Exceptional oxidation activity with size-controlled supported gold clusters of low atomicity

dc.contributor.affiliationInstituto Universitario Mixto de Tecnología Química
dc.contributor.authorCorma Canós, Avelino
dc.contributor.authorConcepción Heydorn, Patricia
dc.contributor.authorBoronat Zaragoza, Mercedes
dc.contributor.authorSabater Picot, Mª José
dc.contributor.authorNavas Escrig, Javieres_ES
dc.contributor.authorYacaman, Miguel Josées_ES
dc.contributor.authorLarios, Eduardoes_ES
dc.contributor.authorPosadas, Álvaroes_ES
dc.contributor.authorLópez Quintela, M. Arturoes_ES
dc.contributor.authorBuceta, Davides_ES
dc.contributor.authorMendoza, Ernestes_ES
dc.contributor.authorGuilera, Gemmaes_ES
dc.contributor.authorMayoral, Álvaroes_ES
dc.contributor.funderNational Institute on Minority Health and Health Disparitieses_ES
dc.contributor.funderMinisterio de Ciencia e Innovaciónes_ES
dc.contributor.funderNational Institutes of Health, EEUUes_ES
dc.contributor.funderNational Science Foundation, EEUUes_ES
dc.contributor.funderXunta de Galiciaes_ES
dc.contributor.funderConsejo Superior de Investigaciones Científicases_ES
dc.date.accessioned2016-07-06T11:52:24Z
dc.date.available2016-07-06T11:52:24Z
dc.date.issued2013-09
dc.description.abstract[EN] The catalytic activity of gold depends on particle size, with the reactivity increasing as the particle diameter decreases. However, investigations into behaviour in the subnanometre regime (where gold exists as small clusters of a few atoms) began only recently with advances in synthesis and characterization techniques. Here we report an easy method to prepare isolated gold atoms supported on functionalized carbon nanotubes and their performance in the oxidation of thiophenol with O-2. We show that single gold atoms are not active, but they aggregate under reaction conditions into gold clusters of low atomicity that exhibit a catalytic activity comparable to that of sulfhydryl oxidase enzymes. When clusters grow into larger nanoparticles, catalyst activity drops to zero. Theoretical calculations show that gold clusters are able to activate thiophenol and O-2 simultaneously, and larger nanoparticles are passivated by strongly adsorbed thiolates. The combination of both reactants activation and facile product desorption makes gold clusters excellent catalysts.en_EN
dc.description.accrualMethodSes_ES
dc.description.bibliographicCitationCorma Canós, A.; Concepción Heydorn, P.; Boronat Zaragoza, M.; Sabater Picot, MJ.; Navas Escrig, J.; Yacaman, MJ.; Larios, E.... (2013). Exceptional oxidation activity with size-controlled supported gold clusters of low atomicity. Nature Chemistry. 5(9):775-781. https://doi.org/10.1038/NCHEM.1721es_ES
dc.description.issue9es_ES
dc.description.referencesHughes, M. D. et al. Tunable gold catalysts for selective hydrocarbon oxidation under mild conditions. Nature 437, 1132–1135 (2005).es_ES
dc.description.referencesHashmi, A. S. K. & Hutchings, G. J. Gold catalysis. Angew. Chem. Int. Ed. 45 7896–7936 (2006).es_ES
dc.description.referencesCorma, A. & Garcia, H. Supported gold nanoparticles as catalysts for organic reactions. Chem. Soc. Rev. 37, 2096–2126 (2008).es_ES
dc.description.referencesHaruta, M. Size- and support-dependency in the catalysis of gold. Catal. Today 36, 153–166 (1997).es_ES
