| 1. |
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| 2. |
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| 3. |
- Nilson, Katharina, et al.
(författare)
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STM and XPS characterization of Zinc Phthalocyanine on InSb(001)
- 2008
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Ingår i: Surface Science. - : Elsevier BV. - 0039-6028 .- 1879-2758. ; 602:2, s. 452-459
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Tidskriftsartikel (refereegranskat)abstract
- Zinc phthalocyanine (ZnPc) adsorbed on the InSb(0 0 1)-c(8 x 2) surface has been studied by scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS). Coverages from sub-monolayer to monolayer (ML) have been investigated. The molecules form ordered structures on the reconstructed rows of the surface with the molecular plane parallel to the surface. A change in the electronic structure between the sub-ML and higher coverages has been observed. Moreover, in order to study the influence of annealing on the electronic and geometric structures, the samples have been heated to elevated temperatures (about 640 K). In addition, multi-layer ZnPc films have been characterized by XPS measurements.
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| 4. |
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| 5. |
- Ahlund, John, et al.
(författare)
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Molecular growth determined by surface domain patterns
- 2008
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 112:17, s. 6887-6890
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Tidskriftsartikel (refereegranskat)abstract
- The growth of iron phthalocyanine (FePc) on InSb(001) c(8 x 2) at submonolayer coverage has been investigated with scanning tunneling microscopy (STM). FePc adsorbs flat centered on the In rows both at 70 K and at room temperature (RT). However, the shapes of the two-dimensional molecular islands are fundamentally different; while the RT growth results in chainlike structures along the [I 10] direction, as already observed for other Pc's adsorbed on the same surface, the islands are prolonged along [110], i.e., perpendicular to the substrate rows, at 70 K. These observations are explained on the basis of a recently observed new surface phase at low temperature, resulting in structural domains on the surface. The molecular growth front follows the propagating domain boundary that freezes at low temperature.
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| 6. |
- Bose, Partha Pratim, et al.
(författare)
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Effects of Congo Red on A beta(1-40) Fibril Formation Process and Morphology
- 2010
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Ingår i: ACS CHEMICAL NEUROSCIENCE. - : American Chemical Society (ACS). - 1948-7193. ; 1:4, s. 315-324
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Tidskriftsartikel (refereegranskat)abstract
- Alzheimer's disease (AD), an age-related neurodegenerative disorder, is the most common form of dementia, and the seventh-leading cause of death in the United States. Current treatments offer only symptomatic relief; thus, there is a great need for new treatments with disease-modifying potential. One pathological hallmark of AD is so-called senile plaques, mainly made up of beta-sheet-rich assemblies of 40- or 42-residue amyloid beta-peptides (A beta). Hence, inhibition of A beta aggregation is actively explored as an option to prevent or treat AD. Congo red (CR) has been widely used as a model antiamyloid agent to prevent A beta aggregation. Herein, we report detailed morphological studies on the effect of CR as an antiamyloid agent, by circular dichroism spectroscopy, photo-induced cross-linking reactions, and atomic force microscopy. We also demonstrate the effect of CR on a preaggregated sample of A beta(1-40). Our result suggests that A beta(1-40) follows a different path for aggregation in the presence of CR.
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| 7. |
- Eriksson, Kristofer L. E., et al.
(författare)
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Performance of a Biomimetic Oxidation Catalyst Immobilized on Silicon Wafers : Comparison with Its Gold Congener
- 2010
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 26:21, s. 16349-16354
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Tidskriftsartikel (refereegranskat)abstract
- With the aim of extending the usefulness of an existing biomimetic catalytic system, cobalt porphyrin catalytic units with thiol linkers were heterogenized via chemical grafting to silicon wafers and utilized for the catalytic oxidation of hydroquinone to p-benzoquinone. Atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) were used to analyze the morphology and composition of the heterogeneous catalyst. The results of the catalytic oxidation of hydroquinone obtained with porphyrins grafted on silicon were compared with those obtained earlier with the same catalyst in homogeneous phase and immobilized on gold. It was found that the catalysis could run over 400 h, without showing any sign of deactivation. The measured catalytic activity is at least 10 times higher than that measured under homogeneous conditions, but also 10 times lower than that observed with the catalytic unit immobilized on gold. The reasons of this discrepancy are discussed in term of substrate influence and overlayer organization. The silicon-immobilized catalyst has potential as an advanced functional material with applications in oxidative heterogeneous catalysis of organic reactions, as it combines long-term relatively high activity with low cost.
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| 8. |
- Eriksson, Kristofer, et al.
