.M.3
Mujsce, A.4
-
25
-
-
0001324126
-
Organized Monolayers on Electrodes
-
Bard, A. J., Rubinstein, I., Eds.; Marcel Dekker: New York, and references therein
-
Finklea, H. O. Organized Monolayers on Electrodes. Electroanalytical Chemistry-A series of advances; Bard, A. J., Rubinstein, I., Eds.; Marcel Dekker: New York, 1996; Vol. 19 and references therein.
-
(1996)
Electroanalytical Chemistry-A Series of Advances
, vol.19
-
-
Finklea, H.O.1
-
28
-
-
0002047167
-
-
Ohtani, M.; Sunagawa, T.; Kuwabata, S.; Yoneyama, H. J. Electroanal. Chem. 1995, 396, 97-102.
-
(1995)
J. Electroanal. Chem.
, vol.396
, pp. 97-102
-
-
Ohtani, M.1
Sunagawa, T.2
Kuwabata, S.3
Yoneyama, H.4
-
29
-
-
0030984988
-
-
Seshadri, K.; Atre, S. V.; Lee, M.-T.; Tao, Y.-T.; Allara, D. L. J. Am. Chem. Soc. 1997, 119, 9, 4698-4711.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, Issue.9
, pp. 4698-4711
-
-
Seshadri, K.1
Atre, S.V.2
Lee, M.-T.3
Tao, Y.-T.4
Allara, D.L.5
-
32
-
-
28044433840
-
-
Blom, N. F.; Neuse, E. W.; Thomas, H. G. Transition Met. Chem. 1987, 12, 301-6.
-
(1987)
Transition Met. Chem.
, vol.12
, pp. 301-306
-
-
Blom, N.F.1
Neuse, E.W.2
Thomas, H.G.3
-
33
-
-
0023849059
-
-
Faraggi, M.; Weinraub, D.; Broitman, F.; DeFelippis, M. R.; Klapper, M. H. Radiat. Phys. Chem. 1988, 32, 293-297.
-
(1988)
Radiat. Phys. Chem.
, vol.32
, pp. 293-297
-
-
Faraggi, M.1
Weinraub, D.2
Broitman, F.3
DeFelippis, M.R.4
Klapper, M.H.5
-
34
-
-
0000831883
-
-
de Boer, T. J.; Backer, H. J. Org. Synth., Coll. Vol. 1963, 4, 250-253.
-
(1963)
Org. Synth., Coll. Vol.
, vol.4
, pp. 250-253
-
-
De Boer, T.J.1
Backer, H.J.2
-
35
-
-
0348076437
-
-
The previous QCM and FRS measurements agree on average within ∼5% (ref 29)
-
The previous QCM and FRS measurements agree on average within ∼5% (ref 29).
-
-
-
-
36
-
-
0004258718
-
-
Ellis Horwood Ltd., Chichester, England, Chapter 6
-
Greef, R.; Peat, R.; Peter, L. M.; Pletcher, D. Robinson, J. In Instrumental Methods in Electrochemistry; Ellis Horwood Ltd., Chichester, England, 1985; Chapter 6.
-
(1985)
Instrumental Methods in Electrochemistry
-
-
Greef, R.1
Peat, R.2
Peter, L.M.3
Pletcher, D.4
Robinson, J.5
-
37
-
-
0039650874
-
-
One must be cautious in interpreting these trends because of the difficulties in determining accurate redox potentials as the voltammograms approach a sigmoidal shape; for example, see: Tokuda, K.; Morita, K.; Shimizu, Y. Anal. Chem. 1989, 61, 1763-8.
-
(1989)
Anal. Chem.
, vol.61
, pp. 1763-1768
-
-
Tokuda, K.1
Morita, K.2
Shimizu, Y.3
-
39
-
-
0000722303
-
-
It has been established from zero-charge potential measurements on gold that the highest surface energies are found for the high-index planes around the (111) point in the stereographic triangle [(554), (332), etc.], the typical planes found at grain boundaries at {111} textured surfaces. Also, the atoms in defect regions have lower coordination numbers and higher energies as calculated from Madelung constants and interparticle attraction, than those on {111} terraces. (See: Hamelin, A.; Lecoeur, J. Surf. Sci. 1976, 57, 771-4.)
-
(1976)
Surf. Sci.
