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Spectroelectrochemistry with Ultrathin Ion-Selective Membranes: Three Distinct Ranges for Analytical Sensing
[Image: see text] We present spectroelectrochemical sensing of the potassium ion (K(+)) at three very distinct analytical ranges—nanomolar, micromolar, and millimolar—when using the same ion-selective electrode (ISE) but interrogated under various regimes. The ISE is conceived in the all-solid-state...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9244873/ https://www.ncbi.nlm.nih.gov/pubmed/35687727 http://dx.doi.org/10.1021/acs.analchem.2c01584 |
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author | Liu, Yujie Crespo, Gastón A. Cuartero, María |
author_facet | Liu, Yujie Crespo, Gastón A. Cuartero, María |
author_sort | Liu, Yujie |
collection | PubMed |
description | [Image: see text] We present spectroelectrochemical sensing of the potassium ion (K(+)) at three very distinct analytical ranges—nanomolar, micromolar, and millimolar—when using the same ion-selective electrode (ISE) but interrogated under various regimes. The ISE is conceived in the all-solid-state format: an ITO glass modified with the conducting polymer poly(3-octylethiophene) (POT) and an ultrathin potassium-selective membrane. The experimental setup is designed to apply a potential in a three-electrode electrochemical cell with the ISE as the working electrode, while dynamic spectral changes in the POT film are simultaneously registered. The POT film is gradually oxidized to POT(+), and this process is ultimately linked to K(+) transfer at the membrane-sample interface, attending to electroneutrality requirements. The spectroelectrochemistry experiment provides two signals: a voltammetric peak and a transient absorbance response, with the latter of special interest because of its correspondence with the generated charge in the POT and thus with the ionic charge expelled from the membrane. By modifying how the ion analyte (K(+) but also others) is initially accumulated into the membrane, we found three ranges of response for the absorbance: 10–950 nM for an accumulation-stripping protocol, 0.5–10 μM in diffusion-controlled cyclic voltammetry, and 0.5–32 mM with thin-layer cyclic voltammetry. This wide response range is a unique feature, one that is rare to find for a sensor and indeed for any analytical technique. Accordingly, the developed sensor is highly appealing for many analytical applications, especially considering the versatility of samples and ion analytes that may be spotted. |
format | Online Article Text |
id | pubmed-9244873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92448732022-07-01 Spectroelectrochemistry with Ultrathin Ion-Selective Membranes: Three Distinct Ranges for Analytical Sensing Liu, Yujie Crespo, Gastón A. Cuartero, María Anal Chem [Image: see text] We present spectroelectrochemical sensing of the potassium ion (K(+)) at three very distinct analytical ranges—nanomolar, micromolar, and millimolar—when using the same ion-selective electrode (ISE) but interrogated under various regimes. The ISE is conceived in the all-solid-state format: an ITO glass modified with the conducting polymer poly(3-octylethiophene) (POT) and an ultrathin potassium-selective membrane. The experimental setup is designed to apply a potential in a three-electrode electrochemical cell with the ISE as the working electrode, while dynamic spectral changes in the POT film are simultaneously registered. The POT film is gradually oxidized to POT(+), and this process is ultimately linked to K(+) transfer at the membrane-sample interface, attending to electroneutrality requirements. The spectroelectrochemistry experiment provides two signals: a voltammetric peak and a transient absorbance response, with the latter of special interest because of its correspondence with the generated charge in the POT and thus with the ionic charge expelled from the membrane. By modifying how the ion analyte (K(+) but also others) is initially accumulated into the membrane, we found three ranges of response for the absorbance: 10–950 nM for an accumulation-stripping protocol, 0.5–10 μM in diffusion-controlled cyclic voltammetry, and 0.5–32 mM with thin-layer cyclic voltammetry. This wide response range is a unique feature, one that is rare to find for a sensor and indeed for any analytical technique. Accordingly, the developed sensor is highly appealing for many analytical applications, especially considering the versatility of samples and ion analytes that may be spotted. American Chemical Society 2022-06-10 2022-06-28 /pmc/articles/PMC9244873/ /pubmed/35687727 http://dx.doi.org/10.1021/acs.analchem.2c01584 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Liu, Yujie Crespo, Gastón A. Cuartero, María Spectroelectrochemistry with Ultrathin Ion-Selective Membranes: Three Distinct Ranges for Analytical Sensing |
title | Spectroelectrochemistry with Ultrathin Ion-Selective
Membranes: Three Distinct Ranges for Analytical Sensing |
title_full | Spectroelectrochemistry with Ultrathin Ion-Selective
Membranes: Three Distinct Ranges for Analytical Sensing |
title_fullStr | Spectroelectrochemistry with Ultrathin Ion-Selective
Membranes: Three Distinct Ranges for Analytical Sensing |
title_full_unstemmed | Spectroelectrochemistry with Ultrathin Ion-Selective
Membranes: Three Distinct Ranges for Analytical Sensing |
title_short | Spectroelectrochemistry with Ultrathin Ion-Selective
Membranes: Three Distinct Ranges for Analytical Sensing |
title_sort | spectroelectrochemistry with ultrathin ion-selective
membranes: three distinct ranges for analytical sensing |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9244873/ https://www.ncbi.nlm.nih.gov/pubmed/35687727 http://dx.doi.org/10.1021/acs.analchem.2c01584 |
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