Attempts to immobilize catalytically active substituted-heteropolytungstates in multilayer film of charged polyelectrolyte poly(allylamine hydrochloride)

A series of transition metal substituted polyoxometalates (POMs) have been attached to carbon electrodes in multilayer films of poly(allylamine hydrochloride) (PAH). These include Wells–Dawson-derived sandwich-type Fe 4 III ( H 2 O ) 2 ( As 2 W 15 O 56 ) 2 12 - , Co 4 II ( H 2 O ) 2 ( As 2 W 15 O 56 ) 2 16 - and Mn 4 II ( H 2 O ) 2 ( As 2 W 15 O 56 ) 2 16 - and Wells–Dawson mono-substituted-type α1-[P2W17VIVO62]8− and α2-[P2W17O61(OH)2FeIII]7−. The modified electrodes were characterized by cyclic voltammetry and UV–Vis spectroscopy. The experimental observations indicate the degradation of the substituted-POMs during their incorporation in the PAH multilayer film, probably as a result of electrostatic repulsions between the positively-charged metal cation substitute (FeIII, MnII or VIV) of the POM and the positively-charged PAH. The degradation mostly results in the formation of lacunary-type POMs. Although the encapsulation does not lead to the entire preservation of the substituted-POMs, the substituted-POMs/PAH films can be used as pH sensors and as efficient electrocatalysts for the reduction of dioxygen, hydrogen peroxide and the oxidation of the NADH coenzyme.