Desalegn Nigatu Gemechu, Aderemi B. Haruna, Ahmed Mustefa Mohammed, Yedilfana Setarge Mekonnen* and Kenneth I. Ozoemena*,
{"title":"氧化铈/类洋葱碳负载pd基催化剂在碱性介质中氧化异丙醇的电催化性能及DFT研究","authors":"Desalegn Nigatu Gemechu, Aderemi B. Haruna, Ahmed Mustefa Mohammed, Yedilfana Setarge Mekonnen* and Kenneth I. Ozoemena*, ","doi":"10.1021/acs.jpcc.5c03686","DOIUrl":null,"url":null,"abstract":"<p >This study investigated the electrocatalytic performance of Pd-based catalysts supported on onion-like carbon (OLC) for isopropanol (IPA) oxidation in alkaline media (a direct isopropanol fuel cells (DIFC)). The synthesized and evaluated catalysts included PdNi/OLC, Pd/CeO<sub>2</sub>/OLC, and PdNi/CeO<sub>2</sub>/OLC, all of which demonstrated performances comparable to that of commercial Pd/C. These samples are characterized by physicochemical analytical methods such as X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) coupled with energy-dispersive X-ray (EDX), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS). Electrochemical measurements were also carried out using cyclic voltammetry (CV), chronoamperometry (CA), linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). The CV tests and Tafel analysis results revealed that PdNi/CeO<sub>2</sub>/OLC exhibited the highest current response with an onset potential of −0.69 V and better kinetic activity of 136.9 mV/dec respectively. Chronoamperometric tests confirmed that PdNi/CeO<sub>2</sub>/OLC maintains superior stability and antipoisoning properties, achieving stable current densities over extended periods. EIS showed the lowest charge transfer resistance (<i>R</i><sub>ct</sub>) for PdNi/CeO<sub>2</sub>/OLC, reflecting more efficient electron transfer. The Ni-containing catalysts also exhibit lower Tafel slopes (121.5 mV/dec for PdNi/OLC and 136.9 mV/dec for PdNi/CeO<sub>2</sub>/OLC), indicating improved reaction kinetics due to Ni. Density functional theory (DFT) calculations suggest that Ni incorporation into Pd enhances electron donation, which is enhanced by the CeO<sub>2</sub> support. This synergy improves IPA adsorption and reaction kinetics, leading to enhanced electrocatalytic performance. These findings demonstrate that alloying Pd with Ni and supporting it on CeO<sub>2</sub> significantly boosts electrocatalytic activity, stability, and mass transport in alcohol oxidation. The PdNi/CeO<sub>2</sub>/OLC catalyst is a promising candidate for DIFC applications, offering high efficiency, durability, and a low onset potential.</p>","PeriodicalId":61,"journal":{"name":"The Journal of Physical Chemistry C","volume":"129 31","pages":"14214–14228"},"PeriodicalIF":3.2000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.jpcc.5c03686","citationCount":"0","resultStr":"{\"title\":\"Electrocatalytic Properties and DFT Studies of Pd-Based Catalysts Supported on Ceria/Onion-like Carbon for Isopropanol Oxidation in Alkaline Medium\",\"authors\":\"Desalegn Nigatu Gemechu, Aderemi B. Haruna, Ahmed Mustefa Mohammed, Yedilfana Setarge Mekonnen* and Kenneth I. Ozoemena*, \",\"doi\":\"10.1021/acs.jpcc.5c03686\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >This study investigated the electrocatalytic performance of Pd-based catalysts supported on onion-like carbon (OLC) for isopropanol (IPA) oxidation in alkaline media (a direct isopropanol fuel cells (DIFC)). The synthesized and evaluated catalysts included PdNi/OLC, Pd/CeO<sub>2</sub>/OLC, and PdNi/CeO<sub>2</sub>/OLC, all of which demonstrated performances comparable to that of commercial Pd/C. These samples are characterized by physicochemical analytical methods such as X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) coupled with energy-dispersive X-ray (EDX), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS). Electrochemical measurements were also carried out using cyclic voltammetry (CV), chronoamperometry (CA), linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). The CV tests and Tafel analysis results revealed that PdNi/CeO<sub>2</sub>/OLC