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1.
  • Magnus, Fridrik, et al. (författare)
  • Sequential magnetic switching in Fe/MgO(001) superlattices
  • 2018
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - : American Physical Society. - 1098-0121 .- 1550-235X. ; 97:17
  • Tidskriftsartikel (refereegranskat)abstract
    • Polarized neutron reflectometry is used to determine the sequence of magnetic switching in interlayer exchangecoupled Fe/MgO(001) superlattices in an applied magnetic field. For 19.6 Å thick MgO layers we obtain a 90◦periodic magnetic alignment between adjacent Fe layers at remanence. In an increasing applied field the toplayer switches first followed by its second-nearest neighbor. For 16.4 Å MgO layers, a 180◦periodic alignment isobtained at remanence and with increasing applied field the layer switching starts from the two outermost layersand proceeds inwards. This sequential tuneable switching opens up the possibility of designing three-dimensionalmagnetic structures with a predefined discrete switching sequence
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2.
  • Malinovskis, Paulius, et al. (författare)
  • Synthesis and characterisation of Mo-B-C thin films deposited by non-reactive DC magnetron sputtering
  • 2017
  • Ingår i: Surface & Coatings Technology. - : ELSEVIER SCIENCE SA. - 0257-8972 .- 1879-3347. ; 309, s. 506-515
  • Tidskriftsartikel (refereegranskat)abstract
    • Thin films in the Mo-B-C system with varying carbon content (up to 37 at.%) were deposited using non-reactive DC magnetron sputtering. The phase composition and microstructure were determined and the potential use of the films in sliding electrical contact applications was evaluated. Films with lower than 23 at.% carbon content consisted of nanocrystalline MoB2 - x grains surrounded by an amorphous tissue phase (a-B for binary, and a-BCx for ternary films). With increasing carbon content grain sizes was found to decrease (from 16 to 5 nm), and above 23 at.% carbon the films deposited at room temperature were X-ray amorphous. Scanning transmission electron microscopy and energy dispersive X-ray spectroscopy reveal that these films contain Mo-rich and Mo-poor regions, and thus are two-phase amorphous nanocomposites. Low-carbon content samples exhibited a friction coefficient against the steel counter surface of 1.1; this was reduced to 0.8 for high carbon-content films. Analysis of the tribofilm revealed formation of molybdenum oxide and amorphous carbon, however without significant lubricating effect at room temperature. Hardness and elastic modulus decrease with carbon content from similar to 29 to similar to 22 GPa and similar to 526 to similar to 326 GPa. These values give an WE ratio of 0.06 to 0.07, indicating brittle material. Resistivity was found to increase with carbon content from similar to 175 mu Omega cm for binary Mo-B to similar to 395 mu Omega cm for Mo-B-C thin film with 37 at.% of C. Therefore all the above results suggest that the Mo-B-C films are not suitable for sliding electrical contacts.
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3.
  • Mockute, A., et al. (författare)
  • Age hardening in (Ti1-xAlx)B2+Delta thin films
  • 2017
  • Ingår i: Scripta Materialia. - : PERGAMON-ELSEVIER SCIENCE LTD. - 1359-6462 .- 1872-8456. ; 127, s. 122-126
  • Tidskriftsartikel (refereegranskat)abstract
    • Thin films of (Ti0.71Al0.29)B2+1.08 have been deposited by magnetron sputtering. Post-deposition annealing at 1000 degrees C for 1 h results in increased hardness and elastic modulus, from 32 to 37 GPa and from 436 to 461 GPa, respectively. In both as-deposited and annealed states the films adhere well to the substrate, indicating no considerable internal stress. The initial high hardness is attributed to a columnar microstructure consisting of crystalline (Ti,Al)B-2 columns separated by an amorphous B matrix. The observed age hardening corresponds to phase separation within the (Ti,Al)B-2 columns including the formation of Ti-deficient crystallites within the grain interior upon annealing.
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4.