(författare)
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Manufacturing of Anisotropic Particles by Site Specific Oxidation of Thiols
- 2012
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Ingår i: Journal of Materials Chemistry. - 0959-9428 .- 1364-5501. ; 22:16, s. 7681-7683
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Tidskriftsartikel (refereegranskat)abstract
- A novel method for the manufacturing of functional anisotropic particles based on an inexpensive and straightforward electrochemical approach is presented. The method enables large-scale manufacturing of anisotropic particles as well as fabrication of multifunctional beads which may be used in the design of barcodes for multiplex diagnostics.
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| 9. |
- Eriksson, Kristofer, et al.
(författare)
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Manufacturing of anisotropic particles by site specific oxidation of thiols
- 2012
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Ingår i: Journal of Materials Chemistry. - : Royal Society of Chemistry (RSC). - 0959-9428 .- 1364-5501. ; 22:16, s. 7681-7683
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Tidskriftsartikel (refereegranskat)abstract
- A novel method for the manufacturing of functional anisotropic particles based on an inexpensive and straightforward electrochemical approach is presented. The method enables large-scale manufacturing of anisotropic particles as well as fabrication of multifunctional beads which may be used in the design of barcodes for multiplex diagnostics.
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| 10. |
- Grand, Laszlo, et al.
(författare)
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Short and long term biocompatibility of NeuroProbes silicon probes
- 2010
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Ingår i: Journal of Neuroscience Methods. - : Elsevier BV. - 0165-0270 .- 1872-678X. ; 189:2, s. 216-229
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Tidskriftsartikel (refereegranskat)abstract
- Brain implants provide exceptional tools to understand and restore cerebral functions. The utility of these devices depends crucially on their biocompatibility and long term viability. We addressed these points by implanting non-functional, NeuroProbes silicon probes, without or with hyaluronic acid (Hya), dextran (Dex), dexamethasone (DexM), Hya + DexM coating, into rat neocortex. Light and transmission electron microscopy were used to investigate neuronal survival and glial response. The surface of explanted probes was examined in the scanning electron microscope. We show that blood vessel disruption during implantation could induce considerable tissue damage. If, however, probes could be inserted without major bleeding, light microscopical evidence of damage to surrounding neocortical tissue was much reduced. At distances less than 100 mu m from the probe track a considerable neuron loss (similar to 40%) occurred at short survival times, while the neuronal numbers recovered close to control levels at longer survival. Slight gliosis was observed at both short and long term survivals. Electron microscopy showed neuronal cell bodies and synapses close (<10 mu m) to the probe track when bleeding could be avoided. The explanted probes were usually partly covered by tissue residue containing cells with different morphology. Our data suggest that NeuroProbes silicon probes are highly biocompatible. If major blood vessel disruption can be avoided, the low neuronal cell loss and gliosis should provide good recording and stimulating results with future functional probes. We found that different bioactive molecule coatings had small differential effects on neural cell numbers and gliosis, with optimal results achieved using the DexM coated probes. (C) 2010 Elsevier B.V. All rights reserved.
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| 11. |
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| 12. |
- Janin, Emmanuelle, et al.
(författare)
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Adsorption and bonding of 2-butenal on Sn/Pt surface alloys
- 2003
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Ingår i: Journal of Catalysis. - : Elsevier BV. - 0021-9517 .- 1090-2694. ; 215:2, s. 245-253
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Tidskriftsartikel (refereegranskat)abstract
- The adsorption of 2-butenal on the Pt(111), Pt(111)Sn-(2 x 2), and Pt(111)Sn-(root3 x root3)R30degrees surfaces has been studied by high-resolution photoelectron spectroscopy and DFT calculations. On Pt(111) 2-butenal adsorbs at a threefold hollow in a eta(3)(C,C,O) configuration. A similar geometry is observed for Pt(111)Sn-(2 x 2), although the oxygen coordinates to tin instead of platinum. As the surface coverage of tin increases, as for Pt(111)Sn-(root3 x root3)R30degrees, the most stable adsorption geometry changes to eta(1)(O), where the carbonyl oxygen once again coordinates to tin. The carbonyl bond thus retains an activated character as Pt/Sn alloys are formed. The alkene/surface interaction is, however, dramatically influenced at increasing surface concentrations of tin.
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| 13. |
- Janin, Emmanuelle, et al.
