| 1. |
- Abelev, Betty, et al.
(författare)
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Long-range angular correlations on the near and away side in p-Pb collisions at root S-NN=5.02 TeV
- 2013
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Ingår i: Physics Letters. Section B: Nuclear, Elementary Particle and High-Energy Physics. - : Elsevier BV. - 0370-2693. ; 719:1-3, s. 29-41
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Tidskriftsartikel (refereegranskat)abstract
- Angular correlations between charged trigger and associated particles are measured by the ALICE detector in p-Pb collisions at a nucleon-nucleon centre-of-mass energy of 5.02 TeV for transverse momentum ranges within 0.5 < P-T,P-assoc < P-T,P-trig < 4 GeV/c. The correlations are measured over two units of pseudorapidity and full azimuthal angle in different intervals of event multiplicity, and expressed as associated yield per trigger particle. Two long-range ridge-like structures, one on the near side and one on the away side, are observed when the per-trigger yield obtained in low-multiplicity events is subtracted from the one in high-multiplicity events. The excess on the near-side is qualitatively similar to that recently reported by the CMS Collaboration, while the excess on the away-side is reported for the first time. The two-ridge structure projected onto azimuthal angle is quantified with the second and third Fourier coefficients as well as by near-side and away-side yields and widths. The yields on the near side and on the away side are equal within the uncertainties for all studied event multiplicity and p(T) bins, and the widths show no significant evolution with event multiplicity or p(T). These findings suggest that the near-side ridge is accompanied by an essentially identical away-side ridge. (c) 2013 CERN. Published by Elsevier B.V. All rights reserved.
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| 2. |
- Abelev, Betty, et al.
(författare)
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Measurement of prompt J/psi and beauty hadron production cross sections at mid-rapidity in pp collisions at root s=7 TeV
- 2012
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Ingår i: Journal of High Energy Physics. - 1029-8479. ; :11
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Tidskriftsartikel (refereegranskat)abstract
- The ALICE experiment at the LHC has studied J/psi production at mid-rapidity in pp collisions at root s = 7 TeV through its electron pair decay on a data sample corresponding to an integrated luminosity L-int = 5.6 nb(-1). The fraction of J/psi from the decay of long-lived beauty hadrons was determined for J/psi candidates with transverse momentum p(t) > 1,3 GeV/c and rapidity vertical bar y vertical bar < 0.9. The cross section for prompt J/psi mesons, i.e. directly produced J/psi and prompt decays of heavier charmonium states such as the psi(2S) and chi(c) resonances, is sigma(prompt J/psi) (p(t) > 1.3 GeV/c, vertical bar y vertical bar < 0.9) = 8.3 +/- 0.8(stat.) +/- 1.1 (syst.)(-1.4)(+1.5) (syst. pol.) mu b. The cross section for the production of b-hadrons decaying to J/psi with p(t) > 1.3 GeV/c and vertical bar y vertical bar < 0.9 is a sigma(J/psi <- hB) (p(t) > 1.3 GeV/c, vertical bar y vertical bar < 0.9) = 1.46 +/- 0.38 (stat.)(-0.32)(+0.26) (syst.) mu b. The results are compared to QCD model predictions. The shape of the p(t) and y distributions of b-quarks predicted by perturbative QCD model calculations are used to extrapolate the measured cross section to derive the b (b) over bar pair total cross section and d sigma/dy at mid-rapidity.
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| 3. |
- Abelev, Betty, et al.
(författare)
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Underlying Event measurements in pp collisions at root s=0.9 and 7 TeV with the ALICE experiment at the LHC
- 2012
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Ingår i: Journal of High Energy Physics. - 1029-8479. ; :7
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Tidskriftsartikel (refereegranskat)abstract
- We present measurements of Underlying Event observables in pp collisions at root s = 0 : 9 and 7 TeV. The analysis is performed as a function of the highest charged-particle transverse momentum p(T),L-T in the event. Different regions are defined with respect to the azimuthal direction of the leading (highest transverse momentum) track: Toward, Transverse and Away. The Toward and Away regions collect the fragmentation products of the hardest partonic interaction. The Transverse region is expected to be most sensitive to the Underlying Event activity. The study is performed with charged particles above three different p(T) thresholds: 0.15, 0.5 and 1.0 GeV/c. In the Transverse region we observe an increase in the multiplicity of a factor 2-3 between the lower and higher collision energies, depending on the track p(T) threshold considered. Data are compared to PYTHIA 6.4, PYTHIA 8.1 and PHOJET. On average, all models considered underestimate the multiplicity and summed p(T) in the Transverse region by about 10-30%.