dc.description.referencesLópez, N. et al. On the origin of the catalytic activity of gold nanoparticles for low-temperature CO oxidation. J. Catal. 223, 232–235 (2004).es_ES
dc.description.referencesHutchings, G. J. Catalysis by gold. Catal. Today 100, 55–61 (2005).es_ES
dc.description.referencesChen, M. S. & Goodman, D. W. Catalytically active gold: from nanoparticles to ultrathin films. Acc. Chem. Res. 39, 739–746 (2006).es_ES
dc.description.referencesRisse, Th., Shaikhutdinov, Sh., Nilius, N., Sterrer, M. & Freund, H. J. Gold supported on thin oxide films: from single atoms to nanoparticles. Acc. Chem. Res. 41, 949–956 (2008).es_ES
dc.description.referencesLiu, Y., Tsunoyama, H., Akita, T., Xie, S. & Tsukuda, T. Aerobic oxidation of cyclohexane catalysed by size-controlled Au clusters on hydroxyapatite: size effect in the sub-2 nm regime. ACS Catal. 1, 2–6 (2011).es_ES
dc.description.referencesHuang, J. et al. Propene epoxidation with O2 and H2: identification of the most active gold clusters. J. Catal. 278, 8–15 (2011).es_ES
dc.description.referencesHaruta, M. et al. Low-temperature oxidation of CO over gold supported on TiO2, α-Fe2O3, and Co3O4 . J. Catal. 144, 175–192 (1993).es_ES
dc.description.referencesTsunoyama, H., Ichikuni, N., Sakurai, H. & Tsukuda, T. Effect of electronic structures of Au clusters stabilized by poly(N-vinyl-2-pyrrolidone) on aerobic oxidation catalysis. J. Am. Chem. Soc. 131, 7086–7093 (2009).es_ES
dc.description.referencesHerzing, A. A., Kiely, C. J., Carley, A. F., Landon, P. & Hutchings, G. J. Identification of active gold nanoclusters on iron oxide supports for CO oxidation. Science 321, 1331–1332 (2008).es_ES
dc.description.referencesLupini A. R., Veith, G. M., Dudney, J. & Pennycook, S. J. Understanding catalyst stability through aberration-corrected STEM. Microsc Microanal. 15, 1408–1409 (2009).es_ES
dc.description.referencesAllard, L. F. et al. Evolution of gold structure during thermal treatment of Au/FeOx catalysts revealed by aberration-corrected electron microscopy. J. Electron Microsc. 58, 199–212 (2009).es_ES
dc.description.referencesUzun, A., Ortalan, V., Hao, Y., Browning, N. D. & Gates, B. C. Imaging gold atoms in site-isolated MgO-supported mononuclear gold complexes. J. Phys. Chem. C 113, 16847–16849 (2009).es_ES
dc.description.referencesLu, J., Aydin, C., Browning, N. D. & Gates, B. C. Imaging isolated gold atom catalytic sites in zeolite NaY. Angew. Chem. 51, 5842–5846 (2012).es_ES
dc.description.referencesYoon, B., Häkkinen, H. & Landman, U. Interaction of O2 with gold clusters: molecular and dissociative adsorption. J. Phys. Chem. A 107, 4066–4071 (2003).es_ES
dc.description.referencesLang, S. M., Bernhardt, T. M., Barnett, R. N., Yoon, B. & Landman, U. Hydrogen-promoted oxygen activation by free gold cluster cations. J. Am. Chem. Soc. 131, 8939–8951 (2009).es_ES
dc.description.referencesHagen, J. et al. Coadsorption of CO and O2 on small free gold cluster anions at cryogenic temperatures: model complexes for catalytic CO oxidation. Phys. Chem. Chem. Phys. 4, 1707–1709 (2002).es_ES
dc.description.referencesMolina, L. M., Lesarri, A. & Alonso, J. A. New insights on the reaction mechanism for CO oxidation on Au catalysts. Chem. Phys. Lett. 468, 201–204 (2009).es_ES
dc.description.referencesJoshi, A. M., Delgass, W. N. & Thomson, K. T. Comparison of the catalytic activity of Au3, Au4+, Au5 and Au5− in the gas-phase reaction of H2 and O2 to form hydrogen peroxide: a density functional theory investigation. J. Phys. Chem. B 109, 22392–22406 (2005).es_ES