(författare)
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Adsorption and bonding of propene and 2-butenal on Pt(111)
- 2001
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Ingår i: Surface Science. - 0039-6028 .- 1879-2758. ; 482, s. 83-89
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Tidskriftsartikel (refereegranskat)abstract
- The adsorption of propene and 2-butenal on the Pt(1 1 1) surface has been studied by high resolution photoelectron spectroscopy, both in the mono-and multi-layer regime. The results obtained indicate an involvement of both aliphatic and carbonyl groups in the bonding of 2-butenal with the platinum surface in the sub-monolayer regime.
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| 14. |
- Karlsson, P. G., et al.
(författare)
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Initial stages of ZrO2 chemical vapor deposition on Si(100)-(2x1) from zirconium tetra-tert-butoxide
- 2008
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Ingår i: Surface Science. - : Elsevier BV. - 0039-6028 .- 1879-2758. ; 602:10, s. 1803-1809
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Tidskriftsartikel (refereegranskat)abstract
- The initial stages of chemical vapor deposition of ZrO2 from zirconium tetra-tert-butoxide (ZTB) on Si(100)-(2 x 1) have been studied by scanning tunnelling microscopy (STM) and synchrotron radiation excited photoelectron spectroscopy (PES). The STM images and core level (PES) spectra indicate that the predominant surface modifications induced by ZTB are due to silicon carbonization and formation of zirconium dioxide. The carbonization reaction leads to formation of subsurface carbon and two types of reconstructions are discussed: dimer vacancies and dimer vacancies in conjunction with a rotated surface Si-dimer. Indications for the formation of small amounts of zirconium silicide are also found. No evidence for silicon oxidation can be observed with PES, in contrast to the interface properties previously found after larger exposures to ZTB.
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| 15. |
- Khatibi, Ali, et al.
(författare)
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Structural and Mechanical Properties of (AlxCr1-x)2+yO3-y Coatings Grown by Reactive Cathodic Arc Evaporation in As-deposited and Annealed States
- 2013
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Ingår i: Acta Materialia. - : Elsevier. - 1359-6454 .- 1873-2453. ; 61:13, s. 4811-4822
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Tidskriftsartikel (refereegranskat)abstract
- Coatings of (AlxCr1-x)2+yO3-y with 0.51≤x≤0.84 and 0.1≤y≤0.5 were deposited on hard cemented carbides substrates in an industrial cathodic arc evaporation system from powder-metallurgy prepared Cr/Al targets in pure O2 and O2+N2 atmospheres. The substrate temperature and bias in all the deposition runs were 575 °C and -120 V, respectively. The composition of the coatings measured by energy dispersive x-ray spectroscopy and elastic recoil detection analysis was the same as that of the targets. Microstructure analyses performed by symmetrical X-ray diffraction and transmission electron microscopy showed that corundum, cubic or mixed-phase coatings formed depending on the Cr/Al ratio of the coatings and O2 flow per activetarget during deposition. The corundum phase was promoted by high Cr content and high O2 flow per target, while the cubic phase was mostly observed for high Al content and low O2 flow per active target. In situ annealing of the cubic coatings resulted in phase transformation from cubic to corundum completed in the temperature range of 900-1100 °C, while corundum coatings retained their structure in the same range of annealing temperatures. Nanoindentation hardness of the coatings with Cr/Al ratio < 0.4 was 26-28 GPa, regardless of the structure. Increasing the Cr content of the coatings resulted in increased hardness of 28-30 GPa for corundum coatings. Wear resistance testing in a turning operation showed that coatings of Al-Cr-O have improved resistance to crater wear at the cost of flank wear compared to TiAlN coatings.
