PM-IRRA Spectroelectrochemistry of Hexacyanoferrate

VILLALBA M.; MENDEZ DE LEO, LUCILA; CALVO EJ,

chemelectrochem

Wiley-VCH

Lugar: Wenheim; Año: 2014 vol. 1 p. 195 - 199

2196-0216

In situ polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS) under potential control is used to study self-assembled layer-by-layer (LbL) poly(allylamine) (PAH) and poly(acrylic acid) (PAA) multilayers containing the hexacyanoferrate redox system on conductive substrates. Two systems were examined, which differ in the way the redox complex is entrapped in the LbL polyelectrolyte multilayer: In system I, the LbL polyelectrolyte multilayer, self-assembled by alternate immersion in PAH and PAA, was exchanged in a 2 mm K3Fe(CN)6 solution of pH 3.5 for 30 min and then thoroughly rinsed with water. In system II, the 2 mm K3Fe(CN)6 solution was complexed with PAA prior to self-assembly with PAA. PMIRRAS studies demonstrate the potential dependence of the vibrational modes of the polyelectrolyte backbones and the CN stretching modes, which are sensitive to the redox charge in the iron center. m K3Fe(CN)6 solution of pH 3.5 for 30 min and then thoroughly rinsed with water. In system II, the 2 mm K3Fe(CN)6 solution was complexed with PAA prior to self-assembly with PAA. PMIRRAS studies demonstrate the potential dependence of the vibrational modes of the polyelectrolyte backbones and the CN stretching modes, which are sensitive to the redox charge in the iron center.