Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method
Autor(a) principal: | |
---|---|
Data de Publicação: | 2017 |
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=S0103-50532017000601091 |
Resumo: | Different mass ratio proportions of PtSn (m/m) electrocatalysts with 20% metal loading on a carbon support were prepared for use in ethanol:methanol solutions oxidation reactions. PtSn/C (3:1) (91% alloy degree, lattice parameter of 0.399 nm and mean crystallite size 4.8 nm) presented the best activity for oxidation of mixed solutions. The highest normalized current (ethanol:methanol 80:20) was 4.2 mA mgPt-1 (measured after 1800 seconds at 0.5 V). Therefore, the PtSn/C (3:1) electrocatalyst with an atomic ratio of 65:35 enhanced both the electronic effect and bifunctional mechanism in (ethanol:methanol 80:20), which resulted in the formation of CO2 at low potentials, as well as the highest amount of by-products than ethanol and methanol. |
id |
SBQ-2_7a0882d922da107121a52dbe02d3e400 |
---|---|
oai_identifier_str |
oai:scielo:S0103-50532017000601091 |
network_acronym_str |
SBQ-2 |
network_name_str |
Journal of the Brazilian Chemical Society (Online) |
repository_id_str |
|
spelling |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor MethodelectrooxidationPtSn/CelectrocatalystsFTIR-ATR in situethanol:methanol solutionsDifferent mass ratio proportions of PtSn (m/m) electrocatalysts with 20% metal loading on a carbon support were prepared for use in ethanol:methanol solutions oxidation reactions. PtSn/C (3:1) (91% alloy degree, lattice parameter of 0.399 nm and mean crystallite size 4.8 nm) presented the best activity for oxidation of mixed solutions. The highest normalized current (ethanol:methanol 80:20) was 4.2 mA mgPt-1 (measured after 1800 seconds at 0.5 V). Therefore, the PtSn/C (3:1) electrocatalyst with an atomic ratio of 65:35 enhanced both the electronic effect and bifunctional mechanism in (ethanol:methanol 80:20), which resulted in the formation of CO2 at low potentials, as well as the highest amount of by-products than ethanol and methanol.Sociedade Brasileira de Química2017-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017000601091Journal of the Brazilian Chemical Society v.28 n.6 2017reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20160266info:eu-repo/semantics/openAccessAmorim,AlineParreira,Luanna S.Silva,Júlio César M.Santos,Mauro C. doseng2017-05-11T00:00:00Zoai:scielo:S0103-50532017000601091Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2017-05-11T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method |
title |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method |
spellingShingle |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method Amorim,Aline electrooxidation PtSn/C electrocatalysts FTIR-ATR in situ ethanol:methanol solutions |
title_short |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method |
title_full |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method |
title_fullStr |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method |
title_full_unstemmed |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method |
title_sort |
Electrooxidation of Mixed Ethanol and Methanol Solutions on PtSn/C Electrocatalysts Prepared by the Polymeric Precursor Method |
author |
Amorim,Aline |
author_facet |
Amorim,Aline Parreira,Luanna S. Silva,Júlio César M. Santos,Mauro C. dos |
author_role |
author |
author2 |
Parreira,Luanna S. Silva,Júlio César M. Santos,Mauro C. dos |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Amorim,Aline Parreira,Luanna S. Silva,Júlio César M. Santos,Mauro C. dos |
dc.subject.por.fl_str_mv |
electrooxidation PtSn/C electrocatalysts FTIR-ATR in situ ethanol:methanol solutions |
topic |
electrooxidation PtSn/C electrocatalysts FTIR-ATR in situ ethanol:methanol solutions |
description |
Different mass ratio proportions of PtSn (m/m) electrocatalysts with 20% metal loading on a carbon support were prepared for use in ethanol:methanol solutions oxidation reactions. PtSn/C (3:1) (91% alloy degree, lattice parameter of 0.399 nm and mean crystallite size 4.8 nm) presented the best activity for oxidation of mixed solutions. The highest normalized current (ethanol:methanol 80:20) was 4.2 mA mgPt-1 (measured after 1800 seconds at 0.5 V). Therefore, the PtSn/C (3:1) electrocatalyst with an atomic ratio of 65:35 enhanced both the electronic effect and bifunctional mechanism in (ethanol:methanol 80:20), which resulted in the formation of CO2 at low potentials, as well as the highest amount of by-products than ethanol and methanol. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-06-01 |
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=S0103-50532017000601091 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017000601091 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.21577/0103-5053.20160266 |
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.28 n.6 2017 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_ |
1750318179576446976 |