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| 16. |
- Landälv, Ludvig, 1982-
(författare)
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Physical vapor deposition and thermal stability of hard oxide coatings
- 2019
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The state-of-the-art tools for machining metals are primarily based on a metal-ceramic composite (WC-Co) coated with different combinations of carbide, nitride, and oxide coatings. Combinations of these coating materials are optimized to withstand specific wear conditions. Oxide coatings, mainly α-Al2O3, are especially desired because of their high hot-hardness, chemical inertness with respect to the workpiece, and their low friction. The search for possible alloy elements, which may facilitate the deposition of such oxides by means of physical vapor deposition (PVD) techniques, has been the goal of this thesis. The sought alloy should form thermodynamically stable or metastable compounds, compatible with the temperature of use in metal cutting application. This thesis deals with process development and coating characterization of such new oxide alloy thin films, focusing on the Al-V-O, Al-Cr-Si-O, and Cr-Zr-O systems.Alloying aluminum oxide with iso-valent vanadium is a candidate for forming the desired alloys. Therefore, coatings of (Al1-xVx)2O3, with x ranging from 0 to 1, were deposited with reactive sputter deposition. X-ray diffraction showed three different crystal structures depending on V-metal fraction in the coating: α-V2O3 rhombohedral structure for 100 at.% V, a defect spinel structure for the intermediate region, (63 - 42 at.% V), and a gamma-alumina-like solid solution at lower V-content, (18 and 7 at.%), were observed, the later was shifted to larger d-spacing compared to the pure γ-Al2O3 sample obtained if deposited with only Al-target. Annealing the Al-rich coatings in air resulted in formation of V2O5 crystals on the surface of the coating after annealing to 500 °C for 42 at.% V and 700 °C for 18 at.% V metal fraction respectively. The highest thermal stability was shown for pure γ-Al2O3-coating which transformed to α-Al2O3 after annealing to 1100° C. Highest hardness was observed for the Al-rich oxides, ~24 GPa. The hardness then decreases with increasing V-content, larger than 7 at.% V metal fraction. Doping the Al2O3 coating with 7 at.% V resulted in a significant surface smoothening compared to the binary oxide. The measured hardness after annealing in air decreased in conjunction with the onset of further oxidation of the coatings. This work increases the understanding of this complicated material system with respect to possible phases formed with pulsed DC magnetron sputtering deposition as well as their response to annealing in air.The inherent difficulties of depositing insulating oxide films with PVD, requiring a closed electrical circuit, makes the investigation of process stability an important part of this research. In this context, I investigated the influence of adding small amount of Si in Al-Cr cathode on the coating properties in a pulsed DC industrial cathodic arc system and the plasma characteristics, process parameters, and coating properties in a lab DC cathodic arc system. Si was chosen here due to a previous study showing improved erosion behavior of Al-Cr-Si over pure Al-Cr cathode without Si incorporation in the coating. The effect of Si in the Al-Cr cathode in the industrial cathodic arc system showed slight improvements on the cathode erosion but Si was found in all coatings where Si was added in the cathode. The Si addition promoted the formation of the B1-like metastable cubic oxide phase and the incorporation led to reduced or equal hardness values compared to the corresponding Si-free processes. The DC-arc plasma study on the same material system showed only small improvements in the cathode erosion and process stability (lower pressure and cathode voltage) when introducing 5 at.% Si in the Al70Cr30-cathode. The presence of volatile SiO species could be confirmed through plasma analysis, but the loss of Si through these species was negligible, since the coating composition matched the cathode composition also under these conditions. The positive effect of added Si on the process stability at the cathode surface, should be weighed against Si incorporation in the coating. This incorporation seems to lead to a reduction in mechanical properties in the as-deposited coatings and promote the formation of a B1-like cubic metastable oxide structure for the (Al,Cr)2O3 oxide. This formation may or may not be beneficial for the final application since literature indicates a slight stabilization of the metastable phase upon Si-incorporation, contrary to the effect of Cr, which stabilizes the α-phase.The thermal stability of alloys for metal cutting application is crucial for their use. Previous studies on another alloy system, Cr-Zr-O, had shown solid solution, for Cr-rich compositions in that material system, in the sought corundum structure. The thermal stability of α-Cr0.28Zr0.10O0.61 coating deposited by reactive radio frequency (RF)-magnetron sputtering at 500 °C was therefore investigated here after annealing in vacuum up to 870 °C. The annealed samples showed transformation of α-(Cr,Zr)2O3 and amorphous ZrOx-rich areas into tetragonal ZrO2 and bcc-Cr. The instability of the α-(Cr,Zr)2O3 is surprising and possibly related to the annealing being done under vacuum, facilitating the loss of oxygen. Further in situ synchrotron XRD annealing studies on the α-Cr0.28Zr0.10O0.61 coating in air and in vacuum showed increased stability for the air annealed sample up to at least 975 °C, accompanied with a slight increase in ex-situ measured nanohardness. The onset temperature for formation of tetragonal ZrO2 was similar to that for isothermally vacuum annealing. The synchrotron-vacuum annealed coating again decomposed into bcc-Cr and t-ZrO2, with an addition of monoclinic–ZrO2 due to grain growth. The stabilization of the room temperature metastable tetragonal ZrO2 phase, due to surface energy effects present with small grains sizes, may prove to be useful for metal cutting applications. The observed phase segregation of α-(Cr,Zr)2O3 and formation of tetragonal ZrO2 with corresponding increase in hardness for this pseudobinary oxide system also opens up design routes for pseudobinary oxides with tunable microstructural and mechanical properties.
