| 1. |
- Andreasson, Jakob, 1975, et al.
(författare)
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Franck-Condon higher order lattice excitations in the LaFe(1-x)Cr(x)O3 (x=0, 0.1, 0.5, 0.9, 1.0) perovskites due to Fe-Cr charge transfer effects
- 2007
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Ingår i: Physical Review B. ; 75, s. 104302-
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Tidskriftsartikel (refereegranskat)abstract
- First and higher order lattice excitiations in the B-site disordered perovskites LaFe(1-x)Cr(x)O3 (x = 0, 0.1, 0.5, 0.9, 1) and La(0.835)Sr(0.165)Fe(0.5)Cr(0.5)O(3-d) are investigated using temperature dependent and polarised inelastic light scattering [lambda = 515 nm (2.41 eV) and 676 nm (1.83 eV)] on oriented crystallites.A peak at approximately 2.4 eV in the imaginary part of the dielectric function of LaFe(0.5)Cr(0.5)O3 is assigned to a charge transfer from Fe 3+ (d5) to Cr 3+ (d3) ions and coupled the appearance of an intense Ag-like mode at approximately 700 cm-1 in the Raman data. This excitation is identified as a symmetric oxygen breathing mode activated by the Fe-Cr charge transfer through an orbital coupling mechanism. Higher order scattering (up to 7th order) of the intrinsic Raman active symmetric breathing mode is also explained by an orbital mediated, electron-phonon coupling, similar to the Franck-Condon effect observed in the Jahn-Teller active perovskite structured manganite LaMnO3. These results show that the Franck-Condon mechanism is a more common mechanism for resonant higher order scattering in solids than previously believed and propose the LaFe(1-x)Cr(x)O(3) system as a model system for electron-phonon coupling and higher order Raman scattering in solids.
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| 2. |
- Andreasson, Jakob, et al.
(författare)
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Franck-Condon higher order lattice excitations in the LaFe1-xCrxO3 (x=0, 0.1, 0.5, 0.9, 1.0) perovskites due to Fe-Cr charge transfer effects
- 2007
-
Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 75
-
Tidskriftsartikel (refereegranskat)abstract
- First and higher order lattice excitations in the B-site disordered perovskites LaFe1-xCrxO3 (x=0, 0.1, 0.5, 0.9, and 1) and La0.835Sr0.165Fe0.5Cr0.5O3-delta are investigated using temperature dependent and polarized inelastic light scattering [lambda=515 nm (2.41 eV) and 676 nm (1.83 eV)] on oriented crystallites. A peak at approximately 2.4 eV in the imaginary part of the dielectric function of LaFe0.5Cr0.5O3 is assigned to a charge transfer from Fe3+ (d(5)) to Cr3+ (d(3)) ions, coupled with the appearance of an intense A(g)-like mode at approximately 700 cm(-1) in the Raman data. This excitation is identified as a symmetric oxygen breathing mode activated by the Fe-Cr charge transfer through an orbital coupling mechanism. Higher order scattering (up to seventh order) of the intrinsic Raman active symmetric breathing mode is also explained by an orbital-mediated electron-phonon coupling, similar to the Franck-Condon effect observed in the Jahn-Teller active-perovskite-structured manganite LaMaO(3). These results show that the Franck-Condon mechanism is a more common mechanism for resonant higher order scattering in solids than previously believed and propose the LaFe1-xCrxO3 system as a model system for electron-phonon coupling and higher order Raman scattering in solids.
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| 3. |
- Budelmann, D., et al.
(författare)
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Antiferromagnetic and superconducting proximity effects in YBa2Cu3O7-delta/PrBa2Cu3O7-delta superlattices
- 2003
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Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 67, s. 140507-
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Tidskriftsartikel (refereegranskat)abstract
- We investigate the interplay between the antiferromagnetic and superconducting order parameters in YBa2Cu3O7-delta/PrBa2Cu3O7-delta superlattices by inelastic light scattering. The ratio of superconducting to antiferromagnetic order is varied through different modulations 4/6, 4/9, and 4/12 of (Y/Pr)Ba2Cu3O7-delta layers. This allows us to identify the proximity effect of the superconducting order parameter into the antiferromagnetic barrier as signified, e.g., by the sharpening of the two-magnon excitation. This proximity effect as well as gap feature and phonon anomalies reveals the delicate interplay between superconducting and antiferromagnetic order parameters.
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| 4. |
- Holmlund, Joakim, 1968, et al.
(författare)
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Resonant two-phonon Raman scattering as a probe of hole crystal formation in Sr14?xCaxCu24O41
- 2006
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Ingår i: Physical Review B - Condensed Matter and Materials Physics. - 2469-9950 .- 2469-9969. ; 74
-
Tidskriftsartikel (refereegranskat)abstract
- The charge dynamics of the spin ladder compound Sr14-xCaxCu24O41 with x=0,6,13.6 has been investigated using wavelength- and temperature-dependent phonon Raman scattering on single crystals. In the unsubstituted, x=0, compound, a set of sharp two-phonon lines shows a strong increase in intensity below T similar to 200 K for light polarized along the ladder layer and with excitation energy close to the charge transfer gap similar to 1.9 eV. The temperature dependence of the strongly enhanced two-phonon bands below 200 K closely follows the recently reported formation of a standing charge density wave in the ladders [P. Abbamonte , Nature 431, 1078 (2004)]. Upon calcium substitution the polarized resonant Raman response rapidly decreases, signaling an increase of hole mobility in the ladder units. Temperature-dependent measurements of the x=13.6 sample indicate mobility of holes down to
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| 5. |
- Abbasi, M., et al.
(författare)
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Fabrication of Spin-Coated Ti/TiHx/Ni-Sb-SnO2 Electrode : Stability and Electrocatalytic Activity
- 2018
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Ingår i: Journal of the Electrochemical Society. - : ELECTROCHEMICAL SOC INC. - 0013-4651 .- 1945-7111. ; 165:9, s. H568-H574
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Tidskriftsartikel (refereegranskat)abstract
- A novel three-layer anode having the composition Ti/TiHx/Ni-Sb-SnO2 (Ti/TiHx/NATO) was successfully prepared by a spin-coating and pyrolysis process aiming at a long service lifetime and good electrocatalytic properties for ozone formation. The TiHx as an interlayer was produced by electrochemical cathodic reduction of a coated layer of the TiOx on the titanium substrate. Spin coating and thermal decomposition were used to deposit the Sn-Sb-Ni precursor on the surface of the prepared Ti/TiHx electrode. Cyclic and linear scanning voltammetry, Raman spectroscopy, scanning electron microscopy (SEM) and X-ray diffraction (XRD) were used to reveal the electrode performance and morphology. Results show that the onset potential for the oxygen evolution reaction (OER) of Ti/TiHx /NATO is higher than for Ti/NATO. They also indicate that the service lifetime of the Ti/TiHx/NATO is twice as long as the Ti/NATO at a current density of 50 mA.cm(-2) at room temperature. Electrochemical ozone generation and degradation of the methylene blue were investigated to confirm selectivity and activity of the electrodes. After 5 min electrolysis, a current efficiency for ozone generation of 56% was obtained the electrode with TiHx while 38% was obtained on Ti/NATO under same conditions. The results also confirm that the Ti/TiH x /NATO has a higher kinetic rate constant and decolorization efficiency for removal of the methylene blue compare to the Ti/NATO. The rate constant for the pseudo-first ordered reaction of methylene blue degradation showed high values of 350 x 10(-3) min(-1) for Ti/NATO and 440 x 10(-3) min(-1) for Ti/TiHx/NATO.
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| 6. |
- Abrashev, M. V., et al.
