Electrochemical operational principles and analytical performance of Pd-based amperometric nanobiosensors

Palladium nanoparticles (Pd-NPs) have been approved as an effective catalyst for hydrogen peroxide decomposition which is released during specific enzymatic reactions. However, the general operational principles and electrochemical performance of Pd-NPs-based nanobiosensors have been poorly exploited. Here, the electrochemical behavior of oxidase-associated peroxide oxidation co-catalysis of the modelled microanalytical system based on screen-printed electrodes modified by electroplated Pd-NPs as an electrocatalyst, glucose oxidase (GOx) or alcohol oxidase (AOx) as a bioreceptor and the ionomer Nafion as a polymeric binding agent was studied in detail. The impact of palladium surface oxides and adsorbed oxygen on the activity and product selectivity in an oxidase type of nanobiosensor was ascertained. To avoid PdO and oxygen electroreduction affecting the entire amperometric response of Pd-NPs-based nanobiosensors, a special two-step polarization procedure was proposed. Under the established electrochemical conditions, Pd-NPs-based nanobiosensors with encapsulated oxidases showed a wide dynamic range towards selective bioanalyte detection, excellent basic line stability, accuracy and resistance to the presence of interfering electrochemical species. This work can serve as a guideline for the search and validation of operational principles of novel biosensors based on nanoparticles.