Electro-Oxidation of Glycerol on Core–Shell M@Pt/C (M = Co, Ni, Sn) Catalysts in Alkaline Medium

This study explores the development of core–shell electrocatalysts for efficient glycerol oxidation in alkaline media. Carbon-supported M@Pt/C (M = Co, Ni, Sn) catalysts with a 1:1 atomic ratio of metal (M) to platinum (Pt) were synthesized using a facile sodium borohydride reduction method. The ana...

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Main Authors: Rudyere Nascimento Silva, Leandro Aparecido Pocrifka, Ermete Antolini, Raimundo Ribeiro Passos
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Energies
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Online Access:https://www.mdpi.com/1996-1073/18/2/305
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author Rudyere Nascimento Silva
Leandro Aparecido Pocrifka
Ermete Antolini
Raimundo Ribeiro Passos
author_facet Rudyere Nascimento Silva
Leandro Aparecido Pocrifka
Ermete Antolini
Raimundo Ribeiro Passos
author_sort Rudyere Nascimento Silva
collection DOAJ
description This study explores the development of core–shell electrocatalysts for efficient glycerol oxidation in alkaline media. Carbon-supported M@Pt/C (M = Co, Ni, Sn) catalysts with a 1:1 atomic ratio of metal (M) to platinum (Pt) were synthesized using a facile sodium borohydride reduction method. The analysis confirmed the formation of the desired core–shell structure, with Pt dominating the surface as evidenced by energy-dispersive X-ray spectroscopy (EDS). X-ray diffraction (XRD) revealed the presence of a face-centered cubic (fcc) Pt structure for Co@Pt/C and Ni@Pt/C. Interestingly, Sn@Pt/C displayed a PtSn alloy formation indicated by shifted Pt peaks and the presence of minor Sn oxide peaks. Notably, no diffraction peaks were observed for the core metals, suggesting their amorphous nature. Electrocatalytic evaluation through cyclic voltammetry (CV) revealed superior glycerol oxidation activity for Co@Pt/C compared to all other catalysts. The maximum current density followed the order Co@Pt/C > Ni@Pt/C > Sn@Pt/C > Pt/C. This highlights the effectiveness of the core–shell design in enhancing activity. Furthermore, Sn@Pt/C displayed remarkable poisoning tolerance attributed to a combined effect: a bifunctional mechanism driven by Sn oxides and an electronic effect within the PtSn alloy. These findings demonstrate the significant potential of core–shell M@Pt/C structures for designing highly active and poisoning-resistant electrocatalysts for glycerol oxidation. The presented approach paves the way for further development of optimized catalysts with enhanced performance and stability aiming at future applications in direct glycerol fuel cells.
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spelling doaj-art-7110ba77bcde401481c5143d6d8105b82025-01-24T13:30:57ZengMDPI AGEnergies1996-10732025-01-0118230510.3390/en18020305Electro-Oxidation of Glycerol on Core–Shell M@Pt/C (M = Co, Ni, Sn) Catalysts in Alkaline MediumRudyere Nascimento Silva0Leandro Aparecido Pocrifka1Ermete Antolini2Raimundo Ribeiro Passos3Department of Chemistry, Environment and Food—DQA, Campus Manaus Centro, Federal Institute of Education, Science and Technology of Amazonas—IFAM, Manaus 69020-120, AM, BrazilLaboratory of Electrochemistry and Energy—LEEN, Department of Chemistry, Federal University of Amazonas—UFAM, Manaus 69088-900, AM, BrazilScuola di Scienza dei Materiali, 16016 Cogoleto, ItalyLaboratory of Electrochemistry and Energy—LEEN, Department of Chemistry, Federal University of Amazonas—UFAM, Manaus 69088-900, AM, BrazilThis study explores the development of core–shell electrocatalysts for efficient glycerol oxidation in alkaline media. Carbon-supported M@Pt/C (M = Co, Ni, Sn) catalysts with a 1:1 atomic ratio of metal (M) to platinum (Pt) were synthesized using a facile sodium borohydride reduction method. The analysis confirmed the formation of the desired core–shell structure, with Pt dominating the surface as evidenced by energy-dispersive X-ray spectroscopy (EDS). X-ray diffraction (XRD) revealed the presence of a face-centered cubic (fcc) Pt structure for Co@Pt/C and Ni@Pt/C. Interestingly, Sn@Pt/C displayed a PtSn alloy formation indicated by shifted Pt peaks and the presence of minor Sn oxide peaks. Notably, no diffraction peaks were observed for the core metals, suggesting their amorphous nature. Electrocatalytic evaluation through cyclic voltammetry (CV) revealed superior glycerol oxidation activity for Co@Pt/C compared to all other catalysts. The maximum current density followed the order Co@Pt/C > Ni@Pt/C > Sn@Pt/C > Pt/C. This highlights the effectiveness of the core–shell design in enhancing activity. Furthermore, Sn@Pt/C displayed remarkable poisoning tolerance attributed to a combined effect: a bifunctional mechanism driven by Sn oxides and an electronic effect within the PtSn alloy. These findings demonstrate the significant potential of core–shell M@Pt/C structures for designing highly active and poisoning-resistant electrocatalysts for glycerol oxidation. The presented approach paves the way for further development of optimized catalysts with enhanced performance and stability aiming at future applications in direct glycerol fuel cells.https://www.mdpi.com/1996-1073/18/2/305fuel cell applicationglycerol oxidationdirect glycerol fuel cellcore–shell catalyst
spellingShingle Rudyere Nascimento Silva
Leandro Aparecido Pocrifka
Ermete Antolini
Raimundo Ribeiro Passos
Electro-Oxidation of Glycerol on Core–Shell M@Pt/C (M = Co, Ni, Sn) Catalysts in Alkaline Medium
Energies
fuel cell application
glycerol oxidation
direct glycerol fuel cell
core–shell catalyst
title Electro-Oxidation of Glycerol on Core–Shell M@Pt/C (M = Co, Ni, Sn) Catalysts in Alkaline Medium
title_full Electro-Oxidation of Glycerol on Core–Shell M@Pt/C (M = Co, Ni, Sn) Catalysts in Alkaline Medium
title_fullStr Electro-Oxidation of Glycerol on Core–Shell M@Pt/C (M = Co, Ni, Sn) Catalysts in Alkaline Medium
title_full_unstemmed Electro-Oxidation of Glycerol on Core–Shell M@Pt/C (M = Co, Ni, Sn) Catalysts in Alkaline Medium
title_short Electro-Oxidation of Glycerol on Core–Shell M@Pt/C (M = Co, Ni, Sn) Catalysts in Alkaline Medium
title_sort electro oxidation of glycerol on core shell m pt c m co ni sn catalysts in alkaline medium
topic fuel cell application
glycerol oxidation
direct glycerol fuel cell
core–shell catalyst
url https://www.mdpi.com/1996-1073/18/2/305
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AT ermeteantolini electrooxidationofglyceroloncoreshellmptcmconisncatalystsinalkalinemedium
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