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Abstract:

A molecular theory is presented to describe chemically modified electrodes by redox polymers. The theory is based on writing the free energy functional of the system which includes the size, shape, charge distribution, and conformations of all of the molecular species as well as all of the inter and intramolecular interactions, the acid-base equilibrium for the ionizable groups of the weak polyelectrolyte, and the redox equilibrium of the electrochemical active sites with the metal. The minimization of the free energy leads to the molecular organization of the film as a function of bulk pH, salt concentration, and applied electrode potential. The approach is applied to the experimental system composed by osmium pyridine-bipyridine complex covalently bound to poly(allylamine) backbone, which is adsorbed onto a mercapto-propane sulfonate thiolated gold electrode. The redox and nonredox capacity of the electrode and its dependence on the electrode potential calculated with the molecular theory shows very good agreement with linear scan voltammetric experiments under reversible conditions (equilibrium scans) without the use of any free adjustable parameter. The predicted film thickness is in line with ellipsometric measurements. Further, the theory predicts the swelling of the film as a function of the electrode potential. The molecular theory provides the link between the molecular organization within the film and the electrochemical behavior. It is shown that the electrostatic, excluded volume, and van der Waals interaction fields are strongly coupled in a nontrivial way. Furthermore, the degree of charge regulation and distribution of oxidized states couples to the molecular distributions and the interaction fields. The application of the theory to different model systems demonstrates the importance of incorporating molecular information into the theoretical approach and the very strong coupling that exists between molecular structure, film organization, interactions fields, and electrochemical behavior. © 2008 American Chemical Society.

Registro:

Documento: Artículo
Título:Molecular theory of chemically modified electrodes by redox polyelectrolytes under equilibrium conditions: Comparison with experiment
Autor:Tagliazucchi, M.; Calvo, E.J.; Szleifer, I.
Filiación:Molecular Electrochemistry Group, INQUIMAE, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina
Department of Chemistry, Purdue University, West Lafayette, IN 47907, United States
Department of Biomedical Engineering, Northwestern University, 2145 Sheridan Rd., Evanston, IL, United States
Palabras clave:Electrode potential; Intramolecular interactions; Molecular theory; Redox polymers; Conformations; Electrodes; Free energy; Redox reactions; Polyelectrolytes
Año:2008
Volumen:112
Número:2
Página de inicio:458
Página de fin:471
DOI: http://dx.doi.org/10.1021/jp073123f
Título revista:Journal of Physical Chemistry C
Título revista abreviado:J. Phys. Chem. C
ISSN:19327447
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19327447_v112_n2_p458_Tagliazucchi

Referencias:

