Abstract :
The goal of our studies was to determine the nature of interactions between catalytic active samples, such as polypyrrole (PPy)
doped with: chloride anions, heteropolyacids such as H5PMo10V2O40, orH4SiW12O40, and oxygen particles. In order to reveal the
mechanismof the linkage between the catalysts and oxygen weprovided the electron paramagnetic resonance (EPR) measurements
of synthesized samples inO2 andN2 flow.Moreover, the X-ray photoelectron spectroscopy (XPS)measurementswere performed to
showthe properties of doped heteropolyacids and the state of nitrogen in polypyrrolematrix. The results of EPR studies of PPy(Cl),
PPy(H4SiW12O40), PPy(H5PMo10V2O40) samples, showthat the polypyrrole doped with chloride anions interactsmuch easierwith
oxygen than polypyrrole doped with heteropolyacids (in the above given order, of preference with the most active polypyrrole
system first). It correlates with XPS results, which show that a molybdenium–vanadium anion is more reduced than a silicon–
tungsten one. The redox reactions of heteropolyacids involve the oxidation–reduction of the conjugated polymer chain, leaving no
or little place for interactions with oxygen. Polypyrrole doped with H4SiW12O40 shows some oxygen sensitivity as observed in the
EPR studies, as opposed to polypyrrole doped with H5PMo10V2O40, which is in line with the XPS results
Keywords :
EPR spectroscopy , Oxygen adsorption , Heterogeneous catalysis , XPS spectroscopy