| 1. |
- Dahlqvist, Martin, et al.
(författare)
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Magnetically driven anisotropic structural changes in the atomic laminate Mn2GaC
- 2016
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Ingår i: Physical Review B. - : AMER PHYSICAL SOC. - 2469-9950 .- 2469-9969. ; 93:1
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Tidskriftsartikel (refereegranskat)abstract
- Inherently layered magnetic materials, such as magnetic M(n+1)AX(n) (MAX) phases, offer an intriguing perspective for use in spintronics applications and as ideal model systems for fundamental studies of complex magnetic phenomena. The MAX phase composition M(n+1)AX(n) consists of M(n+1)AX(n) blocks separated by atomically thin A-layers where M is a transition metal, A an A-group element, X refers to carbon and/or nitrogen, and n is typically 1, 2, or 3. Here, we show that the recently discovered magnetic Mn2GaC MAX phase displays structural changes linked to the magnetic anisotropy, and a rich magnetic phase diagram which can be manipulated through temperature and magnetic field. Using first-principles calculations and Monte Carlo simulations, an essentially one-dimensional (1D) interlayer plethora of two-dimensioanl (2D) Mn-C-Mn trilayers with robust intralayer ferromagnetic spin coupling was revealed. The complex transitions between them were observed to induce magnetically driven anisotropic structural changes. The magnetic behavior as well as structural changes dependent on the temperature and applied magnetic field are explained by the large number of low energy, i.e., close to degenerate, collinear and noncollinear spin configurations that become accessible to the system with a change in volume. These results indicate that the magnetic state can be directly controlled by an applied pressure or through the introduction of stress and show promise for the use of Mn2GaC MAX phases in future magnetoelectric and magnetocaloric applications.
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| 2. |
- Dobrovetska, Oksana, et al.
(författare)
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Electrocatalytic activity of Pd-Au nanoalloys during methanol oxidation reaction
- 2020
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Ingår i: International journal of hydrogen energy. - : Elsevier BV. - 0360-3199 .- 1879-3487. ; 45:7, s. 4444-4456
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Tidskriftsartikel (refereegranskat)abstract
- Methanol fuel cells are very promising power source due to its high efficiency and low emissions of pollutants but their commercialization is hindered by development of the effective catalysts. Bimetallic nanostructured catalysts have been used to increase the effectiveness of methanol electrooxidation. Their high electrocatalytic activity can be accounted largely by the difference in electronegativity of two metals (e.g. Pd and Au), that resulting in gradual Auδ+→Auδ– transition with the increase in Pd content. Therefore, gold-enriched bimetallic Pd-Aunano were recommended as catalysts for oxidation processes since they are characterized by the presence of Auδ+ on their surface. Deposition of Pd, Au and Pd–Au nanoparticles (~50–350 nm) were carried out in dimethyl sulfoxide by pulsed mode of electrolysis directly on electrode surface. Cyclic voltammetry was the main method to study catalytic properties of the modified electrode in the anode oxidation process of methanol. It was found that oxidation rate on the electrode surface modified by bimetallic Pd–Au nanoparticles is ~1.5 times higher as compared to that in the case of electrodes modified by Pd or Au monometallic nanoparticles individually. In order to find highly active, selective, and stable catalysts for methanol electrocatalytic oxidation reaction additional studies are needed to understand the role of electrode surface charge and local OH− ions concentration from alkali solution.
