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- Andersson, Mattias, et al.
(author)
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Conformation sensitive charge transport in conjugated polymers
- 2013
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In: Applied Physics Letters. - : American Institute of Physics (AIP). - 0003-6951 .- 1077-3118. ; 103:21, s. 213303-
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Journal article (peer-reviewed)abstract
- Temperature dependent charge carrier mobility measurements using field effect transistors and density functional theory calculations are combined to show how the conformation dependent frontier orbital delocalization influences the hole-and electron mobilities in a donor-acceptor based polymer. A conformationally sensitive lowest unoccupied molecular orbital results in an electron mobility that decreases with increasing temperature above room temperature, while a conformationally stable highest occupied molecular orbital is consistent with a conventional hole mobility behavior and also proposed to be one of the reasons for why the material works well as a hole transporter in amorphous bulk heterojunction solar cells.
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2. |
- Berggren Kleja, Dan, et al.
(author)
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Characterization of iron in floating surface films of some natural waters using EXAFS
- 2012
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In: Chemical Geology. - : Elsevier. - 0009-2541 .- 1872-6836. ; 326, s. 19-26
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Journal article (peer-reviewed)abstract
- Floating, iron bearing films have been observed in a wide range of environments, including wetlands, seep waters in ground water discharge areas, small rivers and lakes. To date, knowledge about their formation and composition is scarce. We have investigated the form of iron in floating iron-rich films of different origin, including a pond and a brook, as well as seep water pools of a groundwater discharge area. Sampling sites were located in southern (pond, brook) and central (seep pools) Sweden. Synchrotron-based X-ray absorption spectroscopy (EXAFS and XANES) allowed identification of the iron precipitates present in the films, without any pretreatment. The EXAFS data showed that the iron containing phase formed in the floating films varied in composition between the sites investigated. In the films from two ground water discharge areas, characterized by out-flowing iron(II) rich ground water being high in pH and low in DOC, the iron phase was completely dominated by ferrihydrite. In contrast, surface films sampled from the brook and the pond, the iron speciation showed a mixture of iron(III)-organic complexes and iron (hydr)oxide (most likely ferrihydrite). These waters were oxic and contained higher concentration of DOC than the seep water pools in the ground water discharge areas. The position of the pre-edge peak, which is sensitive to the oxidation state of iron, did not indicate occurrence of iron (II) in any of the films. Elemental composition of one film (seep water), suggested that films contained about one third of organic matter. Ferrihydrite is probably present as small particles with humic material sorbed onto surfaces or included in the particles, making the particles sufficiently hydrophobic to not settle without physical disturbance. The films are fragile and break easily down and become suspended upon disturbance. More studies are warranted in order to understand the mechanism of the formation of these fascinating films and their biogeochemical role.
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5. |
- Engvall, Jan, et al.
(author)
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Adenosine stress myocardial perfusion detected with CT compared with attenuation-corrected SPECT
- 2011
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In: EUROPEAN HEART JOURNAL SUPPLEMENTS. - : Oxford University Press. ; , s. A31-A31
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Conference paper (peer-reviewed)abstract
- Purpose: To asses adenosine stress myocardial perfusion by cardiac CT and compare with simultaneously performed attenuation corrected SPECT.Methods: 11 patients, 9 men and 2 women >2months post primary PCI, with manifest myocardial damage and remaining stenoses in the coronary circulation, were studied with myocardial perfusion CT under vasodilatory stress. The investigation started with a topogram followed by a testbolus of iodine whereafter the coronary artery study was performed in sequence mode. Adenosine was then infused for at least five minutes at the standard rate of 140ug/kg/min. After three minutes, 6 MBq/kg of 99mTc-tetrofosmin was injected immediately followed by 80ml iodine contrast. The wash-in of iodine was monitored by CT scanning of a 7cm long cardiac volume segment every other second for 22s. One hour after the CT scan, myocardial SPECT was performed. Scanning required the patients to tolerate breath holding for 22s, have a heart rate <80/min and body weight <85kg, and their kidney function should allow 140ml 370mg iodine contrast to be given.Results: All 11 patients tolerated the full adenosine infusion and scanning was successful. One patient could not be analyzed due to noisy images. In two patients, the limited scanning volume did not cover the entire base of the heart. Three patients had no defect on SPECT. Patients with a defect had on average myocardial blood flow 80ml/100ml tissue/min in the defect area and 142ml in the segments with the highest perfusion, while patients without defect had 98 and 141ml, respectively.Conclusion: Peak myocardial perfusion may be determined with CT under adenosine stress and compared with attenuation corrected SPECT. Initial experience shows that the method is sensitive to timing of bolus, to noisy images and results may diverge from those obtained with SPECT.
