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Platinum Nanocatalysts Prepared With Different Surfactants for C1-C3 Alcohol Oxidations and Their Surface Morphologies by Afm

dc.authorid Ertan, Salih/0000-0001-8852-1879
dc.authorid Sen, Fatih/0000-0001-9929-9556
dc.authorscopusid 55240269100
dc.authorscopusid 8449363400
dc.authorscopusid 36769163600
dc.authorscopusid 6602522546
dc.authorwosid Şen, Fatih/O-9407-2016
dc.authorwosid Ertan, Salih/M-6370-2013
dc.contributor.author Ertan, Salih
dc.contributor.author Sen, Fatih
dc.contributor.author Sen, Selda
dc.contributor.author Gokagac, Gulsun
dc.date.accessioned 2025-05-10T16:48:27Z
dc.date.available 2025-05-10T16:48:27Z
dc.date.issued 2012
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Ertan, Salih; Sen, Fatih; Sen, Selda; Gokagac, Gulsun] Middle E Tech Univ, Dept Chem, TR-06531 Ankara, Turkey; [Sen, Fatih; Sen, Selda] Yuzuncu Yil Univ, Dept Chem, TR-65080 Van, Turkey en_US
dc.description Ertan, Salih/0000-0001-8852-1879; Sen, Fatih/0000-0001-9929-9556 en_US
dc.description.abstract In this study, platinum nanoparticle catalysts have been prepared using PtCl4 as a starting material and 1-octanethiol, 1-decanethiol, 1-dodecanethiol, and 1-hexadecanethiol as surfactants for methanol, ethanol, and 2-propanol oxidation reactions. The structure, particle sizes, and surface morphologies of the catalysts were characterized by X-ray diffraction (XRD), atomic force microscopy and transmission electron microscopy (TEM). XRD and TEM results indicate that all prepared catalysts have a face-centered cubic structure and are homogeneously dispersed on the carbon support with a narrow size distribution (2.0-1.3 nm). X-ray photoelectron spectra of the catalysts were examined and it is found that platinum has two different oxidation states, Pt(0) and Pt(IV), oxygen and sulfur compounds are H2Oads and OHads, bound and unbound thiols. The electrochemical and electrocatalytic properties of these catalysts were investigated with respect to C1-C3 alcohol oxidations by cyclic voltammetry and chronoamperometry. The highest electrocatalytic activity was obtained from catalyst I which was prepared with 1-octanethiol. This may be attributed to a decrease in the ratio of bound to unbound thiol species increase in Pt (0)/Pt(IV), H2Oads/OHads ratios, electrochemical surface area, CO tolerance and percent platinum utility. en_US
dc.description.sponsorship TUBITAK (Turkiye Bilimsel ve Teknik Arastirma Kurumu) [108T065]; Middle East Technical University [BAP-08-11-DPT2002K120510]; TUBITAK en_US
dc.description.sponsorship The authors gratefully acknowledge TUBITAK (Turkiye Bilimsel ve Teknik Arastirma Kurumu, Grant 108T065) for financial support and the Central Laboratory of the Middle East Technical University for acquiring XPS, TEM, and elemental analyses. The authors also thank Dr. Michael W. Pitcher for proofreading of this manuscript. F. S,. and S. S, thank the Middle East Technical University for Grant BAP-08-11-DPT2002K120510 and TUBITAK for 2211 scholarships. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1007/s11051-012-0922-5
dc.identifier.issn 1388-0764
dc.identifier.issn 1572-896X
dc.identifier.issue 6 en_US
dc.identifier.scopus 2-s2.0-84861809944
dc.identifier.scopusquality Q3
dc.identifier.uri https://doi.org/10.1007/s11051-012-0922-5
dc.identifier.uri https://hdl.handle.net/20.500.14720/1541
dc.identifier.volume 14 en_US
dc.identifier.wos WOS:000305328900020
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Springer en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Direct Alcohol Fuel Cells en_US
dc.subject Platinum Catalysts en_US
dc.subject Cyclic Voltammetry en_US
dc.subject Transmission Electron Microscopy en_US
dc.subject X-Ray Photoelectron Spectroscopy en_US
dc.subject Atomic Force Microscopy en_US
dc.title Platinum Nanocatalysts Prepared With Different Surfactants for C1-C3 Alcohol Oxidations and Their Surface Morphologies by Afm en_US
dc.type Article en_US

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