(författare)
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Raman spectroscopy of CaMnO(3) : Mode assignment and relationship between Raman line intensities and structural distortions
- 2002
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Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 65:18, s. 1-9
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Tidskriftsartikel (refereegranskat)abstract
- Polarized Raman spectra of oriented finely twinned CaMnO(3) thin films and nonpolarized Raman spectra of CaMnO(3) ceramics were studied at room temperature using several excitation laser wavelengths. The selection rules for the polarized Raman spectra, obtained from samples consisting of finely twinned orthorhombic domains, were calculated and the symmetry of all observed Raman lines was determined. The relationship between the intensity of the Raman lines and the distortions in the ABO(3) perovskites with GdFeO(3)-type structure is discussed. These distortions can be described as superposition of four simple basic distortions: two MnO(6) octahedral tilts, Jahn-Teller deformation of Mn(3+) O(6) octahedra, and shift of the A ions from their sites in the ideal perovskite. Twenty of the 24 Raman-allowed modes in the real GdFeO(3)-type structure have counterparts in only one of the four simpler structures, obtained by a single basic distortion. The assignment of the Raman lines of CaMnO(3) to definite atomic vibrations, most of them activated by a single basic distortion, was made in close comparison with the results of lattice dynamical calculations and the Raman spectra of isostructural LaMnO(3) and CaGeO(3).
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| 7. |
- Abrashev, M. V., et al.
(författare)
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Raman spectroscopy of the charge- and orbital-ordered state in La0.5Ca0.5MnO3
- 2001
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Ingår i: Physical Review B. ; 64:14
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Tidskriftsartikel (refereegranskat)abstract
- Polarized Raman spectra from microcrystals of La0.5Ca0.5MnO3 were studied as a function of temperature, excitation photon energy, and scattering configuration. At temperatures below the transition from ferromagnetic metallic phase to antiferromagnetic insulating charge- and orbital-ordered (COO) phase, several lines appear in Raman spectra excited with photon energies (h) over bar omega (L)<2.5 eV. We argue that their appearance signals ordering and freezing of the Jahn-Teller distortions at this transition temperature into a superstructure with a doubled elementary cell. We suggest a simplified structural model based on an analysis of the normal phonon modes in the COO phase, neglecting the octahedral tilts and containing ordered Mn4+O6 (undistorted) and Mn3+O6 (Jahn-Teller distorted) octahedra. The symmetries of the experimentally observed Raman lines are determined by comparing their relative intensities to those predicted by the polarization selection rules for a finely twinned quasicubic crystal. The most intensive Raman lines are assigned to definite normal modes in close comparison with corresponding modes in COO layered manganites and undoped RMnO3 (R=La, Y).
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| 8. |
- Andersson, Henrik, et al.
(författare)
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Contacting paper-based supercapacitors to printed electronics on paper substrates
- 2012
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 27:2, s. 476-480
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Tidskriftsartikel (refereegranskat)abstract
- Hybrid printed electronics, in which printed structures and silicon-based components co-exist will likely be among the first commercial solutions. In this case the paper substrate acts much in the same way as circuit boards, containing conductive tracks and acting as a carrier for the electrical components. It is important to consider the contacting of the components to be able to produce low resistance electrical contacts to the conductive tracks. Supercapacitors are able to deliver a large amount of current in a short time and are a good option for short term energy storage and if the printed product is to be used only one, or a few times, it can be the only power source needed. When manufacturing printed electronics, the overall resistance of the printed tracks as well as the contact resistance of the mounted components will add up to the total resistance of the system. A high resistance will cause a voltage drop from the power source to the component. This will waste power that goes to Joule heating and also the voltage and current available to components may be too low to drive them. If the intention is to use a power supply such as batteries or solar cells this becomes a limitation. In this article have been tested several conductive adhesives used to contact paper based supercapacitors to ink jet printed silver tracks on paper. The best adhesive gives about 0.3 Ω per contact, a factor 17 better compared to the worst which gave 5 Ω. The peak power that is possible to take out from a printed system with a flexible battery and super capacitors is about 10 times higher than compared with the same system with only the battery.
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| 9. |
- Andres, Britta, et al.
(författare)
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Supercapacitors with graphene coated paper electrodes
- 2012
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 27:2, s. 481-485
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Tidskriftsartikel (refereegranskat)abstract
- Paper based supercapacitors are prepared by stacking a paper between two graphene electrodes and soaking these in an aqueous electrolyte. We demonstrate that supercapacitors can easily be manufactured by using proven paper technologies. Several different electrode materials were compared and two types of contacting material, silver and graphite foil were tested. The influence of the paper used as separator was also investigated. The supercapacitors with a graphene-gold nanoparticle composite as electrodes showed a specific capacitance of up to 100 F/g and an energy density of 1.27 Wh/kg. The energy density can further be increased by using other electrolytes. The silver contacts showed a pseudo capacitance, which the graphite contacts did not. The papers tested had a minor effect on the capacitance, but they have an influence on the weight and the volume of the supercapacitor.
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| 10. |
- Bjornsson, P., et al.
(författare)
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Lattice and charge excitations in La1-xSrxMnO3
- 2000
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 61, s. 1193-1197
-
Tidskriftsartikel (refereegranskat)abstract
- We employ inelastic Light scattering to study the dependence of the lattice and charge excitations in La1-xSrxMnO3 compounds on doping and temperature. The phonons reveal strong local lattice distortions in the paramagnetic state, which gradually vanish below the ferromagnetic transition. We identify charge excitations in the metallic state. They exhibit a dependence on the doping level and symmetry selection rules typical for a plasmonlike excitation. Their energy scale of 100 meV requires a low-carrier-density component of the plasma outlining the importance of electronic interactions in La1-xSrxMnO3.
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| 11. |
- Blomquist, Nicklas, 1987-, et al.
(författare)
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Metal-free supercapacitor with aqueous electrolyte and low-cost carbon materials
- 2017
-
Ingår i: Scientific Reports. - : Nature Publishing Group. - 2045-2322. ; 7
-
Tidskriftsartikel (refereegranskat)abstract
- Electric double-layer capacitors (EDLCs) or supercapacitors (SCs) are fast energy storage devices with high pulse efficiency and superior cyclability, which makes them useful in various applications including electronics, vehicles and grids. Aqueous SCs are considered to be more environmentally friendly than those based on organic electrolytes. Because of the corrosive nature of the aqueous environment, however, expensive electrochemically stable materials are needed for the current collectors and electrodes in aqueous SCs. This results in high costs for a given energy-storage capacity. To address this, we developed a novel low-cost aqueous SC using graphite foil as the current collector and a mix of graphene, nanographite, simple water-purification carbons and nanocellulose as electrodes. The electrodes were coated directly onto the graphite foil by using casting frames and the SCs were assembled in a pouch cell design. With this approach, we achieved a material cost reduction of greater than 90% while maintaining approximately one-half of the specific capacitance of a commercial unit, thus demonstrating that the proposed SC can be an environmentally friendly, low-cost alternative to conventional SCs.
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| 12. |
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| 13. |
- Bäckström, Joakim, et al.
(författare)
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Optical properties of YBa$_2$Cu$_3$O$_7 - \delta$ and PrBa$_2$Cu$_3$O$_7 - \delta$ films : High-energy correlations and metallicity
- 2004
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 70:17
-
Tidskriftsartikel (refereegranskat)abstract
- We have investigated the temperature dependence of the dielectric functions of a high-Tc superconducting YBa2Cu3O7-- (Y-123) and a nonsuperconducting PrBa2Cu3O7-- (Pr-123) thin film using spectral ellipsometry. We evaluate the data by means of thermal-difference and sum-rule analysis techniques. We find that a spectral-weight transfer into the bands between 4 and 5 eV takes place before Y-123 becomes superconducting. We identify an anomaly around 1 eV that can be explained by a sudden plasma-frequency drop of the order of an meV around Tc. The absence of any sudden effects in the dielectric properties of Pr-123 suggests that both observations are intimately related to the superconducting state. Our findings point out that high-energy degrees of freedom must be considered for the understanding of high-temperature superconductivity.
