Development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cell

Abstract Physical and electrochemical properties of Pd catalysts combined with Ru and Mo on carbon support were investigated. To this end, Pd, Pd1.3Ru1.0, Pd3.2Ru1.3Mo1.0 and Pd1.5Ru0.8Mo1.0 were synthesized on Carbon Vulcan XC72 support by the method of thermal decomposition of polymeric precursors...

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Main Authors: Yonis Fornazier Filho, Ana Caroliny Carvalho da Cruz, Rolando Pedicini, José Ricardo Cezar Salgado, Priscilla Paiva Luz, Josimar Ribeiro
Format: Article
Language:English
Published: SpringerOpen 2021-02-01
Series:Materials for Renewable and Sustainable Energy
Subjects:
Online Access:https://doi.org/10.1007/s40243-020-00187-1
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spelling doaj-d360875a8a174a81b7a896e8ba78fc492021-02-07T12:10:26ZengSpringerOpenMaterials for Renewable and Sustainable Energy2194-14592194-14672021-02-0110111210.1007/s40243-020-00187-1Development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cellYonis Fornazier Filho0Ana Caroliny Carvalho da Cruz1Rolando Pedicini2José Ricardo Cezar Salgado3Priscilla Paiva Luz4Josimar Ribeiro5Departamento de Química-Centro de Ciências Exatas, Universidade Federal Do Espírito Santo (UFES)Departamento de Química-Centro de Ciências Exatas, Universidade Federal Do Espírito Santo (UFES)Istituto Di Tecnologia Avanzate Per L’Energia “Nicola Giordano” (ITAE) - Via S. Lucia Sopra ContesseUniversidade Federal da Integração Latino-Americana (UNILA), Instituto Latino-Americano de Ciências da Vida E da Natureza, Avenida Silvio Américo SadelliDepartamento de Química-Centro de Ciências Exatas, Universidade Federal Do Espírito Santo (UFES)Departamento de Química-Centro de Ciências Exatas, Universidade Federal Do Espírito Santo (UFES)Abstract Physical and electrochemical properties of Pd catalysts combined with Ru and Mo on carbon support were investigated. To this end, Pd, Pd1.3Ru1.0, Pd3.2Ru1.3Mo1.0 and Pd1.5Ru0.8Mo1.0 were synthesized on Carbon Vulcan XC72 support by the method of thermal decomposition of polymeric precursors and then physically and electrochemically characterized. The highest reaction yields are obtained for Pd3.2Ru1.3Mo1.0/C and Pd1.5Ru0.8Mo1.0/C and, as demonstrated by thermal analysis, they also show the smallest metal/carbon ratio compared the other catalysts. XRD (X-ray Diffraction) and Raman analyses show the presence of PdO and RuO2 for the Pd/C and the Pd1.3Ru1.0/C catalysts, respectively, a fact not observed for the Pd3.2Ru1.3 Mo1.0 /C and the Pd1.5Ru0.8Mo1.0/C catalysts. The catalytic activities were tested for the ethanol oxidation in alkaline medium. Cyclic voltammetry (CV) shows Pd1.3Ru1.0/C exhibiting the highest peak of current density, followed by Pd3.2Ru1.3Mo1.0/C, Pd1.5Ru0.8Mo1.0/C and Pd/C. From, chronoamperometry (CA), it is possible to observe the lowest rate of poisoning for the Pd1.3Ru1.0/C, followed by Pd3.2Ru1.3Mo1.0/C, Pd1.5Ru0.8Mo1.0/C and Pd/C. These results suggested that catalytic activity of the binary and the ternary catalysts are improved in comparison with Pd/C. The presence of RuO2 activated the bifunctional mechanism and improved the catalytic activity in the Pd1.3Ru1.0/C catalyst. The addition of Mo in the catalysts enhanced the catalytic activity by the intrinsic mechanism, suggesting a synergistic effect between metals. In summary, we suggest that it is possible to synthesize ternary PdRuMo catalysts supported on Carbon Vulcan XC72, resulting in materials with lower poisoning rates and lower costs than Pd/C. Graphic abstracthttps://doi.org/10.1007/s40243-020-00187-1Palladium-based catalystsRutheniumMolybdenumElectronic interaction mechanismBifunctional mechanism
