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  • 1.
    Dahlqvist, Martin
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Alling, Björn
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Ingason, Per
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Magnus, F.
    2Department of Physics and Astronomy, Uppsala University, Uppsala, Sweden.
    Thore, Andreas
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Mockute, Aurelija
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Meshkian, Rahele
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Sahlberg, M.
    3Department of Chemistry, The Ångström Laboratory, Uppsala University, Uppsala, Sweden.
    Persson, Per O A
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Hjörvarsson, B.
    Department of Physics and Astronomy, Uppsala University, Uppsala, Sweden.
    Abrikosov, A.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Complex magnetism in nanolaminated Mn2GaC2014Manuscript (preprint) (Other academic)
    Abstract [en]

    We have used first-principles calculations and Heisenberg Monte Carlo simulations to search for the magnetic ground state of Mn2GaC, a recently synthesized magnetic nanolaminate. We have, independent on method, identified a range of low energy collinear as well as non-collinear magnetic configurations, indicating a highly frustrated magnetic material with several nearly degenerate magnetic states. An experimentally obtained magnetization of only 0.29 per Mn atom in Mn2GaC may be explained by canted spins in an antiferromagnetic configuration of ferromagnetically ordered sub-layers with alternating spin orientation, denoted AFM[0001]. Furthermore, low temperature X-ray diffraction show a new basal plane peak appearing upon a magnetic transition, which is consistent with the here predicted change in inter-layer spacing for the AFM[0001] configuration.

  • 2.
    Dahlqvist, Martin
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Ingason, Arni Sigurdur
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Alling, Björn
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Magnus, F.
    Uppsala University, Sweden.
    Thore, Andreas
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Mockuté, Aurelija
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Arnalds, U. B.
    University of Iceland, Iceland.
    Sahlberg, M.
    Uppsala University, Sweden.
    Hjorvarsson, B.
    Uppsala University, Sweden.
    Abrikosov, Igor
    Linköping University, Department of Physics, Chemistry and Biology, Theoretical Physics. Linköping University, Faculty of Science & Engineering. National University of Science and Technology MISIS, Russia; Tomsk State University, Russia.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Magnetically driven anisotropic structural changes in the atomic laminate Mn2GaC2016In: Physical Review B, ISSN 2469-9950, E-ISSN 2469-9969, Vol. 93, no 1, p. 014410-Article in journal (Refereed)
    Abstract [en]

    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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  • 3.
    Dahlqvist, Martin
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Lu, Jun
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Hultman, Lars
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Origin of Chemically Ordered Atomic Laminates (i-MAX): Expanding the Elemental Space by a Theoretical/Experimental Approach2018In: ACS Nano, ISSN 1936-0851, E-ISSN 1936-086X, Vol. 12, no 8, p. 7761-7770Article in journal (Refereed)
    Abstract [en]

    With increased chemical diversity and structural complexity comes the opportunities for innovative materials possessing advantageous properties. Herein, we combine predictive first-principles calculations with experimental synthesis, to explore the origin of formation of the atomically laminated i-MAX phases. By probing (Mo2/3M1/32)(2)AC (where M-2 = Sc, Y and A = Al, Ga, In, Si, Ge, In), we predict seven stable i-MAX phases, five of which should have a retained stability at high temperatures. (Mo2/3Sc1/3)(2)GaC and (Mo2/3Y1/3)(2)GaC were experimentally verified, displaying the characteristic in-plane chemical order of Mo and Sc/Y and Kagome-like ordering of the A-element. We suggest that the formation of i-MAX phases requires a significantly different size of the two metals, and a preferable smaller size of the A-element. Furthermore, the population of antibonding orbitals should be minimized, which for the metals herein (Mo and Sc/Y) means that A elements from Group 13 (Al, Ga, In) are favored over Group 14 (Si, Ge, Sn). Using these guidelines, we foresee a widening of elemental space for the family of i-MAX phases and expect more phases to be synthesized, which will realize useful properties. Furthermore, based on i-MAX phases as parent materials for 2D MXenes, we also expect that the range of MXene compositions will be expanded.

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  • 4.
    Flatten, Tim
    et al.
    Forschungszentrum Julich, Germany; JARA, Germany.
    Matthes, Frank
    Forschungszentrum Julich, Germany; JARA, Germany.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Salikhov, Ruslan
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Wiedwald, Ulf
    Univ Duisburg Essen, Germany.
    Farle, Michael
    Univ Duisburg Essen, Germany.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Buergler, Daniel E.
    Forschungszentrum Julich, Germany; JARA, Germany.
    Schneider, Claus M.
    Forschungszentrum Julich, Germany; JARA, Germany; Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Direct measurement of anisotropic conductivity in a nanolaminated (Mn0.5Cr0.5)(2)GaC thin film2019In: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 115, no 9, article id 094101Article in journal (Refereed)
    Abstract [en]

    The direct and parameter-free measurement of anisotropic electrical resistivity of a magnetic M(n+1)AX(n) (MAX) phase film is presented. A multitip scanning tunneling microscope is used to carry out 4-probe transport measurements with variable probe spacing s. The observation of the crossover from the 3D regime for small s to the 2D regime for large s enables the determination of both in-plane and perpendicular-to-plane resistivities rho(ab) and rho(c). A (Cr0.5Mn0.5)(2)GaC MAX phase film shows a large anisotropy ratio rho(c)/rho(ab) = 525 +/- 49. This is a consequence of the complex bonding scheme of MAX phases with covalent M-X and metallic M-M bonds in the MX planes and predominately covalent, but weaker bonds between the MX and A planes. Published under license by AIP Publishing.

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  • 5.
    Ingason, Arni Sigurdur
    et al.
    Linköping University, Department of Physics, Chemistry and Biology. Linköping University, Faculty of Science & Engineering.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Toward Structural Optimization of MAX Phases as Epitaxial Thin Films2016In: MATERIALS RESEARCH LETTERS, ISSN 2166-3831, Vol. 4, no 3, p. 152-160Article in journal (Refereed)
    Abstract [en]

    Prompted by the increased focus on MAX phase materials and their two-dimensional counterparts MXenes, a brief review of the current state of affairs in the synthesis of MAX phases as epitaxial thin films is given. Current methods for synthesis are discussed and suggestions are given on how to increase the material quality even further as well as arrive at those conditions faster. Samples were prepared to exemplify the most common issues involved with the synthesis, and through suggested paths for resolving these issues we attain samples of a quality beyond what has previously been reported.

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  • 6.
    Lai, Chung-Chuan
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Lu, Jun
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Farle, Michael
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany; Immanuel Kant Baltic Fed Univ, Russia.
    Hultman, Lars
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Eklund, Per
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Thermally induced substitutional reaction of Fe into Mo2GaC thin films2017In: MATERIALS RESEARCH LETTERS, ISSN 2166-3831, Vol. 5, no 8, p. 533-539Article in journal (Refereed)
    Abstract [en]

    The first Fe-based MAX phase is realized by solid-state substitution reaction of an Fe/Au/Mo2GaC thin-film diffusion couple, as determined by X-ray diffraction and scanning transmission electron microscopy. Chemical analysis together with elemental mapping reveals that as much as 50 at.% Fe on the A site can be obtained by thermally induced Au and Fe substitution for Ga atomic layers in Mo2GaC. One-sixth of the original Ga is also replaced by Au atoms. When annealing Mo2GaC thin films covered with Fe only, the Mo2GaC phase remains intact, that is, Au acts as a catalyst for the substitution reaction. [GRAPHICS] .