, vol.57
, pp. 771-774
-
-
Hamelin, A.1
Lecoeur, J.2
-
40
-
-
58149364560
-
-
Porter and co-workers also have shown that the defect regions are more active than the terraces in the underpotential deposition of Pb on gold surfaces (Walczak, M. M.; Alves, C. A.; Lamp, B. D.; Porter, M. D. J. Electroanal. Chem. 1995, 396, 103-114.)
-
(1995)
J. Electroanal. Chem.
, vol.396
, pp. 103-114
-
-
Walczak, M.M.1
Alves, C.A.2
Lamp, B.D.3
Porter, M.D.4
-
41
-
-
0023592132
-
-
Ferrocene electrochemistry does not always follow a simple one-electron process. For example, Bond et al (Bond, A. M.; McLennan, E. A.; Stojanovic, R. S.; Thomas, F. G. Anal. Chem. 1987, 59, 2853-2860])-report ferrocene at saturated concentrations in aqueous media show significant deviations of the cathodic to anodic current ratios (JC/JA) from unity at high scan rates. These observations can be associated with weak adsorption of the electroactive species. In our case, FMA was used as the electroactive reagent, and the concentrations were held well below saturation values, thus reducing the possibility of adsorption effects.
-
(1987)
Anal. Chem.
, vol.59
, pp. 2853-2860
-
-
Bond, A.M.1
McLennan, E.A.2
Stojanovic, R.S.3
Thomas, F.G.4
-
42
-
-
0021215936
-
-
2 PM film (~90% passivation), as observed. From this, the theory further predicts r ∼ 4-5 nm, a not unreasonable upper limit.
-
(1984)
J. Electroanal. Chem.
, vol.160
, pp. 27
-
-
Shoup, D.1
Szabo, A.2
-
43
-
-
0000268224
-
-
2 PM film (~90% passivation), as observed. From this, the theory further predicts r ∼ 4-5 nm, a not unreasonable upper limit.
-
(1957)
J. Am. Chem. Soc.
, vol.79
, pp. 6358
-
-
Reinmuth, W.H.1
-
46
-
-
33947483336
-
-
2 PM film (~90% passivation), as observed. From this, the theory further predicts r ∼ 4-5 nm, a not unreasonable upper limit.
-
(1965)
Anal. Chem.
, vol.37
, pp. 1351-1355
-
-
Nicholson, R.S.1
-
47
-
-
0021412692
-
-
Cass, A. E. G.; Davis, G.; Francis, G. D.; Hill, H. A. O.; Aston, W. J.; Higgins, I. J.; Plotkin, E. V.; Scott, L. D. L.; Turner, A. P. F. Anal. Chem. 1984, 56, 667.
-
(1984)
Anal. Chem.
, vol.56
, pp. 667
-
-
Cass, A.E.G.1
Davis, G.2
Francis, G.D.3
Hill, H.A.O.4
Aston, W.J.5
Higgins, I.J.6
Plotkin, E.V.7
Scott, L.D.L.8
Turner, A.P.F.9
-
49
-
-
0001856123
-
-
Cassie, A. B. D. Discuss. Faraday Soc. 1948, 3, 11-16. Adamson, A. W. Physical Chemistry of Surfaces, 5th ed.; John-Wiley & Sons: New York, 1990; pp 385-389.
-
(1948)
Discuss. Faraday Soc.
, vol.3
, pp. 11-16
-
-
Cassie, A.B.D.1
-
50
-
-
0001856123
-
-
John-Wiley & Sons: New York
-
Cassie, A. B. D. Discuss. Faraday Soc. 1948, 3, 11-16. Adamson, A. W. Physical Chemistry of Surfaces, 5th ed.; John-Wiley & Sons: New York, 1990; pp 385-389.
-
(1990)
Physical Chemistry of Surfaces, 5th Ed.
, pp. 385-389
-
-
Adamson, A.W.1
-
51
-
-
33845283225
-
-
Nuzzo, R. G.; Fusco, F. A.; Allara, D. L. J. Am. Chem. Soc. 1987, 709, 2358-2368.
-
(1987)
J. Am. Chem. Soc.
, vol.709
, pp. 2358-2368
-
-
Nuzzo, R.G.1
Fusco, F.A.2
Allara, D.L.3
-
52
-
-
0026237831
-
-
DeRose, J. A.; Thundat, T.; Nagahara, L. A.; Lindsay, S. M. Surf. Sci. 1991, 256, 102-108.
