Abstract

An efficient photoactive spinel NiFe2O4 nanoflakes (NFO NFs) was successfully prepared and integrated into an electrochemical sensor for the sensitive determination of Azithromycin (AZM) under visible light illumination. With the introduction of 532 nm laser illumination, NFO NFs could be easily excited and induce the charge-separation state with electrons in the conduction band and holes in the valence band. Upon illumination, the low band gap value in combination with edge-to-flat-surface/edge-to-edge conjunctions of NFO NFs could form the electron transfer pathway for transferring photogenerated electron-hole pairs to the AZM analyte-NFO electrode interface. Hence, the fabricated visible light-assisted NFO-based electrochemical sensor shows remarkable enhanced analytical performance, with calculated values of electron transfer rate constant, adsorption capacity, diffusion coefficient, and catalytic rate constant under visible light illumination of 1.29, 1.27, 2.08, and 3.40 times higher than in the dark condition, respectively. As a result, the NFO-based electrochemical sensing platform in the presence of visible light illumination possessed a high electrochemical sensitivity of 0.070 μA μM−1 in a wide linear dynamic range of 2.5–150 μM and a detection limit of 1.67 μM and also exhibited excellent anti-interference ability, repeatability, storage stability, reproducibility, and practical feasibility for AZM detection in pharmaceutical tablets.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.