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6. |
- Fredin, Lisa, et al.
(author)
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Exceptional Excited-State Lifetime of an Iron(II)-N-Heterocyclic Carbene Complex Explained
- 2014
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In: The Journal of Physical Chemistry Letters. - : American Chemical Society (ACS). - 1948-7185. ; 5:12, s. 2066-2071
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Journal article (peer-reviewed)abstract
- Earth-abundant transition-metal complexes are desirable for sensitizers in dye-sensitized solar cells or photocatalysts. Iron is an obvious choice, but the energy level structure of its typical polypyridyl complexes, featuring low-lying metal-centered states, has made such complexes useless as energy converters. Recently, we synthesized a novel iron-N-heterocyclic carbene complex exhibiting a remarkable 100-fold increase of the lifetime compared to previously known iron(II) complexes. Here, we rationalize the measured excited-state dynamics with DFT and TD-DFT calculations. The calculations show that the exceptionally long excited-state lifetime (similar to 9 ps) is achieved for this Fe complex through a significant destabilization of both triplet and quintet metal-centered scavenger states compared to other Feu complexes. In addition, a shallow (MLCT)-M-3 potential energy surface with a low-energy transition path from the (MLCT)-M-3 to (MC)-M-3 and facile crossing from the (MC)-M-3 state to the ground state are identified as key features for the excited-state deactivation.
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7. |
- Galynska, Marta, et al.
(author)
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Emerging Polymorphism in Nanostructured TiO2: Quantum Chemical Comparison of Anatase, Rutile, and Brookite Clusters
- 2013
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In: International Journal of Quantum Chemistry. - : Wiley. - 0020-7608. ; 113:24, s. 2611-2620
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Journal article (peer-reviewed)abstract
- Density functional theory (DFT) and time-dependent DFT calculations have been performed on a set of 34 titanium dioxide clusters ((TiO2)(n) with n125) to investigate structural and electronic properties of nanostructured TiO2 (nano-TiO2) materials. The investigated clusters include models of the three low-energy polymorphic forms of TiO2 anatase, rutile, and brookite. A systematic comparison of clusters of increasing size show clear trends for emerging bulk properties in the investigated systems as the surface-to-bulk ratio changes from small clusters dominated by undercoordinated surface atoms to more realistic model nanocrystals with significant bulk components. Differences and similarities in terms of atomic coordination, structural stability, and electronic properties for the three different polymorphic forms of nano-TiO2 are discussed. The calculations provide evidence for emerging polymorphism with increasing cluster sizes so that the different TiO2 forms can be clearly distinguished based on structural characteristics associated with the local bonding environment of the constituent atoms. (c) 2013 Wiley Periodicals, Inc.
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8. |
- Galynska, Marta, et al.
(author)
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Material Dependence of Water Interactions with Metal Oxide Nanoparticles: TiO2, SiO2, GeO2, and SnO2
- 2014
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In: Advances in Quantum Chemistry. - 0065-3276. ; 69, s. 303-332
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Research review (peer-reviewed)abstract
- Surface interactions of water with nano-TiO2 and structurally related group IV metal dioxide nanoparticles have been investigated using density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations. The investigated clusters include 46 and 92 unit models of TiO2 (i.e., (TiO2)(46) and (TiO2)(92)) of the three low-energy polymorphs of TiO2: anatase, rutile, and brookite. The investigation also includes studies of corresponding rutile-type clusters of three structurally related forms of group IV oxides: SnO2, GeO2, and SiO2. The calculations demonstrate the strong influence of water surface adsorption on several important nanoparticle properties including structure, charge distribution, and electronic structure for all investigated materials. Significant differences between the various materials are also revealed by the calculations, including an unusual stability of the electronic structure of TiO2 in the environment of particular relevance for its photoelectrochemical and photocatalytic applications.
