The evolution of model catalytic systems; studies of structure, bonding and dynamics from single crystal metal surfaces to nanoparticles, and from low pressure (< 10(-3) Torr) to high pressure (> 10(-3) Torr) to liquid interfaces

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dc.contributor.authorSomorjai, GAko
dc.contributor.authorYork, RLko
dc.contributor.authorButcher, Dko
dc.contributor.authorPark, JeongYoungko
dc.date.accessioned2013-03-07T15:28:01Z-
dc.date.available2013-03-07T15:28:01Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2007-
dc.identifier.citationPHYSICAL CHEMISTRY CHEMICAL PHYSICS, v.9, no.27, pp.3500 - 3513-
dc.identifier.issn1463-9076-
dc.identifier.urihttp://hdl.handle.net/10203/90532-
dc.description.abstractThe material and pressure gap has been a long standing challenge in the field of heterogeneous catalysis and have transformed surface science and biointerfacial research. In heterogeneous catalysis, the material gap refers to the discontinuity between well-characterized model systems and industrially relevant catalysts. Single crystal metal surfaces have been useful model systems to elucidate the role of surface defects and the mobility of reaction intermediates in catalytic reactivity and selectivity. As nanoscience advances, we have developed nanoparticle catalysts with lithographic techniques and colloidal syntheses. Nanoparticle catalysts on oxide supports allow us to investigate several important ingredients of heterogeneous catalysis such as the metal-oxide interface and the influence of noble metal particle size and surface structure on catalytic selectivity. Monodispersed nanoparticle and nanowire arrays were fabricated for use as model catalysts by lithographic techniques. Platinum and rhodium nanoparticles in the 1 - 10 nm range were synthesized in colloidal solutions in the presence of polymer capping agents. The most catalytically active systems are employed at high pressure or at solid - liquid interfaces. In order to study the high pressure and liquid interfaces on the molecular level, experimental techniques with which we bridged the pressure gap in catalysis have been developed. These techniques include the ultrahigh vacuum system equipped with high pressure reaction cell, high pressure Sum Frequency Generation (SFG) vibration spectroscopy, High Pressure Scanning Tunneling Microscopy (HP-STM), and High Pressure X-ray Photoemission Spectroscopy (HP-XPS), and Quartz Crystal Microbalance (QCM). In this article, we overview the development of experimental techniques and evolution of the model systems for the research of heterogeneous catalysis and biointerfacial studies that can shed light on the long-standing issues of materials and pressure gaps.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectSUM-FREQUENCY-GENERATION-
dc.subjectSCANNING-TUNNELING-MICROSCOPY-
dc.subjectATOMIC-FORCE MICROSCOPY-
dc.subjectELECTRON-BEAM LITHOGRAPHY-
dc.subjectPLATINUM NANOWIRE ARRAYS-
dc.subjectVIBRATIONAL SPECTROSCOPY-
dc.subjectCARBON-MONOXIDE-
dc.subjectETHYLENE HYDROGENATION-
dc.subjectAMMONIA-SYNTHESIS-
dc.subjectCO OXIDATION-
dc.titleThe evolution of model catalytic systems; studies of structure, bonding and dynamics from single crystal metal surfaces to nanoparticles, and from low pressure (&lt; 10(-3) Torr) to high pressure (&gt; 10(-3) Torr) to liquid interfaces-
dc.typeArticle-
dc.identifier.wosid000247800700005-
dc.identifier.scopusid2-s2.0-34447265001-
dc.type.rimsART-
dc.citation.volume9-
dc.citation.issue27-
dc.citation.beginningpage3500-
dc.citation.endingpage3513-
dc.citation.publicationnamePHYSICAL CHEMISTRY CHEMICAL PHYSICS-
dc.identifier.doi10.1039/b618805b-
dc.contributor.localauthorPark, JeongYoung-
dc.contributor.nonIdAuthorSomorjai, GA-
dc.contributor.nonIdAuthorYork, RL-
dc.contributor.nonIdAuthorButcher, D-
dc.type.journalArticleReview-
dc.subject.keywordPlusSUM-FREQUENCY-GENERATION-
dc.subject.keywordPlusSCANNING-TUNNELING-MICROSCOPY-
dc.subject.keywordPlusATOMIC-FORCE MICROSCOPY-
dc.subject.keywordPlusELECTRON-BEAM LITHOGRAPHY-
dc.subject.keywordPlusPLATINUM NANOWIRE ARRAYS-
dc.subject.keywordPlusVIBRATIONAL SPECTROSCOPY-
dc.subject.keywordPlusCARBON-MONOXIDE-
dc.subject.keywordPlusETHYLENE HYDROGENATION-
dc.subject.keywordPlusAMMONIA-SYNTHESIS-
dc.subject.keywordPlusCO OXIDATION-
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