Please use this identifier to cite or link to this item: https://cris.library.msu.ac.zw//handle/11408/4707
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dc.contributor.authorMurinzi, Tafadzwa W.-
dc.contributor.authorWatkins, Gareth M.-
dc.contributor.authorShumba, Munyaradzi-
dc.contributor.authorNyokong, Tebello-
dc.date.accessioned2022-03-17T09:17:48Z-
dc.date.available2022-03-17T09:17:48Z-
dc.date.issued2021-
dc.identifier.issn0095-8972-
dc.identifier.issn1029-0389-
dc.identifier.urihttps://doi.org/10.1080/00958972.2021.1907573-
dc.identifier.urihttp://hdl.handle.net/11408/4707-
dc.description.abstractGlass carbon electrodes (GCE) were modified with metal organic frameworks (MOFs) containing molybdenum polyoxometallates (Mo POMs) in a copper benzene tricarboxylate framework (HKUST-1). The Mo POMs were introduced via one-pot synthesis (Mo2) and post-synthetic modification (Mo1) techniques. The electrode modifiers were characterized by powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and thermal analysis. The modified electrodes’ oxidation capacity toward l-cysteine was studied. Mo POMs significantly improved electron transfer kinetics compared to the bare GCE. The best Mo POM doped electrode (Mo1-GCE) had a catalytic rate constant of 2.2 × 104 M−1 s−1 and a limit of detection of 3.07 × 10−7 M. Under the employed experimental conditions, the detection response for l-cysteine was very fast (within 0.1 s) for all the modified electrodes and selective toward l-cysteine in the presence of other amino acids.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.relation.ispartofseriesJournal of Coordination Chemistry;Vol. 74; No. 9-10: p. 1730-1748-
dc.subjectGlass carbon electrodesen_US
dc.subjectMetal organic frameworksen_US
dc.titleElectrocatalytic detection of l-cysteine using molybdenum POM doped-HKUST-1 metal organic frameworksen_US
dc.typeArticleen_US
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypeArticle-
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