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| 17. |
- Landälv, Ludvig, 1982-
(författare)
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Thin Film and Plasma Characterization of PVD Oxides
- 2017
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The state-of-the-art tools for machining metals are primarily based on a metal-ceramic composite(WC-Co) coated with different combinations of carbide, nitride and oxide coatings. Combinations of these coating materials are optimized to withstand specific wear conditions. Oxide coatings are especially desired because of their possible high hot hardness, chemical inertness with respect to the workpiece, and their low friction.This thesis deals with process and coating characterization of new oxide coatings deposited by physical vapor deposition (PVD) techniques, focusing on the Cr-Zr-O and Al-Cr-Si-O systems.The thermal stability of α-Cr0.28Zr0.10O0.61 deposited by reactive radio frequency (RF)-magnetron sputtering at 500 °C was investigated after annealing up to 870 °C. The annealed samples showed transformation of α-(Cr,Zr)2O3 and amorphous ZrOx-rich areas into tetragonal ZrO2 and bcc Cr. The instability of the α-(Cr,Zr)2O3 is surprising and possibly related to the annealing being done under vacuum, facilitating the loss of oxygen. The stabilization of the room temperature metastable tetragonal ZrO2 phase, due to surface energy effects, may prove to be useful for metal cutting applications. The observed phase segregation of α-(Cr,Zr)2O3 and formation of tetragonal ZrO2 with corresponding increase in hardness for this pseudo-binary oxide system also opens up design routes for pseudo-binary oxides with tunable microstructural and mechanical properties.The inherent difficulties of depositing insulating oxide films with PVD, demanding a closed circuit, makes the investigation of process stability an important part of this research. In this context, we investigated the influence of adding small amount of Si in Al-Cr cathode on plasma characteristics ,process parameters, and coating properties. Si was chosen here due to a previous study showing improved erosion behavior of Al-Cr-Si over pure Al-Cr cathode without Si incorporation in the coating.This work shows small improvements in cathode erosion and process stability (lower pressure and cathode voltage) when introducing 5 at % Si in the Al70Cr30-cathode. This also led to fewer droplets at low cathode current and intermediate O2 flow. A larger positive effect on cathode erosion was observed with respect to cleaning the cathode from oxide contamination by increasing cathode current with 50%. However, higher cathode current also resulted in increased amount of droplets in the coating which is undesirable. Through plasma analysis the presence of volatile SiO species could be confirmed but the loss of Si through volatile SiO species was negligible, since the coating composition matched the cathode composition. The positive effect of added Si on the process stability at the cathode surface should be weighed against Si incorporation in the coating. This incorporation may or may not be beneficial for the final application since literature states that Si promotes the metastable γ-phase over the thermodynamically stable α-phase of pure Al2O3, contrary to the effect of Cr, which stabilizes the α-phase.
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| 18. |
- Ledung, Greger, et al.
(författare)
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The Performance of a Biomimetic Oxidation Catalyst Immobilised on Gold and Silica Substrates
- 2007
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Ingår i: International Symposium on Relations between Homogeneous and Heterogeneous Catalysis. ; , s. 180-
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Konferensbidrag (populärvet., debatt m.m.)abstract
- Thiol-functionalized cobalt porphyrins were used as a model system for investigating catalytic activity in homo-geneous and heterogeneous oxidation catalysis. Self-assembled monolayers of thiol-functionalized cobalt porphyrins were prepared on a gold surface and served as heterogeneous catalysts. The immobilization of the molecules prevented the strong inactivation observed for their homogeneous congener. As a result, the turnover number permolecule in heterogeneous catalysis was at least 100 times higher than that of the corresponding homogeneouscatalyst. It is atypical for a heterogenized catalyst to outperform its homogeneous congener. The properties of themolecular layers were characterized on the molecular level by means of X-ray photoelectron spectroscopy (XPS) and scanning probe microscopy (SPM). The results demonstrate that the performance of these biomimetic catalysts can be dramatically improved if the catalyst arrangement can be controlled on the molecular level. In order to further investigate the influence of the substrate on the catalytic performance, monolayers of the cobalt porphyrins were grafted onto silica surfaces. The observed catalytic activity together with the surface analytical results are interpreted in relation to the supporting substrate. Preliminary results from this investigation (silicon wafer) show that the catalytic activity is similar to that of gold substrates.