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  • 7.
    Lai, Chung-Chuan
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Tao, Quanzheng
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Fashandi, Hossein
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Wiedwald, Ulf
    Univ Duisburg Essen, Germany; Natl Univ Sci and Technol MISIS, Russia.
    Salikhov, Ruslan
    Univ Duisburg Essen, Germany.
    Farle, Michael
    Univ Duisburg Essen, Germany; Immanuel Kant Balt Fed Univ, Russia.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Lu, Jun
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Hultman, Lars
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Eklund, Per
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Magnetic properties and structural characterization of layered (Cr0.5Mn0.5)(2)AuC synthesized by thermally induced substitutional reaction in (Cr0.5Mn0.5)(2)GaC2018In: APL MATERIALS, ISSN 2166-532X, Vol. 6, no 2, article id 026104Article in journal (Refereed)
    Abstract [en]

    The magnetic properties of the new phase (Cr0.5Mn0.5)(2)AuC are compared to the known MAX-phase (Cr0.5Mn0.5)(2)GaC, where the former was synthesized by thermally induced substitution reaction of Au for Ga in (Cr0.5Mn0.5)(2)GaC. The reaction introduced a lattice expansion of similar to 3% along the c-axis, an enhancement of the coercive field from 30 mT to 140 mT, and a reduction of the Curie temperature and the saturation magnetization. Still, (Cr0.5Mn0.5)(2)AuC displays similar features in the magnetic field-and temperature-dependent magnetization curves as previously reported magnetic MAX phases, e.g., (Cr0.5Mn0.5)(2)GaC and (Mo0.5Mn0.5)(2)GaC. Thework suggests a pathway for tuning the magnetic properties of MAX phases. (c) 2018 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license.

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  • 8.
    Meshkian, Rahele
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Sigurdur Ingason, Arni
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Dahlqvist, Martin
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Arnalds, Unnar B.
    University of Iceland, Iceland.
    Magnus, Fridrik
    Uppsala University, Sweden.
    Lu, Jun
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Theoretical stability, thin film synthesis and transport properties of the Mon+1GaCn MAX phase2015In: Physica Status Solidi. Rapid Research Letters, ISSN 1862-6254, E-ISSN 1862-6270, Vol. 9, no 3, p. 197-201Article in journal (Refereed)
    Abstract [en]

    The phase stability of Mon +1GaCn has been investigated using ab-initio calculations. The results indicate stability for the Mo2GaC phase only, with a formation enthalpy of 0.4 meV per atom. Subsequent thin film synthesis of Mo2GaC was performed through magnetron sputtering from elemental targets onto Al2O3 [0001], 6H-SiC [0001] and MgO [111] substrates within the temperature range of 500 degrees C and 750 degrees C. High structural quality films were obtained for synthesis on MgO [111] substrates at 590 degrees C. Evaluation of transport properties showed a superconducting behavior with a critical temperature of approximately 7 K, reducing upon the application of an external magnetic field. The results point towards the first superconducting MAX phase in thin film form.

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  • 9.
    Noroozi, Mohammad
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering. Finisar Sweden AB, Sweden.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Greczynski, Grzegorz
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Eklund, Per
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Structural and mechanical properties of amorphous AlMgB14 thin films deposited by DC magnetron sputtering on Si, Al2O3 and MgO substrates2020In: Applied Physics A: Materials Science & Processing, ISSN 0947-8396, E-ISSN 1432-0630, Vol. 126, no 2, article id 133Article in journal (Refereed)
    Abstract [en]

    AlMgB14 coatings have been deposited by DC magnetron sputtering from elemental targets on Si (001), Al2O3 (0001) and MgO (001) substrates at temperatures in the range of 25-350 degrees C. The structural and mechanical properties of AlMgB14 films were characterized by X-ray diffraction, scanning electron microscopy, nanoindentation, and analyzed as a function of deposition conditions and substrate materials. The results show that all films are X-ray amorphous, and the mechanical properties of the deposited films depend on the substrate and growth temperature. AlMgB14 thin films deposited at 350 degrees C are found to have smoother surfaces and containing more well-formed B-12 icosahedra than the films deposited at lower temperature, which consequently increase the hardness of the deposited films. The maximum hardness and Youngs modulus of the as-deposited films are about 32.3 GPa and 310 GPa, respectively, for films deposited on Al2O3 substrate at 350 degrees C.

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  • 10.
    Novoselova, Iuliia P.
    et al.
    Faculty of Physics and Center for Nanointegration (CENIDE), University of Duisburg-Essen, 47057, Duisburg, Germany..
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Wiedwald, Ulf
    Faculty of Physics and Center for Nanointegration (CENIDE), University of Duisburg-Essen, 47057, Duisburg, Germany.; National University of Science and Technology «MISIS», 119049, Moscow, Russian Federation..
    Ingason, Arni Sigurdur
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering. Grein Research ehf. Dunhaga 5, Reykjavik, Iceland..
    Hase, Thomas
    Department of Physics, University of Warwick, Coventry, CV4 7AL, UK..
    Magnus, Fridrik
    Science Institute, University of Iceland, Dunhaga 3, IS-107, Reykjavik, Iceland.; Division of Materials Physics, Department of Physics and Astronomy, Uppsala University, Box 516, SE-75121, Uppsala, Sweden..
    Kapaklis, Vassilios
    Division of Materials Physics, Department of Physics and Astronomy, Uppsala University, Box 516, SE-75121, Uppsala, Sweden..
    Palisaitis, Justinas
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Spasova, Marina
    Faculty of Physics and Center for Nanointegration (CENIDE), University of Duisburg-Essen, 47057, Duisburg, Germany..
    Farle, Michael
    Faculty of Physics and Center for Nanointegration (CENIDE), University of Duisburg-Essen, 47057, Duisburg, Germany.; Center for Functionalized Magnetic Materials (FunMagMa), Immanuel Kant Baltic Federal University, Kaliningrad, Russian Federation..
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Salikhov, Ruslan
    Faculty of Physics and Center for Nanointegration (CENIDE), University of Duisburg-Essen, 47057, Duisburg, Germany. ruslan.salikhov@uni-due.de.; Zavoisky Physical-Technical Institute, Russian Academy of Sciences, 420029, Kazan, Russian Federation. ruslan.salikhov@uni-due.de..
    Large uniaxial magnetostriction with sign inversion at the first order phase transition in the nanolaminated Mn2GaC MAX phase2018In: Scientific Reports, ISSN 2045-2322, E-ISSN 2045-2322, Vol. 8, no 1, article id 2637Article in journal (Refereed)
    Abstract [en]

    In 2013, a new class of inherently nanolaminated magnetic materials, the so called magnetic MAX phases, was discovered. Following predictive material stability calculations, the hexagonal Mn2GaC compound was synthesized as hetero-epitaxial films containing Mn as the exclusive M-element. Recent theoretical and experimental studies suggested a high magnetic ordering temperature and non-collinear antiferromagnetic (AFM) spin states as a result of competitive ferromagnetic and antiferromagnetic exchange interactions. In order to assess the potential for practical applications of Mn2GaC, we have studied the temperature-dependent magnetization, and the magnetoresistive, magnetostrictive as well as magnetocaloric properties of the compound. The material exhibits two magnetic phase transitions. The Néel temperature is T N  ~ 507 K, at which the system changes from a collinear AFM state to the paramagnetic state. At T t  = 214 K the material undergoes a first order magnetic phase transition from AFM at higher temperature to a non-collinear AFM spin structure. Both states show large uniaxial c-axis magnetostriction of 450 ppm. Remarkably, the magnetostriction changes sign, being compressive (negative) above T t and tensile (positive) below the T t . The sign change of the magnetostriction is accompanied by a sign change in the magnetoresistance indicating a coupling among the spin, lattice and electrical transport properties.

