Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019001002095 |
Resumo: | Herein we sinthesize and investigate Ir-based nanocatalysts (dispersed in carbon) in different atomic compositions combining two (IrRh) and three metals (IrRhSn). These materials were evaluated towards the ethanol electrooxidation in acidic electrolyte in presence of three ethanol concentrations using cyclic voltammetry, while the species produced during the reaction were monitored by in situ Fourier transform infrared spectroscopy (FTIR). Results show that IrRh binary electrocatalysts are selective to the production of CO2 from ethanol, but the catalytic activity is poor. This finding is interpreted in terms of a slow adsorption of ethanol that is assumed to be the rate determining step during the electrooxidation of the alcohol. Ternary catalysts, in turn, present higher electrooxidation currents and anticipate the production of CO2. However, the selectivity towards the CO2 pathway is lost and the higher catalityc activity is justified by a growing production of acetic acid, illustrating the influence of Sn on the eletrooxidation of ethanol. |
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Journal of the Brazilian Chemical Society (Online) |
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Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Mediaethanol electrooxidationelectrocatalysisIrRhSn nanoparticlein situ FTIRHerein we sinthesize and investigate Ir-based nanocatalysts (dispersed in carbon) in different atomic compositions combining two (IrRh) and three metals (IrRhSn). These materials were evaluated towards the ethanol electrooxidation in acidic electrolyte in presence of three ethanol concentrations using cyclic voltammetry, while the species produced during the reaction were monitored by in situ Fourier transform infrared spectroscopy (FTIR). Results show that IrRh binary electrocatalysts are selective to the production of CO2 from ethanol, but the catalytic activity is poor. This finding is interpreted in terms of a slow adsorption of ethanol that is assumed to be the rate determining step during the electrooxidation of the alcohol. Ternary catalysts, in turn, present higher electrooxidation currents and anticipate the production of CO2. However, the selectivity towards the CO2 pathway is lost and the higher catalityc activity is justified by a growing production of acetic acid, illustrating the influence of Sn on the eletrooxidation of ethanol.Sociedade Brasileira de Química2019-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019001002095Journal of the Brazilian Chemical Society v.30 n.10 2019reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20190072info:eu-repo/semantics/openAccessSilva,Fabiano R. P. daSilva-Junior,Luiz C.Camara,Giuseppe A.Giz,Martha Janeteeng2019-10-17T00:00:00Zoai:scielo:S0103-50532019001002095Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2019-10-17T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media |
title |
Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media |
spellingShingle |
Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media Silva,Fabiano R. P. da ethanol electrooxidation electrocatalysis IrRhSn nanoparticle in situ FTIR |
title_short |
Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media |
title_full |
Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media |
title_fullStr |
Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media |
title_full_unstemmed |
Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media |
title_sort |
Iridium-Based Catalysts for the Ethanol Electrooxidation in Acidic Media |
author |
Silva,Fabiano R. P. da |
author_facet |
Silva,Fabiano R. P. da Silva-Junior,Luiz C. Camara,Giuseppe A. Giz,Martha Janete |
author_role |
author |
author2 |
Silva-Junior,Luiz C. Camara,Giuseppe A. Giz,Martha Janete |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Silva,Fabiano R. P. da Silva-Junior,Luiz C. Camara,Giuseppe A. Giz,Martha Janete |
dc.subject.por.fl_str_mv |
ethanol electrooxidation electrocatalysis IrRhSn nanoparticle in situ FTIR |
topic |
ethanol electrooxidation electrocatalysis IrRhSn nanoparticle in situ FTIR |
description |
Herein we sinthesize and investigate Ir-based nanocatalysts (dispersed in carbon) in different atomic compositions combining two (IrRh) and three metals (IrRhSn). These materials were evaluated towards the ethanol electrooxidation in acidic electrolyte in presence of three ethanol concentrations using cyclic voltammetry, while the species produced during the reaction were monitored by in situ Fourier transform infrared spectroscopy (FTIR). Results show that IrRh binary electrocatalysts are selective to the production of CO2 from ethanol, but the catalytic activity is poor. This finding is interpreted in terms of a slow adsorption of ethanol that is assumed to be the rate determining step during the electrooxidation of the alcohol. Ternary catalysts, in turn, present higher electrooxidation currents and anticipate the production of CO2. However, the selectivity towards the CO2 pathway is lost and the higher catalityc activity is justified by a growing production of acetic acid, illustrating the influence of Sn on the eletrooxidation of ethanol. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-10-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019001002095 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019001002095 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.21577/0103-5053.20190072 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.30 n.10 2019 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
_version_ |
1750318182167478272 |