A Sensitive and Selective Non-Enzymatic Dopamine Sensor Based on Nanostructured Co3O4–Fe2O3 Heterojunctions

Author:

Khan Madiha12,Abid Khouloud13,Ferlazzo Angelo1ORCID,Bressi Viviana1ORCID,Espro Claudia1,Hussain Mozaffar2,Foti Antonino3,Gucciardi Pietro Giuseppe3ORCID,Neri Giovanni1ORCID

Affiliation:

1. Department of Engineering, University of Messina, C.da Di Dio, I-98166 Messina, Italy

2. Department of Physics, Air University, PAF Complex, E-9, Islamabad 4400, Pakistan

3. CNR IPCF Istituto per i Processi Chimico-Fisici, Viale F. Stagno D’Alcontres 37, I-98156 Messina, Italy

Abstract

In the present work, a study was carried out with the aim of enhancing the performance of electrochemical biosensors based on Co3O4:Fe2O3 heterojunctions. Specifically, the redox behavior of screen–printed carbon electrodes (SPCEs) modified with Co3O4:Fe2O3 (0.5 wt%:x wt%) nanocomposites, where x ranged from 0.1 to 0.5 wt%, was examined in detail. The hybrid nanocomposites were synthesized using the sol-gel auto-combustion method. Several characterization methods were performed to investigate the morphology, microstructure, and surface area of the pure Co3O4, pure Fe2O3, and the synthesized Co3O4:Fe2O3 nanocomposites. Using cyclic voltammetry (CV) tests, the electrochemical behavior of the modified electrodes toward the dopamine (DA) molecules was investigated. The modified Co3O4:Fe2O3, (0.5 wt%, x = 0.4 wt%)/SPCE resulted in a sensor with the best electrochemical performance toward DA. A high linear relationship between DA concentrations and the faradic current variation (ipa (μA) = 0.0736 + 0.1031 CDA (μA) and R2 = 0.99) was found in the range of 10–100 μM. The sensitivity value was computed to be 0.604 µA µM−1cm−2 and the limit of detection (LOD) 0.24 µM. Based on the characterization and electrochemical results, it can be suggested that the formation of Co3O4:Fe2O3 heterostructures provides a large specific surface area, an increased number of electroactive sites at the metal oxide interface and a p–n heterojunction, thus ensuring a remarkable enhancement in the electrochemical response towards DA.

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Analytical Chemistry

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