Carbon Nanotube-Graphene Supported Bimetallic Electrocatalyst for Direct Borohydride Hydrogen Peroxide Fuel Cells

dc.authoridDEVRIM, YILSER/0000-0001-8430-0702
dc.authoridUZUNDURUKAN, ARIFE/0000-0003-1104-1644
dc.authorscopusid57208702706
dc.authorscopusid57220809867
dc.authorscopusid57201408041
dc.authorscopusid11139445500
dc.authorwosidUzundurukan, Arife/JKH-6503-2023
dc.authorwosidbudak, yağmur/ISA-1148-2023
dc.authorwosidDEVRIM, YILSER/AAF-8790-2019
dc.authorwosidBudak, Yağmur/GOH-1635-2022
dc.contributor.authorUzundurukan, Arife
dc.contributor.authorAkca, Elif Seda
dc.contributor.authorBudak, Yagmur
dc.contributor.authorDevrim, Yilser
dc.contributor.otherEnergy Systems Engineering
dc.date.accessioned2024-07-05T15:21:36Z
dc.date.available2024-07-05T15:21:36Z
dc.date.issued2021
dc.departmentAtılım Universityen_US
dc.department-temp[Uzundurukan, Arife] Univ Sherbrooke, Dept Mech Engn, 2500 Blvd Univ, Sherbrooke, PQ J1K 2R1, Canada; [Akca, Elif Seda] Izmir Inst Technol, Dept Energy Syst Engn, Izmir, Turkey; [Budak, Yagmur] Atilim Univ, Dept Mech Engn, TR-06836 Ankara, Turkey; [Devrim, Yilser] Atilim Univ, Dept Energy Syst Engn, TR-06836 Ankara, Turkeyen_US
dc.descriptionDEVRIM, YILSER/0000-0001-8430-0702; UZUNDURUKAN, ARIFE/0000-0003-1104-1644en_US
dc.description.abstractAt present study, carbon nanotube-graphene (CNT-G) supported PtAu, Au and Pt catalysts were prepared by microwave-assisted synthesis method to investigate the direct liquid-fed sodium borohydride/hydrogen peroxide (NaBH4/H2O2) fuel cell performance. Prepared catalysts were characterized by TGA, XRD, TEM, ICP-OES, cyclic voltammetry and rotating disc electrode (RDE) voltammetry. The catalysts were tested in a single NaBH4/H2O2 fuel cell with 25 cm(2) active area to evaluate fuel cell performance. The effects of temperature and fuel concentration on fuel cell performance were examined to observed best operating conditions. As a result of direct NaBH4/H2O2 fuel cell experiments, maximum power densities of 139 mW/cm(2), 125 mW/cm(2) and 113 mW/cm(2) were obtained for PtAu/CNT-G, Au/CNT-G and Pt/CNT-G catalysts, respectively. PtAu/CNT-G catalyst showed the enhanced NaBH4/H2O2 fuel cell performance, which was higher than the Pt/CNT-G catalyst and Au/CNT-G catalyst at 50 degrees C. The enhanced NaBH4/H2O2 performance can be attributed to synergistic effects between Pt and Au particles on CNT-G support providing a better catalyst utilization and interaction. These results suggest that the prepared PtAu/CNT-G catalyst is a promising anode catalyst for NaBH4/H2O2 fuel cell application. (c) 2020 Elsevier Ltd. All rights reserved.en_US
dc.description.sponsorshipAtilim University [ATU-LAP-1819-01]en_US
dc.description.sponsorshipThe authors gratefully acknowledge funding from the Atilim University (Grant Number: ATU-LAP-1819-01). The authors would like to thank to TEKSIS Company (Turkey) for providing technical support on manufacturing of GDE's by the ultrasonic coating system.en_US
dc.identifier.citationcount24
dc.identifier.doi10.1016/j.renene.2020.12.003
dc.identifier.endpage1364en_US
dc.identifier.issn0960-1481
dc.identifier.issn1879-0682
dc.identifier.scopus2-s2.0-85097676039
dc.identifier.startpage1351en_US
dc.identifier.urihttps://doi.org/10.1016/j.renene.2020.12.003
dc.identifier.urihttps://hdl.handle.net/20.500.14411/2110
dc.identifier.volume172en_US
dc.identifier.wosWOS:000641142500005
dc.identifier.wosqualityQ1
dc.institutionauthorDevrim, Yılser
dc.institutionauthorUzundurukan, Arife
dc.language.isoenen_US
dc.publisherPergamon-elsevier Science Ltden_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.scopus.citedbyCount35
dc.subjectDirect borohydride-hydrogen peroxide fuel cellen_US
dc.subjectBimetallic catalysten_US
dc.subjectHydrogen peroxideen_US
dc.subjectSodium borohydrideen_US
dc.subjectLiquid fuels fuel cellen_US
dc.titleCarbon Nanotube-Graphene Supported Bimetallic Electrocatalyst for Direct Borohydride Hydrogen Peroxide Fuel Cellsen_US
dc.typeArticleen_US
dc.wos.citedbyCount36
dspace.entity.typePublication
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