| 1. |
- Arman, Alif, et al.
(författare)
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Adsorption of hydrogen on stable and metastable Ir(100) surfaces
- 2017
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Ingår i: Surface Science. - : Elsevier BV. - 0039-6028. ; 656, s. 66-76
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Using the combination of high resolution core level spectroscopy and density functional theory we present adetailed spectroscopic study for all clean and hydrogen covered phases of Ir(100). The results are complementedby an investigation of the hydrogen desorption process from various phases using temperature programmeddesorption spectroscopy and scanning tunneling microscopy. In total, all experimentally determined core levelshifts match very well with those predicted by density functional theory based on established structural models.In particular, we find for the (bridge site) adsorption on the unreconstructed 1×1 phase that the initial core levelshift of surface Ir atoms is altered by +0.17 eV for each Ir–H bond formed. In the submonolayer regime we findevidence for island formation at low temperatures. For the H-induced deconstructed 5×1-H phase we identifyfour different surface core level shifts with two of them being degenerate. Finally, for the reconstructed 5×1-hexphase also four surface components are identified, which undergo a rather rigid core level shift of +0.15 eV uponhydrogen adsorption suggesting a similarly homogeneous charge transfer to all Ir surface atoms.Thermodesorption experiments for the 5×1-H phase reveal two different binding states for hydrogenindependent of the total coverage. We conclude that the surface always separates into patches of fully covereddeconstructed and uncovered reconstructed phases. We could also show by tunneling microscopy that with thedesorption of the last hydrogen atom from the deconstructed unit cell the surface instantaneously reverts intothe reconstructed state. Eventually, we could determine the saturation coverage upon molecular adsorption forall phases to be θmax = 1.0 ML1×1−H , θ = 0.8 ML max5×1−H , and θ ≥ 1.0 ML max5×1−hex−H .
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| 2. |
- Arman, Alif, et al.
(författare)
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Co3O4(100) films grown on Ag(100): Structure and chemical properties
- 2017
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Ingår i: Surface Science. - : Elsevier BV. - 0039-6028. ; 657, s. 90-95
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Tidskriftsartikel (refereegranskat)abstract
- Spinel type Co3O4(100) is successfully grown on Ag(100) at ultrahigh vacuum conditions and its structure, electronic and chemical properties are compared with those of Co3O4(111) grown on Ir(100). We find that the Co3O4(100) is unreconstructed. In contrast to the defect free Co3O4(111) surface the Co3O4(100) surface contains a high concentration of defects that we assign to subsurface cation vacancies analogous to those observed for Fe3O4(100). Our photoemission and absorption spectroscopy experiments reveal a very similar electronic structure of the Co3O4(111) and Co3O4(100) surfaces. The similar electronic structure of the two surfaces is reflected in the CO adsorption properties at low temperatures, as we observe adsorption of molecular CO as well as the formation of carbonate (CO3) species on both surfaces upon CO exposure at 85 K.
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| 3. |
- Barbier, Antoine, et al.
(författare)
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Editorial
- 2016
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Ingår i: Physics Procedia. - : Elsevier BV. - 1875-3884 .- 1875-3892. ; 85, s. 1-3
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Tidskriftsartikel (refereegranskat)abstract
- Editorial comments about the proceedings of EMRS Symposium C: In situ studies of functional nano materials at large scale facilities: From model systems to applications, EMRS Spring Meeting.
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| 4. |
- Blomberg, Sara, et al.