dc.description.referencesLee, S. et al. Selective propene epoxidation on immobilized Au6–10 clusters: the effect of hydrogen and water on activity and selectivity. Angew. Chem. Int. Ed. 48, 1467–1471 (2009).es_ES
dc.description.referencesGuzman, J. & Gates, B. C. Structure and reactivity of a mononuclear gold-complex catalyst supported on magnesium oxide. Angew. Chem. Int. Ed. 42, 690–693 (2003).es_ES
dc.description.referencesRobinson, P. S. D., Khairallah, G. N., da Silva, G., Lioe, H. & O'Hair, R. A. J. Gold-mediated C–I bond activation of iodobenzene. Angew. Chem. Int. Ed. 51, 3812–3817 (2012).es_ES
dc.description.referencesJia, C. J. & Schüth, F. Colloidal metal nanoparticles as a component of designed catalyst. Phys. Chem. Chem. Phys. 13, 2457–2487 (2011).es_ES
dc.description.referencesTran, M. L., Zvyagin, A. V. & Plakhotnik, T. Synthesis and spectroscopic observation of dendrimer-encapsulated gold nanoclusters. Chem. Commun. 2400–2401 (2006).es_ES
dc.description.referencesLedo-Suárez, A. et al. Facile synthesis of stable subnanosized silver clusters in microemulsions. Angew. Chem. Int. Ed. 46, 8823–8827 (2007).es_ES
dc.description.referencesTurner, M. et al. Selective oxidation with dioxygen by gold nanoparticle catalysts derived from 55-atom clusters. Nature 454, 981–983 (2008).es_ES
dc.description.referencesLiu, Y. M., Tsunoyama, H., Akita, T. & Tsukuda, T. Chem. Commun. 46, 550–552 (2010).es_ES
dc.description.referencesShichibu, Y. & Konishi, K. HCl-induced nuclearity convergence in diphosphine-protected ultrasmall gold clusters: a novel synthetic route to ‘magic-number’ Au13 clusters. Small 6, 1216–1220 (2010).es_ES
dc.description.referencesXie, S., Tsunoyama, H., Kurashige, W., Negishi, Y. & Tsukuda, T. Enhancement in aerobic alcohol oxidation catalysis of Au25 clusters by single Pd atom doping. ACS Catal. 2, 1519–1523 (2012).es_ES
dc.description.referencesSanchez, A. et al. When gold is not noble: nanoscale gold catalysts. J. Phys. Chem. A 103, 9573–9578 (1999).es_ES
dc.description.referencesHoober, K. L. & Thorpe, C. Egg white sulfhydryl oxidase: kinetic mechanism of the catalysis of disulfide bond formation. Biochemistry 38, 3211–3217 (1999).es_ES
dc.description.referencesJaje, J. et al. A flavin-dependent sulfhydryl oxidase in bovine milk. Biochemistry 46, 13031–13040 (2007).es_ES
dc.description.referencesDumont, E., Michel, C. & Sautet, P. Unraveling gold(I)-specific action towards peptidic disulfide cleavage: a DFT investigation. ChemPhysChem 12, 2596–2603 (2011).es_ES
dc.description.referencesBarton, D. G. & Podkolzin, S. G. Kinetic study of a direct water synthesis over silica-supported gold nanoparticles. J. Phys. Chem. B 109, 2262–2274 (2005).es_ES
dc.description.referencesNtainjua, E. N. et al. The role of the support in achieving high selectivity in the direct formation of hydrogen peroxide. Green Chem. 10, 1162–1169 (2008).es_ES
dc.description.referencesJadzinsky, P. D., Calero, G., Ackerson, C. J., Bushnell, D. A. & Kornberg, R. D. Structure of a thiol monolayer-protected gold nanoparticle at 1.1 Å resolution. Science 318, 430–433 (2007).es_ES
dc.description.referencesHäkkinen, H. The gold–sulfur interface at the nanoscale. Nature Chem. 4, 443–455 (2012).es_ES