  • Moses, P.R., Wier, L., Murray, R.W., (1975) Anal. Chem, 47, p. 1882
  • Murray, R.W., (1980) Acc Chem. Res, 13, p. 135
  • Murray, R.W., Chemically Modified Electrodes (1984) Electroanalytical Chemistry, 13, p. 191. , Bard, A. J, Ed, Marcel Dekker: New York
  • Murray, R.W., Introduction to Molecularly Designed Electrode Surfaces (1992) Molecular Design of Electrode Surfaces, , Murray, R. W, Ed, John Wiley and Sons, Inc, New York
  • Bard, A.J., (1994) Integrated Chemical Systems. A Chemical Approach to Nanotechnology, 1. , John Wiley & Sons: New York
  • Hodak, J., Etchenique, R., Calvo, E.J., Singhal, K., Bartlett, P.N., (1997) Langmuir, 13, p. 2708
  • Lyons, M.E.G., (1994) Electroactive Polymer Electrochemistry, 1. , Plenum Press: New York
  • Bard, A.J., Faulkner, L.R., (2001) Electrochemical Methods: Fundamentals and Applications, , 2nd. ed, John Wiley & Sons: New York
  • Doblhofer, K., Vorotyntsev, M., Fundamentals (1994) Electroactive Polymer Electrochemistry, p. 375. , Lyons, M. E. G, Ed, Plenum: New York
  • Naegeli, R., Redepenning, J., Anson, F.C., (1986) J. Phys. Chem, 90, p. 6227
  • Redepenning, J., Anson, F.C., (1987) J. Phys. Chem, 91, p. 4549
  • Laviron, E., (1979) J. Electroanal. Chem, 100, p. 263
  • Andrieux, C.P., Savéant, J.M., (1988) J. Phys. Chem, 92, p. 6761
  • Anson, F.C., Blauch, D.N., Savéant, J.-M., Shu, C.-F., (1991) J. Am. Chem. Soc, 113, p. 1922
  • Blauch, D.N., Savéant, J.M., (1993) J. Phys. Chem, 97, p. 6444
  • Savéant, J.M., (1988) J. Phys. Chem, 92, p. 4526
  • Laviron, E., (1980) J. Electroanal. Chem, 112, p. 1
  • Chidsey, C.E.D., Murray, R.W., (1986) J. Phys. Chem, 90, p. 1479
  • Bowden, E.F., Dautartas, M.F., Evans, J.F., (1987) J. Electroanal. Chem, 219, p. 49
  • Dautartas, M.F., Bowden, E.F., Evans, J.F., (1987) J. Electroanal. Chem, 219, p. 71
  • Bowden, E.F., Dautartas, M.F., Evans, J.F., (1987) J. Electroanal. Chem. Interfacial Electrochem, J219, p. 91
  • Posadas, D., Florit, M.I., (2004) J. Phys. Chem. B, 108, p. 15470
  • Lizarraga, L., Andrade, E.M., Florit, M.I., Molina, F.V., (2005) J. Phys. Chem. B, 109, p. 18815
  • Hill, T.L., (1986) An Introduction to Statistical Thermodynamics, , Dover Publications: New York
  • Netz, R.R., Andelman, D., (2003) Phys. Rep, 380, p. 1
  • Tagliazucchi, M., Calvo, E.J., (2007) J. Electroanal. Chem, 599, p. 249
  • Calvo, E.J., Wolosiuk, A., (2002) J. Am. Chem. Soc, 124, p. 8490
  • Calvo, E.J., Danilowicz, C., Wolosiuk, A., (2002) J. Am. Chem. Soc, 124, p. 2452
  • Calvo, E.J., Etchenique, R., Pietrasanta, L., Wolosiuk, A., (2001) Anal. Chem, 73, p. 1161
  • Flexer, V., Forzani, E.S., Calvo, E.J., Luduena, S.J., Pietrasanta, L.I., (2006) Anal. Chem, 78, p. 399
  • Calvo, E.J., Danilowicz, C.B., Wolosiuk, A., (2005) Phys. Chem. Chem. Phys, 7, p. 1800
  • Calvo, E.J., Wolosiuk, A., (2004) ChemPhysChem, 5, p. 235
  • By reversible conditions, we mean the equilibrium behavior of the electrodes; the generalization to study the kinetics of the electrochemical process is left to future work; Szleifer, I., Carignano, M.A., (1996) Adv. Chem. Phys, 96, p. 165
  • Szleifer, I., Carignano, M.A., (2000) Macromol. Rapid Commun, 21, p. 423
  • Nap, R., Gong, P., Szleifer, I., (2006) J. Polym. Sci. Part B, 44, p. 2638
  • Wu, T., Genzer, J., Gong, P., Szleifer, I., Vlcek, P., Subr, V., (2004) Behavior of surface-anchored poly(acrylic acid) brushes with grafting density gradients on solid substrates In Polymer, p. 287. , Brushes; Brittain, B, Advincula, R, Caster, K, Eds, Wiley & Sons: New York
  • McPherson, T., Kidane, A., Szleifer, I., Park, K., (1998) Langmuir, 14, p. 176
  • Satulovsky, J., Carignano, M.A., Szleifer, I., (2000) Proc Natl. Acad. Sci, 97, p. 9037
  • Trasatti, S., (1986) Pure Appl. Chem, 58, p. 956
  • de Gennes, P.G., (1991) Scaling Concepts in Polymer Physics, , Cornell University Press: Ithaca, NY
  • Flory, P.J., (1953) Principles of Polymer Chemistry, , Cornell University Press: Ithaca, NY
  • Carignano, M.A., Szleifer, I., (1994) J. Chem. Phys, 100, p. 3210
  • Croze, O., Cates, M., (2005) Langmuir, 21, p. 5627
  • Schwinger, J., DeRaad, L.J., Milton, K., Tsai, W.-Y., (1998) Classical Electrodynamics, , Persus Books: Reading, MA
  • Llano, J., Eriksson, L.A., (2002) J. Chem. Phys, 117, p. 10193
  • Israelachvili, J., (1992) Intermolecular and Surface Forces, , Academic Press: San Diego, CA
  • Mokrani, C., Fatisson, J., Guérente, L., Labbé, P., (2005) Langmuir, 21, p. 4400
  • Love, J.C., Estroff, L.A., Kriebel, J.K., Nuzzo, R.G., Whitesides, G.M., (2005) Chem. Rev, 105, p. 1103
  • Ninham, B.W., Parsegian, V.A.J., (1971) Theor. Biol, 31, p. 405
  • Tagliazucchi, M., Williams, F., Calvo, E.J., (2007) J. Phys. Chem. B, 111, p. 8105
  • Szleifer, I., Brinke, G.T., (1996) J. Chem. Phys, 104, p. 6343
  • Forzani, E.S., Pérez, M.A., Teijelo, M.L., Calvo, E.J., (2002) Langmuir, 18, p. 9867
  • Messina, R., (2004) Macromolecules, 37, p. 621
  • Carrillo, J.-M.Y., Dobrynin, A.V., (2007) Langmuir, 23, p. 2472
  • Danilowicz, C., Corton, E., Battaglini, F., (1998) J. Electroanal. Chem, 445, p. 89
  • Finklea, H.O., Snider, D.A., Fedyk, J., (1990) Langmuir, 6, p. 371
  • Trassati, S., (1974) J. Electroanal. Chem, 54, p. 19
  • This is an approximation since it is known that the potential of zero charge of polycristalline gold (which depends on its work function) varies upon thiol adsorption. For further details, see: Iwami, Y, Hobara, D, Yamamoto, M, Kakiuchi, T. J. Electroanal. Chem. 2004, 564, 77-83 and references therein; Brown, A.P., Anson, F.C., (1977) Anal. Chem, 49, p. 1589
  • Albery, W.J., Boutelle, M.G., Colby, P.J., Hillman, A.R., (1982) J. Electroanal. Chem, 133, p. 135
  • Redepenning, J., Miller, B.R., Burham, S., (1994) Anal. Chem, 66, p. 1560
  • Calvo, E.J., Etchenique, R., Danilowicz, C., Diaz, L., (1996) Anal. Chem, 68, p. 4186
  • Ohshima, H., Ohki, S., (1985) Biophys. J, 47, p. 673
  • Garcia-Morales, V., Cervera, J., Manzanares, J.A., (2007) J. Electroanal. Chem, 599, p. 203
  • Castelnovo, M., Joanny, J.-F., (2000) Langmuir, 2000, p. 7524
  • Solis, F.J., Olvera de la Cruz, M., (1999) J. Chem. Phys, 110, p. 11517
  • Israels, R., Leermakers, F., Fleer, G.J., Zhulina, E.B., (1994) Macromolecules, 27, p. 3249
  • Rühe, J., (2004) Adv. Polym. Sci, 165, pp. 79-150
  • v.Klitzing, R.; Möwald, H. Langmuir 1995, 11, 3554; Tagliazucchi, M., Grumelli, D., Bonazzola, C., Calvo, E.J., (2006) J. Nanosci. Nanotechnol, 6, p. 1731
  • Grumelli, D.E., Garay, F., Barbero, C.A., Calvo, E.J., (2006) J. Phys. Chem. B, 110, p. 15345
  • Grumelli, D.E., Wolosiuk, A., Forzani, E., Planes, G.A., Barbero, C., Calvo, E., (2003) J. Chem. Commun, 9, p. 3014

