The detection of nitrate using in-situ copper nanoparticle deposition at a boron doped diamond electrode.
Electrochemical deposition from a 0.1 M sodium sulphate solution, containing Cu2+ (adjusted to pH 3 with hydrochloric acid) produced a well defined copper nanoparticle deposit on the surface of a boron doped diamond electrode. Changing conditions such as potential (-0.8, -1.0 and -1.2 V), time (5, 2...
| Autori principali: | , , , |
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| Natura: | Journal article |
| Lingua: | English |
| Pubblicazione: |
2005
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| _version_ | 1826278552740298752 |
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| author | Welch, C Hyde, M Banks, C Compton, R |
| author_facet | Welch, C Hyde, M Banks, C Compton, R |
| author_sort | Welch, C |
| collection | OXFORD |
| description | Electrochemical deposition from a 0.1 M sodium sulphate solution, containing Cu2+ (adjusted to pH 3 with hydrochloric acid) produced a well defined copper nanoparticle deposit on the surface of a boron doped diamond electrode. Changing conditions such as potential (-0.8, -1.0 and -1.2 V), time (5, 2 and 0.5 s) and concentration of Cu2+ (500, 250 and 100 microM) was found to give copper nanoparticles of varying size and particle density. The electrocatalytic properties of the copper surface towards nitrate reduction were explored. An in-situ copper nanoparticle production method was developed for the detection of nitrate; this involves electrodeposition, followed by linear sweep voltammetry for the reduction of nitrate and then application of a stripping potential to renew the electrode surface. The linear sweep was discovered to have homogenised the size of the nanoparticles but their number density was still dependant on the initial conditions of deposition. Some particles were still present at the surface after the stripping potential had been applied but repetitions of the procedure showed these did not have an effect on subsequent deposits. Optimisation of the method lead to applying a deposition potential of -0.8 V, at a BDD electrode for 5 s in a 0.1 M sodium sulphate solution (pH 3) containing 100 microM Cu2+ followed by a linear sweep at 1 V/s; this yielded a limit of detection of 1.5 microM nitrate. The analytical applicability of the technique was evaluated for nitrate detection in a natural mineral water sample and was found to agree well with that stated by the manufacturer. |
| first_indexed | 2024-03-06T23:45:37Z |
| format | Journal article |
| id | oxford-uuid:70ca35b5-f8ba-461d-a322-168b1fdc4104 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T23:45:37Z |
| publishDate | 2005 |
| record_format | dspace |
| spelling | oxford-uuid:70ca35b5-f8ba-461d-a322-168b1fdc41042022-03-26T19:39:33ZThe detection of nitrate using in-situ copper nanoparticle deposition at a boron doped diamond electrode.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:70ca35b5-f8ba-461d-a322-168b1fdc4104EnglishSymplectic Elements at Oxford2005Welch, CHyde, MBanks, CCompton, RElectrochemical deposition from a 0.1 M sodium sulphate solution, containing Cu2+ (adjusted to pH 3 with hydrochloric acid) produced a well defined copper nanoparticle deposit on the surface of a boron doped diamond electrode. Changing conditions such as potential (-0.8, -1.0 and -1.2 V), time (5, 2 and 0.5 s) and concentration of Cu2+ (500, 250 and 100 microM) was found to give copper nanoparticles of varying size and particle density. The electrocatalytic properties of the copper surface towards nitrate reduction were explored. An in-situ copper nanoparticle production method was developed for the detection of nitrate; this involves electrodeposition, followed by linear sweep voltammetry for the reduction of nitrate and then application of a stripping potential to renew the electrode surface. The linear sweep was discovered to have homogenised the size of the nanoparticles but their number density was still dependant on the initial conditions of deposition. Some particles were still present at the surface after the stripping potential had been applied but repetitions of the procedure showed these did not have an effect on subsequent deposits. Optimisation of the method lead to applying a deposition potential of -0.8 V, at a BDD electrode for 5 s in a 0.1 M sodium sulphate solution (pH 3) containing 100 microM Cu2+ followed by a linear sweep at 1 V/s; this yielded a limit of detection of 1.5 microM nitrate. The analytical applicability of the technique was evaluated for nitrate detection in a natural mineral water sample and was found to agree well with that stated by the manufacturer. |
| spellingShingle | Welch, C Hyde, M Banks, C Compton, R The detection of nitrate using in-situ copper nanoparticle deposition at a boron doped diamond electrode. |
| title | The detection of nitrate using in-situ copper nanoparticle deposition at a boron doped diamond electrode. |
| title_full | The detection of nitrate using in-situ copper nanoparticle deposition at a boron doped diamond electrode. |
| title_fullStr | The detection of nitrate using in-situ copper nanoparticle deposition at a boron doped diamond electrode. |
| title_full_unstemmed | The detection of nitrate using in-situ copper nanoparticle deposition at a boron doped diamond electrode. |
| title_short | The detection of nitrate using in-situ copper nanoparticle deposition at a boron doped diamond electrode. |
| title_sort | detection of nitrate using in situ copper nanoparticle deposition at a boron doped diamond electrode |
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