Activity of carbon supported Pt3Ru2 nanocatalyst in CO oxidation

The electrocatalytic activity of Pt3Ru2/C nanocatalyst toward the electro-oxidation of bulk CO was examined in acid and alkaline solution at ambient temperature using the thin-film, rotating disk electrode (RDE) method. The catalyst was characterized by XRD analysis. The XRD pattern revealed that th...

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Main Authors: Popović Ksenija Đ., Lović Jelena D., Tripković Amalija V., Olszewski Piotr K.
Format: Article
Language:English
Published: Serbian Chemical Society 2009-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
xrd
Online Access:http://www.doiserbia.nb.rs/img/doi/0352-5139/2009/0352-51390909965P.pdf
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spelling doaj-3a66107b1eda44508637b130990f30e92020-12-30T07:57:52ZengSerbian Chemical Society Journal of the Serbian Chemical Society0352-51391820-74212009-01-01748-996597510.2298/JSC0909965P0352-51390909965PActivity of carbon supported Pt3Ru2 nanocatalyst in CO oxidationPopović Ksenija Đ.0Lović Jelena D.1Tripković Amalija V.2Olszewski Piotr K.3IHTM - Centar za elektrohemiju, BeogradIHTM - Centar za elektrohemiju, BeogradIHTM - Centar za elektrohemiju, BeogradInstitute of Catalysis and Surface Chemistry, Polish Academy of Sciences, Krakow, PolandThe electrocatalytic activity of Pt3Ru2/C nanocatalyst toward the electro-oxidation of bulk CO was examined in acid and alkaline solution at ambient temperature using the thin-film, rotating disk electrode (RDE) method. The catalyst was characterized by XRD analysis. The XRD pattern revealed that the Pt3Ru2/C catalyst consisted of two structures, i.e., Pt-Ru-fcc and Ruhcp (a solid solution of Ru in Pt and a small amount of Ru or a solid solution of Pt in Ru). Electrocatalytic activities were measured by applying potentiodynamic and steady state techniques. The oxidation of CO on the Pt3Ru2/C catalyst was influenced by pH and anions from the supporting electrolytes. The Pt3Ru2/C was more active in alkaline than in acid solution, as well as in perchloric than in sulfuric acid. Comparison of CO oxidation on Pt3Ru2/C and Pt/C revealed that the Pt3Ru2/C was more active than Pt/C in acid solution, while both catalysts had a similar activity in alkaline solution.http://www.doiserbia.nb.rs/img/doi/0352-5139/2009/0352-51390909965P.pdfco oxidationpt3ru2/c nanocatalystxrdph effectanion effect
collection DOAJ
language English
format Article
sources DOAJ
author Popović Ksenija Đ.
Lović Jelena D.
Tripković Amalija V.
Olszewski Piotr K.
spellingShingle Popović Ksenija Đ.
Lović Jelena D.
Tripković Amalija V.
Olszewski Piotr K.
Activity of carbon supported Pt3Ru2 nanocatalyst in CO oxidation
Journal of the Serbian Chemical Society
co oxidation
pt3ru2/c nanocatalyst
xrd
ph effect
anion effect
author_facet Popović Ksenija Đ.
Lović Jelena D.
Tripković Amalija V.
Olszewski Piotr K.
author_sort Popović Ksenija Đ.
title Activity of carbon supported Pt3Ru2 nanocatalyst in CO oxidation
title_short Activity of carbon supported Pt3Ru2 nanocatalyst in CO oxidation
title_full Activity of carbon supported Pt3Ru2 nanocatalyst in CO oxidation
title_fullStr Activity of carbon supported Pt3Ru2 nanocatalyst in CO oxidation
title_full_unstemmed Activity of carbon supported Pt3Ru2 nanocatalyst in CO oxidation
title_sort activity of carbon supported pt3ru2 nanocatalyst in co oxidation
publisher Serbian Chemical Society
series Journal of the Serbian Chemical Society
issn 0352-5139
1820-7421
publishDate 2009-01-01
description The electrocatalytic activity of Pt3Ru2/C nanocatalyst toward the electro-oxidation of bulk CO was examined in acid and alkaline solution at ambient temperature using the thin-film, rotating disk electrode (RDE) method. The catalyst was characterized by XRD analysis. The XRD pattern revealed that the Pt3Ru2/C catalyst consisted of two structures, i.e., Pt-Ru-fcc and Ruhcp (a solid solution of Ru in Pt and a small amount of Ru or a solid solution of Pt in Ru). Electrocatalytic activities were measured by applying potentiodynamic and steady state techniques. The oxidation of CO on the Pt3Ru2/C catalyst was influenced by pH and anions from the supporting electrolytes. The Pt3Ru2/C was more active in alkaline than in acid solution, as well as in perchloric than in sulfuric acid. Comparison of CO oxidation on Pt3Ru2/C and Pt/C revealed that the Pt3Ru2/C was more active than Pt/C in acid solution, while both catalysts had a similar activity in alkaline solution.
topic co oxidation
pt3ru2/c nanocatalyst
xrd
ph effect
anion effect
url http://www.doiserbia.nb.rs/img/doi/0352-5139/2009/0352-51390909965P.pdf
work_keys_str_mv AT popovicksenijađ activityofcarbonsupportedpt3ru2nanocatalystincooxidation
AT lovicjelenad activityofcarbonsupportedpt3ru2nanocatalystincooxidation
AT tripkovicamalijav activityofcarbonsupportedpt3ru2nanocatalystincooxidation
AT olszewskipiotrk activityofcarbonsupportedpt3ru2nanocatalystincooxidation
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