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| 19. |
- Nilson, Katharina, 1977-
(författare)
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Phthalocyanines on Surfaces : Monolayers, Films and Alkali Modified Structures
- 2007
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The Phthalocyanines (Pc’s) are a group of macro-cyclic molecules, widely investigated due to the possibility to use them in a variety of applications. Electronic and geometrical structure investigations of molecular model systems of Pc’s adsorbed on surfaces are important for a deeper understanding of the functionality of different Pc-based devices. Here, Pc’s monolayers and films, deposited on different surfaces, were investigated by X-ray Photoelectron Spectroscopy (XPS), X-ray Absorption Spectroscopy (XAS) and Scanning Tunneling Microscopy (STM). In addition Density Functional Theory (DFT) simulations were performed. For molecular films of Metal-free (H2Pc) and Iron (FePc) Pc’s, on surfaces, it is found that the intermolecular interaction is weak and the molecules arrange with their molecular plane mainly perpendicular to the surface. Several monolayer systems were characterized, namely H2Pc and FePc adsorbed on Graphite, ZnPc on InSb(001)-c(8x2), H2Pc on Al(110) and on Au(111). For all the studied monolayers it was found that the molecules are oriented with their molecular plane parallel to the surface. The electronic structure of the molecules is differently influenced by interaction with the surfaces. For H2Pc adsorbed on Graphite the nearly negligible effect of the surface on the molecular electronic structure allowed STM characterization of different molecular orbitals. A strong interaction is instead found in the case of H2Pc on Al(110) resulting in molecules strongly adsorbed, and partly dissociated. Modifications of the electronic and geometrical structure induced by alkali doping of H2Pc films and monolayers were characterized. It is found both for the H2Pc film on Al(110) and monolayer adsorbed on Au(111), that the molecular arrangement is changed upon doping by Potassium and Rubidium, respectively. Potassium doping of the H2Pc films results in a filling of previously empty molecular orbitals by a charge transfer from the alkali to the molecule, with significant modification of the molecular electronic structure.
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| 20. |
- Nilson, Katharina, et al.
(författare)
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Rubidium Doped Metal-Free Phthalocyanine Monolayer Structures on Au(111)
- 2010
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 114:28, s. 12166-12172
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Tidskriftsartikel (refereegranskat)abstract
- Scanning tunneling microscopy (STM) studies of monolayer of metal-free phthalocyanine (H2Pc) adsorbed on Au(111) have shown ordered arrangement of the molecules on the surface. Evaporation of H2Pc onto the Au(111) surface and post annealing of the sample to 670 K results in a densely packed structure of the molecules. The monolayer is characterized by molecules adsorbed with the molecular plane parallel to the substrate surface in a square adsorption unit cell. Furthermore, the high resolution images revealed the orientation of individual molecules. The H2Pc/Au(111) system has also been doped by rubidum and compared to the undoped layers. The Rb affects the molecular adsorption geometry, and a hexagonal unit cell is found for the coadsorption of H2Pc and Rb. Upon doping, highly ordered Rb-induced protrusions are observed at the benzene site of adsorbed molecules.
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| 21. |
- Nilson, Katharina, et al.
(författare)
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Scanning tunneling microscopy study of metal-free phthalocyanine monolayer structures on graphite
- 2007
-
Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 127:11, s. 114702-
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Tidskriftsartikel (refereegranskat)abstract
- Low temperature scanning tunneling microscopy (STM) studies of metal-free phthalocyanine (H2Pc) adsorbed on highly oriented pyrolytic graphite (HOPG) have shown ordered arrangement of molecules for low coverages up to 1 ML. Evaporation of H2Pc onto HOPG and annealing of the sample to 670 K result in a densely packed structure of the molecules. Arrangements of submonolayer, monolayer, and monolayer with additional adsorbed molecules have been investigated. The high resolution of our investigations has permitted us to image single molecule orientation. The molecular plane is found to be oriented parallel to the substrate surface and a square adsorption unit cell of the molecules is reported. In addition, depending on the bias voltage, different electronic states of the molecules have been probed. The characterized molecular states are in excellent agreement with density functional theory ground state simulations of a single molecule. Additional molecules adsorbed on the monolayer structures have been observed, and it is found that the second layer molecules adsorb flat and on top of the molecules in the first layer. All STM measurements presented here have been performed at a sample temperature of 70 K.
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| 22. |
- Pratim Bose, Partha, et al.
