Voltammetry at Micropipet Electrodes

摘要

The use of micropipet electrodes for quantitative voltammetric measurements of ion-transfer (IT) and electron-transfer (Er) reactions at the interface between two immiscible electrolyte solutions (1TIES) requires knowledge of geometry of the liquid interface. The shape of the meniscus formed at the pipet tip was studied in situ by video microscopy under controlled pressure. The shape of the interface can be changed from a complete sphere to a concave spherical cap by varying the pressure applied to the pipet, and the diffusion current to the pipet changes accordingly. With no external pressure applied, the water/organic interface turned out to be fiat, and the voltammetric response of a pipet must follow the well-known theory for a microdisk electrode. The large deviations from this theory observed previously can be attributed to a small mount of the filling aqueous solution which escapes from the pipet and forms a thin layer on its outer wall. This effect can be eliminated by making the outer pipet wall hydrophobic. Procedures have been developed for independent silanization of the inner and outer walls of the pipet. Pipets with a silanized inner wall can be filled with an organic solvent (e.g., 1,2-dichloroethane) and be used for voltammetric measurements in aqueous solutions. Another mode of voltammetry is based on trapping of a thin layer of organic solvent in- the narrow shaft of a pipet between the filling solution and the aqueous outer phase. This arrangement is potentially useful for electrochemical catalysis and sensor applications.