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| 14. |
- Bäckström, Joakim, 1971
(författare)
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Raman Scattering and Neutron Diffraction Studies of Manganites and Cuprates
- 2001
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- This thesis is devoted to experimental studies of two classes of strongly correlated transition metal oxides, namely cuprates and manganite perovskites. Manganites generally display complex phase diagrams, including the so-called colossal magnetoresistance effect. Some cuprates show high-temperature superconductivity, a phenomenon that is poorly understood in spite of many years of intense research. It is clear, though, that a delicate interplay between the atomic structure, magnetism and charge carriers is important in these materials. Experimental investigations have been done using Raman spectroscopy, a powerful technique for these studies since it is able to simultaneously probe vibrational, magnetic and electronic excitations. Neutron diffraction in combination with Reverse Monte Carlo modelling have been used to study both structural and magnetic ordering on a local scale. We demonstrate that an anomaly of the Ba-phonon mode in YBa2Cu4O8 is directly correlated to the opening of a pseudogap well above the superconducting critical temperature. A similar anomaly in the non-superconductor PrBa2Cu4O8 indicates that the pseudogap state is not a sufficient prerequisite for superconductivity. Following neutron diffraction studies of PrBa2Cu4O8 reveal a Ba-site instability, which we link to anomalies in the electronic properties. In the high-temperature superconductor YBa2Cu3O6+x, we investigate the influence of light irradiation on the Raman spectra and propose a simplistic model for photoinduced effects. We show effects of interactions between charge and lattice degrees of freedom in the manganites La0.5Ca0.5MnO3 and La1-xSrxMnO3. In the latter compound, we discovered a low-energy electronic excitation suggesting the existence of a two-component metallic state.
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| 15. |
- Bäckström, Joakim, et al.
(författare)
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Raman scattering in \RmYBa$_2$Cu$_4$O$_8$ and PrBa$_2$Cu$_4$O$_8$ : Indications of pseudogap effects in non-superconducting \RmPrBa$_2$Cu$_4$O$_8$
- 2000
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 61, s. 7049-7054
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Tidskriftsartikel (refereegranskat)abstract
- By analysis of the Raman spectra of superconducting YBa2Cu4O8 (Y-124), we observe a suppression of low-energy electronic density of states that we link to changes in the linewidth of the Ba-phonon mode. These effects occur at a temperature below 150 K, where also anomalies in resistivity and other physical properties take place. We argue that these changes in the Raman spectra of Y-124 are connected to the opening of a pseudogap. Analogous anomalies in resistivity and the Ba-phonon width in the nonsuperconducting homologue PrBa2Cu4O8 (Pr-124) below 150 K suggest that similar pseudogap effects can occur without a following transition to a superconducting state at a lower temperature.
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| 16. |
- Bäckström, Joakim, et al.
(författare)
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Raman scattering in YBa2Cu4O8 and PrBa2Cu4O8 - indications of pseudogap effects in non-superconducting PrBa2Cu4O8
- 2000
-
Ingår i: Physica. C, Superconductivity. - 0921-4534 .- 1873-2143. ; 341, s. 2251-2252
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Tidskriftsartikel (refereegranskat)abstract
- By analysis of the temperature evolution of Raman spectra, we connect an observed supression in low-energy electronic density of states to an anomalous sharpening of the Ba-phonon mode in superconducting YBa2Cu4O8 (Y-124) at around T=150 K. We link the supression of electronic excitations to an opening of a pseudogap. Similar effects observed for the Ba-phonon mode at roughly the same temperature in non-superconducting PrBa2Cu4O8 (Pr-124) suggests that a pseduogap opens up around 150 K also in this material.
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| 17. |
- Bäckström, Pontus, 1983-, et al.
(författare)
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Kanon eller inte kanon? En enkätstudie bland samhällskunskapslärare i årskurs 7–9
- 2021
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Ingår i: Nordidactica. - Karlstad : CSD Karlstad. - 2000-9879. ; 11:2021:2, s. 20-56
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Tidskriftsartikel (refereegranskat)abstract
- The aim of the present study is to investigate whether social studies in compulsory school grades 7–9 can be perceived as having a clear canon regarding subject content, methods, used sources and examination methods. Previous research has suggested that social studies is unclear, vague and that it lacks a subject canon. The results of the present study points in both directions. On the one hand, the study shows that there is a clear core of content around which lower secondary social studies teaching revolves and a common foundation regarding how this content is mainly conveyed and examined. On the other hand, the study shows that there is also great variation between different teachers, variation that can be partly explained by the teachers' preferences. Different teachers seem to have different preferences when it comes to how they teach, what methods and sources they use and how sections are examined. For example, there are significant correlations between how teachers who use group-based methods also use group-based examinations. An important factor for the variation between teachers can be traced to gender. At group level, we see differences regarding male and female teachers based on subject matter, methods, sources and examination methods. In general, there is a common core for most social studies teachers, regardless of gender, but female teachers tend to cover a broader subject content, use a wider array of methods and sources and more varied forms of examination.
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| 18. |
- Eivazihollagh, Alireza, et al.
(författare)
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Electrochemical recovery of copper complexed by DTPA and C12-DTPA from aqueous solution using a membrane cell
- 2018
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Ingår i: Journal of chemical technology and biotechnology (1986). - : Wiley. - 0268-2575 .- 1097-4660. ; 93:5, s. 1421-1431
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Tidskriftsartikel (refereegranskat)abstract
- BACKGROUNDThe electrochemical recovery of copper from DTPA and C12-DTPA (a surface-active derivative of DTPA) complex solutions was investigated in a membrane flow cell. Electrolysis time, solution flow rate, applied current density, and solution pH were evaluated.RESULTSThe chelating surfactant C12-DTPA can promote the kinetics of copper electrodeposition more than DTPA depending on the experimental conditions. At a current density of 30 A m–2, a solution flow rate of 0.6 L min–1, and pH 10 after 180 min treatment, the copper recovery and current efficiency were 50% and 43.3%, respectively, in the Cu(II)-DTPA system and about 65% and 53.6%, respectively, in the Cu(II)-C12-DTPA system. The differences in the amount of recovery could be explained in terms of differences in the diffusion of copper complexes with DTPA and C12-DTPA to the cathode, as well as their solution behavior and pH-dependent conditional stability constants (log10 K’CuDTPA3-).CONCLUSIONElectrochemical methods could be effectively combined with foam flotation for the chelating surfactant C12-DTPA, to recover copper and C12-DTPA. This makes the overall treatment more sustainable, and can be helpful in complying with the increasingly stringent environmental regulations
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| 19. |
- Eivazihollagh, Alireza, et al.
(författare)
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Influences of the operational variables on electrochemical treatment of chelated Cu(II) in alkaline solutions using a membrane cell
- 2017
-
Ingår i: Journal of chemical technology and biotechnology (1986). - : Wiley. - 0268-2575 .- 1097-4660. ; 92:6, s. 1436-1445
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Tidskriftsartikel (refereegranskat)abstract
- BACKGROUNDThe electrochemical recovery of copper and chelating agent from their complex solution using a membrane flow cell was investigated. The parameters electrolysis time, solution pH, current density, and temperature were investigated.RESULTSElectrochemical investigation indicated that chelating ligands can be recovered by the electrodeposition of copper ions on the cathode. For copper and EDTA recovery, the results indicated that recovery efficiency was affected by time, current density, and temperature. The recovery process was not influenced by pH in the range studied (pH 8–12), which can be explained by the low variation in the conditional stability constant, i.e. Δlog10 K' ≤ 0.7, over the pH range. However, when NTA, EDTA, and DTPA were compared, the results indicated that the recovery efficiency decreased as the conditional stability constant of the chelating agent–Cu(II) complex increased. The maximum current efficiency of copper and EDTA recovery after 5 h of treatment was approximately 85%, whereas the recovery was 80% of the initial concentration (0.05 mol L−1) at a current density of 1 A dm−2, temperature of 333 K, and pH of 10.CONCLUSIONRelatively high recovery efficiency makes the process fairly sustainable and hinders the discharge of copper ions and chelating ligands as pollutants into the environment.