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  • 11.
    Novoselova, Iuliia P.
    et al.
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Wiedwald, Ulf
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany; Natl Univ Sci and Technol MISIS, Russia.
    Weller, Dieter
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Farle, Michael
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Salikhov, Ruslan
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Long-term stability and thickness dependence of magnetism in thin (Cr0.5Mn0.5)(2)GaC MAX phase films2019In: MATERIALS RESEARCH LETTERS, ISSN 2166-3831, Vol. 7, no 4, p. 159-163Article in journal (Refereed)
    Abstract [en]

    The thickness dependence and long-term stability of the magnetic properties of epitaxial (Cr0.5Mn0.5)(2)GaC MAX phase films on MgO (111) were investigated. For 12.5- to 156-nm-thick films, which corresponds to 10-125 c-axis unit cells, samples were found to be phase pure with negligible c-axis lattice strain of less than 10(-4) nm even for the thinnest films. No influence of the interface layers on the magnetic anisotropy, the magnetization or the para- to ferromagnetic phase transition was observed. All samples remained stable for more than one year in ambient conditions. [GRAPHICS] IMPACT STATEMENT The complex temperature- and magnetic field-dependent magnetism of electrically conducting (Cr0.5Mn0.5)(2)GaC MAX phase films is environmentally robust over one year and independent on interface effects.

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  • 12.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Synthesis and characterization of Ga-containing MAX phase thin films2014Licentiate thesis, comprehensive summary (Other academic)
    Abstract [en]

    The study of magnetic Mn+1AXn (MAX) phases (n = 1 − 3, M – a transition metal, A – an A group element, X – C or N) is a recently established research area, fuelled by theoretical predictions and first confirmed experimentally through alloying of Mn into the well-known Cr2AlC and Cr2GeC. Theoretical phase stability investigations suggested a new magnetic MAX phase, Mn2GaC, containing Ga which is liquid close to room temperature. Hence, alternative routes for MAX phase synthesis were needed, motivating a further development of magnetron sputtering from liquid targets.

    In this thesis, (Cr1-xMnx)2GaC 0 ≤ x ≤ 1  MAX phase thin films have been synthesized from elemental and/or compound targets, using ultra high vacuum magnetron sputtering. Initial thin film synthesis of Cr2GaC was performed using elemental targets, including liquid Ga. Process optimization ensured optimal target size and crucible geometry for containing the Ga. Films were deposited at 650 °C on MgO(111) substrates. X-ray diffraction and transmission electron microscopy confirms the growth of epitaxial Cr2GaC MAX phase with minor inclusions of Cr3Ga.

    To explore the magnetic characteristics upon Mn alloying, synthesis of (Cr0.5Mn0.5)2GaC thin films was performed from elemental Ga and C and a composite Cr/Mn target of 1:1 composition. Films were deposited on MgO(111), Al2O3(0001) (with or without NbN seed layer), and 4° off-cut 4H-SiC(0001) substrates. The films are smooth and of high structural quality as confirmed by X-ray diffraction and transmission electron microscopy. The film composition measured by high resolution energy dispersive X-ray spectroscopy confirms a composition corresponding to (Cr0.5Mn0.5)2GaC. The magnetic response, as measured with vibrating sample magnetometry, displays a ferromagnetic component, however, the temperature dependence of the magnetic moments and saturation fields suggests competing magnetic interaction and possible non-collinear magnetic ordering.

    Finally, inspired by theoretical predictions, a new member of the MAX phase family, Mn2GaC, was synthesized. This is the first MAX phase containing Mn as a sole M element. X-ray diffraction and transmission electron microscopy confirms the characteristic MAX phase structure with a 2:1:1 composition. Theoretical work suggests that the magnetic ground state is almost degenerate between ferromagnetic and anti-ferromagnetic. Vibrating sample magnetometry shows ferromagnetic response with a transition temperature Tc of 230 K. However, also for this phase, complex magnetism is suggested. Altogether, the results indicate a new family of magnetic nanolaminates with a rich variation of magnetic ground states.

    List of papers
    1. Phase stability of Crn+1GaCn MAX phases from first principles and Cr2GaC thin-film synthesis using magnetron sputtering from elemental targets
    Open this publication in new window or tab >>Phase stability of Crn+1GaCn MAX phases from first principles and Cr2GaC thin-film synthesis using magnetron sputtering from elemental targets
    Show others...
    2013 (English)In: Physica Status Solidi. Rapid Research Letters, ISSN 1862-6254, E-ISSN 1862-6270, Vol. 7, no 11, p. 971-974Article in journal (Refereed) Published
    Abstract [en]

    Ab-initio calculations have been used to investigate the phase stability and magnetic state of Crn+ 1GaCn MAX phase. Cr2GaC (n = 1) was predicted to be stable, with a ground state corresponding to an antiferromagnetic spin configuration. Thin-film synthesis by magnetron sputtering from elemental targets, including liquid Ga, shows the formation of Cr2GaC, previously only attained from bulk synthesis methods. The films were deposited at 650 degrees C on MgO(111) substrates. X-ray diffraction and high-resolution transmission electron microscopy show epitaxial growth of (000) MAX phase.

    Place, publisher, year, edition, pages
    Wiley-VCH Verlag, 2013
    Keywords
    MAX phases; ab-initio calculations; magnetron sputtering; epitaxial thin films
    National Category
    Engineering and Technology
    Identifiers
    urn:nbn:se:liu:diva-103307 (URN)10.1002/pssr.201308025 (DOI)000328321700009 ()
    Available from: 2014-01-16 Created: 2014-01-16 Last updated: 2018-03-15
    2. Synthesis and characterization of magnetic (Cr0.5Mn0.5)2GaC thin films
    Open this publication in new window or tab >>Synthesis and characterization of magnetic (Cr0.5Mn0.5)2GaC thin films
    Show others...
    2015 (English)In: Journal of Materials Science, ISSN 0022-2461, E-ISSN 1573-4803, Vol. 50, no 13, p. 4495-4502Article in journal (Refereed) Published
    Abstract [en]

    Growth of (Cr0.5Mn0.5)2GaC thin films from C, Ga, and compound Cr0.5Mn0.5 targets is reported for depositions on MgO (111), 4H-SiC (0001), and Al2O3 (0001) with and without a NbN (111) seed layer. Structural quality is found to be highly dependent on the choice of substrate with MgO (111) giving the best results as confirmed by X-ray diffraction and transmission electron microscopy. Phase pure, high crystal quality MAX phase thin films are realized, with a Cr:Mn ratio of 1:1. Vibrating sample magnetometry shows a ferromagnetic component from 30 K up to 300 K, with a measured net magnetic moment of 0.67 μB per metal (Cr + Mn) atom at 30 K and 5 T. The temperature dependence of the magnetic response suggests competing magnetic interactions with a resulting non-collinear magnetic ordering.