Citas:

---------- APA ----------
Tagliazucchi, M., Calvo, E.J. & Szleifer, I. (2008) . Molecular theory of chemically modified electrodes by redox polyelectrolytes under equilibrium conditions: Comparison with experiment. Journal of Physical Chemistry C, 112(2), 458-471.
http://dx.doi.org/10.1021/jp073123f
---------- CHICAGO ----------
Tagliazucchi, M., Calvo, E.J., Szleifer, I. "Molecular theory of chemically modified electrodes by redox polyelectrolytes under equilibrium conditions: Comparison with experiment" . Journal of Physical Chemistry C 112, no. 2 (2008) : 458-471.
http://dx.doi.org/10.1021/jp073123f
---------- MLA ----------
Tagliazucchi, M., Calvo, E.J., Szleifer, I. "Molecular theory of chemically modified electrodes by redox polyelectrolytes under equilibrium conditions: Comparison with experiment" . Journal of Physical Chemistry C, vol. 112, no. 2, 2008, pp. 458-471.
http://dx.doi.org/10.1021/jp073123f
---------- VANCOUVER ----------
Tagliazucchi, M., Calvo, E.J., Szleifer, I. Molecular theory of chemically modified electrodes by redox polyelectrolytes under equilibrium conditions: Comparison with experiment. J. Phys. Chem. C. 2008;112(2):458-471.
http://dx.doi.org/10.1021/jp073123f