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| 20. |
- Eivazihollagh, Alireza
(författare)
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Metal-Chelate Complexes in Alkaline Solution : On Recovery Techniques and Cellulose-based Hybrid Material Synthesis
- 2018
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- For decades, aminopolycarboxylate chelating agents have been extensively used in various industrial applications. The ability of chelating agents to form stable metal-chelate complexes is the main reason for using them to manage metal ions within water-based industrial processes. Considerable quantities of industrial effluent containing chelating agents and heavy metals are produced and often discharged into the environment. The toxicity of heavy metals and the non-biodegradability of the chelating agents, as well as their accumulation in the environment, has become cause for concern. The main purpose of this thesis was to evaluate and develop processes for recovery of chelated metal complexes from aqueous solution. In this regard, the membrane electrolysis technique was evaluated for recovery of copper and aminopolycarboxylic chelating ligands such as ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), diethylenetriaminepentaacetic acid (DTPA), and a surface-active derivative of DTPA, 2-dodecyldiethylenetriaminepentaacetic acid (C12-DTPA) from aqueous solution. By using this method, it was possible to simultaneously recover the chelating ligand for further reuse and collect the metals by electrodeposition, making the process more cost-effective and hindering the discharge of copper ions and chelating ligands as pollutants into the environment. In addition, the ion flotation technique with the chelating surfactant C12-DTPA could be employed to separate metal ions, especially from their dilute solutions, and concentrate them in a foam phase. This is because C12-DTPA has a purpose-built functionality; besides forming strong coordination complexes with metal ions, it is also surface-active and will readily adsorb at air-water interfaces. In this study, C12-DTPA was effectively used in combination with foaming agents for the removal of toxic metal ions such as Cd2+, Zn2+, and Sr2+ from aqueous solution using ion flotation. From an economical perspective, this method could be combined with the membrane electrolysis technique to recover metal and regenerate chelating surfactant so that it can be reused.The present work also shows the synthesis of metal and metal oxide(s) nanoparticles (NPs) in alkaline aqueous solution containing chelated metal ions, in order to fabricate metal NPs–cellulose hybrid materials. Cellulose is the most abundant renewable material, with good mechanical performance and chemical resistivity in a wide range of solvents, which makes it a promising material to support metal NPs. In this respect, we developed a rapid and inexpensive one-pot synthesis of spherical copper NPs in a cellulose matrix. The hybrid material displayed antibacterial properties for both the gram-negative and gram-positive bacteria. The synthesis was further developed by studying the influence of various chelating ligands and surfactants on the NPs’ morphology and chemical composition. According to the results, DDAO, a zwitterionic surfactant, was found to mediate the formation of pure octahedral Cu2O NPs. In addition, a hybrid material film composed of regenerated cellulose and synthesized Cu2O nano-octahedrons was fabricated by spin-coating.
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| 21. |
- Eivazihollagh, Alireza, et al.
(författare)
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One-pot synthesis of cellulose-templated copper nanoparticles with antibacterial properties
- 2017
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Ingår i: Materials letters (General ed.). - : Elsevier BV. - 0167-577X .- 1873-4979. ; 187, s. 170-172
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Tidskriftsartikel (refereegranskat)abstract
- We report a facile in situ synthesis of spherical copper nanoparticles (NPs) templated by a gelled cellulose II matrix under alkaline aqueous reaction conditions. In under 20 min, the hybrid material could be obtained in a one-pot reaction. Field-emission scanning electron microscopy (FE-SEM) revealed that the polycrystalline NPs of 200–500 nm were well distributed in the regenerated cellulose matrix. The average Cu crystallite size was of the order of 20 nm, as estimated from both X-ray diffraction (XRD) and FE-SEM. XRD data also indicated that the composite contained up to approximately 20% Cu2O. In suspensions containing the hybrid material, growth of Escerichia coli and Staphylococcus aureus strains was inhibited by 80% and 95%, respectively, after 72 h. The synthesis procedure offers a general approach to designing various low-cost hybrid materials of almost any shape, and the concept could be extended to utilization areas such as catalysis, functional textiles, and food packaging as well as to electronic applications.
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| 22. |
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| 23. |
- Forsberg, Viviane, 1981-, et al.
(författare)
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Exfoliated MoS2 in Water without Additives
- 2016
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Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 11:4
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Tidskriftsartikel (refereegranskat)abstract
- Many solution processing methods of exfoliation of layered materials have been studied during the last few years; most of them are based on organic solvents or rely on surfactants andother funtionalization agents. Pure water should be an ideal solvent, however, it is generallybelieved, based on solubility theories that stable dispersions of water could not be achievedand systematic studies are lacking. Here we describe the use of water as a solvent and thestabilization process involved therein. We introduce an exfoliation method of molybdenumdisulfide (MoS2) in pure water at high concentration (i.e., 0.14±0.01 g L−1). This was achieved by thinning the bulk MoS2by mechanical exfoliation between sand papers and dis-persing it by liquid exfoliation through probe sonication in water. We observed thin MoS2nanosheets in water characterized by TEM, AFM and SEM images. The dimensions of thenanosheets were around 200 nm, the same range obtained in organic solvents. Electropho-retic mobility measurements indicated that electrical charges may be responsible for the sta-bilization of the dispersions. A probability decay equation was proposed to compare thestability of these dispersions with the ones reported in the literature. Water can be used as asolvent to disperse nanosheets and although the stability of the dispersions may not be ashigh as in organic solvents, the present method could be employed for a number of applications where the dispersions can be produced on site and organic solvents are not desirable.
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| 24. |
- Forsberg, Viviane, 1981-, et al.
(författare)
-
Liquid Exfoliation of Layered Materials in Water for Inkjet Printing
- 2016
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Ingår i: Printing for Fabrication 2016. - USA : Curran Associates, Inc.. - 9780892083220 - 9780892083237 - 9780892083213 ; 60:4, s. 1-7
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Konferensbidrag (refereegranskat)abstract
- MoS2 is a layered material which is abundant and non-toxic and has been increasingly studied during the last few years as a semiconducting alternative to graphene. While most studies have been performed on single MoS2 nanosheets, for example to demonstrate high-performance electronic transistors, more work is needed to explore the use of MoS2 in printed electronics. The importance of using MoS2 as a printed electronic material could be understood by considering the several orders higher electron mobility in MoS2, even in several nanometer thick layers, compared to the organic and other materials used today. In the few studies performed so far on printing MoS2, the developed dispersions used mainly organic solvents that might be detrimental for the environment. Here, we show an environmentally friendly liquid-based exfoliation method in water where the solution was stabilized by sodium dodecyl sulfate (SDS) surfactant. The dispersions consisted of very thin MoS2 nanosheets with average lateral size of about 150 nm, surface tension of 28 mN m-1 and a shelf life of a year. Although both the concentration and viscosity was less than optimal, we were able to inkjet print the MoS2 solution on paper and on PET films, using multiple printing passes. By tuning the concentration/viscosity, this approach might lead to an environmentally friendly MoS2 ink suitable for printed electronics.
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| 25. |
- Forsberg, Viviane, 1981-
(författare)
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Liquid Exfoliation of Molybdenum Disulfide for Inkjet Printing
- 2016
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Since the discovery of graphene, substantial effort has been put toward the synthesis and production of 2D materials. Developing scalable methods for the production of high-quality exfoliated nanosheets has proved a significant challenge. To date, the most promising scalable method for achieving these materials is through the liquid-based exfoliation (LBE) of nanosheetsin solvents. Thin films of nanosheets in dispersion can be modified with additives to produce 2D inks for printed electronics using inkjet printing. This is the most promising method for the deposition of such materials onto any substrate on an industrial production level. Although well-developed metallic and organic printed electronic inks exist on the market, there is still a need to improve or develop new inks based on semiconductor materials such as transition metal dichalcogenides (TMDs) that are stable, have good jetting conditions and deliver good printing quality.The inertness and mechanical properties of layered materials such as molybdenum disulfide (MoS2) make them ideally suited for printed electronics and solution processing. In addition,the high electron mobility of the layered semiconductors, make them a candidate to become a high-performance semiconductor material in printed electronics. Together, these features make MoS2 a simple and robust material with good semiconducting properties that is also suitable for solution coating and printing. It is also environmentally safe.The method described in this thesis could be easily employed to exfoliate many types of 2D materials in liquids. It consists of two exfoliation steps, one based on mechanical exfoliation of the bulk powder utilizing sand paper, and the other inthe liquid dispersion, using probe sonication to liquid-exfoliate the nanosheets. The dispersions, which were prepared in surfactant solution, were decanted, and the supernatant was collected and used for printing tests performed with a Dimatix inkjetprinter. The printing test shows that it is possible to use the MoS2 dispersion as a printed electronics inkjet ink and that optimization for specific printer and substrate combinations should be performed. There should also be advances in ink development, which would improve the drop formation and break-off at the inkjet printing nozzles, the ink jetting and, consequently, the printing quality.