    Place, publisher, year, edition, pages
    Springer Berlin/Heidelberg, 2015
    Keywords
    magnetism, thin films, magnetron sputtering, MAX phase
    National Category
    Condensed Matter Physics
    Identifiers
    urn:nbn:se:liu:diva-118837 (URN)10.1007/s10853-015-8999-8 (DOI)000354093500005 ()
    Note

    At the time for thesis presentation publication was in status: Manuscript

    Funding Agencies|European Research Council under the European Community [258509]; Swedish Research Council (VR) [642-2013-8020, 621-2012-4425]; KAW Fellowship program; SSF synergy grant FUNCASE; Icelandic University Research fund

    Available from: 2015-06-08 Created: 2015-06-04 Last updated: 2018-03-15Bibliographically approved
    3. A Nanolaminated Magnetic Phase: Mn2GaC
    Open this publication in new window or tab >>A Nanolaminated Magnetic Phase: Mn2GaC
    Show others...
    2014 (English)In: Materials Research Letters, ISSN 2166-3831, Vol. 2, no 2, p. 89-93Article in journal (Refereed) Published
    Abstract [en]

    Layered magnetic materials are fascinating from the point of view of fundamental science as well as applications. Discoveries such as giant magnetoresistance (GMR) in magnetic multilayers have revolutionized data storage and magnetic recording, and concurrently initiated the search for new layered magnetic materials. One group of inherently nanolaminated compounds are the so called Mn+1AXn (MAX) phases. Due to the large number of isostructural compositions, researchers are exploring the wide range of interesting properties, and not primarily functionalization through optimization of structural quality. Magnetic MAX phases have been discussed in the literature, though this is hitherto an unreported phenomenon. However, such materials would be highly interesting, based on the attractive and useful properties attained with layered magnetic materials to date. Here we present a new MAX phase, (Cr1–xMnx)2GeC, synthesized as thin film in heteroepitaxial form, showing single crystal material with unprecedented structural MAX phase quality. The material was identified using first-principles calculations to study stability of hypothetical MAX phases, in an eort to identify a potentially magnetic material. The theory predicts a variety of magnetic behavior depending on the Mn concentration and Cr/Mn atomic conguration within the sublattice. The analyzed thin films display a magnetic signal well above room temperature and with partly ferromagnetic ordering. These very promising results open up a field of new layered magnetic materials, with high potential for electronics and spintronics applications.

    Place, publisher, year, edition, pages
    Taylor & Francis, 2014
    Keywords
    MAX phases, sputtering, transmission electron microscopy (TEM), ab initio calculation
    National Category
    Natural Sciences
    Identifiers
    urn:nbn:se:liu:diva-77774 (URN)10.1080/21663831.2013.865105 (DOI)
    Note

    On the day of the defence date the status of this article was previous Manuscript. The original title of the Manuscript was Magnetic nanoscale laminates from first principles and thin film synthesis.

    Available from: 2012-05-29 Created: 2012-05-29 Last updated: 2018-03-15Bibliographically approved
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    Synthesis and characterization of Ga-containing MAX phase thin films
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  • 13. Order onlineBuy this publication >>
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Synthesis and characterization of magnetic nanolaminated carbides2018Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    MAX phases are a group of nanolaminated ternary carbides and nitrides, with a composition expressed by the general formula Mn+1AXn (𝑛 = 1 − 3), where M is a transition metal, A is an A-group element, and X is carbon and/or nitrogen. MAX phases have attracted interest due to their unique combination of metallic and ceramic properties, related to their inherently laminated structure of a transition metal carbide (Mn+1Xn) layer interleaved by an A-group metal layer.

    This Thesis explores synthesis and characterization of magnetic MAX phases, where the A-group element is gallium (Ga). Due to the low melting point of Ga (T = 30 °C), conventional thin film synthesis methods become challenging, as the material is in liquid form at typical process temperatures. Development of existing methods has therefore been investigated, for reliable/reproducible synthesis routes, including sputtering from a liquid target, and resulting high quality material. Routes for minimizing trial-and-error procedures during optimization of thin film synthesis have also been studied, allowing faster identification of optimal deposition conditions and a simplified transfer of essential deposition parameters between different deposition systems.

    A large part of this Thesis is devoted towards synthesis of MAX phase thin films in the Cr-Mn-Ga-C system. First, through process development, thin films of Cr2GaC were deposited by magnetron sputtering. The films were epitaxial, however with small amount of impurity phase Cr3Ga, as confirmed by X-ray diffraction (XRD) measurements. The film structure was confirmed by scanning transmission electron microscopy (STEM) and the composition by energy dispersive X-ray spectroscopy (EDX) inside the TEM.

    Inspired by predictive ab initio calculations, the new MAX phase Mn2GaC was successfully synthesized in thin film form by magnetron sputtering. Structural parameters and magnetic properties were analysed. The material was found to have two magnetic transitions in the temperature range 3 K to 750 K, with a first order transition at around 214 K, going from non-collinear antiferromagnetic state at lower temperature to an antiferromagnetic state at higher temperature. The Neél temperature was determined to be 507 K, changing from an antiferromagnetic to a paramagnetic state. Above 800 K, Mn2GaC decomposes. Furthermore, magnetostrictive, magnetoresistive and magnetocaloric properties of the material were iv determined, among which a drastic change in lattice parameters upon the first magnetic transition was observed. This may be of interest for magnetocaloric applications.

    Synthesis of both Cr2GaC and Mn2GaC in thin film form opens the possibility to tune the magnetic properties through a solid solution on the transition metal site, by alloying the aforementioned Cr2GaC with Mn, realizing (Cr1-xMnx)2GaC. From a compound target with a Cr:Mn ratio of 1:1, thin films of (Cr0.5Mn0.5)2GaC were synthesized, confirmed by TEM-EDX. Optimized structure was obtained by deposition on MgO substrates at a deposition temperature of 600 ºC. The thin films were phase pure and of high structural quality, allowing magnetic measurements. Using vibrating sample magnetometry (VSM), it was found that (Cr0.5Mn0.5)2GaC has a ferromagnetic component in the temperature range from 30 K to 300 K, with the measured magnetic moment at high field decreasing by increasing temperature. The remanent moment and coercive field is small, 0.036 μB, and 12 mT at 30 K, respectively. Using ferromagnetic resonance spectroscopy, it was also found that the material has pure spin magnetism, as indicated by the determined spectroscopic splitting factor g = 2.00 and a negligible magnetocrystalline anisotropy energy.

    Fuelled by the recent discoveries of in-plane chemically ordered quaternary MAX phases, so called i-MAX phases, and guided by ab initio calculations, new members within this family, based on Cr and Mn, were synthesized by pressureless sintering methods, realizing (Cr2/3Sc1/3)2GaC and (Mn2/3Sc1/3)2GaC. Their structural properties were determined. Through these phases, the Mn content is the highest obtained in a bulk MAX phase to date.

    This work has further developed synthesis processes for sputtering from liquid material, for an optimized route to achieve thin films of controlled composition and a high structural quality. Furthermore, through this work, Mn has been added as a new element in the family of MAX phase elements. It has also been shown, that alloying with different content of Mn gives rise to varying magnetic properties in MAX phases. As a result of this Thesis, it is expected that the MAX phase family can be further expanded, with more members of new compositions and new properties.