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| 4. |
- Beket, Gulzada, et al.
(författare)
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Overcoming the voltage losses caused by the acceptor-based interlayer in laminated indoor OPVs
- 2023
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Ingår i: SMARTMAT. - : WILEY. - 2766-8525.
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Tidskriftsartikel (refereegranskat)abstract
- Harvesting indoor light to power electronic devices for the Internet of Things has become an application scenario for emerging photovoltaics, especially utilizing organic photovoltaics (OPVs). Combined liquid- and solid-state processing, such as printing and lamination used in industry for developing indoor OPVs, also provides a new opportunity to investigate the device structure, which is otherwise hardly possible based on the conventional approach due to solvent orthogonality. This study investigates the impact of fullerene-based acceptor interlayer on the performance of conjugated polymer-fullerene-based laminated OPVs for indoor applications. We observe open-circuit voltage (V-OC) loss across the interface despite this arrangement being presumed to be ideal for optimal device performance. Incorporating insulating organic components such as polyethyleneimine (PEI) or polystyrene (PS) into fullerene interlayers decreases the work function of the cathode, leading to better energy level alignment with the active layer (AL) and reducing the V-OC loss across the interface. Neutron reflectivity studies further uncover two different mechanisms behind the V-OC increase upon the incorporation of these insulating organic components. The self-organized PEI layer could hinder the transfer of holes from the AL to the acceptor interlayer, while the gradient distribution of the PS-incorporated fullerene interlayer eliminates the thermalization losses. This work highlights the importance of structural dynamics near the extraction interfaces in OPVs and provides experimental demonstrations of interface investigation between solution-processed cathodic fullerene layer and bulk heterojunction AL.
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| 5. |
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| 6. |
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| 7. |
- Matsubara, Nami, et al.
(författare)
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Magnetism and ion diffusion in honeycomb layered oxide K 2Ni 2TeO 6
- 2020
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Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322 .- 2045-2322. ; 10:1
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Tidskriftsartikel (refereegranskat)abstract
- In the quest for developing novel and efficient batteries, a great interest has been raised for sustainable K-based honeycomb layer oxide materials, both for their application in energy devices as well as for their fundamental material properties. A key issue in the realization of efficient batteries based on such compounds, is to understand the K-ion diffusion mechanism. However, investigation of potassium-ion (K+) dynamics in materials using e.g. NMR and related techniques has so far been very challenging, due to its inherently weak nuclear magnetic moment, in contrast to other alkali ions such as lithium and sodium. Spin-polarised muons, having a high gyromagnetic ratio, make the muon spin rotation and relaxation (μ+SR) technique ideal for probing ions dynamics in these types of energy materials. Here we present a study of the low-temperature magnetic properties as well as K+ dynamics in honeycomb layered oxide material K 2Ni 2TeO 6 using mainly the μ+SR technique. Our low-temperature μ+SR results together with complementary magnetic susceptibility measurements find an antiferromagnetic transition at TN≈ 27 K. Further μ+SR studies performed at higher temperatures reveal that potassium ions (K+) become mobile above 200 K and the activation energy for the diffusion process is obtained as Ea= 121 (13) meV. This is the first time that K+ dynamics in potassium-based battery materials has been measured using μ+SR. Assisted by high-resolution neutron diffraction, the temperature dependence of the K-ion self diffusion constant is also extracted. Finally our results also reveal that K-ion diffusion occurs predominantly at the surface of the powder particles. This opens future possibilities for potentially improving ion diffusion as well as K-ion battery device performance using nano-structuring and surface coatings of the particles.
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| 8. |
- Matsubara, Nami, et al.