(författare)
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2D and 3D imaging of the gas phase close to an operating model catalyst by planar laser induced fluorescence
- 2016
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Ingår i: Journal of Physics: Condensed Matter. - : IOP Publishing. - 0953-8984 .- 1361-648X. ; 28:45
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Forskningsöversikt (refereegranskat)abstract
- In recent years, efforts have been made in catalysis related surface science studies to explore the possibilities to perform experiments at conditions closer to those of a technical catalyst, in particular at increased pressures. Techniques such as high pressure scanning tunneling/atomic force microscopy (HPSTM/AFM), near ambient pressure x-ray photoemission spectroscopy (NAPXPS), surface x-ray diffraction (SXRD) and polarization-modulation infrared reflection absorption spectroscopy (PM-IRAS) at semi-realistic conditions have been used to study the surface structure of model catalysts under reaction conditions, combined with simultaneous mass spectrometry (MS). These studies have provided an increased understanding of the surface dynamics and the structure of the active phase of surfaces and nano particles as a reaction occurs, providing novel information on the structure/activity relationship. However, the surface structure detected during the reaction is sensitive to the composition of the gas phase close to the catalyst surface. Therefore, the catalytic activity of the sample itself will act as a gas-source or gas-sink, and will affect the surface structure, which in turn may complicate the assignment of the active phase. For this reason, we have applied planar laser induced fluorescence (PLIF) to the gas phase in the vicinity of an active model catalysts. Our measurements demonstrate that the gas composition differs significantly close to the catalyst and at the position of the MS, which indeed should have a profound effect on the surface structure. However, PLIF applied to catalytic reactions presents several beneficial properties in addition to investigate the effect of the catalyst on the effective gas composition close to the model catalyst. The high spatial and temporal resolution of PLIF provides a unique tool to visualize the on-set of catalytic reactions and to compare different model catalysts in the same reactive environment. The technique can be applied to a large number of molecules thanks to the technical development of lasers and detectors over the last decades, and is a complementary and visual alternative to traditional MS to be used in environments difficult to asses with MS. In this article we will review general considerations when performing PLIF experiments, our experimental set-up for PLIF and discuss relevant examples of PLIF applied to catalysis.
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| 5. |
- Blomberg, Sara, et al.
(författare)
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Combining synchrotron light with laser technology in catalysis research
- 2018
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Ingår i: Journal of Synchrotron Radiation. - 1600-5775 .- 0909-0495. ; 25:5, s. 1389-1394
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Tidskriftsartikel (refereegranskat)abstract
- High-energy surface X-ray diffraction (HESXRD) provides surface structural information with high temporal resolution, facilitating the understanding of the surface dynamics and structure of the active phase of catalytic surfaces. The surface structure detected during the reaction is sensitive to the composition of the gas phase close to the catalyst surface, and the catalytic activity of the sample itself may affect the surface structure, which in turn may complicate the assignment of the active phase. For this reason, planar laser-induced fluorescence (PLIF) and HESXRD have been combined during the oxidation of CO over a Pd(100) crystal. PLIF complements the structural studies with an instantaneous two-dimensional image of the CO2 gas phase in the vicinity of the active model catalyst. Here the combined HESXRD and PLIF operandomeasurements of CO oxidation over Pd(100) are presented, allowing for an improved assignment of the correlation between sample structure and the CO2distribution above the sample surface with sub-second time resolution.
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| 6. |
- Blomberg, Sara, et al.
(författare)
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Real-Time Gas-Phase Imaging over a Pd(110) Catalyst during CO Oxidation by Means of Planar Laser-Induced Fluorescence.
- 2015
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Ingår i: ACS Catalysis. - : American Chemical Society (ACS). - 2155-5435. ; 5:4, s. 2028-2034
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Tidskriftsartikel (refereegranskat)abstract
- The gas composition surrounding a catalytic sample has direct impact on its surface structure, which is essential when in situ investigations of model catalysts are performed. Herein a study of the gas phase close to a Pd(110) surface during CO oxidation under semirealistic conditions is presented. Images of the gas phase, provided by planar laser-induced fluorescence, clearly visualize the formation of a boundary layer with a significantly lower CO partial pressure close to the catalytically active surface, in comparison to the overall concentration as detected by mass spectrometry. The CO partial pressure variation within the boundary layer will have a profound effect on the catalysts' surface structure and function and needs to be taken into consideration for in situ model catalysis studies.
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| 7. |
- Blomberg, Sara, et al.