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| 3. |
- Fang, Hailiang, 1985-
(författare)
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Structural Studies of Mn-X (X=Al, Bi): Permanent Magnetic Materials without Rare Earth Metals
- 2019
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- How to generate and use electricity in a more efficient way is a major challenge for humankind. In this context, permanent magnets play an important role within a very broad range of electric power applications. The strongest magnets used today are mainly based on alloys that contain rare-earth metals, which are neither economical nor sustainable. The search for new alternative alloys with satisfactory magnetic properties is the major motivation for the investigations summarized in this thesis. Interesting candidates for alternative rare-earth free alloys were selected with τ-MnAl as the basis. Theoretical studies suggest that such alloys may show good magnetic properties after chemical modifications to optimize them. Another compound with promising magnetic properties is MnBi, included in this study.MnAl-Z (Z= C, B, Ga as doping elements) and MnBi compounds were synthesized through carefully devised high-temperature methods, followed by various milling and annealing steps. The structural phase analysis of the samples was based on X-ray and neutron diffraction. A systematic microstructural investigation was also performed for selected samples. The phase transitions of MnAl and MnBi during heating and cooling at different rates were studied by in situ X-ray diffraction from a synchrotron source. The magnetic properties were characterized by various methods.By strict control of experimental parameters, the metastable τ-MnAl was found to be directly obtainable using a "drop synthesis” process. A cooling rate of 10 K/min yielded an almost pure ferromagnetic τ-MnAl phase. A microstructural characterization of similarly synthesized MnAl-C samples revealed the presence of phase segregation, a Mn-rich region and an Al-rich grain boundary phase.A cryomilling process was employed which decreased the particle size of the MnAl-C sample. Neutron diffraction data disclosed accompanying amorphous features, related to changes in Mn and Al atom occupancies during the milling process. A flash heating procedure regenerated the structural ordering between Mn and Al in the structure, where the initial magnetic properties were recovered.The MnBi compound was synthesized by a self-flux method in order to isolate single crystals. As for τ-MnAl, in situ diffraction studies were applied for following phase transitions and the magnetic properties were studied.
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| 4. |
- Jacobsson, Jesper T., et al.
(författare)
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A monolithic device for solar water splitting based on series interconnected thin film absorbers reaching over 10% solar-to-hydrogen efficiency
- 2013
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Ingår i: Energy & Environmental Science. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 6:12, s. 3676-3683
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Tidskriftsartikel (refereegranskat)abstract
- Efficient production of hydrogen from solar energy is anticipated to be an important component in a future sustainable post-carbon energy system. Here we demonstrate that series interconnected absorbers in a PV-electrolysis configuration based on the compound semiconductor CIGS, CuInxGa1-xSe2, are a highly interesting concept for solar water splitting applications. The band gap energy of CIGS can be adjusted to a value close to optimum for efficient absorption of the solar spectrum, but is too low to drive overall water splitting. Therefore we connect three cells in series, into a monolithic device, which provides sufficient driving force for the full reaction. Integrated with a catalyst this forms a stable PV/photo-electrochemical device, which when immersed in water reaches over 10% solar-to-hydrogen efficiency for unassisted water splitting. The results show that series interconnected device concepts, which enable use of a substantial part of the solar spectrum, provide a simple route towards highly efficient water splitting and could be used also for other solar absorbers with similar electro-optical properties. We discuss how the efficiency could be increased for this particular device, as well as the general applicability of the concepts used in this work. We also briefly discuss advantages and disadvantages of photo-electrochemical cells in relation to PV-electrolysis with respect to our results.
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| 5. |
- Popova, Gergana, et al.
(författare)
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Optimization of Tetrahydroindazoles as Inhibitors of Human Dihydroorotate Dehydrogenase and Evaluation of Their Activity and In Vitro Metabolic Stability
- 2020
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Ingår i: Journal of Medicinal Chemistry. - : American Chemical Society (ACS). - 0022-2623 .- 1520-4804. ; 63:8, s. 3915-3934
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Tidskriftsartikel (refereegranskat)abstract
- Human dihydroorotate dehydrogenase (DHODH), an enzyme in the de novo pyrimidine synthesis pathway, is a target for the treatment of rheumatoid arthritis and multiple sclerosis and is re-emerging as an attractive target for cancer therapy. Here we describe the optimization of recently identified tetrahydroindazoles (HZ) as DHODH inhibitors. Several of the HZ analogues synthesized in this study are highly potent inhibitors of DHODH in an enzymatic assay, while also inhibiting cancer cell growth and viability and activating p53-dependent transcription factor activity in a reporter cell assay. Furthermore, we demonstrate the specificity of the compounds toward the de novo pyrimidine synthesis pathway through supplementation with an excess of uridine. We also show that induction of the DNA damage marker gamma-H2AX after DHODH inhibition is preventable by cotreatment with the pancaspase inhibitor Z-VAD-FMK. Additional solubility and in vitro m etabolic stability profiling revealed compound 51 as a favorable candidate for preclinical efficacy studies.
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