(författare)
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Magnetism and ion diffusion in honeycomb layered oxide K2Ni2TeO6
- 2020
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Ingår i: Scientific Reports. - : Springer Nature. - 2045-2322. ; 10:1
-
Tidskriftsartikel (refereegranskat)abstract
- In the quest for developing novel and efficient batteries, a great interest has been raised for sustainable K-based honeycomb layer oxide materials, both for their application in energy devices as well as for their fundamental material properties. A key issue in the realization of efficient batteries based on such compounds, is to understand the K-ion diffusion mechanism. However, investigation of potassium-ion (K+) dynamics in materials using e.g. NMR and related techniques has so far been very challenging, due to its inherently weak nuclear magnetic moment, in contrast to other alkali ions such as lithium and sodium. Spin-polarised muons, having a high gyromagnetic ratio, make the muon spin rotation and relaxation (mu+SR) technique ideal for probing ions dynamics in these types of energy materials. Here we present a study of the low-temperature magnetic properties as well as K+ dynamics in honeycomb layered oxide material K2Ni2TeO6 using mainly the mu+SR technique. Our low-temperature mu+SR results together with complementary magnetic susceptibility measurements find an antiferromagnetic transition at T-N approximate to 27 K. Further mu+SR studies performed at higher temperatures reveal that potassium ions (K+) become mobile above 200 K and the activation energy for the diffusion process is obtained as E-a = 121(13) meV. This is the first time that K+ dynamics in potassium-based battery materials has been measured using mu+SR. Assisted by high-resolution neutron diffraction, the temperature dependence of the K-ion self diffusion constant is also extracted. Finally our results also reveal that K-ion diffusion occurs predominantly at the surface of the powder particles. This opens future possibilities for potentially improving ion diffusion as well as K-ion battery device performance using nano-structuring and surface coatings of the particles.
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| 9. |
- Nocerino, Elisabetta, et al.
(författare)
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Na-ion Dynamics in the Solid Solution NaxCa1-xCr2O4 Studied by Muon Spin Rotation and Neutron Diffraction
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Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- In this work we present systematic set of measurements carried out by muon spin rotation/relaxation (μ+SR) and neutron powder diffraction (NPD) on the solid solution NaxCa1−xCr2O4. This study investigates Na-ion dynamics in the quasi-1D (Q1D) diffusion channels created by the honeycomb-like arrangement of CrO6 octahedra, in the presence of defects introduced by Ca doping. With increasing Ca content, the size of the diffusion channels is enlarged, however, this effect does not enhance the Na ion mobility. Instead the overall diffusivity is hampered by the local defects and the Na hopping probability is lowered. The diffusion mechanism in NaxCa1−xCr2O4 was found to be interstitial and the activation energy as well as diffusion coefficient were determined for all the members of the solid solution.
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| 10. |
- Nocerino, Elisabetta, et al.
(författare)
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Na-ion dynamics in the solid solution NaxCa1−xCr2O4 studied by muon spin rotation and neutron diffraction
- 2024
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Ingår i: Sustainable Energy & Fuels. - : ROYAL SOC CHEMISTRY. - 2398-4902. ; 8:7
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Tidskriftsartikel (refereegranskat)abstract
- In this work we present a systematic set of measurements carried out by muon spin rotation/relaxation (mu+SR) and neutron powder diffraction (NPD) on the solid solution NaxCa1-xCr2O4. This study investigates Na-ion dynamics in the quasi-1D (Q1D) diffusion channels created by the honeycomb-like arrangement of CrO6 octahedra, in the presence of defects introduced by Ca substitution. With increasing Ca content, the size of the diffusion channels is enlarged; however, this effect does not enhance the Na ion mobility. Instead the overall diffusivity is hampered by the local defects and the Na hopping probability is lowered. The diffusion mechanism in NaxCa1-xCr2O4 is proposed to be interstitial and the activation energy as well as diffusion coefficient are determined for all the members of the solid solution.
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| 11. |
- Nocerino, Elisabetta, et al.
