Publication:
A facile synthesis of ternary PtCuNi nanoalloys as catalysts for the hydrogen evolution and oxygen evolution reactions both in alkaline and acidic media

dc.contributor.coauthorBaldan Isik, Ilknur
dc.contributor.coauthorKaya, Dogan
dc.contributor.coauthorKaradag, Faruk
dc.contributor.coauthorEkicibil, Ahmet
dc.contributor.departmentDepartment of Chemistry
dc.contributor.departmentKUYTAM (Koç University Surface Science and Technology Center)
dc.contributor.kuauthorEroğlu, Zafer
dc.contributor.kuauthorMetin, Önder
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2025-12-31T08:18:44Z
dc.date.available2025-12-31
dc.date.issued2025
dc.description.abstractTernary PtCuNi nanoalloys with different Pt/Cu/Ni ratios were synthesized by using one-pot modified polyol method, and their electrocatalytic performance in hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) was investigated in detail. The structural analysis of as-synthesized PtCuNi nanoalloys performed by using Rietveld refinement and X-ray diffraction (XRD) analyses confirmed that they have the cubic crystal phase with a space group of the face-centered cubic (fcc)—Fm3¯m, where the increasing Pt ratio increased the lattice parameter to 3.712 Å and decreased the crystal size to 1.59 ± 0.39 nm. All prepared nanoalloys showed a uniform spherical shape with an average particle size between 3 and 9 nm. The Pt58Cu15Ni27 nanocatalyst with an average particle size of 3.62 nm shows that lowest Tafel slopes of 40 and 62 mV dec−1 for HER region both in alkaline and acidic media, respectively. Chronoamperometry tests of Pt58Cu15Ni27 nanocatalysts were performed at −0.3 mV (vs. RHE) in both acidic and alkaline solution displayed that they all exhibited excellent cycle stability. The Pt58Cu15Ni27 nanocatalysts also exhibited the lowest overpotentials (η) at 10 mA cm−2 of 1.36 V for OER in alkaline solution, while the Pt9Cu39Ni52 demonstrated the lowest Tafel slopes of 30 and 44 mV dec−1 for OER in both alkaline and acidic media, respectively. The enhanced electrocatalytic activity of the PtCuNi nanocatalysts is attributed to the stabilization of Pt through electron transfer from Cu and Ni in both reaction media, as well as their critical role in facilitating the cleavage of HO–H bonds during water splitting.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipThis work was financially supported by Cukurova University, Adana, Turkey, under Scientific Research Funding No: FBA-2021-14176. Ö.M. thanks to the Turkish Academy of Sciences (TUBA) for the financial support.
dc.identifier.doi10.1007/s12598-025-03579-2
dc.identifier.eissn1867-7185
dc.identifier.embargoNo
dc.identifier.issn1001-0521
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-105016213073
dc.identifier.urihttps://doi.org/10.1007/s12598-025-03579-2
dc.identifier.urihttps://hdl.handle.net/20.500.14288/31394
dc.identifier.wos001571504200001
dc.keywordsPtCuNi nanoalloy
dc.keywordsHydrogen evolution reaction
dc.keywordsOxygen evolution reaction
dc.keywordsWater splitting
dc.keywordsElectrocatalysis
dc.language.isoeng
dc.publisherSpringer Nature
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofRare Metals
dc.relation.openaccessYes
dc.rightsCC BY-NC-ND (Attribution-NonCommercial-NoDerivs)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectMaterials science
dc.subjectMetallurgy and metallurgical engineering
dc.titleA facile synthesis of ternary PtCuNi nanoalloys as catalysts for the hydrogen evolution and oxygen evolution reactions both in alkaline and acidic media
dc.typeJournal Article
dspace.entity.typePublication
person.familyNameEroğlu
person.familyNameMetin
person.givenNameZafer
person.givenNameÖnder
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relation.isOrgUnitOfPublicationd41f66ba-d7a4-4790-9f8f-a456c391209b
relation.isOrgUnitOfPublication.latestForDiscovery035d8150-86c9-4107-af16-a6f0a4d538eb
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