Abstract

Deposition of alternating layers of phosphomolybdic acid, PMo 12, and generation-4 polyamidoamine dendrimer, PAMAM, on a gold electrode is demonstrated. The gold is first coated with a self-assembled monolayer of 4-aminothiophenol. Based on the charge under cyclic voltammetric peaks, at least 12 layers of PMo 12 are deposited with an estimated quantity of 5.2×10 −11 mol cm −2 in each. The voltammetry of PMo 12 is consistent with that for solution studies, in that three two-electron processes are observed with formal potentials of 0.381, 0.238 and 0.012 V. However, the dependence of peak current on scan rate is indicative of redox surface-confined species. The PAMAM provided a spacer that led to a multilayer assembly with high conductivity and, because of its size, apparently high permeability. Regarding the latter, efficient catalysis of the reduction of nitrite and the oxidation of arsenite is achieved.

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