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  • 1
    Publication Date: 2003-01-18
    Description: We report the design of surfaces that exhibit dynamic changes in interfacial properties, such as wettability, in response to an electrical potential. The change in wetting behavior was caused by surface-confined, single-layered molecules undergoing conformational transitions between a hydrophilic and a moderately hydrophobic state. Reversible conformational transitions were confirmed at a molecular level with the use of sum-frequency generation spectroscopy and at a macroscopic level with the use of contact angle measurements. This type of surface design enables amplification of molecular-level conformational transitions to macroscopic changes in surface properties without altering the chemical identity of the surface. Such reversibly switching surfaces may open previously unknown opportunities in interfacial engineering.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lahann, Joerg -- Mitragotri, Samir -- Tran, Thanh-Nga -- Kaido, Hiroki -- Sundaram, Jagannathan -- Choi, Insung S -- Hoffer, Saskia -- Somorjai, Gabor A -- Langer, Robert -- New York, N.Y. -- Science. 2003 Jan 17;299(5605):371-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemical Engineering, Massachusetts Institute of Technology (MIT), 45 Carleton Street, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/12532011" target="_blank"〉PubMed〈/a〉
    Keywords: Adsorption ; Chemistry, Physical ; Electricity ; Electrochemistry ; Esters ; Gold ; Hydrogen-Ion Concentration ; Hydrophobic and Hydrophilic Interactions ; Molecular Conformation ; Molecular Structure ; Palmitic Acids/*chemistry ; Physicochemical Phenomena ; Spectrum Analysis ; *Surface Properties ; Thermodynamics ; Wettability
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2004-05-01
    Description: Hollow nanocrystals can be synthesized through a mechanism analogous to the Kirkendall Effect, in which pores form because of the difference in diffusion rates between two components in a diffusion couple. Starting with cobalt nanocrystals, we show that their reaction in solution with oxygen and either sulfur or selenium leads to the formation of hollow nanocrystals of the resulting oxide and chalcogenides. This process provides a general route to the synthesis of hollow nanostructures of a large number of compounds. A simple extension of the process yielded platinum-cobalt oxide yolk-shell nanostructures, which may serve as nanoscale reactors in catalytic applications.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yin, Yadong -- Rioux, Robert M -- Erdonmez, Can K -- Hughes, Steven -- Somorjai, Gabor A -- Alivisatos, A Paul -- New York, N.Y. -- Science. 2004 Apr 30;304(5671):711-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, University of California at Berkeley, and Materials Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15118156" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 1994-09-02
    Description: The platinum-rhodium tip of a scanning tunneling microscope that operates inside of an atmospheric-pressure chemical reactor cell has been used to locally rehydrogenate carbonaceous fragments deposited on the (111) surface of platinum. The carbon fragments were produced by partial dehydrogenation of propylene. The reactant gas environment inside the cell consisted of pure H(2) or a 1:9 mixture of CH(3)CHCH(2) and H(2) at 300 kelvin. The platinum-rhodium tip acted as a catalyst after activation by short voltage pulses. In this active state, the clusters in the area scanned by the tip were reacted away with very high spatial resolution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McIntyre, B J -- Salmeron, M -- Somorjai, G A -- New York, N.Y. -- Science. 1994 Sep 2;265(5177):1415-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17833813" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2008-10-11
    Description: Heterogeneous catalysts that contain bimetallic nanoparticles may undergo segregation of the metals, driven by oxidizing and reducing environments. The structure and composition of core-shell Rh(0.5)Pd(0.5) and Pt(0.5)Pd(0.5) nanoparticle catalysts were studied in situ, during oxidizing, reducing, and catalytic reactions involving NO, O2, CO, and H2 by x-ray photoelectron spectroscopy at near-ambient pressure. The Rh(0.5)Pd(0.5) nanoparticles underwent dramatic and reversible changes in composition and chemical state in response to oxidizing or reducing conditions. In contrast, no substantial segregation of Pd or Pt atoms was found in Pt(0.5)Pd(0.5) nanoparticles. The different behaviors in restructuring and chemical response of Rh(0.5)Pd(0.5) and Pt(0.5)Pd(0.5) nanoparticle catalysts under the same reaction conditions illustrates the flexibility and tunability of the structure of bimetallic nanoparticle catalysts during catalytic reactions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tao, Feng -- Grass, Michael E -- Zhang, Yawen -- Butcher, Derek R -- Renzas, James R -- Liu, Zhi -- Chung, Jen Y -- Mun, Bongjin S -- Salmeron, Miquel -- Somorjai, Gabor A -- New York, N.Y. -- Science. 2008 Nov 7;322(5903):932-4. doi: 10.1126/science.1164170. Epub 2008 Oct 9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Materials Sciences and Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18845713" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2010-02-13
    Description: Stepped single-crystal surfaces are viewed as models of real catalysts, which consist of small metal particles exposing a large number of low-coordination sites. We found that stepped platinum (Pt) surfaces can undergo extensive and reversible restructuring when exposed to carbon monoxide (CO) at pressures above 0.1 torr. Scanning tunneling microscopy and photoelectron spectroscopy studies under gaseous environments near ambient pressure at room temperature revealed that as the CO surface coverage approaches 100%, the originally flat terraces of (557) and (332) oriented Pt crystals break up into nanometer-sized clusters and revert to the initial morphology after pumping out the CO gas. Density functional theory calculations provide a rationale for the observations whereby the creation of increased concentrations of low-coordination Pt edge sites in the formed nanoclusters relieves the strong CO-CO repulsion in the highly compressed adsorbate film. This restructuring phenomenon has important implications for heterogeneous catalytic reactions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tao, Feng -- Dag, Sefa -- Wang, Lin-Wang -- Liu, Zhi -- Butcher, Derek R -- Bluhm, Hendrik -- Salmeron, Miquel -- Somorjai, Gabor A -- New York, N.Y. -- Science. 2010 Feb 12;327(5967):850-3. doi: 10.1126/science.1182122.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Materials Science Division, Lawrence Berkeley National Lab, Berkeley, CA 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20150498" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2014-03-01