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| 26. |
- Gustavsson, John, et al.
(författare)
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In-situ activated hydrogen evolution by molybdate addition to neutral and alkaline electrolytes
- 2012
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Ingår i: Journal of Electrochemical Science and Engineering. - : International Association of Physical Chemists (IAPC). - 1847-9286. ; 2:3, s. 105-120
-
Tidskriftsartikel (refereegranskat)abstract
- Activation of the hydrogen evolution reaction (HER) by in-situ addition of Mo(VI) to the electrolyte has been studied in alkaline and pH neutral electrolytes, the latter with the chlorate process in focus. Catalytic molybdenum containing films formed on the cathodes during polarization were investigated using scanning electron microscopy (SEM), energy-dispersive X ray analysis (EDS), X-ray photoelectron spectroscopy (XPS), and X ray fluorescence (XRF). In-situ addition of Mo(VI) activates the HER on titanium in both alkaline and neutral electrolytes and makes the reaction kinetics independent of the substrate material. Films formed in neutral electrolyte consisted of molybdenum oxides and contained more molybdenum than those formed in alkaline solution. Films formed in neutral electrolyte in the presence of phosphate buffer activated the HER, but were too thin to be detected by EDS. Since molybdenum oxides are generally not stable in strongly alkaline electrolyte, films formed in alkaline electrolyte were thinner and probably co-deposited with iron. A cast iron molybdenum alloy was also investigated with respect to activity for HER. When polished in the same way as iron, the alloy displayed a similar activity for HER as pure iron.
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| 27. |
- Gustavsson, John, 1979-, et al.
(författare)
-
In-situ Activated Hydrogen Evolution by Molybdate Addition to Neutral and Alkaline Electrolytes
-
Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- Activation of the hydrogen evolution reaction (HER) by in-situ addition of Mo(VI) to the electrolyte has been studied in alkaline and pH neutral electrolytes, the latter with the chlorate process in focus. Catalytic molybdenum containing films formed on the cathodes during polarization were investigated using scanning electron microscopy (SEM), energy-dispersive X‑ray analysis (EDS), X-ray photoelectron spectroscopy (XPS), and X‑ray fluorescence (XRF). In-situ addition of Mo(VI) activates the HER on titanium in both alkaline and neutral electrolytes and makes the reaction kinetics independent of the substrate material. Films formed in neutral electrolyte consisted of molybdenum oxides and contained more molybdenum than those formed in alkaline solution. Films formed in neutral electrolyte in the presence of phosphate buffer activated the HER, but were too thin to be detected by EDS. Since molybdenum oxides are generally not stable in strongly alkaline electrolyte, films formed in alkaline electrolyte were thinner and probably co-deposited with iron. A cast iron‑molybdenum alloy was also investigated with respect to activity for HER. When polished in the same way as iron, the alloy displayed a similar activity for HER as pure iron.
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| 28. |
- Gustavsson, John, et al.
(författare)
-
On the suppression of cathodic hypochlorite reduction by electrolyte additions of molybdate and chromate ions
- 2012
-
Ingår i: Journal of electrochemical science and engineering. - : International Association of Physical Chemists (IAPC). - 1847-9286. ; 2:4, s. 185-198
-
Tidskriftsartikel (refereegranskat)abstract
- The goal of this study was to gain a better understanding of the feasibility of replacing Cr(VI) in the chlorate process by Mo(VI), focusing on the cathode reaction selectivity for hydrogen evolution on steel and titanium in a hypochlorite containing electrolyte. To evaluate the ability of Cr(VI) and Mo(VI) additions to hinder hypochlorite reduction, potential sweep experiments on rotating disc electrodes and cathodic current efficiency (CE) measurements on stationary electrodes were performed. Formed electrode films were investigated with scanning electron microscopy and energy-dispersive X-ray spectroscopy. Cathodic hypochlorite reduction is hindered by the Mo-containing films formed on the cathode surface after Mo(VI) addition to the electrolyte, but much less efficient compared to Cr(VI) addition. Very low levels of Cr(VI), in the mM range, can efficiently suppress hypochlorite reduction on polished titanium and steel. Phosphate does not negatively influence the CE in the presence of Cr(VI) or Mo(VI) but the Mo-containing cathode films become thinner if the electrolyte during the film build-up also contains phosphate. For a RuO2-TiO2 anode polarized in electrolyte with 40 mM Mo(VI), the anode potential increased and increased molybdenum levels were detected on the electrode surface
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| 29. |
- Gustavsson, John, 1979-, et al.
(författare)
-
On the Suppression of Cathodic Hypochlorite Reduction by ElectrolyteAdditions of Molybdate and Chromate Ions
-
Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- The goal of this study was to gain a better understanding of the feasibility of replacing Cr(VI) in the chlorate process by Mo(VI), focusing on the cathode reaction selectivity for hydrogen evolution on steel and titanium in a hypochlorite containing electrolyte. To evaluate the ability of Cr(VI) and Mo(VI) additions to hinder hypochlorite reduction, potential sweep experiments on rotating disc electrodes and cathodic current efficiency (CE) measurements on stationary electrodes were performed. Formed electrode films were investigated with scanning electron microscopy and energy-dispersive X-ray spectroscopy. Cathodic hypochlorite reduction is hindered by the Mo-containing films formed on the cathode surface after Mo(VI) addition to the electrolyte, but much less efficient compared to Cr(VI) addition. Very low levels of Cr(VI), in the mM range, can efficiently suppress hypochlorite reduction on polished titanium and steel. Phosphate does not negatively influence the CE in the presence of Cr(VI) or Mo(VI) and the Mo-containing cathode films become thinner if the electrolyte during the film build-up also contains phosphate. For a RuO2-TiO2 anode polarized in electrolyte with 40 mM Mo(VI), the anode potential increased and on the electrode surface, increased molybdenum levels were detected. In an earlier study 40 mM Mo(VI) gave increased by-product oxygen.
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| 30. |
- Hadjiev, V. G., et al.
(författare)
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Symmetry of phonon, magnetic, and spin-phonon excitations in GdSr2RuCu2O8 single crystals
- 2001
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 64
-
Tidskriftsartikel (refereegranskat)abstract
- We present a polarized Raman scattering study of GdSr2RuCu2O8 single crystals. In this compound, the RuO6 octahedra are rotated around the c axis that in turn gives some Raman activity of the oxygen (O-Ru) vibrations at 265 cm(-1) (A(1g)), 411 cm(-1) (B-2g) and 607 cm(-1) (B-1g). These vibrations, as well as those of the apical oxygen of RuO6, at 654 cm(-1) (A(1g)) and the Cu-plane oxygen at 318 cm(-1) (B-2g), clearly respond to the onset of magnetic ordering at T-m approximate to 140 K. In particular, the 265 cm(-1) mode hardens anomalously with decreasing temperature below T-m. Notably, the corresponding phonon line is absent in the Raman spectra of GdSr2NbCu2O8 (Nb5+:4d(0)), a compound isomorphic to GdSr2RuCu2O8 (Ru5+:4d(3)). We argue that the eigenvector of the 265 cm(-1) phonon (rotational mode) facilitates efficient modulation of the Ru(t(1g))-O-Ru (p) bands. This modulation gives both Raman scattering strength to the 265 cm(-1) mode and strong spin-phonon coupling.
