Pr3+ surface fraction in CePr mixed oxides determined by XPS analysis
CePr mixed oxides were previously studied as supports for Water Gas Shift catalysts, considering their promising textural and redox properties arising from the presence of a non-stoichiometric oxide. A very small Ce3+ fraction was observed on those oxides, suggesting that Pr3+ion could be responsibl...
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03682048_v222_n_p1_PoggioFraccari http://hdl.handle.net/20.500.12110/paper_03682048_v222_n_p1_PoggioFraccari |
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paper:paper_03682048_v222_n_p1_PoggioFraccari2023-06-08T15:36:12Z Pr3+ surface fraction in CePr mixed oxides determined by XPS analysis Oxidation state Pr XPS Binary alloys Cerium alloys D region Ions Praseodymium Water gas shift X ray photoelectron spectroscopy Mixed oxide Non-stoichiometric Oxidation state Pr ions Redox property Surface fraction Water gas shift catalysts XPS analysis Praseodymium alloys CePr mixed oxides were previously studied as supports for Water Gas Shift catalysts, considering their promising textural and redox properties arising from the presence of a non-stoichiometric oxide. A very small Ce3+ fraction was observed on those oxides, suggesting that Pr3+ion could be responsible for the enhanced activity. Therefore, in-depth XPS analysis is conducted in the present work in order to determine the Pr3+ fraction by fitting the XPS Pr 3d region. Much higher values of reduced Pr ions than Ce ions were observed, confirming the promoter role of the former. © 2017 Elsevier B.V. 2018 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03682048_v222_n_p1_PoggioFraccari http://hdl.handle.net/20.500.12110/paper_03682048_v222_n_p1_PoggioFraccari |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Oxidation state Pr XPS Binary alloys Cerium alloys D region Ions Praseodymium Water gas shift X ray photoelectron spectroscopy Mixed oxide Non-stoichiometric Oxidation state Pr ions Redox property Surface fraction Water gas shift catalysts XPS analysis Praseodymium alloys |
spellingShingle |
Oxidation state Pr XPS Binary alloys Cerium alloys D region Ions Praseodymium Water gas shift X ray photoelectron spectroscopy Mixed oxide Non-stoichiometric Oxidation state Pr ions Redox property Surface fraction Water gas shift catalysts XPS analysis Praseodymium alloys Pr3+ surface fraction in CePr mixed oxides determined by XPS analysis |
topic_facet |
Oxidation state Pr XPS Binary alloys Cerium alloys D region Ions Praseodymium Water gas shift X ray photoelectron spectroscopy Mixed oxide Non-stoichiometric Oxidation state Pr ions Redox property Surface fraction Water gas shift catalysts XPS analysis Praseodymium alloys |
description |
CePr mixed oxides were previously studied as supports for Water Gas Shift catalysts, considering their promising textural and redox properties arising from the presence of a non-stoichiometric oxide. A very small Ce3+ fraction was observed on those oxides, suggesting that Pr3+ion could be responsible for the enhanced activity. Therefore, in-depth XPS analysis is conducted in the present work in order to determine the Pr3+ fraction by fitting the XPS Pr 3d region. Much higher values of reduced Pr ions than Ce ions were observed, confirming the promoter role of the former. © 2017 Elsevier B.V. |
title |
Pr3+ surface fraction in CePr mixed oxides determined by XPS analysis |
title_short |
Pr3+ surface fraction in CePr mixed oxides determined by XPS analysis |
title_full |
Pr3+ surface fraction in CePr mixed oxides determined by XPS analysis |
title_fullStr |
Pr3+ surface fraction in CePr mixed oxides determined by XPS analysis |
title_full_unstemmed |
Pr3+ surface fraction in CePr mixed oxides determined by XPS analysis |
title_sort |
pr3+ surface fraction in cepr mixed oxides determined by xps analysis |
publishDate |
2018 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03682048_v222_n_p1_PoggioFraccari http://hdl.handle.net/20.500.12110/paper_03682048_v222_n_p1_PoggioFraccari |
_version_ |
1768542989643153408 |