    List of papers
    1. Phase stability of Crn+1GaCn MAX phases from first principles and Cr2GaC thin-film synthesis using magnetron sputtering from elemental targets
    Open this publication in new window or tab >>Phase stability of Crn+1GaCn MAX phases from first principles and Cr2GaC thin-film synthesis using magnetron sputtering from elemental targets
    Show others...
    2013 (English)In: Physica Status Solidi. Rapid Research Letters, ISSN 1862-6254, E-ISSN 1862-6270, Vol. 7, no 11, p. 971-974Article in journal (Refereed) Published
    Abstract [en]

    Ab-initio calculations have been used to investigate the phase stability and magnetic state of Crn+ 1GaCn MAX phase. Cr2GaC (n = 1) was predicted to be stable, with a ground state corresponding to an antiferromagnetic spin configuration. Thin-film synthesis by magnetron sputtering from elemental targets, including liquid Ga, shows the formation of Cr2GaC, previously only attained from bulk synthesis methods. The films were deposited at 650 degrees C on MgO(111) substrates. X-ray diffraction and high-resolution transmission electron microscopy show epitaxial growth of (000) MAX phase.

    Place, publisher, year, edition, pages
    Wiley-VCH Verlag, 2013
    Keywords
    MAX phases; ab-initio calculations; magnetron sputtering; epitaxial thin films
    National Category
    Engineering and Technology
    Identifiers
    urn:nbn:se:liu:diva-103307 (URN)10.1002/pssr.201308025 (DOI)000328321700009 ()
    Available from: 2014-01-16 Created: 2014-01-16 Last updated: 2018-03-15
    2. A Nanolaminated Magnetic Phase: Mn2GaC
    Open this publication in new window or tab >>A Nanolaminated Magnetic Phase: Mn2GaC
    Show others...
    2014 (English)In: Materials Research Letters, ISSN 2166-3831, Vol. 2, no 2, p. 89-93Article in journal (Refereed) Published
    Abstract [en]

    Layered magnetic materials are fascinating from the point of view of fundamental science as well as applications. Discoveries such as giant magnetoresistance (GMR) in magnetic multilayers have revolutionized data storage and magnetic recording, and concurrently initiated the search for new layered magnetic materials. One group of inherently nanolaminated compounds are the so called Mn+1AXn (MAX) phases. Due to the large number of isostructural compositions, researchers are exploring the wide range of interesting properties, and not primarily functionalization through optimization of structural quality. Magnetic MAX phases have been discussed in the literature, though this is hitherto an unreported phenomenon. However, such materials would be highly interesting, based on the attractive and useful properties attained with layered magnetic materials to date. Here we present a new MAX phase, (Cr1–xMnx)2GeC, synthesized as thin film in heteroepitaxial form, showing single crystal material with unprecedented structural MAX phase quality. The material was identified using first-principles calculations to study stability of hypothetical MAX phases, in an eort to identify a potentially magnetic material. The theory predicts a variety of magnetic behavior depending on the Mn concentration and Cr/Mn atomic conguration within the sublattice. The analyzed thin films display a magnetic signal well above room temperature and with partly ferromagnetic ordering. These very promising results open up a field of new layered magnetic materials, with high potential for electronics and spintronics applications.

    Place, publisher, year, edition, pages
    Taylor & Francis, 2014
    Keywords
    MAX phases, sputtering, transmission electron microscopy (TEM), ab initio calculation
    National Category
    Natural Sciences
    Identifiers
    urn:nbn:se:liu:diva-77774 (URN)10.1080/21663831.2013.865105 (DOI)
    Note

    On the day of the defence date the status of this article was previous Manuscript. The original title of the Manuscript was Magnetic nanoscale laminates from first principles and thin film synthesis.

    Available from: 2012-05-29 Created: 2012-05-29 Last updated: 2018-03-15Bibliographically approved
    3. Large uniaxial magnetostriction with sign inversion at the first order phase transition in the nanolaminated Mn2GaC MAX phase
    Open this publication in new window or tab >>Large uniaxial magnetostriction with sign inversion at the first order phase transition in the nanolaminated Mn2GaC MAX phase
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    2018 (English)In: Scientific Reports, ISSN 2045-2322, E-ISSN 2045-2322, Vol. 8, no 1, article id 2637Article in journal (Refereed) Published
    Abstract [en]

    In 2013, a new class of inherently nanolaminated magnetic materials, the so called magnetic MAX phases, was discovered. Following predictive material stability calculations, the hexagonal Mn2GaC compound was synthesized as hetero-epitaxial films containing Mn as the exclusive M-element. Recent theoretical and experimental studies suggested a high magnetic ordering temperature and non-collinear antiferromagnetic (AFM) spin states as a result of competitive ferromagnetic and antiferromagnetic exchange interactions. In order to assess the potential for practical applications of Mn2GaC, we have studied the temperature-dependent magnetization, and the magnetoresistive, magnetostrictive as well as magnetocaloric properties of the compound. The material exhibits two magnetic phase transitions. The Néel temperature is T N  ~ 507 K, at which the system changes from a collinear AFM state to the paramagnetic state. At T t  = 214 K the material undergoes a first order magnetic phase transition from AFM at higher temperature to a non-collinear AFM spin structure. Both states show large uniaxial c-axis magnetostriction of 450 ppm. Remarkably, the magnetostriction changes sign, being compressive (negative) above T t and tensile (positive) below the T t . The sign change of the magnetostriction is accompanied by a sign change in the magnetoresistance indicating a coupling among the spin, lattice and electrical transport properties.

    Place, publisher, year, edition, pages
    London: Nature Publishing Group, 2018
    National Category
    Condensed Matter Physics
    Identifiers
    urn:nbn:se:liu:diva-145680 (URN)10.1038/s41598-018-20903-2 (DOI)
    Available from: 2018-03-15 Created: 2018-03-15 Last updated: 2018-03-15Bibliographically approved
    4. Synthesis and characterization of magnetic (Cr0.5Mn0.5)2GaC thin films
    Open this publication in new window or tab >>Synthesis and characterization of magnetic (Cr0.5Mn0.5)2GaC thin films
    Show others...
    2015 (English)In: Journal of Materials Science, ISSN 0022-2461, E-ISSN 1573-4803, Vol. 50, no 13, p. 4495-4502Article in journal (Refereed) Published
    Abstract [en]

    Growth of (Cr0.5Mn0.5)2GaC thin films from C, Ga, and compound Cr0.5Mn0.5 targets is reported for depositions on MgO (111), 4H-SiC (0001), and Al2O3 (0001) with and without a NbN (111) seed layer. Structural quality is found to be highly dependent on the choice of substrate with MgO (111) giving the best results as confirmed by X-ray diffraction and transmission electron microscopy. Phase pure, high crystal quality MAX phase thin films are realized, with a Cr:Mn ratio of 1:1. Vibrating sample magnetometry shows a ferromagnetic component from 30 K up to 300 K, with a measured net magnetic moment of 0.67 μB per metal (Cr + Mn) atom at 30 K and 5 T. The temperature dependence of the magnetic response suggests competing magnetic interactions with a resulting non-collinear magnetic ordering.

    Place, publisher, year, edition, pages
    Springer Berlin/Heidelberg, 2015
    Keywords
    magnetism, thin films, magnetron sputtering, MAX phase
    National Category
    Condensed Matter Physics
    Identifiers
    urn:nbn:se:liu:diva-118837 (URN)10.1007/s10853-015-8999-8 (DOI)000354093500005 ()
    Note

    At the time for thesis presentation publication was in status: Manuscript

    Funding Agencies|European Research Council under the European Community [258509]; Swedish Research Council (VR) [642-2013-8020, 621-2012-4425]; KAW Fellowship program; SSF synergy grant FUNCASE; Icelandic University Research fund

    Available from: 2015-06-08 Created: 2015-06-04 Last updated: 2018-03-15Bibliographically approved
    5. Magnetic Anisotropy in the (Cr0.5Mn0.5)(2)GaC MAX Phase
    Open this publication in new window or tab >>Magnetic Anisotropy in the (Cr0.5Mn0.5)(2)GaC MAX Phase
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    2015 (English)In: MATERIALS RESEARCH LETTERS, ISSN 2166-3831, Vol. 3, no 3, p. 156-160Article in journal (Refereed) Published
    Abstract [en]

    Magnetic MAX phase (Cr0.5Mn0.5)(2)GaC thin films grown epitaxially on MgO(111) substrates were studied by ferromagnetic resonance at temperatures between 110 and 300 K. The spectroscopic splitting factor g = 2.00 +/- 0.01 measured at all temperatures indicates pure spin magnetism in the sample. At all temperatures we find the magnetocrystalline anisotropy energy to be negligible which is in agreement with the identified pure spin magnetism.