collection DOAJ
language English
format Article
sources DOAJ
author Yonis Fornazier Filho
Ana Caroliny Carvalho da Cruz
Rolando Pedicini
José Ricardo Cezar Salgado
Priscilla Paiva Luz
Josimar Ribeiro
spellingShingle Yonis Fornazier Filho
Ana Caroliny Carvalho da Cruz
Rolando Pedicini
José Ricardo Cezar Salgado
Priscilla Paiva Luz
Josimar Ribeiro
Development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cell
Materials for Renewable and Sustainable Energy
Palladium-based catalysts
Ruthenium
Molybdenum
Electronic interaction mechanism
Bifunctional mechanism
author_facet Yonis Fornazier Filho
Ana Caroliny Carvalho da Cruz
Rolando Pedicini
José Ricardo Cezar Salgado
Priscilla Paiva Luz
Josimar Ribeiro
author_sort Yonis Fornazier Filho
title Development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cell
title_short Development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cell
title_full Development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cell
title_fullStr Development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cell
title_full_unstemmed Development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cell
title_sort development of palladium catalysts modified by ruthenium and molybdenum as anode in direct ethanol fuel cell
publisher SpringerOpen
series Materials for Renewable and Sustainable Energy
issn 2194-1459
2194-1467
publishDate 2021-02-01
description Abstract Physical and electrochemical properties of Pd catalysts combined with Ru and Mo on carbon support were investigated. To this end, Pd, Pd1.3Ru1.0, Pd3.2Ru1.3Mo1.0 and Pd1.5Ru0.8Mo1.0 were synthesized on Carbon Vulcan XC72 support by the method of thermal decomposition of polymeric precursors and then physically and electrochemically characterized. The highest reaction yields are obtained for Pd3.2Ru1.3Mo1.0/C and Pd1.5Ru0.8Mo1.0/C and, as demonstrated by thermal analysis, they also show the smallest metal/carbon ratio compared the other catalysts. XRD (X-ray Diffraction) and Raman analyses show the presence of PdO and RuO2 for the Pd/C and the Pd1.3Ru1.0/C catalysts, respectively, a fact not observed for the Pd3.2Ru1.3 Mo1.0 /C and the Pd1.5Ru0.8Mo1.0/C catalysts. The catalytic activities were tested for the ethanol oxidation in alkaline medium. Cyclic voltammetry (CV) shows Pd1.3Ru1.0/C exhibiting the highest peak of current density, followed by Pd3.2Ru1.3Mo1.0/C, Pd1.5Ru0.8Mo1.0/C and Pd/C. From, chronoamperometry (CA), it is possible to observe the lowest rate of poisoning for the Pd1.3Ru1.0/C, followed by Pd3.2Ru1.3Mo1.0/C, Pd1.5Ru0.8Mo1.0/C and Pd/C. These results suggested that catalytic activity of the binary and the ternary catalysts are improved in comparison with Pd/C. The presence of RuO2 activated the bifunctional mechanism and improved the catalytic activity in the Pd1.3Ru1.0/C catalyst. The addition of Mo in the catalysts enhanced the catalytic activity by the intrinsic mechanism, suggesting a synergistic effect between metals. In summary, we suggest that it is possible to synthesize ternary PdRuMo catalysts supported on Carbon Vulcan XC72, resulting in materials with lower poisoning rates and lower costs than Pd/C. Graphic abstract
topic Palladium-based catalysts
Ruthenium
Molybdenum
Electronic interaction mechanism
Bifunctional mechanism
url https://doi.org/10.1007/s40243-020-00187-1
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