dc.description.referencesAlves, L. et al. Synthesis and stabilization of subnanometric gold oxide nanoparticles on multiwalled carbon nanotubes and their catalytic activity. J. Am. Chem. Soc. 133, 10251–10261 (2011).es_ES
dc.description.referencesSantiago-González, B. et al. One step synthesis of the smallest photoluminescent and paramagnetic PVP-protected gold atomic clusters. Nano Lett. 10, 4217–4221 (2010).es_ES
dc.description.referencesBecke, A. D. Density-functional thermochemistry. III. The role of exact exchange. J. Chem. Phys. 98, 5648–5652 (1993).es_ES
dc.description.referencesLee, C., Yang, W. & Parr, R. G. Development of the Colle–Salvetti correlation-energy formula into a functional of the electron density. Phys. Rev. B 37, 785–789 (1988).es_ES
dc.description.referencesFrisch, M. J. et al. Gaussian 03, Revision B.04 (Gaussian, 2003).es_ES
dc.description.referencesMcLean A. D. & Chandler G. S. Contracted Gaussian basis sets for molecular calculations. I. Second row atoms, Z = 11–18. J. Chem. Phys. 72 5639–5648 (1980).es_ES
dc.description.referencesKrishnan, R., Binkley, J. S., Seeger, R. &. Pople, J. A. Self-consistent molecular orbital methods. XX. A basis set for correlated wave functions. J. Chem. Phys. 72 650–654 (1980).es_ES
dc.description.referencesHay P. J. & Wadt, W. R. Ab initio effective core potentials for molecular calculations. Potentials for the transition metal atoms Sc to Hg. J. Chem. Phys. 82, 270–283 (1985).es_ES
dc.description.referencesReed, A. E., Weinstock, R. B. & Weinhold, F. Natural population analysis. J. Chem. Phys. 83, 735–747 (1985).es_ES
dc.description.sponsorshipFinancial support from the Spanish Science and Innovation Ministry (Consolider Ingenio 2010-MULTICAT CSD2009-00050, Subprograma de apoyo a Centros y Universidades de Excelencia Severo Ochoa SEV 2012 0267, MAT2011-28009 and MAT2010-20442 projects) and Xunta de Galicia (Grupos Ref.Comp.2010/41) is acknowledged. M.J.Y. and E. L. acknowledge the support of the National Centre for Research Resources (5 G12RR013646-12) and the National Institute on Minority Health and Health Disparities (G12MD007591) from the National Institutes of Health and of the National Science Foundation for support with grants DMR-1103730 and PREM: NSF PREM Grant # DMR 0934218. We also acknowledge the support of Consejo Nacional De Ciencia y Tecnologia. J.N. expresses his gratitude to Consejo Superior de Investigaciones Cientificas for a JAE Fellowship.en_EN
dc.description.upvformatpfin781es_ES
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dc.description.volume5es_ES
dc.identifier.doi10.1038/NCHEM.1721
dc.identifier.issn1755-4330
dc.identifier.urihttps://riunet.upv.es/handle/10251/67246
dc.languageIngléses_ES
dc.publisherNature Publishing Groupes_ES
dc.relation.ispartofNature Chemistryes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN//CSD2009-00050/ES/Desarrollo de catalizadores más eficientes para el diseño de procesos químicos sostenibles y produccion limpia de energia/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/NIH//5G12RR013646-12/US/CORE 1- BIOPHOTONICS CORE/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/NIMHD//G12MD007591/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/NSF//1103730/US/Alloys at the Nanoscale; The Case of Nanoparticles Second Phase/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/NSF//0934218/US/Oxide and Metal Nanoparticles-The Interface between Life Sciences and Physical Sciences/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//SEV-2012-0267/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN//MAT2011-28009/ES/CATALIZADORES MONO- Y MULTIFUNCIONALES BASADOS EN NANOPARTICULAS METALICAS DIRIGIDOS A TRANSFORMACIONES SECUENCIALES O REACCIONES EN CASCADA/es_ES