exhibited the highest current response with an onset potential of −0.69 V and better kinetic activity of 136.9 mV/dec respectively. Chronoamperometric tests confirmed that PdNi/CeO<sub>2</sub>/OLC maintains superior stability and antipoisoning properties, achieving stable current densities over extended periods. EIS showed the lowest charge transfer resistance (<i>R</i><sub>ct</sub>) for PdNi/CeO<sub>2</sub>/OLC, reflecting more efficient electron transfer. The Ni-containing catalysts also exhibit lower Tafel slopes (121.5 mV/dec for PdNi/OLC and 136.9 mV/dec for PdNi/CeO<sub>2</sub>/OLC), indicating improved reaction kinetics due to Ni. Density functional theory (DFT) calculations suggest that Ni incorporation into Pd enhances electron donation, which is enhanced by the CeO<sub>2</sub> support. This synergy improves IPA adsorption and reaction kinetics, leading to enhanced electrocatalytic performance. These findings demonstrate that alloying Pd with Ni and supporting it on CeO<sub>2</sub> significantly boosts electrocatalytic activity, stability, and mass transport in alcohol oxidation. The PdNi/CeO<sub>2</sub>/OLC catalyst is a promising candidate for DIFC applications, offering high efficiency, durability, and a low onset potential.</p>\",\"PeriodicalId\":61,\"journal\":{\"name\":\"The Journal of Physical Chemistry C\",\"volume\":\"129 31\",\"pages\":\"14214–14228\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-07-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acs.jpcc.5c03686\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Physical Chemistry C\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jpcc.5c03686\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpcc.5c03686","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Electrocatalytic Properties and DFT Studies of Pd-Based Catalysts Supported on Ceria/Onion-like Carbon for Isopropanol Oxidation in Alkaline Medium
This study investigated the electrocatalytic performance of Pd-based catalysts supported on onion-like carbon (OLC) for isopropanol (IPA) oxidation in alkaline media (a direct isopropanol fuel cells (DIFC)). The synthesized and evaluated catalysts included PdNi/OLC, Pd/CeO2/OLC, and PdNi/CeO2/OLC, all of which demonstrated performances comparable to that of commercial Pd/C. These samples are characterized by physicochemical analytical methods such as X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) coupled with energy-dispersive X-ray (EDX), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS). Electrochemical measurements were also carried out using cyclic voltammetry (CV), chronoamperometry (CA), linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). The CV tests and Tafel analysis results revealed that PdNi/CeO2/OLC exhibited the highest current response with an onset potential of −0.69 V and better kinetic activity of 136.9 mV/dec respectively. Chronoamperometric tests confirmed that PdNi/CeO2/OLC maintains superior stability and antipoisoning properties, achieving stable current densities over extended periods. EIS showed the lowest charge transfer resistance (Rct) for PdNi/CeO2/OLC, reflecting more efficient electron transfer. The Ni-containing catalysts also exhibit lower Tafel slopes (121.5 mV/dec for PdNi/OLC and 136.9 mV/dec for PdNi/CeO2/OLC), indicating improved reaction kinetics due to Ni. Density functional theory (DFT) calculations suggest that Ni incorporation into Pd enhances electron donation, which is enhanced by the CeO2 support. This synergy improves IPA adsorption and reaction kinetics, leading to enhanced electrocatalytic performance. These findings demonstrate that alloying Pd with Ni and supporting it on CeO2 significantly boosts electrocatalytic activity, stability, and mass transport in alcohol oxidation. The PdNi/CeO2/OLC catalyst is a promising candidate for DIFC applications, offering high efficiency, durability, and a low onset potential.
期刊介绍:
The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.