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Carbon Nanotube PtSn Nanoparticles for Enhanced Complete Biocatalytic Oxidation of Ethylene Glycol in Biofuel Cells
[Image: see text] We report a hybrid catalytic system containing metallic PtSn nanoparticles deposited on multiwalled carbon nanotubes (Pt(65)Sn(35)/MWCNTs), prepared by the microwave-assisted method, coupled to the enzyme oxalate oxidase (OxOx) for complete ethylene glycol (EG) electrooxidation. Pt...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9888613/ https://www.ncbi.nlm.nih.gov/pubmed/36855769 http://dx.doi.org/10.1021/acsmaterialsau.1c00029 |
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author | Antonio, Jesimiel Glaycon Rodrigues Franco, Jefferson Honorio Almeida, Paula Z. Almeida, Thiago S. Teixeira de Morais Polizeli, Maria de Lourdes Minteer, Shelley D. Rodrigues de Andrade, Adalgisa |
author_facet | Antonio, Jesimiel Glaycon Rodrigues Franco, Jefferson Honorio Almeida, Paula Z. Almeida, Thiago S. Teixeira de Morais Polizeli, Maria de Lourdes Minteer, Shelley D. Rodrigues de Andrade, Adalgisa |
author_sort | Antonio, Jesimiel Glaycon Rodrigues |
collection | PubMed |
description | [Image: see text] We report a hybrid catalytic system containing metallic PtSn nanoparticles deposited on multiwalled carbon nanotubes (Pt(65)Sn(35)/MWCNTs), prepared by the microwave-assisted method, coupled to the enzyme oxalate oxidase (OxOx) for complete ethylene glycol (EG) electrooxidation. Pt(65)Sn(35)/MWCNTs, without OxOx, showed good electrochemical activity toward EG oxidation and all the byproducts. Pt(65)Sn(35)/MWCNTs cleaved the glyoxilic acid C–C bond, producing CO(2) and formic acid, which was further oxidized at the electrode. Concerning EG oxidation, the catalytic activity of the hybrid system (Pt(65)Sn(35)/MWCNTs+OxOx) was twice the catalytic activity of Pt(65)Sn(35)/MWCNTs. Long-term electrolysis revealed that Pt(65)Sn(35)/MWCNTs+OxOx was much more active for EG oxidation than Pt(65)Sn(35)/MWCNTs: the charge increased by 65%. The chromatographic results proved that Pt(65)Sn(35)/MWCNTs+OxOx collected all of the 10 electrons per molecule of the fuel and was able to catalyze EG oxidation to CO(2) due to the associative oxidation between the metallic nanoparticles and the enzymatic pathway. Overall, Pt(65)Sn(35)/MWCNTs+OxOx proved to be a promising system to enhance the development of enzymatic biofuel cells for further application in the bioelectrochemistry field. |
format | Online Article Text |
id | pubmed-9888613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98886132023-02-27 Carbon Nanotube PtSn Nanoparticles for Enhanced Complete Biocatalytic Oxidation of Ethylene Glycol in Biofuel Cells Antonio, Jesimiel Glaycon Rodrigues Franco, Jefferson Honorio Almeida, Paula Z. Almeida, Thiago S. Teixeira de Morais Polizeli, Maria de Lourdes Minteer, Shelley D. Rodrigues de Andrade, Adalgisa ACS Mater Au [Image: see text] We report a hybrid catalytic system containing metallic PtSn nanoparticles deposited on multiwalled carbon nanotubes (Pt(65)Sn(35)/MWCNTs), prepared by the microwave-assisted method, coupled to the enzyme oxalate oxidase (OxOx) for complete ethylene glycol (EG) electrooxidation. Pt(65)Sn(35)/MWCNTs, without OxOx, showed good electrochemical activity toward EG oxidation and all the byproducts. Pt(65)Sn(35)/MWCNTs cleaved the glyoxilic acid C–C bond, producing CO(2) and formic acid, which was further oxidized at the electrode. Concerning EG oxidation, the catalytic activity of the hybrid system (Pt(65)Sn(35)/MWCNTs+OxOx) was twice the catalytic activity of Pt(65)Sn(35)/MWCNTs. Long-term electrolysis revealed that Pt(65)Sn(35)/MWCNTs+OxOx was much more active for EG oxidation than Pt(65)Sn(35)/MWCNTs: the charge increased by 65%. The chromatographic results proved that Pt(65)Sn(35)/MWCNTs+OxOx collected all of the 10 electrons per molecule of the fuel and was able to catalyze EG oxidation to CO(2) due to the associative oxidation between the metallic nanoparticles and the enzymatic pathway. Overall, Pt(65)Sn(35)/MWCNTs+OxOx proved to be a promising system to enhance the development of enzymatic biofuel cells for further application in the bioelectrochemistry field. American Chemical Society 2021-10-18 /pmc/articles/PMC9888613/ /pubmed/36855769 http://dx.doi.org/10.1021/acsmaterialsau.1c00029 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Antonio, Jesimiel Glaycon Rodrigues Franco, Jefferson Honorio Almeida, Paula Z. Almeida, Thiago S. Teixeira de Morais Polizeli, Maria de Lourdes Minteer, Shelley D. Rodrigues de Andrade, Adalgisa Carbon Nanotube PtSn Nanoparticles for Enhanced Complete Biocatalytic Oxidation of Ethylene Glycol in Biofuel Cells |
title | Carbon Nanotube PtSn Nanoparticles for Enhanced Complete
Biocatalytic Oxidation of Ethylene Glycol in Biofuel Cells |
title_full | Carbon Nanotube PtSn Nanoparticles for Enhanced Complete
Biocatalytic Oxidation of Ethylene Glycol in Biofuel Cells |
title_fullStr | Carbon Nanotube PtSn Nanoparticles for Enhanced Complete
Biocatalytic Oxidation of Ethylene Glycol in Biofuel Cells |
title_full_unstemmed | Carbon Nanotube PtSn Nanoparticles for Enhanced Complete
Biocatalytic Oxidation of Ethylene Glycol in Biofuel Cells |
title_short | Carbon Nanotube PtSn Nanoparticles for Enhanced Complete
Biocatalytic Oxidation of Ethylene Glycol in Biofuel Cells |
title_sort | carbon nanotube ptsn nanoparticles for enhanced complete
biocatalytic oxidation of ethylene glycol in biofuel cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9888613/ https://www.ncbi.nlm.nih.gov/pubmed/36855769 http://dx.doi.org/10.1021/acsmaterialsau.1c00029 |
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