    Place, publisher, year, edition, pages
    TAYLOR & FRANCIS INC, 2015
    Keywords
    Magnetic MAX Phase; Ferromagnetic Resonance; g-Factor; Magnetic Anisotropy
    National Category
    Physical Sciences
    Identifiers
    urn:nbn:se:liu:diva-127070 (URN)10.1080/21663831.2015.1036324 (DOI)000372219300006 ()
    Note

    Funding Agencies|EC [280670]; UDE; ERC [258509]; Swedish Research Council (VR) [642-2013-8020]; SSF synergy grant FUNCASE

    Available from: 2016-04-13 Created: 2016-04-13 Last updated: 2018-03-15
    6. Toward Structural Optimization of MAX Phases as Epitaxial Thin Films
    Open this publication in new window or tab >>Toward Structural Optimization of MAX Phases as Epitaxial Thin Films
    2016 (English)In: MATERIALS RESEARCH LETTERS, ISSN 2166-3831, Vol. 4, no 3, p. 152-160Article in journal (Refereed) Published
    Abstract [en]

    Prompted by the increased focus on MAX phase materials and their two-dimensional counterparts MXenes, a brief review of the current state of affairs in the synthesis of MAX phases as epitaxial thin films is given. Current methods for synthesis are discussed and suggestions are given on how to increase the material quality even further as well as arrive at those conditions faster. Samples were prepared to exemplify the most common issues involved with the synthesis, and through suggested paths for resolving these issues we attain samples of a quality beyond what has previously been reported.

    Place, publisher, year, edition, pages
    TAYLOR & FRANCIS INC, 2016
    Keywords
    MAX Phase; Thin Films; Reproducible Materials Synthesis; Sample Quality
    National Category
    Inorganic Chemistry
    Identifiers
    urn:nbn:se:liu:diva-132496 (URN)10.1080/21663831.2016.1157525 (DOI)000385011000004 ()
    Note

    Funding Agencies|European Research Council under the European Community Seventh Framework Program (FP7)/ERC Grant [258509]; Swedish Research Council (VR); Knut and Alice Wallenberg (KAW) Fellowship program; SSF synergy grant FUNCASE

    Available from: 2016-11-13 Created: 2016-11-12 Last updated: 2018-03-15
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    Synthesis and characterization of magnetic nanolaminated carbides
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  • 14.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Synthesis of atomically layered and chemically ordered rare-earth (RE) i-MAX phases; (Mo2/3RE1/3)2GaC with RE = Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu2019In: Materials Research Letters, ISSN 2166-3831, Vol. 7, no 11, p. 446-452Article in journal (Refereed)
    Abstract [en]

    We report the synthesis of eight new members of the i-MAX family, of the formula (Mo2/3RE1/3)2GaC, where RE = Gd, Tb, Dy, Ho, Er, Tm, Lu, and Yb, the latter not previously incorporated in a MAX phase. The structure and composition of powder samples were investigated by X-ray diffraction, scanning transmission electron microscopy, and energy dispersive X-ray analysis combined with scanning electron microscopy. All phases showed evidence of an orthorhombic (Cmcm) structure, and the phases based on Er and Yb also crystallized in a monoclinic (C2/c) arrangement. The chemical order of the magnetic elements suggests interesting magnetic characteristics, with a high tuning potential through the range of attainable lanthanide elements.

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  • 15.
    Petruhins, Andrejs
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Dahlqvist, Martin
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Lu, Jun
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Hultman, Lars
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Theoretical Prediction and Experimental Verification of the Chemically Ordered Atomic-Laminate i-MAX Phases (Cr2/3Sc1/3)(2)GaC and (Mn2/3Sc1/3)(2)GaC2020In: Crystal Growth & Design, ISSN 1528-7483, E-ISSN 1528-7505, Vol. 20, no 1, p. 55-61Article in journal (Refereed)
    Abstract [en]

    We combine predictive ab initio calculations with experimental verification of bulk materials synthesis for exploration of new and potentially magnetic atomically laminated i-MAX phases. Two such phases are discovered: (Cr2/3Sc1/3)(2)GaC and (Mn2/3Sc1/3)(2)GaC synthesized by the solid state reaction from elemental constituents. The latter compound displays a 2-fold increase in Mn content compared to previously reported bulk MAX phases. Both new compounds exhibit the characteristic in-plane chemical order of Cr(Mn) and Sc, and crystallize in an orthorhombic structure, space group Cmcm, as confirmed by scanning transmission electron microscopy. From density functional theory calculations of the magnetic ground state, including the electron-interaction parameter U, we suggest an antiferromagnetic ground state, close to degenerate with the ferromagnetic state.

    The full text will be freely available from 2020-12-02 15:15
  • 16.
    Petruhins, Andrejs
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Ingason, Arni Sigurdur
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Dahlqvist, Martin
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Mockuté, Aurelija
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Junaid, Muhammad
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Birch, Jens
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Lu, Jun
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Hultman, Lars
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Persson, Per O A
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Phase stability of Crn+1GaCn MAX phases from first principles and Cr2GaC thin-film synthesis using magnetron sputtering from elemental targets2013In: Physica Status Solidi. Rapid Research Letters, ISSN 1862-6254, E-ISSN 1862-6270, Vol. 7, no 11, p. 971-974Article in journal (Refereed)
    Abstract [en]

    Ab-initio calculations have been used to investigate the phase stability and magnetic state of Crn+ 1GaCn MAX phase. Cr2GaC (n = 1) was predicted to be stable, with a ground state corresponding to an antiferromagnetic spin configuration. Thin-film synthesis by magnetron sputtering from elemental targets, including liquid Ga, shows the formation of Cr2GaC, previously only attained from bulk synthesis methods. The films were deposited at 650 degrees C on MgO(111) substrates. X-ray diffraction and high-resolution transmission electron microscopy show epitaxial growth of (000) MAX phase.

    Download full text (pdf)
    fulltext
  • 17.
    Petruhins, Andrejs
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Ingason, Arni Sigurdur
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Lu, Jun
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Magnus, Fridrik
    Department of Physics and Astronomy, Uppsala University, Uppsala, Sweden.
    Olafsson, Sveinn
    Science Institute, University of Iceland, Reykjavik, Iceland.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Synthesis and characterization of magnetic (Cr0.5Mn0.5)2GaC thin films2015In: Journal of Materials Science, ISSN 0022-2461, E-ISSN 1573-4803, Vol. 50, no 13, p. 4495-4502Article in journal (Refereed)
    Abstract [en]

    Growth of (Cr0.5Mn0.5)2GaC thin films from C, Ga, and compound Cr0.5Mn0.5 targets is reported for depositions on MgO (111), 4H-SiC (0001), and Al2O3 (0001) with and without a NbN (111) seed layer. Structural quality is found to be highly dependent on the choice of substrate with MgO (111) giving the best results as confirmed by X-ray diffraction and transmission electron microscopy. Phase pure, high crystal quality MAX phase thin films are realized, with a Cr:Mn ratio of 1:1. Vibrating sample magnetometry shows a ferromagnetic component from 30 K up to 300 K, with a measured net magnetic moment of 0.67 μB per metal (Cr + Mn) atom at 30 K and 5 T. The temperature dependence of the magnetic response suggests competing magnetic interactions with a resulting non-collinear magnetic ordering.