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| 31. |
- Hedenstedt, Kristoffer, 1979, et al.
(författare)
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In-situ Raman spectroscopy of α- and γ-FeOOH during cathodic load
- 2017
-
Ingår i: Journal of the Electrochemical Society. - : The Electrochemical Society. - 0013-4651 .- 1945-7111. ; 164:9
-
Tidskriftsartikel (refereegranskat)abstract
- Water reduction on corroded iron surfaces is technologically and fundamentally important. Here, the technological interest originates from the chlorate process where water reduction is the main cathodic process. Fundamentally, water reduction on oxide surfaces raises questions on the stability of the oxide and the nature of electrocatalytic surface sites. Two iron oxyhydroxides, alpha- and gamma-FeOOH, were electrodeposited on titanium substrate and their reduction processes were followed in detail with in-situ Raman spectroscopy, using low incident laser power to avoid sample damaging. Polarization to negative potentials show two reduction peaks for gamma-FeOOH and one peak for alpha-FeOOH prior to hydrogen evolution. The characteristic Raman peaks gradually disappear as the potential is made more negative but no new peaks can be observed. delta-FeOOH was detected as an intermediate phase upon oxidation of the reduced surface layer. This indicates that Fe(OH)(2) is formed during cathodic polarization and initially re-oxidized to the isostructural delta-FeOOH. Characteristic Raman signals of the original phases appear upon further oxidation in air. (C) The Author(s) 2017. Published by ECS. All rights reserved.
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| 32. |
- Hummelgård, Christine
(författare)
-
Nanoscaled Structures of Chlorate Producing Electrodes
- 2012
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Sodium chlorate is mainly used for production of chlorine dioxide (a pulp bleaching agent). Sodium chlorate is produced by an electrochemical process where chloride ions (from sodium chloride dissolved in water) are oxidized to chlorine on the anodes and hydrogen is evolved on the cathodes. The anode of this process consists of a metal plate coated with a catalytically active metal oxide film. The electrocatalytic properties of the anode coating film have been widely investigated due to the great importance of these electrodes in the electrochemical industry. The material properties are, however, not as well investigated, and the studies described in this thesis are an attempt to remedy this.Several standard material characterization methods were used, such as SEM, TEM, AFM, EDX, XRD, porosimetry and DSC. Also, a novel model system based on spin coated electrode films on smooth substrates was developed. The model system provided a way to design samples suitable for e.g. TEM, where the sample thickness is limited to maximum of 100 nm. This is possible due to the ability to control the film thickness by the spinning velocity when using the spin coating technique.It was shown here that the anode coating has a nanostructure. It consists of grains, a few tens of nanometers across. The nanostructure leads to a large effective area and thus provides an explanation of the superior catalytic properties of these coatings. The grains were also shown to be monocrystalline. The size of these grains and its origin was investigated. The calcination temperature, the precursor salt and (if any) doping material all affected the grain size. A higher calcination temperature yielded larger grains and doping with cobalt resulted in smaller grains and therefore a larger real area of the coating. Some preparation conditions also affected the microstructure of the coating; such as substrate roughness. The microstructure is for example the cracked-mud structure. A smoother substrate gave a lower crack density.The cathode of chlorate production is usually an uncoated metal plate, therefore 'less catalytically active'. It is, however, possible to activate the cathode by for example in situ additions to the electrolyte. It was shown here that sufficient addition of molybdate to the electrolyte resulted in a molybdenum film deposited on the cathode and thereby an increase of its surface area and an activation the hydrogen evolution reaction.
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| 33. |
- Hummelgård, Christine, et al.
(författare)
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Physical and electrochemical properties of cobalt doped (Ti,Ru)O-2 electrode coatings
- 2013
-
Ingår i: Materials Science & Engineering B: Solid-State Materials for Advanced Technology. - : Elsevier BV. - 0921-5107 .- 1873-4944. ; 178:20, s. 1515-1522
-
Tidskriftsartikel (refereegranskat)abstract
- The physical and electrochemical properties of ternary oxides Ti0.7Ru0.3-xCoxO2 (x = 0.093 and x = 0) have been investigated and compared. Samples of three different thicknesses were prepared by spin-coating onto polished titanium to achieve uniform and well-defined coatings. The resulting electrodes were characterized with a variety of methods, including both physical and electrochemical methods. Doping with cobalt led to a larger number of micrometer-sized cracks in the coating, and coating grains half the size compared to the undoped samples (10 instead of 20 nm across). This is in agreement with a voltammetric charge twice as high, as estimated from cyclic voltammetry. There is no evidence of a Co3O4 spinel phase, suggesting that the cobalt is mainly incorporated in the overall rutile structure of the (Ti,Ru)O-2. The doped electrodes exhibited a higher activity for cathodic hydrogen evolution compared to the undoped electrodes, despite the fact that one third of the active ruthenium was substituted with cobalt. For anodic chlorine evolution, the activity was similar for both electrode types. (C) 2013 The Authors. Published by Elsevier B.V. All rights reserved.
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| 34. |
- Hummelgård, Christine, et al.
(författare)
-
Spin coated titanium-ruthenium oxide thin films
- 2013
-
Ingår i: Thin Solid Films. - : Elsevier BV. - 0040-6090 .- 1879-2731. ; 536, s. 74-80
-
Tidskriftsartikel (refereegranskat)abstract
- Substrates of different roughness spin coated with Ti0.7Ru0.3O2 films have been evaluated as model system for fundamental studies of the industrially and scientifically interesting (Ti, Ru)O-2 based electrodes. The approach allowed for much more accurate control over the material synthesis than the traditionally used brush-, dip-, or spray-coating, on titanium-metal substrates. It moreover yielded well-defined samples suitable for basic studies of the surface properties that are of fundamental importance for understanding the electrochemical functionality of the electrode. We have compared the films on silicon substrates to films prepared by spin coating the same material on titanium-metal substrates. Samples have been characterized using atomic force microscopy (AFM), X-ray diffraction, scanning electronmicroscopy (SEM), and cyclic voltammetry. The samples displayed a uniformity of the films appropriate for AFM characterization. The smoother the substrate the less cracks in the coating. Using easily broken silicon wafers as substrate, a straightforward sample preparation technique was demonstrated for cross-section SEM. In addition, using high spinning velocities we have deposited the oxide films directly on silicon-nitride grids, thin enough to allow for studies with transmission electron microscopy without further sample preparation.
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| 35. |
- Iliev, M. N., et al.
(författare)
-
Comparative Raman studies of Sr$_2$RuO$_4$, Sr$_3$Ru$_2$O$_7$ and Sr$_4$Ru$_3$O$_10$
- 2005
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 358:1--4
-
Tidskriftsartikel (refereegranskat)abstract
- The polarized Raman spectra of layered ruthenates of the Srn+1RunO3n+1 (n=1,2,3) Ruddlesden-Popper series were measured between 10 and 300 K. The phonon spectra of Sr3Ru2O7 and Sr4Ru3O10 confirmed earlier reports for correlated rotations of neighboring RuO6 octahedra within double or triple perovskite blocks. The observed Raman lines of Ag or B1g symmetry were assigned to particular atomic vibrations by considering the Raman modes in simplified structures with only one double or triple RuO6 layer per unit cell and by comparison to the predictions of lattice dynamical calculations for the real Pban and Pbam structures. Along with discrete phonon lines, a continuum scattering, presumably of electronic origin, is present in the zz, xx and xy, but not in the x'y' and zx spectra. Its interference with phonons results in Fano shape for some of the lines in the xx and xy spectra. The temperature dependences of phonon parameters of Sr3Ru2O7 exhibit no anomaly between 10 and 300 K where no magnetic transition occur. In contrast, two B1g lines in the spectra of Sr4Ru3O10, corresponding to oxygen vibrations modulating the Ru-O-Ru bond angle, show noticeable hardening with ferromagnetic ordering at 105 K, thus indicating strong spin-phonon interaction.
