Abstract

A kinetic framework is introduced for a pseudocapacitive potentiometric biosensor. Mathematical derivation and kinetic modeling demonstrate that experimentally observed linearity in analyte-OCP response arises from a dynamic equilibrium between competing redox reactions on a single electrode. This system can be expanded to develop a new generation of biosensors.

Department(s)

Chemistry

Publication Status

Open Access

International Standard Serial Number (ISSN)

1364-548X; 1359-7345

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2025 Royal Society of Chemistry, All rights reserved.

Publication Date

01 Jan 2025

Included in

Chemistry Commons

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