    Download full text (pdf)
    fulltext
  • 18.
    Salikhov, Ruslan
    et al.
    University of Duisburg Essen, Germany.
    Semisalova, Anna S.
    University of Duisburg Essen, Germany; Moscow MV Lomonosov State University, Russia; Helmholtz Zentrum Dresden Rossendorf, Germany.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Ingason, Arni Sigurdur
    Linköping University, Department of Physics, Chemistry and Biology. Linköping University, Faculty of Science & Engineering.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Wiedwald, Ulf
    University of Duisburg Essen, Germany.
    Farle, Michael
    University of Duisburg Essen, Germany.
    Magnetic Anisotropy in the (Cr0.5Mn0.5)(2)GaC MAX Phase2015In: MATERIALS RESEARCH LETTERS, ISSN 2166-3831, Vol. 3, no 3, p. 156-160Article in journal (Refereed)
    Abstract [en]

    Magnetic MAX phase (Cr0.5Mn0.5)(2)GaC thin films grown epitaxially on MgO(111) substrates were studied by ferromagnetic resonance at temperatures between 110 and 300 K. The spectroscopic splitting factor g = 2.00 +/- 0.01 measured at all temperatures indicates pure spin magnetism in the sample. At all temperatures we find the magnetocrystalline anisotropy energy to be negligible which is in agreement with the identified pure spin magnetism.

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  • 19.
    Tao, Quanzheng
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Lu, Jun
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Dahlqvist, Martin
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Mockuté, Aurelija
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering. Oak Ridge Natl Lab, TN 37831 USA.
    Calder, Stuart
    Oak Ridge Natl Lab, TN 37831 USA.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Meshkian, Rahele
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Rivin, Oleg
    Nucl Res Ctr Negev, Israel; Helmholtz Zentrum Berlin Mat and Energie, Germany.
    Potashnikov, Daniel
    Technion Israeli Inst Technol, Israel; Israel Atom Energy Commiss, Israel.
    Caspi, Elad N.
    Nucl Res Ctr Negev, Israel.
    Shaked, Hagai
    Ben Gurion Univ Negev, Israel.
    Hoser, Andreas
    Helmholtz Zentrum Berlin Mat and Energie, Germany.
    Opagiste, Christine
    Univ Grenoble Alpes, France.
    Galera, Rose-Marie
    Univ Grenoble Alpes, France.
    Salikhov, Ruslan
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Wiedwald, Ulf
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Ritter, Clemens
    Inst Laue Langevin, France.
    Wildes, Andrew R.
    Inst Laue Langevin, France.
    Johansson, Boerje
    Uppsala Univ, Sweden; Humboldt Univ, Germany.
    Hultman, Lars
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Fade, Michael
    Univ Duisburg Essen, Germany; Univ Duisburg Essen, Germany.
    Barsoum, Michel
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering. Drexel Univ, PA 19104 USA.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Atomically Layered and Ordered Rare-Earth i-MAX Phases: A New Class of Magnetic Quaternary Compounds2019In: Chemistry of Materials, ISSN 0897-4756, E-ISSN 1520-5002, Vol. 31, no 7, p. 2476-2485Article in journal (Refereed)
    Abstract [en]

    In 2017, we discovered quaternary i-MAX phases atomically layered solids, where M is an early transition metal, A is an A group element, and X is C-with a ((M2/3M1/32)-M-1)(2)AC chemistry, where the M-1 and M-2 atoms are in-plane ordered. Herein, we report the discovery of a class of magnetic i-MAX phases in which bilayers of a quasi-2D magnetic frustrated triangular lattice overlay a Mo honeycomb arrangement and an Al Kagome lattice. The chemistry of this family is (Mo2/3RE1/3)(2)AlC, and the rare-earth, RE, elements are Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, and Lu. The magnetic properties were characterized and found to display a plethora of ground states, resulting from an interplay of competing magnetic interactions in the presence of magnetocrystalline anisotropy.

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  • 20.
    Zhirkov, Igor
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Eriksson, Anders
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Dahlqvist, Martin
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Ingason, Arni Sigurdur
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, The Institute of Technology.
    Effect of Ti-Al cathode composition on plasma generation and plasma transport in direct current vacuum arc2014In: Journal of Applied Physics, ISSN 0021-8979, E-ISSN 1089-7550, Vol. 115, no 12, p. 123301-Article in journal (Refereed)
    Abstract [en]

    DC arc plasma from Ti, Al, and Ti1-xAlx (x = 0.16, 0.25, 0.50, and 0.70) compound cathodes was characterized with respect to plasma chemistry and charge-state-resolved ion energy. Scanning electron microscopy, X-ray diffraction, and Energy-dispersive X-ray spectroscopy of the deposited films and the cathode surfaces were used for exploring the correlation between cathode-, plasma-, and film composition. Experimental work was performed at a base pressure of 10(-6) Torr, to exclude plasma-gas interaction. The plasma ion composition showed a reduction of Al of approximately 5 at. % compared to the cathode composition, while deposited films were in accordance with the cathode stoichiometry. This may be explained by presence of neutrals in the plasma/vapour phase. The average ion charge states (Ti = 2.2, Al = 1.65) were consistent with reference data for elemental cathodes, and approximately independent on the cathode composition. On the contrary, the width of the ion energy distributions (IEDs) were drastically reduced when comparing the elemental Ti and Al cathodes with Ti0.5Al0.5, going from similar to 150 and similar to 175 eV to similar to 100 and similar to 75 eV for Ti and Al ions, respectively. This may be explained by a reduction in electron temperature, commonly associated with the high energy tail of the IED. The average Ti and Al ion energies ranged between similar to 50 and similar to 61 eV, and similar to 30 and similar to 50 eV, respectively, for different cathode compositions. The attained energy trends were explained by the velocity rule for compound cathodes, which states that the most likely velocities of ions of different mass are equal. Hence, compared to elemental cathodes, the faster Al ions will be decelerated, and the slower Ti ions will be accelerated when originating from compound cathodes. The intensity of the macroparticle generation and thickness of the deposited films were also found to be dependent on the cathode composition. The presented results may be of importance for choice of cathodes for thin film depositions involving compound cathodes.

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  • 21.
    Zhirkov, Igor
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Näslund, Lars-Åke
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Kolozsvari, Szilard
    PLANSEE Composite Mat GmbH, Germany.
    Polcik, Peter
    PLANSEE Composite Mat GmbH, Germany.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Vacuum arc plasma generation and thin film deposition from a TiB2 cathode2015In: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 107, no 18, p. 184103-Article in journal (Refereed)
    Abstract [en]

    We have studied the utilization of TiB2 cathodes for thin film deposition in a DC vacuum arc system. We present a route for attaining a stable, reproducible, and fully ionized plasma flux of Ti and B by removal of the external magnetic field, which leads to dissipation of the vacuum arc discharge and an increased active surface area of the cathode. Applying a magnetic field resulted in instability and cracking, consistent with the previous reports. Plasma analysis shows average energies of 115 and 26 eV, average ion charge states of 2.1 and 1.1 for Ti and B, respectively, and a plasma ion composition of approximately 50% Ti and 50% B. This is consistent with measured resulting film composition from X-ray photoelectron spectroscopy, suggesting a negligible contribution of neutrals and macroparticles to the film growth. Also, despite the observations of macroparticle generation, the film surface is very smooth. These results are of importance for the utilization of cathodic arc as a method for synthesis of metal borides. (C) 2015 AIP Publishing LLC.