(författare)
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Strain Dependent Light-off Temperature in Catalysis Revealed by Planar Laser-Induced Fluorescence
- 2017
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Ingår i: ACS Catalysis. - : American Chemical Society (ACS). - 2155-5435. ; 7:1, s. 110-114
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Tidskriftsartikel (refereegranskat)abstract
- Understanding how specific atom sites on metal surfaces lower the energy barrier for chemical reactions is vital in catalysis. Studies on simplified model systems have shown that atoms arranged as steps on the surface play an important role in catalytic reactions, but a direct comparison of how the light-off temperature is affected by the atom orientation on the step has not yet been possible due to methodological constraints. Here we report in situ spatially resolved measurements of the CO2 production over a cylindrical-shaped Pd catalyst and show that the light-off temperature at different parts of the crystal depends on the step orientation of the two types of steps (named A and B). Our finding is supported by density functional theory calculations, revealing that the steps, in contrast to what has been previously reported in the literature, are not directly involved in the reaction onset but have the role of releasing stress.
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| 8. |
- Busch, Michael, 1983, et al.
(författare)
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Adsorption of NO on Fe3O4(111)
- 2018
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Ingår i: Chemical Physics Letters. - : Elsevier BV. - 0009-2614 .- 1873-4448. ; 693, s. 84-87
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Tidskriftsartikel (refereegranskat)abstract
- Adsorption of NO on Fe 3 O 4 (111) is studied by density functional theory (DFT) calculations. NO is preferably adsorbed atop the octahedral site which has a clearly higher adsorption energy than the tetrahedral site. The difference in adsorption energy correlates with differences in adsorption geometries and N–O stretch vibrations. The results are in good agreement with temperature programmed desorption (TPD) and reflection-adsorption IR spectroscopy (RAIRS) measurements and provide an explanation of the observation of only one vibrational mode despite two distinct TPD features.
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| 9. |
- Evertsson, Jonas, et al.
(författare)
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Anodization of Al(100), Al(111) and Al Alloy 6063 studied in situ with X-ray reflectivity and electrochemical impedance spectroscopy
- 2017
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Ingår i: Journal of Electroanalytical Chemistry. - : Elsevier BV. - 1572-6657. ; 799, s. 556-562
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Tidskriftsartikel (refereegranskat)abstract
- We present results from the anodization of single crystal Al(100) and Al(111) surfaces and the aluminum alloy AA 6063 studied in situ by X-ray reflectivity and electrochemical impedance spectroscopy. We observe that the anodic oxide layer grows linearly with the anodization potential and that the thicknesses are similar for all samples. However, the thicknesses obtained from X-ray reflectivity are higher than that obtained from electrochemical impedance spectroscopy. We attribute the higher thicknesses to an outer porous oxide layer, which is not detected by electrochemical impedance spectroscopy. Both, electrochemical impedance spectroscopy and X-ray reflectivity suggests that a more heterogeneous and rough oxide is formed on AA 6063 due to the influence of the alloying elements and intermetallic particles during the growth.
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| 10. |
- Evertsson, Jonas, et al.
(författare)
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Self-organization of porous anodic alumina films studied in situ by grazing-incidence transmission small-angle X-ray scattering
- 2018
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Ingår i: RSC Advances. - 2046-2069. ; 8:34, s. 18980-18991
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Tidskriftsartikel (refereegranskat)abstract
- Self-ordered porous anodic alumina (PAA) films are studied extensively due to a large number of possible applications in nanotechnology and low cost of production. Whereas empirical relationships between growth conditions and produced oxides have been established, fundamental aspects regarding pore formation and self-organization are still under debate. We present in situ structural studies of PAA films using grazing-incidence transmission small-angle X-ray scattering. We have considered the two most used recipes where the pores self-organize: 0.3 M H2SO4 at 25 V and 0.3 M C2H2O4 at 40 V. During anodization we have followed the evolution of the structural parameters: average interpore distance, length of ordered pores domains, and thickness of the porous oxide layer. Compared to the extensively used ex situ investigations, our approach gives an unprecedented temporal accuracy in determination of the parameters. By using of Al(100), Al(110) and Al(111) surfaces, the influence of surface orientation on the structural evolution was studied, and no significant differences in the interpore distance and domain length could be observed. However, the rate of oxide growth in 0.3 M C2H2O4 at 40 V was significantly influenced by the surface orientation, where the slowest growth occurs for Al(111). In 0.3 M H2SO4 at 25 V, the growth rates were higher, but the influence of surface orientation was not obvious. The structural evolution was also studied on pre-patterned aluminum surfaces. These studies show that although the initial structures of the oxides are governed by pre-patterning geometry, the final structures are dictated by the anodization conditions.
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