  • Mockute, A., et al. (författare)
  • Synthesis and characterization of (Ti1-xAlx)B2+Delta thin films from combinatorial magnetron sputtering
  • 2019
  • Ingår i: Thin Solid Films. - : ELSEVIER SCIENCE SA. - 0040-6090 .- 1879-2731. ; 669, s. 181-187
  • Tidskriftsartikel (refereegranskat)abstract
    • (Ti1-xAlx)B2+Delta films with a lateral composition gradient of x = [0.30-0.66] and Delta = [0.07-1.22] were deposited on an Al2O3 wafer by dual magnetron sputtering at 400 degrees C from sintered TiB2 and AlB2 targets. Composition analysis indicates that higher Ti:Al ratios favor overstoichiometry in B and a reduced incorporation of O. Transmission electron microscopy reveals distinctly different microstructures of Ti- and Al-rich compositions, with formation of characteristic conical growth features for the latter along with a lower degree of crystallinity and significantly less tissue phase from B segregation at the grain boundaries. For Al-rich films, phase separation into Ti- and Al-rich diboride nanometer-size domains is observed and interpreted as surface-initiated spinodal decomposition. The hardness of the films ranges from 14 to 28 GPa, where the higher values were obtained for the Ti-rich regions of the metal boride.
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5.
  • Moubah, Reda, et al. (författare)
  • Discrete Layer-by-Layer Magnetic Switching in Fe/MgO(001) Superlattices
  • 2016
  • Ingår i: Physical Review Applied. - : American physical society. - 2331-7019. ; 5:4
  • Tidskriftsartikel (refereegranskat)abstract
    • We report on a discrete layer-by-layer magnetic switching in Fe/MgO superlattices driven by an antiferromagnetic interlayer exchange coupling. The strong interlayer coupling is mediated by tunneling through MgO layers with thicknesses up to at least 1.8 nm, and the coupling strength varies with MgO thickness. Furthermore, the competition between the interlayer coupling and magnetocrystalline anisotropy stabilizes both 90 degrees and 180 degrees periodic alignment of adjacent layers throughout the entire superlattice. The tunable layer-by-layer switching, coupled with the giant tunneling magnetoresistance of Fe/MgO/Fe junctions, is an appealing combination for three-dimensional spintronic memories and logic devices.
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6.
  • Adam, Rania Elhadi, 1978-, et al. (författare)
  • Graphene-based plasmonic nanocomposites for highly enhanced solar-driven photocatalytic activities
  • 2019
  • Ingår i: RSC Advances. - Cambridge : Royal Meteorological Society. - 2046-2069 .- 2046-2069. ; 9:52, s. 30585-30598
  • Tidskriftsartikel (refereegranskat)abstract
    • High-efficiency photocatalysts are crucial for the removal of organic pollutants and environmental sustainability. In the present work, we report on a new low-temperature hydrothermal chemical method, assisted by ultrasonication, to synthesize disruptive plasmonic ZnO/graphene/Ag/AgI nanocomposites for solar-driven photocatalysis. The plasmonic nanocomposites were investigated by a wide range of characterization techniques, confirming successful formation of photocatalysts with excellent degradation efficiency. Using Congo red as a model dye molecule, our experimental results demonstrated a photocatalytic reactivity exceeding 90% efficiency after one hour simulated solar irradiation. The significantly enhanced degradation efficiency is attributed to improved electronic properties of the nanocomposites by hybridization of the graphene and to the addition of Ag/AgI which generates a strong surface plasmon resonance effect in the metallic silver further improving the photocatalytic activity and stability under solar irradiation. Scavenger experiments suggest that superoxide and hydroxyl radicals are responsible for the photodegradation of Congo red. Our findings are important for the fundamental understanding of the photocatalytic mechanism of ZnO/graphene/Ag/AgI nanocomposites and can lead to further development of novel efficient photocatalyst materials.
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7.
  • Adam, Rania E., et al. (författare)
  • Graphene-based plasmonic nanocomposites for highly enhanced solar-driven photocatalytic activities
  • 2019
  • Ingår i: RSC Advances. - : Royal Society of Chemistry. - 2046-2069. ; 9:52, s. 30585-30598
  • Tidskriftsartikel (refereegranskat)abstract
    • High-efficiency photocatalysts are crucial for the removal of organic pollutants and environmental sustainability. In the present work, we report on a new low-temperature hydrothermal chemical method, assisted by ultrasonication, to synthesize disruptive plasmonic ZnO/graphene/Ag/AgI nanocomposites for solar-driven photocatalysis. The plasmonic nanocomposites were investigated by a wide range of characterization techniques, confirming successful formation of photocatalysts with excellent degradation efficiency. Using Congo red as a model dye molecule, our experimental results demonstrated a photocatalytic reactivity exceeding 90% efficiency after one hour simulated solar irradiation. The significantly enhanced degradation efficiency is attributed to improved electronic properties of the nanocomposites by hybridization of the graphene and to the addition of Ag/AgI which generates a strong surface plasmon resonance effect in the metallic silver further improving the photocatalytic activity and stability under solar irradiation. Scavenger experiments suggest that superoxide and hydroxyl radicals are responsible for the photodegradation of Congo red. Our findings are important for the fundamental understanding of the photocatalytic mechanism of ZnO/graphene/Ag/AgI nanocomposites and can lead to further development of novel efficient photocatalyst materials.
