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dc.contributor.authorLee, SHen_US
dc.contributor.authorFang, HYen_US
dc.contributor.authorChen, WCen_US
dc.contributor.authorLin, HMen_US
dc.contributor.authorChang, CAen_US
dc.date.accessioned2014-12-08T15:18:19Z-
dc.date.available2014-12-08T15:18:19Z-
dc.date.issued2005-10-01en_US
dc.identifier.issn1618-2642en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s00216-005-0034-5en_US
dc.identifier.urihttp://hdl.handle.net/11536/13212-
dc.description.abstractThe remarkable enhancement of electron transfer on screen-printed carbon electrodes (SPCEs) with modification by iron nanoparticles (Fe-nano), coupled with Fe(CN)(6)(4-/3-) redox species, was characterized with an increase of electroactive area (A(ea)) at electrode surface together with a decrease of heterogeneous. electron transfer rate constant (k degrees) in the system. Hence, Fe-nano-Fe(CN)(6)(3-) SPCEs with deposition of glucose oxidase (GOD) demonstrated a higher sensitivity to various glucose concentrations than Fe(CN)(6)(3-)/GOD-deposited SPCEs. In addition, an inhibited diffusion current from cyclic voltammograms was also observed with an increase in redox concentration and complicated the estimation of A(ea). Further analysis by the electrochemical impedance method, it was shown that this effect might be resulted from the electrode surface blocking by the products of activated complex decomposition.en_US
dc.language.isoen_USen_US
dc.subjectheterogeneous electron transfer rate constanten_US
dc.subjectelectroactive areaen_US
dc.subjectscreen-printed carbon electrodeen_US
dc.subjectiron nanoparticlesen_US
dc.subjectFe(CN)(6) (4-/3) redox coupleen_US
dc.titleElectrochemical study on screen-printed carbon electrodes with modification by iron nanoparticles in Fe(CN)(6)(4-/3-) redox systemen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s00216-005-0034-5en_US
dc.identifier.journalANALYTICAL AND BIOANALYTICAL CHEMISTRYen_US
dc.citation.volume383en_US
dc.citation.issue3en_US
dc.citation.spage532en_US
dc.citation.epage538en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000233457800024-
dc.citation.woscount4-
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