Publication:
Discovery of superior cu-gaox-hooy catalysts for the reduction of carbon dioxide to methanol at atmospheric pressure

dc.contributor.coauthorZohour, Bahman
dc.contributor.coauthorGulgun, Mehmet A.
dc.contributor.coauthorLeidholm, Craig
dc.contributor.coauthorSenkan, Selim
dc.contributor.departmentKUYTAM (Koç University Surface Science and Technology Center)
dc.contributor.facultymemberYes
dc.contributor.kuauthorBirer, Özgür
dc.contributor.kuauthorÜnal, Uğur
dc.contributor.kuauthorYılgör, İskender
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2024-11-09T23:18:31Z
dc.date.issued2016
dc.description.abstractCatalytic conversion of carbon dioxide to liquid fuels and basic chemicals by using solar-derived hydrogen at, or near, ambient pressure is a highly desirable goal in heterogeneous catalysis. If realized, this technology could lead to a more sustainable society together with decentralized power generation. A novel class of holmium-containing multi-metal oxide Cu catalysts, discovered through the application of high-throughput methods, is reported. In particular, ternary systems of Cu-GaOx-HoOy>Cu-CeOx-HoOy approximate to Cu-LaOx-HoOy supported on -Al2O3 exhibited superior methanol production (10x) with less CO formation than previously reported catalysts at 1atm pressure. Holmium was shown to be highly dispersed as few-atom clusters, suggesting that the formation of trimetallic sites could be the key for the promotion of methanol synthesis by Ho.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.openaccessNO
dc.description.peerreviewstatusPeer-Reviewed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipLaboratory Catalyst Systems (LCS), LLC We thank Laboratory Catalyst Systems (LCS), LLC for funding and access to their high-throughput equipment and catalyst data base. We also thank Dr. Selim Alayoglu and Dr. Kwangjin An of the Lawrence Berkeley National Laboratory for providing the hybrid MgO<INF>x</INF>/CoO<INF>y</INF> catalyst. Author contributions: BZ, CL, and SS initiated and performed the original catalyst discovery work at LCS. IY, OB, and UU performed and interpreted the XRD and XPS analysis. MAG performed and interpreted the HRTEM analysis.
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.WoSQuartileQ2
dc.identifier.doi10.1002/cctc.201600020
dc.identifier.eissn1867-3899
dc.identifier.embargoN/A
dc.identifier.endpage1469
dc.identifier.issn1867-3880
dc.identifier.issue8
dc.identifier.scopus2-s2.0-84977950732
dc.identifier.startpage1464
dc.identifier.urihttps://doi.org/10.1002/cctc.201600020
dc.identifier.urihttps://hdl.handle.net/20.500.14288/10386
dc.identifier.volume8
dc.identifier.wos000374763200006
dc.keywordsCarbon dioxide
dc.keywordsDimethyl ether
dc.keywordsHeterogeneous catalysis
dc.keywordsHigh-throughput testing
dc.keywordsMethanol synthesis
dc.keywordsGas shift reaction
dc.keywordsOxide
dc.keywordsPerformance
dc.keywordsCo2
dc.keywordsHydrogenation
dc.keywordsTechnologies
dc.keywordsConversion
dc.keywordsSupport
dc.keywordsOil
dc.keywordsZno
dc.language.isoeng
dc.publisherWiley Blackwell
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofChemcatchem
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectPhysical chemistry
dc.subjectTheoretical chemistry
dc.titleDiscovery of superior cu-gaox-hooy catalysts for the reduction of carbon dioxide to methanol at atmospheric pressure
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorYılgör, İskender
local.contributor.kuauthorBirer, Özgür
local.contributor.kuauthorÜnal, Uğur
relation.isGoalOfPublication33fc53ce-3b0a-4f77-913b-c44bfa9a02a5
relation.isGoalOfPublication.latestForDiscovery33fc53ce-3b0a-4f77-913b-c44bfa9a02a5
relation.isOrgUnitOfPublicationd41f66ba-d7a4-4790-9f8f-a456c391209b
relation.isOrgUnitOfPublication.latestForDiscoveryd41f66ba-d7a4-4790-9f8f-a456c391209b
relation.isParentOrgUnitOfPublicationd437580f-9309-4ecb-864a-4af58309d287
relation.isParentOrgUnitOfPublication.latestForDiscoveryd437580f-9309-4ecb-864a-4af58309d287

Files