Expanded Electrochemical Capabilities of the Electrospray Ion Source Using Porous Flow-Through Electrodes as the Upstream Ground and Emitter High-Voltage Contact

Abstract

Use of a porous flow-through electrode at the upstream ground contact or at both the upstream ground contact and the high-voltage emitter contact in an electrospray ion source was shown to provide for new types of electrochemical experiments utilizing only the electrochemistry inherent to electrospray. The normal stainless steel bore-through union serving as the upstream grounding point in a floated electrospray emitter system was replaced with a high surface area porous flow-through electrode assembly to achieve effective electrochemical reduction of analytes at this point in positive ion mode, and effective electrochemical oxidation of analytes in negative ion mode. This was demonstrated by the oxidation of 3,4-dihydroxybenzoic acid and reserpine in negative ion mode and by the reduction of thionine in positive ion mode. In the case of reversible oxidation (3,4-dihydroxybenzoic acid) and reduction (thionine) processes, partial rereduction and reoxidation of the products due to reaction with products generated by cathodic and anodic processes at the emitter were observed, respectively. By implementing two high surface area porous flow-through electrodes in the system, one as the upstream grounding point and the other as the emitter electrode, a multiple-step reaction scheme was achieved that included consecutive electrochemical reduction and oxidation reactions and a following chemical reaction as demonstrated by the hydroquinone tagging of an initially disulfide-linked peptide.