S. Irazoque, A. López-Suárez, C. K. Zagal-Padilla, S. A. Gamboa
{"title":"直接乙醇燃料电池用Pd-Cu/TPPCu电催化剂的合成","authors":"S. Irazoque, A. López-Suárez, C. K. Zagal-Padilla, S. A. Gamboa","doi":"10.1007/s10800-023-02003-w","DOIUrl":null,"url":null,"abstract":"Abstract In this study, the electro-oxidation reaction of ethanol over Pd–Cu supported on Cu porphyrin (TPPCu) was investigated. The catalyst was synthesized using the microwave-assisted polyol method and physicochemically characterized by XRD, XPS, SEM, EDS, TEM, EDAX, UV–Vis, FTIR, and RBS. A Cu-enriched catalyst with Cu 3 Pd, Pd,Cu, and TPPCu phases was identified using XRD and XPS. However, according to the RBS results, the catalytic surface was enriched with Pd, indicating that the interaction between TPPCu and Pd–Cu allowed the presence of Pd on the surface, thus enhancing the catalytic response of the material. This synthesis prevented the deprotonation of porphyrin on the electrocatalyst, as confirmed by XPS analysis. Electrochemical studies based on cyclic voltammetry and electrochemical impedance spectroscopy were used to investigate the response of the catalyst to variations in the scan rate and increasing ethanol concentration. The electrochemical response of PdCu/TPPCu improved with an increasing number of cycles, indicating improved mass transport, thus improving its electrochemical response and tolerance to CO contamination. This catalyst exhibited a high electroactive surface area of 49.4 m 2 /g, which could be related to the presence of TPPCu as a support. The behavior of the catalyst on the anode of a fuel cell fed with ethanol, bioethanol, and bioethanol residues was evaluated. Graphical Abstract","PeriodicalId":14887,"journal":{"name":"Journal of Applied Electrochemistry","volume":"36 14","pages":"0"},"PeriodicalIF":2.4000,"publicationDate":"2023-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of Pd-Cu/TPPCu electrocatalyst for direct ethanol fuel cell applications\",\"authors\":\"S. Irazoque, A. López-Suárez, C. K. Zagal-Padilla, S. A. Gamboa\",\"doi\":\"10.1007/s10800-023-02003-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract In this study, the electro-oxidation reaction of ethanol over Pd–Cu supported on Cu porphyrin (TPPCu) was investigated. The catalyst was synthesized using the microwave-assisted polyol method and physicochemically characterized by XRD, XPS, SEM, EDS, TEM, EDAX, UV–Vis, FTIR, and RBS. A Cu-enriched catalyst with Cu 3 Pd, Pd,Cu, and TPPCu phases was identified using XRD and XPS. However, according to the RBS results, the catalytic surface was enriched with Pd, indicating that the interaction between TPPCu and Pd–Cu allowed the presence of Pd on the surface, thus enhancing the catalytic response of the material. This synthesis prevented the deprotonation of porphyrin on the electrocatalyst, as confirmed by XPS analysis. Electrochemical studies based on cyclic voltammetry and electrochemical impedance spectroscopy were used to investigate the response of the catalyst to variations in the scan rate and increasing ethanol concentration. The electrochemical response of PdCu/TPPCu improved with an increasing number of cycles, indicating improved mass transport, thus improving its electrochemical response and tolerance to CO contamination. This catalyst exhibited a high electroactive surface area of 49.4 m 2 /g, which could be related to the presence of TPPCu as a support. The behavior of the catalyst on the anode of a fuel cell fed with ethanol, bioethanol, and bioethanol residues was evaluated. Graphical Abstract\",\"PeriodicalId\":14887,\"journal\":{\"name\":\"Journal of Applied Electrochemistry\",\"volume\":\"36 14\",\"pages\":\"0\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2023-11-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Applied Electrochemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s10800-023-02003-w\",\"RegionNum\":4,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Electrochemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s10800-023-02003-w","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
Synthesis of Pd-Cu/TPPCu electrocatalyst for direct ethanol fuel cell applications
Abstract In this study, the electro-oxidation reaction of ethanol over Pd–Cu supported on Cu porphyrin (TPPCu) was investigated. The catalyst was synthesized using the microwave-assisted polyol method and physicochemically characterized by XRD, XPS, SEM, EDS, TEM, EDAX, UV–Vis, FTIR, and RBS. A Cu-enriched catalyst with Cu 3 Pd, Pd,Cu, and TPPCu phases was identified using XRD and XPS. However, according to the RBS results, the catalytic surface was enriched with Pd, indicating that the interaction between TPPCu and Pd–Cu allowed the presence of Pd on the surface, thus enhancing the catalytic response of the material. This synthesis prevented the deprotonation of porphyrin on the electrocatalyst, as confirmed by XPS analysis. Electrochemical studies based on cyclic voltammetry and electrochemical impedance spectroscopy were used to investigate the response of the catalyst to variations in the scan rate and increasing ethanol concentration. The electrochemical response of PdCu/TPPCu improved with an increasing number of cycles, indicating improved mass transport, thus improving its electrochemical response and tolerance to CO contamination. This catalyst exhibited a high electroactive surface area of 49.4 m 2 /g, which could be related to the presence of TPPCu as a support. The behavior of the catalyst on the anode of a fuel cell fed with ethanol, bioethanol, and bioethanol residues was evaluated. Graphical Abstract
期刊介绍:
The Journal of Applied Electrochemistry is the leading journal on technologically orientated aspects of electrochemistry. The interface between electrochemical science and engineering is highlighted, emphasizing the application of electrochemistry to technological development and practice, and documenting properties and data of materials; design factors, design methodologies, scale-up, economics and testing of electrochemical devices and processes. The broad range of technologies includes energy conversion, conservation, and storage, new battery systems, fuel cells, super capacitors, solar cells, power delivery, industrial synthesis, environmental remediation, cell design, corrosion, electrochemical reaction engineering, medical applications of electrochemistry and bio-electrochemistry, the electrochemical treatment of effluents, hydrometallurgy, molten salt and solid state electrochemistry, surface finishing, electroplating, electrodeposition, sensors, and applications of molecular electrochemistry. It also publishes invited reviewed articles, book reviews and news items and a comprehensive electrochemical events calendar.