Publication:
Atomically dispersed zeolite-supported rhodium complex: selective and stable catalyst for acetylene semi-hydrogenation

dc.contributor.coauthorSu Yordanli, Melisa
dc.contributor.coauthorHoffman, Adam S.
dc.contributor.coauthorHong, Jiyun
dc.contributor.coauthorPerez-Aguilar, Jorge E.
dc.contributor.coauthorSaltuk, Aylin
dc.contributor.coauthorAkgül, Deniz
dc.contributor.coauthorDemircan, Oktay
dc.contributor.coauthorAteşin, Tülay A.
dc.contributor.coauthorAviyente, Viktorya
dc.contributor.coauthorGates, Bruce C.
dc.contributor.coauthorBare, Simon R.
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.kuauthorZhao, Yuxin
dc.contributor.kuauthorBozkurt, Özge Deniz
dc.contributor.kuauthorÖztulum, Samira Fatma Kurtoğlu
dc.contributor.kuauthorUzun, Alper
dc.contributor.otherDepartment of Chemical and Biological Engineering
dc.contributor.researchcenterKoç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM)
dc.contributor.researchcenterKoç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM)
dc.contributor.schoolcollegeinstituteGraduate School of Sciences and Engineering
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.date.accessioned2024-12-29T09:38:17Z
dc.date.issued2024
dc.description.abstractSupported rhodium catalysts are known to be unselective for semi-hydrogenation reactions. Here, by tuning the electronic structure of supported mononuclear rhodium sites determined by the metal nuclearity and the electron-donor properties of the support, we report that atomically dispersed HY zeolite-supported rhodium with reactive acetylene ligands affords a stable ethylene selectivity > 90 % for acetylene semi-hydrogenation at 373 K and atmospheric pressure, even when ethylene is present in a large excess over acetylene. Infrared and X-ray absorption spectra and measurements of rates of the catalytic reaction complemented with calculations at the level of density functional theory show how the catalyst performance depends on the electronic structure of the rhodium, influenced by the support as a ligand that is a weak electron donor.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorsThe work at Koç University was supported by Koç University TUPRAS Energy Center (KUTEM). A.U. thanks the Fulbright Türkiye's Visiting Scholar Program and the TUBA-GEBIP Award of the Turkish Academy of Sciences. Y.Z. acknowledges the Fung Scholarship. We acknowledge the use of STEM services and facilities of the Central Research Infrastructure Directorate at Koç University. Computing resources performed in the investigation were provided by the National Center for High Performance Computing of Turkey (UHEM) under grant number 1006502019 and by TUBITAK ULAKBIM, High Performance and Grid Computing Center (TRUBA resources) and the Texas Advanced Computing Center (TACC) at The University of Texas at Austin. M.Y. and V.A. thank TUBITAK (Project Number: 121Z092);T.A. thanks the Welch Foundation (Grant No. BX-0048) for support. Work at the Stanford Synchrotron Radiation Light source of the SLAC National Accelerator Laboratory was supported by the U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES), under Contract DE-AC02-76SF00515 and by Co-ACCESS, supported by DOE BES, Chemical Sciences, Geosciences, and Biosciences Division, which also supported the work at the University of California (B.C.G.;DEFG02-04ER15513).
dc.description.volume429
dc.identifier.doi10.1016/j.jcat.2023.115196
dc.identifier.eissn1090-2694
dc.identifier.issn0021-9517
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85178049621
dc.identifier.urihttps://doi.org/10.1016/j.jcat.2023.115196
dc.identifier.urihttps://hdl.handle.net/20.500.14288/22642
dc.identifier.wos1132798800001
dc.keywordsAcetylene semi-hydrogenation
dc.keywordsDensity functional theory
dc.keywordsElectronic structure effect
dc.keywordsSupported rhodium complexes
dc.keywordsZeolite
dc.languageen
dc.publisherAcademic Press Inc.
dc.relation.grantnoKUTEM
dc.relation.grantnoKoç University TUPRAS Energy Center
dc.relation.grantnoTUBITAK ULAKBIM
dc.relation.grantnoTexas Advanced Computing Center
dc.relation.grantnoU.S. Department of Energy, USDOE
dc.relation.grantnoWelch Foundation, (BX-0048)
dc.relation.grantnoUniversity of California, UC, (DEFG02-04ER15513)
dc.relation.grantnoOffice of Science, SC
dc.relation.grantnoBasic Energy Sciences, BES, (DE-AC02-76SF00515)
dc.relation.grantnoUniversity of Texas at Austin, UT
dc.relation.grantnoChemical Sciences, Geosciences, and Biosciences Division, CSGB
dc.relation.grantnoTürkiye Bilimsel ve Teknolojik Araştırma Kurumu, TÜBİTAK, (121Z092)
dc.relation.grantnoTürkiye Bilimler Akademisi, (1006502019)
dc.sourceJournal of Catalysis
dc.subjectChemistry
dc.subjectPhysical chemistry
dc.subjectEngineering
dc.subjectChemical engineering
dc.titleAtomically dispersed zeolite-supported rhodium complex: selective and stable catalyst for acetylene semi-hydrogenation
dc.typeJournal article
dspace.entity.typePublication
local.contributor.kuauthorZhao, Yuxin
local.contributor.kuauthorBozkurt, Özge Deniz
local.contributor.kuauthorÖztulum, Samira Fatma Kurtoğlu
local.contributor.kuauthorUzun, Alper
relation.isOrgUnitOfPublicationc747a256-6e0c-4969-b1bf-3b9f2f674289
relation.isOrgUnitOfPublication.latestForDiscoveryc747a256-6e0c-4969-b1bf-3b9f2f674289

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