Spectroelectrochemical sensing based on multimode selectivity simultaneously achievable in a single device: 14. Enhancing sensitivity of a metal complex ion by ligand exchange

Abstract

Enhancement of the sensitivity of a spectroelectrochemical sensor by ligand exchange within the sensing film during spectroelectrochemical modulation is demonstrated in this paper. This concept is illustrated with a sensor for Cu(en) 2 2+, where en = ethylenediamine, in aqueous solution. A ligand exchange reaction increases the difference in the molar absorptivities of the two complex ions involved in spectroelectrochemical modulation, thus giving a larger optical response. The spectroelectrochemical sensor consists of a cation-selective Nafion-SiO 2 composite film spin-coated onto an indium tin oxide (ITO) glass optically transparent electrode (OTE). The film was loaded with 2,9-dimethyl-1,10-phenanthroline (neocuproine, or nc) for the ligand exchange reaction. Reduction of Cu(en) 2 2+ at the OTE is accompanied by ligand exchange with nc to form Cu(nc) 2 1+, which has a molar absorptivity of 7950 M −1 cm −1 at λ max = 454 nm. Detection within the sensing film using attenuated total reflectance (ATR) at 454 nm during modulation was accomplished by potential cycling between 0.8 and −0.9 V versus Ag/AgCl. The effects of nc concentration in the film and potential scan rate on the absorbance–time profile for spectroelectrochemical modulation were studied. The calibration curve for Cu(en) 2 2+ was linear within the range of 5 × 10 −6 M to 1 × 10 −3 M.