    Description: Control of structure at the atomic level can precisely and effectively tune catalytic properties of materials, enabling enhancement in both activity and durability. We synthesized a highly active and durable class of electrocatalysts by exploiting the structural evolution of platinum-nickel (Pt-Ni) bimetallic nanocrystals. The starting material, crystalline PtNi3 polyhedra, transforms in solution by interior erosion into Pt3Ni nanoframes with surfaces that offer three-dimensional molecular accessibility. The edges of the Pt-rich PtNi3 polyhedra are maintained in the final Pt3Ni nanoframes. Both the interior and exterior catalytic surfaces of this open-framework structure are composed of the nanosegregated Pt-skin structure, which exhibits enhanced oxygen reduction reaction (ORR) activity. The Pt3Ni nanoframe catalysts achieved a factor of 36 enhancement in mass activity and a factor of 22 enhancement in specific activity, respectively, for this reaction (relative to state-of-the-art platinum-carbon catalysts) during prolonged exposure to reaction conditions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chen, Chen -- Kang, Yijin -- Huo, Ziyang -- Zhu, Zhongwei -- Huang, Wenyu -- Xin, Huolin L -- Snyder, Joshua D -- Li, Dongguo -- Herron, Jeffrey A -- Mavrikakis, Manos -- Chi, Miaofang -- More, Karren L -- Li, Yadong -- Markovic, Nenad M -- Somorjai, Gabor A -- Yang, Peidong -- Stamenkovic, Vojislav R -- New York, N.Y. -- Science. 2014 Mar 21;343(6177):1339-43. doi: 10.1126/science.1249061. Epub 2014 Feb 27.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, University of California, Berkeley, CA 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24578531" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
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  • 7
    Publication Date: 2016-01-30
    Description: The (111) surface of copper (Cu), its most compact and lowest energy surface, became unstable when exposed to carbon monoxide (CO) gas. Scanning tunneling microscopy revealed that at room temperature in the pressure range 0.1 to 100 Torr, the surface decomposed into clusters decorated by CO molecules attached to edge atoms. Between 0.2 and a few Torr CO, the clusters became mobile in the scale of minutes. Density functional theory showed that the energy gain from CO binding to low-coordinated Cu atoms and the weakening of binding of Cu to neighboring atoms help drive this process. Particularly for softer metals, the optimal balance of these two effects occurs near reaction conditions. Cluster formation activated the surface for water dissociation, an important step in the water-gas shift reaction.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Eren, Baran -- Zherebetskyy, Danylo -- Patera, Laerte L -- Wu, Cheng Hao -- Bluhm, Hendrik -- Africh, Cristina -- Wang, Lin-Wang -- Somorjai, Gabor A -- Salmeron, Miquel -- New York, N.Y. -- Science. 2016 Jan 29;351(6272):475-8. doi: 10.1126/science.aad8868.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Materials Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA. ; Materials Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA. CNR-IOM, Laboratorio TASC, Strada Statale 14, Km. 163.5, I-34149 Trieste, Italy. Physics Department and CENMAT, University of Trieste, via A. Valerio 2, I-34127 Trieste, Italy. ; Materials Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA. Department of Chemistry, University of California, Berkeley, CA, USA. ; Chemical Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA. ; CNR-IOM, Laboratorio TASC, Strada Statale 14, Km. 163.5, I-34149 Trieste, Italy. ; Materials Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA. Department of Materials Science and Engineering, University of California, Berkeley, CA, USA. mbsalmeron@lbl.gov.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26823421" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
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  • 8
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1978-08-11
    Description: During the past 15 years, surfaces have been increasingly studied on the atomic scale. As a result, their atomic structure and composition and the dynamics of gas-surface interactions are much better understood. Modern surface science is beginning to have an impact on many technologies. Techniques are readily available to study solid-vacuum and solid-gas interfaces. Studies of solid-liquid and solid-solid interfaces are difficult and appear to be challenging frontier areas of research. Surface science is at the heart of most research and development problems in energy conversion and storage.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Somorjai, G A -- New York, N.Y. -- Science. 1978 Aug 11;201(4355):489-97.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17790425" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-02-22
    Description: During the last 20 years, surface scientists have developed a variety of techniques that make it possible to study, on the molecular level, the structure, composition, and chemical bonding in the surface monolayer. Both single-crystal model catalysts and real catalyst systems that are active in important chemical processes have been investigated by a combination of ultrahigh-vacuum surface science techniques and high-pressure kinetic techniques in an effort to determine the relation between the structure and composition of the surface and the rates of reaction and selectivities. The structure of the atomic surface, a strongly adsorbed overlayer, and the oxidation states of surface atoms are the important molecular features of an active catalyst. As a consequence of modern surface science, the design and preparation of catalysts has developed from an art into a high technology.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Somorjai, G A -- New York, N.Y. -- Science. 1985 Feb 22;227(4689):902-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17821221" target="_blank"〉PubMed〈/a〉
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  • 10
    Publication Date: 1985-04-01
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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