1989
DOI: 10.1021/la00087a020
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Adsorption and micellization influence the electrochemistry of redox surfactants derived from ferrocene

Abstract: for estimating double-layer effects when the admittance of the background electrolyte alone is measured.Acknowledgment. The financial support of the Office of Naval Research, Washington, DC, is gratefully acknowledged.

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Cited by 58 publications
(31 citation statements)
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“…At these low solution concentrations, the contribution to the voltanimetric response from solution phase C16 is negligible, so only the surface wave for adsorbed C16 is observed. Quite similar behavior was previously described for the C12 and C14 derivatives (5,8,9), although their tendency towards adsorption is somewhat lower, so that larger concentrations are required to achieve similar surface coverages. The EQCM frequency data obtained during the voltammetric scan indicate a monotonic mass decrease during the oxidation of the adsorbed redox surfactant, behavior which is also similar to that observed for C12 (5,8,9) and C14 (5).…”
Section: Resultssupporting
confidence: 80%
See 1 more Smart Citation
“…At these low solution concentrations, the contribution to the voltanimetric response from solution phase C16 is negligible, so only the surface wave for adsorbed C16 is observed. Quite similar behavior was previously described for the C12 and C14 derivatives (5,8,9), although their tendency towards adsorption is somewhat lower, so that larger concentrations are required to achieve similar surface coverages. The EQCM frequency data obtained during the voltammetric scan indicate a monotonic mass decrease during the oxidation of the adsorbed redox surfactant, behavior which is also similar to that observed for C12 (5,8,9) and C14 (5).…”
Section: Resultssupporting
confidence: 80%
“…The instrumentation for the EQCM measurements has been described in considerable detail elsewhere (5,7), as have the considerations pertinent to application of the EQCM to measurement of mass changes at electrode surfaces for species such as those studied here (5,(7)(8)(9). We deter discussion of details to a later section, but point out that the EQCM is capable of detecting mass changes at the electrode surface by virtue of changes in its resonant frequency caused by these mass changes.…”
Section: Methodsmentioning
confidence: 99%
“…As can been seen in Figure 2, the peak potential for FeTMUA-polyanion is higher than that for FeTMUA-Cl. According to the adsorption model of redox surfactant at electrode [14,15], the peak potential reflects free energy difference between the oxidizing agent adsorbed and the reducing agent adsorbed. When the free energy of the reducing agent is fairly small, peak potentials depends upon the stability of FeTMUA complex at electrode.…”
Section: Adsorption State Of Polyanion-cationic Surfactantmentioning
confidence: 99%
“…In the case of a dielectric substrate, for the calculation of S = (R p /R s ), Eq. [11] is used, while for S 0 = (R p /R s ) 0 , Eq. [10] is employed.…”
Section: Reflectometrymentioning
confidence: 99%