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8.
  • Alnoor, Hatim, et al. (författare)
  • Exploring MXenes and their MAX phase precursors by electron microscopy
  • 2021
  • Ingår i: Materials Today Advances. - : Elsevier. - 2590-0498. ; 9
  • Tidskriftsartikel (refereegranskat)abstract
    • This review celebrates the width and depth of electron microscopy methods and how these have enabled massive research efforts on MXenes. MXenes constitute a powerful recent addition to 2-dimensional materials, derived from their parent family of nanolaminated materials known as MAX phases. Owing to their rich chemistry, MXenes exhibit properties that have revolutionized ranges of applications, including energy storage, electromagnetic interference shielding, water filtering, sensors, and catalysis. Few other methods have been more essential in MXene research and development of corresponding applications, compared with electron microscopy, which enables structural and chemical identification at the atomic scale. In the following, the electron microscopy methods that have been applied to MXene and MAX phase precursor research are presented together with research examples and are discussed with respect to advantages and challenges. (C) 2020 The Author(s). Published by Elsevier Ltd.
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9.
  • Amloy, Supaluck, et al. (författare)
  • Excitons and biexcitons in InGaN quantum dot like localization centers
  • Annan publikation (övrigt vetenskapligt)abstract
    • Indium segregation in a narrow InGaN single quantum well creates quantum dot (QD) like exciton localization centers. Cross section transmission electron microscopy reveals varying shapes and lateral sizes in the range ~1-5 nm of the QD-like features, while scanning near field optical microscopy demonstrates a highly inhomogeneous spatial distribution of optically active individual localization centers. Microphotoluminescence spectroscopy confirms the spectrally inhomogeneous distribution of localization centers, in which the exciton and the biexciton related emissions from single centers of varying geometry could be identified by means of excitation power dependencies. Interestingly, the biexciton binding energy (Ebxx) was found to vary from center to center, between 3 to -22 meV, in correlation with the exciton emission energy. Negative binding energies justify the three-dimensional quantum confinement, which confirms QD-like properties of the localization centers.! The observed energy correlation is proposed to be understood as variations of the lateral extension of the confinement potential, which would yield smaller values of Ebxx for reduced lateral extension and higher exciton emission energy. The proposed relation between lateral extension and Ebxx is further supported by the exciton and the biexciton recombination lifetimes of a single QD, which suggest a lateral extension of merely ~3 nm for a QD with strongly negative Ebxx = -15.5 meV.
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10.
  • Amloy, Supaluck, et al. (författare)
  • Excitons and biexcitons in InGaN quantum dot like localization centers
  • 2014
  • Ingår i: Nanotechnology. - : IOP Publishing. - 0957-4484. ; 25:49, s. 495702-
  • Tidskriftsartikel (refereegranskat)abstract
    • Indium segregation in a narrow InGaN single quantum well creates quantum dot (QD) like exciton localization centers. Cross-section transmission electron microscopy reveals varying shapes and lateral sizes in the range ∼1–5 nm of the QD-like features, while scanning near field optical microscopy demonstrates a highly inhomogeneous spatial distribution of optically active individual localization centers. Microphotoluminescence spectroscopy confirms the spectrally inhomogeneous distribution of localization centers, in which the exciton and the biexciton related emissions from single centers of varying geometry could be identified by means of excitation power dependencies. Interestingly, the biexciton binding energy (Ebxx) was found to vary from center to center, between 3 to −22 meV, in correlation with the exciton emission energy. Negative binding energies are only justified by a three-dimensional quantum confinement, which confirms QD-like properties of the localization centers. The observed energy correlation is proposed to be understood as variations of the lateral extension of the confinement potential, which would yield smaller values of Ebxx for reduced lateral extension and higher exciton emission energy. The proposed relation between lateral extension and Ebxx is further supported by the exciton and the biexciton recombination lifetimes of a single QD, which suggest a lateral extension of merely ∼3 nm for a QD with strongly negative Ebxx = −15.5 meV. 
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