(författare)
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Poly-N-methylated Amyloid β-Peptide (Aβ) C-Terminal Fragments Reduce Aβ Toxicity in Vitro and in Drosophila melanogaster
- 2009
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Ingår i: Journal of Medicinal Chemistry. - : American Chemical Society (ACS). - 0022-2623 .- 1520-4804. ; 52:24, s. 8002-8009
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Tidskriftsartikel (refereegranskat)abstract
- Alzheimer’s disease (AD), an age related neurodegenerative disorder, threatens to become a major health-economic problem. Assembly of 40- or 42-residue amyloid β-peptides (Aβ) into neurotoxic oligo-/polymeric β-sheet structures is an important pathogenic feature in AD, thus, inhibition of this process has been explored to prevent or treat AD. The C-terminal part plays an important role in Aβ aggregation, but most Aβ aggregation inhibitors have targeted the central region around residues 16−23. Herein, we synthesized hexapeptides with varying extents of N-methylation based on residues 32−37 of Aβ, to target its C-terminal region. We measured the peptides' abilities to retard β-sheet and fibril formation of Aβ and to reduce Aβ neurotoxicity. A penta-N-methylated peptide was more efficient than peptides with 0, 2, or 3 N-methyl groups. This penta-N-methylated peptide moreover increased life span and locomotor activity in Drosophila melanogaster flies overexpressing human Aβ1−42.
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| 23. |
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| 24. |
- Shakeri, Mozaffar, et al.
(författare)
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Small Pd Nanoparticles Supported in Large Pores of Mesocellular Foam : An Excellent Catalyst for Racemization of Amines
- 2011
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Ingår i: Chemistry - A European Journal. - : Wiley. - 0947-6539 .- 1521-3765. ; 17:47, s. 13269-13273
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Tidskriftsartikel (refereegranskat)abstract
- Highly dispersed palladium nanoparticles (1–2 nm) supported in large-pore mesocellular foam (MCF; 29 nm) were synthesized. The Pd-nanocatalyst/MCF system was characterized by transmission electron microscopy (TEM), powder X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The performance of the Pd nanocatalyst obtained was examined for amine racemization. The Pd nanocatalyst showed higher activity and selectivity toward racemization of (S)-1-phenylethyl amine than any other amine racemization catalyst reported so far and it could be reused several times. Our data from TEM and XRD suggest a restructuring of the Pd nanocatalyst from amorphous to crystalline and an increase in Pd nanocatalyst size during the racemization reaction. This led to an unexpected increase of activity after the first use. The Pd nanocatalyst obtained can be integrated with other resolving processes of racemic organic compounds to increase the yield of chiral organic products.
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| 25. |
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| 26. |
- Shariati, Masumeh-Nina, et al.
(författare)
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Photoelectron and Absorption Spectroscopy Studies of Metal-Free Phthalocyanine on Au(111) : Experiment and Theory
- 2013
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 117:14, s. 7018-7025
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Tidskriftsartikel (refereegranskat)abstract
- The adsorption of monolayers and multilayers of metal-free phthalocyanine molecules on the Au(111) (root 3 x 22) reconstructed surface has been investigated by X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS). Our results for the monolayer show that the molecules are arranged tightly onto the surface with their molecular plane parallel to it. In addition, the X-ray absorption spectra of the monolayer have been modeled by density functional theory, which could enlighten new aspect of the interaction between molecules and substrate. The XAS results evidence that also in the multilayer the molecules keep the orientation with the molecular plane parallel to the surface. These results are discussed in the framework of moleculemolecule/moleculeadsorbate interactions.
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| 27. |
- Surpi, Alessandro, et al.
(författare)
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Localised modifications of anatase TiO2 thin films by a Focused Ion Beam
- 2010
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Ingår i: Nuclear Instruments and Methods in Physics Research Section B. - : Elsevier BV. - 0168-583X .- 1872-9584. ; 268:19, s. 3142-3146
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Tidskriftsartikel (refereegranskat)abstract
- A Focused Ion Beam (FIB) has been used to implant micrometer-sized areas of polycrystalline anatase TiO2 thin films with Ga+ ions using fluencies from 10(15) to 10(17) ions/cm(2). The evolution of the surface morphology was studied by scanning electron microscopy (SEM) and atomic force microscopy (AFM). In addition, the chemical modifications of the surface were followed by X-ray photoelectron spectroscopy (XPS). The implanted areas show a noticeable change in surface morphology as compared to the as-deposited surface. The surface loses its grainy morphology to gradually become a smooth surface with a RMS roughness of less than 1 nm for the highest ion fluence used. The surface recession or depth of the irradiated area increases with ion fluence, but the rate with which the depth increases changes at around 5 x 10(16) ions/cm(2). Comparison with implantation of a pre-irradiated surface indicates that the initial surface morphology may have a large effect on the surface recession rate. Detailed analysis of the XPS spectra shows that the oxidation state of Ti and O apparently does not change, whereas the implanted gallium exists in an oxidation state related to Ga2O3.