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| 36. |
- Iliev, M. N., et al.
(författare)
-
Comparative Raman studies of Sr2RuO4, Sr 3Ru2O7 and Sr4Ru3O 10
- 2005
-
Ingår i: Physica B: Condensed Matter. - : Elsevier BV. - 0921-4526. ; 358:1-4, s. 138-152
-
Tidskriftsartikel (refereegranskat)abstract
- The polarized Raman spectra of layered ruthenates of the Srn+1RunO3n+1 (n=1,2,3) Ruddlesden-Popper series were measured between 10 and 300 K. The phonon spectra of Sr3Ru2O7 and Sr4Ru3O10 confirmed earlier reports for correlated rotations of neighboring RuO6 octahedra within double or triple perovskite blocks. The observed Raman lines of Ag or B1g symmetry were assigned to particular atomic vibrations by considering the Raman modes in simplified structures with only one double or triple RuO6 layer per unit cell and by comparison to the predictions of lattice dynamical calculations for the real Pban and Pbam structures. Along with discrete phonon lines, a continuum scattering, presumably of electronic origin, is present in the zz, xx and xy, but not in the x′y′ and zx spectra. Its interference with phonons results in Fano shape for some of the lines in the xx and xy spectra. The temperature dependences of phonon parameters of Sr3Ru2O7 exhibit no anomaly between 10 and 300 K where no magnetic transition occur. In contrast, two B1g lines in the spectra of Sr4Ru3O10, corresponding to oxygen vibrations modulating the Ru-O-Ru bond angle, show noticeable hardening with ferromagnetic ordering at 105 K, thus indicating strong spin-phonon interaction.
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| 37. |
- Johansson, Malin E V, 1971, et al.
(författare)
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Composition and functional role of the mucus layers in the intestine.
- 2011
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Ingår i: Cellular and Molecular Life Sciences. - : Springer Science and Business Media LLC. - 1420-682X .- 1420-9071. ; 68, s. 3635-3641
-
Forskningsöversikt (refereegranskat)abstract
- In discussions on intestinal protection, the protective capacity of mucus has not been very much considered. The progress in the last years in understanding the molecular nature of mucins, the main building blocks of mucus, has, however, changed this. The intestinal enterocytes have their apical surfaces covered by transmembrane mucins and the whole intestinal surface is further covered by mucus, built around the gel-forming mucin MUC2. The mucus of the small intestine has only one layer, whereas the large intestine has a two-layered mucus where the inner, attached layer has a protective function for the intestine, as it is impermeable to the luminal bacteria.
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| 38. |
- Kakihana, M., et al.
(författare)
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A simple and reproducible way to synthesize PrBa2Cu4O8 under 1 atm of oxygen by amorphous citrate method
- 1999
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Ingår i: Physica. C, Superconductivity. - 0921-4534 .- 1873-2143. ; 321, s. 74-80
-
Tidskriftsartikel (refereegranskat)abstract
- A simple aqueous solution technique utilizing citric acid (CA) as a complexant was applied to prepare PrBa2Cu4O8 (Pr124) at ambient oxygen pressure. Heating of a mixed-solution of CA, water (H2O) and ions of Pr, Ba and Cu with a molar ratio of [CA]:[H2O]:[Pr + Ba + Cu] = 3.6:40:1 on a hot-plate set at 200 degrees C produced a transparent amorphous citrate "gel" without any precipitation, which after heat-treatment at 450 degrees C was converted to a precursor for Pr124. The Pr124 compound with only minor traces of BaCuO2, PrBaO3 and CuO formed after heat-treating the precursor twice at 850 degrees C for 60 h under 1 atm oxygen pressure. The amount of impurities in the citrate-derived Pr124 was approximately half of that in the best sample previously prepared by the more elaborate high-pressure technique. (C) 1999 Elsevier Science B.V. All rights reserved.
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| 39. |
- Kall, M., et al.
(författare)
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Resonance Raman scattering as a probe of oxygen dynamics in YBa2Cu3Ox
- 1998
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Ingår i: Journal of Physics and Chemistry of Solids. - 0022-3697 .- 1879-2553. ; 59, s. 1988-1990
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Tidskriftsartikel (refereegranskat)abstract
- We report on the metastable photo-bleaching of the 2.15 eV yellow Raman resonance in oxygen deficient YBa2Cu3Ox (x = 6.35-6.87), extending investigations by Wake ct al. (Phys. Rev. Lett., 1991,67, 3728) for x approximate to 7. Polarization, x dependence and phonon spectra indicate that the resonance is localized at oxygen vacancies in long CuO-chains. The resonance is thermally reactivated from the metastable bleached state with a relaxation time tau similar to exp[Delta/k(B)T] with Delta approximate to 1 eV. The resulting temperature dependent equilibrium resonance intensity essentially miners the oxygen superstructure disordering around T* approximate to 100 degrees C observed in the same crystals by hard X-ray diffraction, thus offering a new effective probe of chain-oxygen dynamics in YBa2Cu3Ox. (C) 1998 Elsevier Science Ltd. All rights reserved.
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| 40. |
- Karlsson, Joakim, 1984-
(författare)
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Optimization of Electron Beam Melting for Production of Small Components in Biocompatible Titanium Grades
- 2015
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Additive manufacturing (AM), also called 3D-printing, are technologies where parts are formed from the bottom up by adding material layer-by-layer on top of each other. Electron Beam Melting (EBM) is an AM technique capable of manufacturing fully solid metallic parts, using a high-intensity electron beam to melt powder particles in layers to form finished components. Compared to conventional machining, EBM offers enhanced efficiency for production of customized and patient specific parts such as e.g. dental prosthetics. However, dental prosthetics are challenging to produce by EBM, as their small sizes mean that mechanical and surface properties may be altered as part sizes decreases.The aim of this thesis is to gain new insights that could lead to optimization for production of small sized components in the EBM. The work is focused to understand the process-property relationships for small size components production.To improve the surface resolution and part detailing, a smaller sized powder was used for production and compared to parts made with standard sized powder. The surface-, chemical and mechanical properties were evaluated for parts produced with both types of powders. The results indicate that the surface roughness may be influenced by powder and build layer thickness size, whereas the mechanical properties showed no influence of the layer-wise production. However, the mechanical properties are dependent on part size. The outermost surface of the parts consists of a surface oxide dominated by TiO2, formed as a result of reaction between the surface and residual gases in the EBM build chamber. The surface oxide thickness is comparable to that of a conventionally machined surface, but is dependent on build height.This work concludes that the surface resolution and component detailing can be improved by various measures. Provided that proper process themes are used, the EBM manufactured material is homogenous with properties comparable to conventional produced titanium. It has also been shown that the material properties will be altered for small components. The results point towards different ways of optimizing manufacturing of dental prosthetics by EBM, which will make dental prosthetics available for an increased number of patients.
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| 41. |
- Kruger, R., et al.
(författare)
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Orbital ordering in LaMnO3 investigated by resonance Raman spectroscopy
- 2004
-
Ingår i: Physical Review Letters. - 0031-9007 .- 1079-7114. ; 92
-
Tidskriftsartikel (refereegranskat)abstract
- Orbital ordering leads to an unconventional excitation spectrum that we investigate by resonance Raman scattering using incident photon energies between 1.7 and 5.0 eV. We use spectral ellipsometry to determine the corresponding dielectric function. Our results show resonant behavior of the phonon Raman cross section when the laser frequency is close to the orbiton-excitation energy of 2 eV in LaMnO3. We show an excellent agreement between theoretical calculations based on the Franck-Condon mechanism activating multiphonon Raman scattering in first order of the electron-phonon coupling and the experimental data of phonons with different symmetries.
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| 42. |
- Kunze, J., et al.
