Electrochemical determination of nitrite at a bare glassy carbon electrode; why chemically modify electrodes?
The oxidation of nitrite was studied at a bare glassy carbon (GC) electrode in aqueous solution using cyclic voltammetry, square wave voltammetry and chronoamperometry. A mechanism for the electrode reaction is proposed. A limit of detection (LOD) of 4 × 1 0- 7 M was obtained for amperometry and thi...
Main Authors: | , , |
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Format: | Journal article |
Language: | English |
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2010
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_version_ | 1797077014266511360 |
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author | Kozub, B Rees, N Compton, R |
author_facet | Kozub, B Rees, N Compton, R |
author_sort | Kozub, B |
collection | OXFORD |
description | The oxidation of nitrite was studied at a bare glassy carbon (GC) electrode in aqueous solution using cyclic voltammetry, square wave voltammetry and chronoamperometry. A mechanism for the electrode reaction is proposed. A limit of detection (LOD) of 4 × 1 0- 7 M was obtained for amperometry and this is evaluated with reference to literature reports for NO2- detection; in particular, the possible merits of using chemically modified electrodes as compared to 'bare' unmodified electrodes are critically assessed. © 2009 Elsevier B.V. All rights reserved. |
first_indexed | 2024-03-07T00:11:42Z |
format | Journal article |
id | oxford-uuid:7974d673-2607-41c9-9fc0-a1ca4c70e6af |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T00:11:42Z |
publishDate | 2010 |
record_format | dspace |
spelling | oxford-uuid:7974d673-2607-41c9-9fc0-a1ca4c70e6af2022-03-26T20:37:34ZElectrochemical determination of nitrite at a bare glassy carbon electrode; why chemically modify electrodes?Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7974d673-2607-41c9-9fc0-a1ca4c70e6afEnglishSymplectic Elements at Oxford2010Kozub, BRees, NCompton, RThe oxidation of nitrite was studied at a bare glassy carbon (GC) electrode in aqueous solution using cyclic voltammetry, square wave voltammetry and chronoamperometry. A mechanism for the electrode reaction is proposed. A limit of detection (LOD) of 4 × 1 0- 7 M was obtained for amperometry and this is evaluated with reference to literature reports for NO2- detection; in particular, the possible merits of using chemically modified electrodes as compared to 'bare' unmodified electrodes are critically assessed. © 2009 Elsevier B.V. All rights reserved. |
spellingShingle | Kozub, B Rees, N Compton, R Electrochemical determination of nitrite at a bare glassy carbon electrode; why chemically modify electrodes? |
title | Electrochemical determination of nitrite at a bare glassy carbon electrode; why chemically modify electrodes? |
title_full | Electrochemical determination of nitrite at a bare glassy carbon electrode; why chemically modify electrodes? |
title_fullStr | Electrochemical determination of nitrite at a bare glassy carbon electrode; why chemically modify electrodes? |
title_full_unstemmed | Electrochemical determination of nitrite at a bare glassy carbon electrode; why chemically modify electrodes? |
title_short | Electrochemical determination of nitrite at a bare glassy carbon electrode; why chemically modify electrodes? |
title_sort | electrochemical determination of nitrite at a bare glassy carbon electrode why chemically modify electrodes |
work_keys_str_mv | AT kozubb electrochemicaldeterminationofnitriteatabareglassycarbonelectrodewhychemicallymodifyelectrodes AT reesn electrochemicaldeterminationofnitriteatabareglassycarbonelectrodewhychemicallymodifyelectrodes AT comptonr electrochemicaldeterminationofnitriteatabareglassycarbonelectrodewhychemicallymodifyelectrodes |