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Room-Temperature One-Pot Synthesis of pH-Responsive Pyridine-Functionalized Carbon Surfaces
[Image: see text] Carbon surfaces (glassy carbon, graphite, and boron-doped diamond) were functionalized with layers composed of linked pyridinium and pyridine moieties using simple electrochemical reduction of trifluoroacetylpyridinium. The pyridinium species was generated in situ in solution by th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061597/ https://www.ncbi.nlm.nih.gov/pubmed/37008109 http://dx.doi.org/10.1021/acsomega.2c06847 |
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author | Wilson, Isobel M. Padamati, Sandeep K. Bobitan, Antonia D. Porter, Michael J. Holt, Katherine B. |
author_facet | Wilson, Isobel M. Padamati, Sandeep K. Bobitan, Antonia D. Porter, Michael J. Holt, Katherine B. |
author_sort | Wilson, Isobel M. |
collection | PubMed |
description | [Image: see text] Carbon surfaces (glassy carbon, graphite, and boron-doped diamond) were functionalized with layers composed of linked pyridinium and pyridine moieties using simple electrochemical reduction of trifluoroacetylpyridinium. The pyridinium species was generated in situ in solution by the reaction of trifluoroacetic anhydride and pyridine precursors and underwent electrochemical reduction at −1.97 V vs Fc/Fc(+), as determined by cyclic voltammetry. The pyridine/pyridinium films were electrodeposited at room temperature, on a timescale of minutes, and were characterized using X-ray photoelectron spectroscopy. The as-prepared films have a net positive charge in aqueous solution at pH 9 and below due to the pyridinium content, confirmed by the electrochemical response of differently charged redox molecules at the functionalized surfaces. The positive charge can be enhanced further through protonation of the neutral pyridine component by controlling the solution pH. Moreover, the nitrogen–acetyl bond can be cleaved through base treatment to purposefully increase the neutral pyridine proportion of the film. This results in a surface that can be “switched” from functionally near neutral to a positive charge by treatment in basic and acidic solutions, respectively, through manipulation of the protonation state of the pyridine. The functionalization process demonstrated here is readily achievable at a fast timescale at room temperature and hence can allow for rapid screening of surface properties. Such functionalized surfaces present a means to test in isolation the specific catalytic performance of pyridinic groups toward key processes such as oxygen and CO(2) reduction. |
format | Online Article Text |
id | pubmed-10061597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100615972023-03-31 Room-Temperature One-Pot Synthesis of pH-Responsive Pyridine-Functionalized Carbon Surfaces Wilson, Isobel M. Padamati, Sandeep K. Bobitan, Antonia D. Porter, Michael J. Holt, Katherine B. ACS Omega [Image: see text] Carbon surfaces (glassy carbon, graphite, and boron-doped diamond) were functionalized with layers composed of linked pyridinium and pyridine moieties using simple electrochemical reduction of trifluoroacetylpyridinium. The pyridinium species was generated in situ in solution by the reaction of trifluoroacetic anhydride and pyridine precursors and underwent electrochemical reduction at −1.97 V vs Fc/Fc(+), as determined by cyclic voltammetry. The pyridine/pyridinium films were electrodeposited at room temperature, on a timescale of minutes, and were characterized using X-ray photoelectron spectroscopy. The as-prepared films have a net positive charge in aqueous solution at pH 9 and below due to the pyridinium content, confirmed by the electrochemical response of differently charged redox molecules at the functionalized surfaces. The positive charge can be enhanced further through protonation of the neutral pyridine component by controlling the solution pH. Moreover, the nitrogen–acetyl bond can be cleaved through base treatment to purposefully increase the neutral pyridine proportion of the film. This results in a surface that can be “switched” from functionally near neutral to a positive charge by treatment in basic and acidic solutions, respectively, through manipulation of the protonation state of the pyridine. The functionalization process demonstrated here is readily achievable at a fast timescale at room temperature and hence can allow for rapid screening of surface properties. Such functionalized surfaces present a means to test in isolation the specific catalytic performance of pyridinic groups toward key processes such as oxygen and CO(2) reduction. American Chemical Society 2023-03-17 /pmc/articles/PMC10061597/ /pubmed/37008109 http://dx.doi.org/10.1021/acsomega.2c06847 Text en © 2023 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 | Wilson, Isobel M. Padamati, Sandeep K. Bobitan, Antonia D. Porter, Michael J. Holt, Katherine B. Room-Temperature One-Pot Synthesis of pH-Responsive Pyridine-Functionalized Carbon Surfaces |
title | Room-Temperature
One-Pot Synthesis of pH-Responsive
Pyridine-Functionalized Carbon Surfaces |
title_full | Room-Temperature
One-Pot Synthesis of pH-Responsive
Pyridine-Functionalized Carbon Surfaces |
title_fullStr | Room-Temperature
One-Pot Synthesis of pH-Responsive
Pyridine-Functionalized Carbon Surfaces |
title_full_unstemmed | Room-Temperature
One-Pot Synthesis of pH-Responsive
Pyridine-Functionalized Carbon Surfaces |
title_short | Room-Temperature
One-Pot Synthesis of pH-Responsive
Pyridine-Functionalized Carbon Surfaces |
title_sort | room-temperature
one-pot synthesis of ph-responsive
pyridine-functionalized carbon surfaces |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061597/ https://www.ncbi.nlm.nih.gov/pubmed/37008109 http://dx.doi.org/10.1021/acsomega.2c06847 |
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