-
(1991)
Surf. Sci.
, vol.256
, pp. 102-108
-
-
DeRose, J.A.1
Thundat, T.2
Nagahara, L.A.3
Lindsay, S.M.4
-
53
-
-
0002516541
-
-
Chidsey, C. E. D.; Loiacono, D. N.; Sleator, T.; Nakahara, S. Surf. Sci. 1988, 200, 45-66.
-
(1988)
Surf. Sci.
, vol.200
, pp. 45-66
-
-
Chidsey, C.E.D.1
Loiacono, D.N.2
Sleator, T.3
Nakahara, S.4
-
55
-
-
0017539369
-
-
Painter, P. C.; Runt, J.; Coleman, M. M.; Harrison, I. R. J. Polym. Sci., Polym. Phys. Ed. 1977, 15, 1647-1654.
-
(1977)
J. Polym. Sci., Polym. Phys. Ed.
, vol.15
, pp. 1647-1654
-
-
Painter, P.C.1
Runt, J.2
Coleman, M.M.3
Harrison, I.R.4
-
56
-
-
5244297041
-
-
Snyder, R. G.; Strauss, H. L.; Elliger, C. A. J. Phys. Chem. 1982, 86, 5145-5150.
-
(1982)
J. Phys. Chem.
, vol.86
, pp. 5145-5150
-
-
Snyder, R.G.1
Strauss, H.L.2
Elliger, C.A.3
-
58
-
-
0348076435
-
-
Note that the contact angle hysteresis for PM/(sputtered Au) is consistently higher by as much as 30° than for PM/(evaporated Au), as expected from the increased surface roughness for the former.
-
Note that the contact angle hysteresis for PM/(sputtered Au) is consistently higher by as much as 30° than for PM/(evaporated Au), as expected from the increased surface roughness for the former.
-
-
-
-
59
-
-
0346815515
-
-
note
-
The procedure involved the introduction of PM-modified substrates into 2 mM solutions of the thiol in ethanol. The substrates were taken out after a 24-h immersion period and washed sequentially in ethanol, hexanes, water, and ethanol, under sonication, and then spectra were taken.
-
-
-
-
61
-
-
0346815514
-
-
The C-H spectra are not reported as the strong C-H modes of the PM interfere with the thiol component.
-
The C-H spectra are not reported as the strong C-H modes of the PM interfere with the thiol component.
-
-
-
-
62
-
-
0346185164
-
-
note
-
However, note that the intensities of the progression bands appear to increase with increasing PM coverage (Figure 7a), in contrast to the decrease of the C - O stretching peak. The source of this contrary effect is not clear but may be due to chain orientation effects. Since the transition moment of the progression series is parallel to the chain axis, this would imply a more vertical alignment of the alkanethiolate chains as the PM pore sizes decrease.
-
-
-
-
63
-
-
0347446318
-
-
note
-
The origin of this effect is unclear but could be a combination of chain orientation effects and local electromagnetic field effects induced by the atomic-level surface roughness of the sputtered surface. Further studies are in progress to clarify this issue. Also, see footnote 52.
-
-
-
-
64
-
-
0023592132
-
-
The smallest cylindrical pore into which an alkanethiol chain would fit would be ∼0.5 nm, the diameter of an all-trans extended alkyl chain. In comparison note that the size of an FMA moiety is about 30 Å or ∼0.5 nm across (Bond, A. M., McLennan, E. A., Stojanovic, R. S., Thomas, F. G. Anal. Chem. 1987, 59, 2853-2860).
-
(1987)
Anal. Chem.
, vol.59
, pp. 2853-2860
-
-
Bond, A.M.1
McLennan, E.A.2
Stojanovic, R.S.3
Thomas, F.G.4
-
65
-
-
0001367153
-
-
Guiseppi-Elie, A., Pradhan, S. R., Wilson, A. M., Allara, D. L.; Zhang, P.; Collins, R. W.; Kim, Y.-T. Chem. Mater. 1993, 5, 1474-1480.
-
(1993)
Chem. Mater.
, vol.5
, pp. 1474-1480
-
-
Guiseppi-Elie, A.1
Pradhan, S.R.2
Wilson, A.M.3
Allara, D.L.4
Zhang, P.5
Collins, R.W.6
Kim, Y.-T.7
|