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dc.relation.projectIDinfo:eu-repo/grantAgreement/Xunta de Galicia//Comp.2010%2F41/es_ES
dc.relation.publisherversionhttps://dx.doi.org/10.1038/nchem.1721es_ES
dc.relation.references10.1038/nature04190es_ES
dc.relation.references10.1002/anie.200602454es_ES
dc.relation.references10.1039/b707314nes_ES
dc.relation.references10.1016/S0920-5861(96)00208-8es_ES
dc.relation.references10.1016/j.jcat.2004.01.001es_ES
dc.relation.references10.1016/j.cattod.2004.12.016es_ES
dc.relation.references10.1021/ar040309des_ES
dc.relation.references10.1021/ar800078mes_ES
dc.relation.references10.1021/cs100043jes_ES
dc.relation.references10.1016/j.jcat.2010.11.012es_ES
dc.relation.references10.1006/jcat.1993.1322es_ES
dc.relation.references10.1021/ja810045yes_ES
dc.relation.references10.1126/science.1159639es_ES
dc.relation.references10.1017/S143192760909833Xes_ES
dc.relation.references10.1093/jmicro/dfp016es_ES
dc.relation.references10.1021/jp906754jes_ES
dc.relation.references10.1002/anie.201107391es_ES
dc.relation.references10.1021/jp027596ses_ES
dc.relation.references10.1021/ja9022368es_ES
dc.relation.references10.1039/b201236ges_ES
dc.relation.references10.1016/j.cplett.2008.11.087es_ES
dc.relation.references10.1021/jp052653des_ES
dc.relation.references10.1002/anie.200804154es_ES
dc.relation.references10.1002/anie.200390191es_ES
dc.relation.references10.1002/anie.201108502es_ES
dc.relation.references10.1039/c0cp02680hes_ES
dc.relation.references10.1039/b602079hes_ES
dc.relation.references10.1002/anie.200702427es_ES
dc.relation.references10.1038/nature07194es_ES
dc.relation.references10.1039/B921082Bes_ES
dc.relation.references10.1002/smll.200902398es_ES
dc.relation.references10.1021/cs300252ges_ES
dc.relation.references10.1021/jp9935992es_ES
dc.relation.references10.1021/bi9820816es_ES
dc.relation.references10.1021/bi7016975es_ES
dc.relation.references10.1002/cphc.201100336es_ES
dc.relation.references10.1021/jp048837ues_ES
dc.relation.references10.1039/b809881fes_ES
dc.relation.references10.1126/science.1148624es_ES
dc.relation.references10.1038/nchem.1352es_ES
dc.relation.references10.1021/ja202862kes_ES
dc.relation.references10.1021/nl1026716es_ES
dc.relation.references10.1063/1.464913es_ES
dc.relation.references10.1103/PhysRevB.37.785es_ES
dc.relation.references10.1063/1.438980es_ES
dc.relation.references10.1063/1.438955es_ES
dc.relation.references10.1063/1.448799es_ES
dc.relation.references10.1063/1.449486es_ES
dc.relation.senia254813es_ES
dc.rightsReserva de todos los derechoses_ES
dc.rights.accessRightsAbiertoes_ES
dc.subjectGoldes_ES
dc.subjectGold, clusters, atomicity, oxidation, disulfideses_ES
dc.subjectClusterses_ES
dc.subjectAtomicityes_ES
dc.subjectOxidationes_ES
dc.subjectDisulfideses_ES
dc.subject.classificationQUIMICA ORGANICAes_ES
dc.titleExceptional oxidation activity with size-controlled supported gold clusters of low atomicityes_ES
dc.typeArtículoes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
dspace.entity.typePublication
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