(författare)
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Optical study of competition between ordering and metallicity in La(2-2x)Sr(1+2x)Mn(2)O(7)
- 2003
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 67
-
Tidskriftsartikel (refereegranskat)abstract
- We study by spectroscopic ellipsometry the optical in-plane anisotropies in La(2-2x)Sr(1+2x)Mn(2)O(7) with 0.32less than or equal toxless than or equal to0.40 above and below the metal to insulator (MI) transition. Spectral-weight changes in the optical conductivity occur at a cross-over temperature T(’)=280 K for all dopings. Local ordering of orbital and charge degrees of freedom sets in doping dependently at temperatures of 145 Kless than or equal toT(*)less than or equal to310 K. Below the MI transition we observe for all dopings except x=0.36 a vanishing of the charge ordering and an isotropic and metallic state at low frequencies, whereas the local orbital ordering persists. For x=0.36 we observe two different characteristic developments of the ordering processes, one being compatible with the parabolic doping dependence on T(*) established by the other doping levels and the second showing ordering at a temperature slightly above the MI transition. We argue that our observations are compatible with a phase separation scenario.
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| 43. |
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| 44. |
- Malmgren, Christine, et al.
(författare)
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Nanocrystallinity in RuO2 coatings-Influence of precursor and preparation temperature
- 2010
-
Ingår i: Thin Solid Films. - : Elsevier BV. - 0040-6090 .- 1879-2731. ; 518:14, s. 3615-3618
-
Tidskriftsartikel (refereegranskat)abstract
- The effects of precursor and calcination temperature on the nano morphology of ruthenium dioxide on titanium, prepared from thermal decomposition of aqueous salt solutions were investigated. Transmission electron microscopy. X-ray diffraction, gas porosimetry and cyclic voltammetry showed that lower calcination temperature yielded smaller crystallites. The crystallites were between 6 and 22 nm in diameter. When using ruthenium nitrosyl nitrate the firing temperature had a large impact on the grain size, but for chloride there was only a minor effect in the temperature range 350-550 degrees C.
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| 45. |
- Malmgren, Christine, et al.
(författare)
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Nanoscale characterization of crystallinity in DSA (R) coating
- 2008
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Ingår i: Journal of Physics, Conference Series. - : IOP Publishing. - 1742-6588 .- 1742-6596. ; 100:Part 5, s. 052026-, s. 4-4
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Tidskriftsartikel (refereegranskat)abstract
- Dimensionally Stable Anodes (DSA (R)) are used for industrial production of e. g. chlorine and chlorate. It is known that the superior electrocatalytical properties of DSA (R) is due to the large effective area of the porous coating. However, this knowledge is mainly found from in situ electrochemical measurements. Here, we used ex situ methods, AFM, TEM and gas porosimetry, for characterization at the nanoscale. The DSA (R) coating was found to consist of mono-crystalline grains with a size of 20-30 nm and with pores of about 10 nm in diameter. Using a simple geometrical model an effective area was calculated. For a typical coating thickness, an increase of about 1000 times in the effective surface area was found, which is consistent with in situ estimations. These results suggest that the dominating source of surface enlargement is due to nano-crystallinity.
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| 46. |
- Malmgren, Christine
(författare)
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Nanoscaled Structures in Ruthenium Dioxide Coatings
- 2009
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- An essential ingredient in the generation of environmentally compatible pulp bleaching chemicals is sodium chlorate. Chlorate is produced in electrochemical cells, where the electrodes are the key components. In Sweden the so-called DSA !R electrodes with catalytic coatings have been produced for more than 35 years. The production of chlorate uses a large amount of electric energy, and a decrease of just five percent of this consumption would, globally, decrease the consumption of electrical energy corresponding to half a nuclear power reactor. The aim of this project is to improve the electrode design on the nanoscale to decrease the energy consumption. The success of the DSA!R depends on the large catalytic area of the coating, however, little is known about the actual structure at the nanometer level. To increase the understanding of the nanostructure of these coatings, we used a number of methods, including atomic force microscopy, transmission electron microscopy, X-ray diffraction, porosimetry, and voltammetric charge. We found that the entire coating is built up of loosely packed rutile mono-crystalline 20 − 30 nm sized grains. The small grain sizes give a the large area, and consequently, lower cell-voltage and reduced energy consumption. A method to control the grain size would thus be a way to control the electrode efficiency. To alter the catalytically active area, we made changes in the coating process parameters. We found a dependency of the crystal-grain sizes on the choice of ruthenium precursor and processing temperature. The use of ruthenium nitrosyl nitrate resulted in smaller grains than ruthenium chloride and lowering the temperature tended to favour smaller grains. A more radical way would be to create a totally different type of electrode, manufactured in another way than using the 1965 DSA !R recipe. Such new types of electrodes based on, for example, nanowires or nanoimprint lithography, are discussed as future directions.
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| 47. |
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| 48. |
- Neuber, G., et al.
(författare)
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Generalized magneto-optical ellipsometry in ferromagnetic metals
- 2004
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Ingår i: Thin Solid Films. - 0040-6090 .- 1879-2731. ; 455, s. 39-42
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Tidskriftsartikel (refereegranskat)abstract
- We present spectral generalized magneto-optical ellipsometry as an optical tool to investigate magnetic and electronic properties of ferromagnetic materials. The advantage of the simultaneous observation of the dielectric and the magnetic responses within one measurement procedure is crucial for materials with coupled degrees of freedom near a phase transition or during annealing procedures to improve the film quality by removing grain boundaries. Moreover, we show the implementation of this technique within an UHV-cryostat for a temperature range between 4.2 and 800 K and fields up to 40 mT. Examplary measurements on iron and Permalloy demonstrate the comfortable application of this technique. (C) 2003 Elsevier B.V. All rights reserved.
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| 49. |
- Neuber, G., et al.
(författare)
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Temperature-dependent spectral generalized magneto-optical ellipsometry
- 2003
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Ingår i: Applied Physics Letters. - 0003-6951 .- 1077-3118. ; 83, s. 4509-4511
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Tidskriftsartikel (refereegranskat)abstract
- We present a setup for temperature-dependent spectral generalized magneto-optical ellipsometry (SGME). This technique gives access to the electronic as well as the magnetic properties of ferromagnetic materials within one single magneto-optical measurement. It also allows the determination of the orientation of the magnetization. We show spectra of the real and the imaginary part of the refractive index N as well as the magneto-optical coupling parameter Q of permalloy and iron films for in-plane magnetization. Our findings demonstrate the relevance of SGME for the understanding of the interplay between electronic and magnetic properties of ferromagnetics. (C) 2003 American Institute of Physics.
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| 50. |
- Näslund, Lars-Åke, et al.
(författare)
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The Role of TiO2 Doping on RuO2-Coated Electrodes for the Water Oxidation Reaction
- 2013
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 117:12, s. 6126-6135
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Tidskriftsartikel (refereegranskat)abstract
- Electrochemical water splitting into H-2 and O-2 presents a significant and challenging energy loss due to the high overpotential required at the anode. Today, in industrially relevant applications, dimensionally stable anodes (DSA) based on the electrocatalytic active RuO2 are conventionally utilized. To enhance the resistance against corrosion, incorporation of TiO2 in the RuO2-coated electrodes is widely employed. In the present work we have used scanning electrochemical microscopy (SECM) to demonstrate that TiO2-doped RuO2-coated electrodes, in addition to being more durable, also show an electrocatalytic activity that is, on average, 13% higher as compared to the pure RuO2-coated electrodes. We also demonstrate that cracks in the pure RuO2 coating are the most active zones, probably because Ti from the Ti support has diffused into the first applied layer of the RuO2 coating. To reveal the nature of this enhanced activity for water oxidation displayed on TiO2-doped RuO2 electrodes, we have employed X-ray photoelectron spectroscopy (XPS) for material characterization. The results show that the electrocatalytic activity enhancement displayed on the mixed (Ru1-x:Ti-x)O-2 coating is promoted through a charge transfer from the RuO2 to the TiO2, which provides new and more reactive sites designated as activated RuO2 delta+.
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