Author ORCID Identifier:

https://orcid.org/0009000380782638

Date of Graduation

5-2026

Document Type

Thesis

Degree Name

Master of Science in Chemistry (MS)

Degree Level

Graduate

Department

Chemistry & Biochemistry

Advisor/Mentor

Fritsch, Ingrid

Committee Member

Dong, Bin

Second Committee Member

Stenken, Julie

Keywords

Electrochemistry; Generation-Collection; Microband Electrode Arrays; Redox Monitoring

Abstract

Snapshot redox cycling voltammetry (Snapshot RCV) is introduced as a rapid electrochemical technique that reconstructs the current-potential profile of a redox active species using a microband electrode array. By simultaneously biasing individual generator electrodes alternating in the array to different voltages across the analyte’s potential range while individually holding collector electrodes at a reversing potential, “spatial” voltammetry is achieved in as little as 1 s with the temporal speed of chronoamperometry, rapidly capturing the steady-state redox cycling (RC) profiles. During RC (a mode of generation-collection), the analyte is oxidized (or reduced) at generator electrodes and converted back at neighboring collector electrodes held at a constant potential, yielding two current signals. This reveals information about diffusion-dominated systems, heterogeneous electron transfer kinetics, and following chemical reactions. Furthermore, as electrode spacing decreases, current amplifies from overlapping diffusion layers that increase concentration gradients. In contrast to conventional RC voltammetry (Conventional RCV) that slowly sweeps the generator potential, Snapshot RCV applies a distribution of potentials across individual generator electrodes instead. Snapshot RCV was validated using 0.50 mM Ru(NH3)6Cl3 in 0.10 M KCl on a seven-electrode subset of a nine-electrode gold microband chip, (NE = 7, w = 4.08 µm, wgap = 4.14 µm, length = 97.17 µm). Snapshot RCV was then applied to pure solutions of 0.50 mM dopamine (DA), 3,4-dihydroxyphenylalanine (L-DOPA), 3,4-dihydroxyphenylacetic acid (DOPAC), and ascorbic acid (AA) in artificial cerebral spinal fluid (aCSF). This applies the technique to systems where subsequent chemical reactions lower collection efficiency (DA, L-DOPA, DOPAC), or where irreversible products are generated (AA). Snapshot RCV is shown to capture the voltammetric shape for the electrochemical behavior of the analyte with an increase in collection efficiency by 10%-60% over Conventional RCV. This distinction in collection efficiencies and response shapes of biologically relevant molecules, driven by their thermodynamics, kinetics, and following chemical mechanisms could make Snapshot RCV a promising qualitative and quantitative technique, enabling rapid sensing in confined spaces.

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