Effective Carbon Nanotube Supported Metal (M=au, Ag, Co, Mn, Ni, V, Zn) Core Pd Shell Bimetallic Anode Catalysts for Formic Acid Fuel Cells

dc.contributor.author Caglar, Aykut
dc.contributor.author Cogenli, Mehmet Selim
dc.contributor.author Yurtcan, Aye Bayrakceken
dc.contributor.author Kivrak, Hilal
dc.date.accessioned 2025-05-10T17:04:33Z
dc.date.available 2025-05-10T17:04:33Z
dc.date.issued 2020
dc.description Kivrak, Hilal/0000-0001-8001-7854; Bayrakceken, Ayse/0000-0002-8964-0869; Cogenli, Mehmed Selim/0000-0002-1228-5256 en_US
dc.description.abstract At present, CNT supported Pd and core-shell Pd-based catalysts are synthesized by employing the NaBH4 reduction method to investigate on formic acid electrooxidation (FAEO) activity. These catalysts are characterized by XRD, TEM, HRTEM, and XPS. The XRD results display that the electronic state of catalysts changed by second metal addition to Pd. TEM results reveal that Au and Pd are homogeneously distributed. XPS results of AucorePdshell/CNT catalyst show that Au and Pd atoms used in the preparation of the catalyst are obtained mainly in elemental state. The FAEO activity, stability, and resistance of these catalysts are investigated by employing cyclic voltammetry (CV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS). The CV results show that AucorePdshell/CNT catalyst having 16.42 mAcm(-2) specific activity and 4978.23 mA mg(-1) Pd mass activity is better than other catalysts. In addition, the AucorePdshell/CNT (21 m(2)/g) catalyst has better electrochemical active surface area (ECSA) value as 5.25 times compared with Pd/CNT catalyst. Direct formic acid fuel cell (DFAFC) performances are performed at different temperatures for AucorePdshell/CNT and NicorePdshell/CNT catalysts. The specific activity of AucorePdshen/CNT catalyst is 2.5 times higher than the value for NicorePdshell/CNT catalyst. AucorePdshell catalyst is a promising catalyst for DFAFCs. (C) 2019 Elsevier Ltd. All rights reserved. en_US
dc.description.sponsorship Scientific and Technological Research Council of Turkey TUBITAK [114M156] en_US
dc.description.sponsorship Hilal Kivrak would like to thank for the financial support for The Scientific and Technological Research Council of Turkey TUBITAK projects (project no: 114M156). en_US
dc.identifier.doi 10.1016/j.renene.2019.12.104
dc.identifier.issn 0960-1481
dc.identifier.scopus 2-s2.0-85078155073
dc.identifier.uri https://doi.org/10.1016/j.renene.2019.12.104
dc.identifier.uri https://hdl.handle.net/20.500.14720/6049
dc.language.iso en en_US
dc.publisher Pergamon-elsevier Science Ltd en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Au en_US
dc.subject Pd en_US
dc.subject Ni en_US
dc.subject Co en_US
dc.subject Formic Acid Electrooxidation en_US
dc.subject Nabh4 Reduction en_US
dc.title Effective Carbon Nanotube Supported Metal (M=au, Ag, Co, Mn, Ni, V, Zn) Core Pd Shell Bimetallic Anode Catalysts for Formic Acid Fuel Cells en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Kivrak, Hilal/0000-0001-8001-7854
gdc.author.id Bayrakceken, Ayse/0000-0002-8964-0869
gdc.author.id Cogenli, Mehmed Selim/0000-0002-1228-5256
gdc.author.scopusid 57201153766
gdc.author.scopusid 56183828300
gdc.author.scopusid 23468849600
gdc.author.scopusid 25959155500
gdc.author.wosid Kivrak, Hilal/Hji-7095-2023
gdc.author.wosid Kivrak, Hilal/Aaq-8663-2021
gdc.author.wosid Bayrakceken, Ayse/F-9342-2015
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Caglar, Aykut; Kivrak, Hilal] Van Yuzuncu Yil Univ, Fac Engn, Dept Chem Engn, TR-65000 Van, Turkey; [Cogenli, Mehmet Selim; Yurtcan, Aye Bayrakceken] Ataturk Univ, Dept Chem Engn, TR-25240 Erzurum, Turkey en_US
gdc.description.endpage 90 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 78 en_US
gdc.description.volume 150 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.wos WOS:000518874500007
gdc.index.type WoS
gdc.index.type Scopus

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