Abstract
This study developed an electrochemical sensor for ascorbic acid (AA) using dendritic nanostructured (DN) bismuth/bismuth oxide thin films with oxygen-deficient (SOD) surfaces (SOD-DN Bi/Bi2O3-x thin films) that were successfully fabricated through electrodeposition on fluorine-doped tin oxide (FTO) substrates. Using cyclic voltammetry and amperometry, we assessed electrocatalytic activity in neutral media. The prepared SOD-DN Bi/Bi2O3-x thin film was used, for the first time, as electrodes in a highly sensitive and selective electrochemical AA sensor. The SOD-DN Bi/Bi2O3-x thin film with optimal characteristics was shown to be ultrasensitive in AA detection in neutral conditions, whereby high detection sensitivity ∼ 2.30 µA µM-1cm−2 over a wide range of AA concentration ∼ 0.01 µM to 1.0 mM and working potential range ∼ 0.3–1.0 V vs. SCE. The results indicate that SOD-DN Bi/Bi2O3-x can provide large amounts of active reaction sites, thereby enhancing electrocatalytic activity and electrochemical sensitivity. Due to this, it is a unique electrochemical sensor able to detect AA without interference from DA, UA, or other contaminants. A further amperometric test demonstrated that this sensor was capable of detecting AA even under conditions of dopamine and uric acid. Accordingly, the proposed sensor provides a promising avenue for developing electrochemical sensing for AA determination. This strategy introduces a novel type of high-efficiency electrocatalyst for ultrasensitive detection of medical and environmental biomarkers.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.