Abstract
The electrochemical sensors with the ability of biomolecule detection can be used for human life and health monitoring. In this work, we developed an electrochemical sensor with a Schottky junction by electrostatic interaction, composed of Nb2C MXene and MnFe2O4. Large reactive groups (O, OH, Cl, or F) are observed at the ends of the Nb2C MXene surface. Meanwhile, there are abundant oxygen vacancies and surfaces of MnFe2O4 which bring it favorable heterogeneous catalytic properties. Among them, the chemical self-assembly of MnFe2O4 nanoparticles on Nb2C MXene enhances the binding strength of the material through electrostatic interaction, promotes charge transfer across the interface, and modulates the electronic and nanostructural characteristics of the N-MFO (MnFe2O4/Nb2C MXene). The results demonstrate that the sensing performance of N-MFO4 for Acetaminophen (AP) and Dopamine (DA) is significantly improved compared to Nb2C MXene and MnFe2O4 modified electrodes, respectively. The obtained limits of detection (LOD) of N-MFO4 modified electrode for AP and DA being 0.079 and 0.070 μM, respectively. The combination of electrodes modified with highly active nanomaterials is supposed to build a portable electrochemical analysis system with high sensitivity, good selectivity, favorable stability, simple operation and low cost, and promote the application of electrochemical sensors in related fields.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Colloids and Surfaces A: Physicochemical and Engineering Aspects
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.