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| 28. |
- Wang, Qin, et al.
(författare)
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Analysis of surface oxides on narrow bandgap III-V semiconductors leading towards surface leakage free IR photodetectors
- 2012
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Ingår i: Proceedings of SPIE, the International Society for Optical Engineering. - : SPIE. - 0277-786X .- 1996-756X. ; 8353, s. 835311-
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Tidskriftsartikel (refereegranskat)abstract
- Narrow bandgap semiconductors GaSb, InAs, and InSb are important building blocks for infrared photodetectors based on type-II InSb quantum dots or an InAs/GaSb strained layer superlattice. Understanding the surface chemical composition of these materials can provide valuable information that enables optimization of device surface passivation techniques leading towards surface leakage free IR photodetectors. We report on an investigation into Ga-, In-, Sb-, and As-oxides and other chemical species on the surface of untreated, dry etched and thermally treated GaSb, InAs and InSb samples by x-ray photoelectron spectroscopy. The experimental results reveal the presence of Sb- and Ga-oxides on the surfaces of the untreated and treated GaSb samples. Both Sb- and In-oxides were observed on the surface of all InSb samples, and especially the dry etched sample had thicker oxide layers. In the case of the InAs samples, not only In-and As-oxides XPS signals were obtained, but also AsCl species were found on the ICP dry etched sample. These results helped to analyze the dark current of our fabricated IR detectors.
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| 29. |
- Watcharinyanon, Somsakul, 1978-, et al.
(författare)
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Molecular orientation of thiol-derivatized tetraphenylporphyrin on gold studied by XPS and NEXAFS
- 2009
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Ingår i: Surface Science. - Amsterdam : Elsevier BV. - 0039-6028 .- 1879-2758. ; 603:7, s. 1026-1033
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Tidskriftsartikel (refereegranskat)abstract
- Tetraphenylporphyrins bearing four linkers consisting of thioacetyl-functionalized carbon chains were immobilized on a gold surface via thiolate-gold bonds using two different preparation routes. The structure of these molecular layers was characterized in detail with synchrotron radiation based core-level spectroscopy, X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. The results show that the geometry of the molecular layers and the number of linkers that bind to the gold surface depends on the preparation schemes. The deprotection of the linkers through removal of the terminal acetyl group before the molecular adsorption (deprotected systems) resulted in porphyrins bound to the gold surface with on the average three linkers, their normal axis being tilted similar to 38 degrees with respect to the surface normal. On the other hand, porphyrin layers prepared directly with the acetyl group still in place on the linkers (protected systems) are made of molecules bound to the gold surface via two linkers on the average. The resulting orientation is more upright, with the normal axis of the porphyrin plane tilted similar to 50 degrees with respect to the surface normal. Moreover, NEXAFS measurements revealed that the acetyl deprotected porphyrin layers have a higher degree of ordering than the protected systems. (C) 2009 Elsevier B.V. All rights reserved.
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| 30. |
- Åhlund, John, et al.
(författare)
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The adsorption of iron phthalocyanine on graphite : A scanning tunnelling microscopy study
- 2007
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Ingår i: Surface Science. - : Elsevier BV. - 0039-6028 .- 1879-2758. ; 601:17, s. 3661-3667
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Tidskriftsartikel (refereegranskat)abstract
- Different adsorption phases of iron phthalocyanine (FePc) on highly oriented pyrolitic graphite (HOPG) have been characterized by scanning tunnelling microscopy (STM). Evaporation of FePc onto the graphite (0 0 0 1) surface, kept at room temperature, results in the formation of three-dimensional molecular islands.After annealing to 400 °C different two-dimensional features are identified, depending on the initial coverage. At low doses, domains with well defined boundaries have been observed, within which molecules tend to organise in chains. At higher coverage, islands exhibiting well-ordered densely-packed square or hexagonal molecular arrangement have been resolved. For the adsorption structures corresponding to one monolayer islands our results show that the molecules adsorb with the molecular plane parallel to the surface. The high resolution STM images allow us to resolve the orientation of single molecules and subsequently we suggest that the molecular monolayer is stabilized by van der Waals interactions. The characterization of the observed Moiré contrast and a comparison with other similar systems underlines the importance of the central metal in the molecule–molecule and molecule–substrate interactions, which govern the molecular adsorption geometry.
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