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9. |
- Gustafsson, Jon Petter, 1964-, et al.
(author)
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Chromium (III) and bismuth (III) complexation to organic matter : EXAFS Spectroscopy and equilibrium modeling
- 2013
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In: Mineralogical magazine. - 0026-461X .- 1471-8022. ; 77:5, s. 1235-
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Journal article (peer-reviewed)abstract
- The complexation of chromium(III) and bismuth(III) to organic matter was investigated by batch equilibrations with Suwannee River Fulvic Acid (SRFA) and with mor layer material (Risbergshöjden Oe). In the SRFA systems, 3 mM chromium(III) solutions were equilibrated with 9 g L-1 SRFA and equilibrated at different pH values ranging from 2 to 6. Characterization of the reaction products was made at MAX-Lab, Lund, Sweden, using Cr K-edge EXAFS spectroscopy at 5 989 eV. The spectra were interpreted using both conventional data treatment using EXAFSPAK and with wavelet transform (WT) analysis. The results show that chromium(III) formed monomeric organic complexes with SRFA. There was no evidence of polymerization with the exception of the particulate phase at pH 6, which was attributed to a limited extent of Cr(OH)3 formation.The mor layer material was equilibrated with chromium(III) and bismuth(III) solutions as a function of pH, time and competing ions (iron(III), aluminium(III), copper(II)). Again CrK-edge and Bi L3-edge EXAFS spectroscopy was used, at 5 989 and 13 419 eV. The experiments showed a predominance of monomeric organic complexes for chromium(III). The sorption of chromium(III) was pH-dependent and to some extent found to be influenced by competition from aluminium(III) and copper(II). Chromium(III) complexation was found to be very slow at pH < 4, and equilibration times of three months or longer were required to reach equilibrium under these conditions. Concerning bismuth(III), complexation was quicker and found to be very strong, with more than 94 % bound at pH 1.2 at a high bismuth(III) loading. EXAFS spectroscopy showed that two complexes were involved, one monomeric and one di- or trimeric, with the latter being predominant at higher pH values, although it was present already at pH 1.2. In the organic bismuth(III) complexes, the bismuth(III) octahedron was found to be strongly distorted, which implies strong binding to organic acid functional groups. The complexation of bismuth(III) remained essentially unchanged even in the presence of a potent competitor such as iron(III).The results from the spectroscopic investigation and from the quantitative solution data were used to calibrate new and improved complexation models for the Stockholm Humic (SHM) and the NICA-Donnan models. In the case of the Stockholm Humic Model, both complexes as found by EXAFS spectroscopy were considered explicitly; this ensured the model to predict minimum competition effects in agreement with the laboratory results.
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10. |
- Gustafsson, Jon Petter, et al.
(author)
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Chromium(III) complexation to natural organic matter : Mechanisms and modeling
- 2014
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In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 48:3, s. 1753-1761
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Journal article (peer-reviewed)abstract
- Chromium is a common soil contaminant, and it often exists as chromium(III). However, limited information exists on the coordination chemistry and stability of chromium(III) complexes with natural organic matter (NOM). Here, the complexation of chromium(III) to mor layer material and to Suwannee River Fulvic Acid (SRFA) was investigated using EXAFS spectroscopy and batch experiments. The EXAFS results showed a predominance of monomeric chromium(III)-NOM complexes at low pH (<5), in which only Cr··C and Cr-O-C interactions were observed in the second coordination shell. At pH > 5 there were polynuclear chromium(III)-NOM complexes with Cr···Cr interactions at 2.98 Å and for SRFA also at 3.57 Å, indicating the presence of dimers (soil) and tetramers (SRFA). The complexation of chromium(III) to NOM was intermediate between that of iron(III) and aluminum(III). Chromium(III) complexation was slow at pH < 4: three months or longer were required to reach equilibrium. The results were used to constrain chromium-NOM complexation in the Stockholm Humic Model (SHM): a monomeric complex dominated at pH < 5, whereas a dimeric complex dominated at higher pH. The optimized constant for the monomeric chromium(III) complex was in between those of the iron(III) and aluminum(III) NOM complexes. Our study suggests that chromium(III)-NOM complexes are important for chromium speciation in many environments.
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