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  • 22.
    Zhirkov, Igor
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Polcik, Peter
    PLANSEE Composite Mat GmbH, Germany.
    Kolozsvari, Szilard
    PLANSEE Composite Mat GmbH, Germany.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Effect of Ti-Al cathode grain size on plasma generation and thin film synthesis from a direct current vacuum arc plasma source2019In: AIP Advances, ISSN 2158-3226, E-ISSN 2158-3226, Vol. 9, no 4, article id 045008Article in journal (Refereed)
    Abstract [en]

    Herein, we investigate the influence of powder metallurgical manufactured Ti0.5Al0.5 cathode grain size (45-150 mu m) on the properties of a DC arc discharge, for N-2 pressures in the range 10(-5) Torr (base pressure) up to 3x10(-2) Torr. Intermetallic TiAl cathodes are also studied. The arc plasma is characterized with respect to ion composition, ion charge state, and ion energy, and is found to change with pressure, independent on choice of cathode. Scanning electron microscopy, X-ray diffraction, and Energy-dispersive X-ray spectroscopy of the cathode surfaces and the concurrently deposited films are used for exploring the correlation between cathode-, plasma-, and film composition. The plasma has a dominating Al ion content at elevated pressures, while the film composition is consistent with the cathode composition, independent on cathode grain size. Cross-sections of the used cathodes are studied, and presence of a converted layer, up to 10 mu m, is shown, with an improved intermixing of the elements on the cathode surface. This layer is primarily explained by condensation of cathode material from the melting and splashes accompanying the arc spot movement, as well as generated plasma ions being redeposited upon returning to the cathode. The overall lack of dependence on grain size is likely due to similar physical properties of Ti, Al and TiAl grains, as well as the formation of a converted layer. The presented findings are of importance for large scale manufacturing and usage of Ti-Al cathodes in industrial processes. (C) 2019 Author(s).

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  • 23.
    Zhirkov, Igor
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Polcik, Peter
    PLANSEE Composite Mat GmbH, Germany.
    Kolozsvari, Szilard
    PLANSEE Composite Mat GmbH, Germany.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Generation of super-size macroparticles in a direct current vacuum arc discharge from a Mo-Cu cathode2016In: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 108, no 5, p. 054103-Article in journal (Refereed)
    Abstract [en]

    An inherent property of cathodic arc is the generation of macroparticles, of a typical size ranging from submicrometer up to a few tens of mu m. In this work, we have studied macroparticle generation from a Mo0.78Cu0.22 cathode used in a dc vacuum arc discharge, and we present evidence for super-size macroparticles of up to 0.7mm in diameter. All analyzed particles are found to be rich in Mo (>= 98 at. %). The particle generation is studied by visual observation of the cathode surface during arcing, by analysis of composition and geometrical features of the used cathode surface, and by examination of the generated macroparticles with respect to shape and composition. A mechanism for super-size macroparticle generation is suggested based on observed segregated layers of Mo and Cu identified in the topmost part of the cathode surface, likely due to the discrepancy in melting and evaporation temperatures of Mo and Cu. The results are of importance for increasing the fundamental understanding of macroparticle generation, which in turn may lead to increased process control and potentially provide paths for tuning, or even mitigating, macroparticle generation. (C) 2016 AIP Publishing LLC.

  • 24.
    Zhirkov, Igor
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Rosén, Jakob
    Linköping University, Department of Computer and Information Science, ESLAB - Embedded Systems Laboratory. Linköping University, The Institute of Technology.
    Effect of cathode composition and nitrogen pressure on macroparticle generation and type of arc discharge in a DC arc source with Ti-Al compound cathodes2015In: Surface & Coatings Technology, ISSN 0257-8972, E-ISSN 1879-3347, Vol. 281, p. 20-26Article in journal (Refereed)
    Abstract [en]

    Thin films deposited with unfiltered DC arc plasma from Ti, Ti0.75Al0.25, Ti0.50Al0.50, Ti0.30Al0.70, and Al cathodes were characterized with a scanning electron microscope for quantification of extent of macroparticle incorporation. Depositions were performed in N-2 atmosphere in the pressure range from 10(-6) Torr up to 3 . 10(-2) Torr, and the formation of cathode surface nitride contamination was identified from X-ray diffraction analysis. Visual observation and photographic fixation of the arc spot behavior was simultaneously performed. A reduction in macroparticle generation with decreasing Al content and increasing N-2 pressure was demonstrated. A correlated transformation of the arc from type 2 to the type 1 was visually detected and found to be a function of N-2 pressure and at of Al in the cathode. For the Ti cathode, no arc transformation was detected. These observations can be explained by a comparatively high electrical resistivity and high melting point of Al rich surface nitrides, promoting an arc transformation and a reduction in macropartide generation. (C) 2015 Elsevier B.V. All rights reserved.

  • 25.
    Zhirkov, Igor
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Polcik, Peter
    PLANSEE Composite Mat GmbH, Germany.
    Petruhins, Andrejs
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Kolozsvari, Szilard
    PLANSEE Composite Mat GmbH, Germany.
    Rosén, Johanna
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Effect of Mo-Cu cathode composition on process stability, macroparticle formation, plasma generation, and thin-film deposition in DC arc synthesis2020In: Journal of Applied Physics, ISSN 0021-8979, E-ISSN 1089-7550, Vol. 127, no 1, article id 013301Article in journal (Refereed)
    Abstract [en]

    In this work, we present the correlation between cathode composition and features of the arcing process for Mo1-xCux [x = 0.0, 0.07 (0.05), 0.14 (0.10), 0.21 (0.15), 0.40 (0.3), 0.73 (0.63), 0.97 (0.95), and 1.00, atomic fraction (weight fraction)] cathodes used in a DC vacuum-arc deposition system. It is found that the stability of the arcing process crucially depends on the cathode composition. The most stable arc spot and the lowest cathode potential (similar to 19 V) are detected for the Mo0.27Cu0.73 cathode, while the Mo0.93Cu0.07 cathode shows the most unstable arcing process with the highest cathode potential (similar to 28 V). The properties of the generated plasma are also strongly dependent on the relative ratio of the cathode elements. The metal ions from the Mo and Cu cathodes have peak kinetic energies around 136 and 62 eV, respectively, while for a Mo0.79Cu0.21 cathode, the corresponding energies are only 45 and 28 eV. The average charge states decreased from 2.1 to 1.6 for Mo ions and from 2 to 1.2 for Cu ions. The intensity of macroparticle generation and the size of the droplets correlate with the relative fraction of Cu. However, it is shown that, typically for the cathodes with a low amount of Cu, an increased abundance of visually observed macroparticles leads to droplet-free films. The film thicknesses and their compositions also demonstrate dependencies on the elemental composition of the cathode. These results are discussed in the light of no solubility between Mo and Cu and the high temperature of the cathode surface during the arcing process. Published under license by AIP Publishing.

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