172 research outputs found
Exploring Zeolite Chemistry with the Tools of Surface Science: Challenges, Opportunities, and Limitations
The complexity of catalysts that the surface science community has been able to address has increased substantially in a systematic manner, starting with metal and oxide single crystal surfaces and evolving to an atomistic description of clusters and nanoparticles on well-defined, planar supports. The next step in adding complexity is now to address surfaces of porous oxide materials, in particular of zeolites, which are the most extensively used catalysts in the industry. The recently reported successful fabrication of well-ordered thin films, consisting of planar arrangement of aluminosilicate polygonal prisms on a metal substrate counting with highly acidic bridging hydroxyl groups on the surface, represents the limiting case of infinitely large pore and cages in zeolites. This model system allows one to study reactions catalyzed by zeolites using the toolkit of surface science. In this Perspective, we describe the zeolitic model system, with its virtues and limitations, as well as the challenges, opportunities and expectations for the future in modelling porous catalysts by a surface science approach
Stabilization of Ultrathin Zinc Oxide Films on Metals: Reconstruction versus Hydroxylation
Thin (0001)-oriented films of ZnO on metals may exhibit interlayer relaxations, resulting in the hexagonal boron nitride-like crystal structure. The driving force for such reconstruction is the polar instability of either Zn- or O- terminated surfaces of ZnO(0001). Here, we examined surface hydroxylation as another possible stabilization mechanism. Zinc oxide films grown on Pt(111) were studied by infrared reflectionâabsorption spectroscopy (IRAS) as a function of film thickness and morphology as imaged by scanning tunneling microscopy. Despite prepared in pure oxygen ambient, the âas grownâ films on Pt(111) expose hydroxyl groups. In contrast, the bilayer films on Ag(111) do not exhibit OH species, not even upon dosing of hydrogen or water. The results show that hydrogen may efficiently be provided by a Pt support, even for the multilayer films, via hydrogen dissociation and subsequent diffusion of H atoms through the film. Thermal stability of the OH-terminated surfaces depends on the film thickness, with a monolayer film being the least stable. Removal of OH species from a monolayer film proceeds through water desorption and may be accompanied by hydrogen spillover onto more stable multilayer structures. Stabilization of the polar ZnO surface in the metal-supported films seems to be a delicate balance between interlayer relaxation and hydroxylation and depends on the metal support
Low pressure CO2 hydrogenation to methanol over gold nanoparticles activated on a CeOx/TiO2 Interface
Capture and recycling of CO2 into valuable chemicals such as alcohols could help mitigate its emissions into the atmosphere. Due to its inert nature, the activation of CO2 is a critical step in improving the overall reaction kinetics during its chemical conversion. Although pure gold is an inert noble metal and cannot catalyze hydrogenation reactions, it can be activated when deposited as nanoparticles on the appropriate oxide support. In this combined experimental and theoretical study, it is shown that an electronic polarization at the metal-oxide interface of Au nanoparticles anchored and stabilized on a CeOx/TiO2 substrate generates active centers for CO2 adsorption and its low pressure hydrogenation, leading to a higher selectivity toward methanol. This study illustrates the importance of localized electronic properties and structure in catalysis for achieving higher alcohol selectivity from CO2 hydrogenation.U.S. Department of Energy DE-AC02- 98CH10886, DE-AC02-05CH11231Brookhaven National Laboratory DE-SC001270
Thin silica films on Ru(0001): monolayer, bilayer and three-dimensional networks of [SiO<sub>4</sub>] tetrahedra
The atomic structure of thin silica films grown over a Ru(0001) substrate was studied by X-ray photoelectron spectroscopy, infrared reflection absorption spectroscopy, low energy electron diffraction, helium ion scattering spectroscopy, CO temperature programmed desorption, and scanning tunneling microscopy in combination with density functional theory calculations. The films were prepared by Si vapor deposition and subsequent oxidation at high temperatures. The silica film first grows as a monolayer of corner-sharing [SiO4] tetrahedra strongly bonded to the Ru(0001) surface through the SiâOâRu linkages. At increasing amounts of Si, the film forms a bilayer of corner-sharing [SiO4] tetrahedra which is weakly bonded to Ru(0001). The bilayer film can be grown in either the crystalline or vitreous state, or both coexisting. Further increasing the film thickness leads to the formation of vitreous silica exhibiting a three-dimensional network of [SiO4]. The principal structure of the films can be monitored by infrared spectroscopy, as each structure shows a characteristic vibrational band, i.e., [similar]1135 cm-1 for a monolayer film, [similar]1300 cmâ»-1 for the bilayer structures, and [similar]1250 cmâ»-1 for the bulk-like vitreous silica
Atomically-thin micas as proton conducting membranes
Monolayers of graphene and hexagonal boron nitride (hBN) are highly permeable
to thermal protons. For thicker two-dimensional (2D) materials, proton
conductivity diminishes exponentially so that, for example, monolayer MoS2 that
is just three atoms thick is completely impermeable to protons. This seemed to
suggest that only one-atom-thick crystals could be used as proton conducting
membranes. Here we show that few-layer micas that are rather thick on the
atomic scale become excellent proton conductors if native cations are
ion-exchanged for protons. Their areal conductivity exceeds that of graphene
and hBN by one-two orders of magnitude. Importantly, ion-exchanged 2D micas
exhibit this high conductivity inside the infamous gap for proton-conducting
materials, which extends from 100 C to 500 C. Areal conductivity of
proton-exchanged monolayer micas can reach above 100 S cm-2 at 500 C, well
above the current requirements for the industry roadmap. We attribute the fast
proton permeation to 5 A-wide tubular channels that perforate micas' crystal
structure which, after ion exchange, contain only hydroxyl groups inside. Our
work indicates that there could be other 2D crystals with similar nm-scale
channels, which could help close the materials gap in proton-conducting
applications
Supramolecular binding and separation of hydrocarbons within a functionalised porous metal-organic framework
Supramolecular interactions are fundamental to host-guest binding in chemical and biological processes. Direct visualisation of such supramolecular interactions within host-guest systems is extremely challenging but crucial for the understanding of their function. We report a comprehensive study combining neutron scattering with synchrotron X-ray and neutron diffraction, coupled with computational modelling, to define the detailed binding at a molecular level of acetylene, ethylene and ethane within the porous host NOTT-300. This study reveals the simultaneous and cooperative hydrogen-bonding, ÏÂ·Â·Â·Ï stacking interactions and inter-molecular dipole interactions in the binding of acetylene and ethylene to give up to twelve individual weak supramolecular interactions aligned within the host to form an optimal geometry for intelligent, selective binding of hydrocarbons. We also report, for the first time, the cooperative binding of a mixture of acetylene and ethylene within the porous host together with the corresponding breakthrough experiment and analysis of mixed gas adsorption isotherms
Site-Specific Sodiation Mechanisms of Selenium in Microporous Carbon Host
We combined advanced TEM (HRTEM, HAADF, EELS) with solid-state (SS)MAS NMR and electroanalytical techniques (GITT, etc.) to understand the site-specific sodiation of selenium (Se) encapsulated in a nanoporous carbon host. The architecture employed is representative of a wide number of electrochemically stable and rate-capable Se-based sodium metal battery (SMB) cathodes. SSNMR demonstrates that during the first sodiation, the Se chains are progressively cut to form an amorphous mixture of polyselenides of varying lengths, with no evidence for discrete phase transitions during sodiation. It also shows that Se nearest the carbon pore surface is sodiated first, leading to the formation of a coreâshell compositional profile. HRTEM indicates that the vast majority of the pore-confined Se is amorphous, with the only localized presence of nanocrystalline equilibrium Na2Se2 (hcp) and Na2Se (fcc). A nanoscale fracture of terminally sodiated NaâSe is observed by HAADF, with SSNMR, indicating a physical separation of some Se from the carbon host after the first cycle. GITT reveals a 3-fold increase in Na+ diffusivity at cycle 2, which may be explained by the creation of extra interfaces. These combined findings highlight the complex phenomenology of electrochemical phase transformations in nanoconfined materials, which may profoundly differ from their âfreeâ counterparts
Non-Antioxidant Properties of α-Tocopherol Reduce the Anticancer Activity of Several Protein Kinase Inhibitors In Vitro
The antioxidant properties of α-tocopherol have been proposed to play a beneficial chemopreventive role against cancer. However, emerging data also indicate that it may exert contrasting effects on the efficacy of chemotherapeutic treatments when given as dietary supplement, being in that case harmful for patients. This dual role of α-tocopherol and, in particular, its effects on the efficacy of anticancer drugs remains poorly documented. For this purpose, we studied here, using high throughput flow cytometry, the direct impact of α-tocopherol on apoptosis and cell cycle arrest induced by different cytotoxic agents on various models of cancer cell lines in vitro. Our results indicate that physiologically relevant concentrations of α-tocopherol strongly compromise the cytotoxic and cytostatic action of various protein kinase inhibitors (KI), while other classes of chemotherapeutic agents or apoptosis inducers are unaffected by this vitamin. Interestingly, these anti-chemotherapeutic effects of α-tocopherol appear to be unrelated to its antioxidant properties since a variety of other antioxidants were completely neutral toward KI-induced cell cycle arrest and cell death. In conclusion, our data suggest that dietary α-tocopherol could limit KI effects on tumour cells, and, by extent, that this could result in a reduction of the clinical efficacy of anti-cancer treatments based on KI molecules
Surface Composition and Catalytic Evolution of Au x Pd1âx (x = 0.25, 0.50 and 0.75) Nanoparticles Under CO/O2 Reaction in Torr Pressure Regime and at 200 °C
Exploring Zeolite Chemistry with the Tools of Surface Science: Challenges, Opportunities, and Limitations
- âŠ