(författare)
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Nuclear and magnetic spin structure of the antiferromagnetic triangular lattice compound LiCrTe 2 investigated by μ + SR, neutron and X-ray diffraction
- 2022
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Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322 .- 2045-2322. ; 12:1
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Tidskriftsartikel (refereegranskat)abstract
- Two-dimensional (2D) triangular lattice antiferromagnets (2D-TLA) often manifest intriguing physical and technological properties, due to the strong interplay between lattice geometry and electronic properties. The recently synthesized 2-dimensional transition metal dichalcogenide LiCrTe2, being a 2D-TLA, enriched the range of materials which can present such properties. In this work, muon spin rotation (μ+SR) and neutron powder diffraction (NPD) have been utilized to reveal the true magnetic nature and ground state of LiCrTe2. From high-resolution NPD the magnetic spin order at base-temperature is not, as previously suggested, helical, but rather collinear antiferromagnetic (AFM) with ferromagnetic (FM) spin coupling within the ab-plane and AFM coupling along the c-axis. The value if the ordered magnetic Cr moment is established as μCr=2.36μB. From detailed μ+SR measurements we observe an AFM ordering temperature TN≈ 125 K. This value is remarkably higher than the one previously reported by magnetic bulk measurements. From μ+SR we are able to extract the magnetic order parameter, whose critical exponent allows us to categorize LiCrTe2 in the 3D Heisenberg AFM universality class. Finally, by combining our magnetic studies with high-resolution synchrotron X-ray diffraction (XRD), we find a clear coupling between the nuclear and magnetic spin lattices. This suggests the possibility for a strong magnon–phonon coupling, similar to what has been previously observed in the closely related compound LiCrO2.
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| 12. |
- Nocerino, Elisabetta, et al.
(författare)
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Nuclear and magnetic spin structure of the antiferromagnetic triangular lattice compound LiCrTe2 investigated by µ+SR, neutron and X-ray diffraction
-
Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- Two−dimensional (2D) triangular lattices antiferromagnets (2D−TLA) often manifest intriguing physical and technological properties, due to the strong interplay between lattice geometry and electronic properties. The recently synthesized 2−dimensional transition metal dichalcogenide LiCrTe2, being a 2D−TLA, enriched the range of materials which can present such properties. In this work, muon spin rotation (μ+SR) and neutron powder diffraction (NPD) have been utilized to reveal the true magnetic nature and ground state of LiCrTe2. From high−resolution NPD the magnetic spin order at base−temperature is not, as previously suggested, helical, but rather collinear antiferromagnetic (AFM) with ferromagnetic (FM) spin coupling within the ab−plane and AFM coupling along the c−axis. The ordered magnetic Cr moment is established as μCr= 2.36 μB. From detailed μ+SR measurements we observe an AFM ordering temperature TN≈ 125 K. This value is remarkably higher than the one previously reported by magnetic bulk measurements. From μ+SR we are able to extract the magnetic order parameter, whose critical exponent allows us to categorize LiCrTe2 in the 3D Heisenberg AFM universality class. Finally, by combining our magnetic studies with high−resolution synchrotron X−ray diffraction (XRD), we find a clear coupling between the nuclear and magnetic spin lattices. This suggests the possibility for a strong magnon−phonon coupling, similar to what has been previously observed in the closely related compound LiCrO2.
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| 13. |
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| 14. |
- Nocerino, E., et al.
(författare)
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Unusually large magnetic moment and tricritical behavior of the CMR compound NaCr 2 O 4 revealed with high resolution neutron diffraction and μ + SR
- 2023
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Ingår i: JPhys Materials. - 2515-7639. ; 6:3
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Tidskriftsartikel (refereegranskat)abstract
- The mixed valence Cr3+/Cr4+ compound NaCr2O4, hosts a plethora of unconventional electronic properties. In the present study, muon spin rotation/relaxation ( μ + SR) and high-resolution time-of-flight neutron powder diffraction measurements were carried out on high-quality samples to clarify the complex magnetic ground state of this unique material. We identified a commensurate canted antiferromagnetic order (C-AFM) with a canting angle of the Cr spin axial vector equal to θ c = ( 8.8 ± 0.5 ) ∘ , and an estimated Cr moment μ C r C ∼ ( 4.30 ± 0.01 ) μ B . Such an unusually large value of μ C r C is compatible with the existence of high-spin Cr sites created by the presence of an unconventional negative charge transfer state in NaCr2O4. In addition to the C-AFM structure, a novel magnetic supercell was also revealed. Such supercell display an incommensurate (IC)-AFM propagation vector (0 0 1 2 − δ ), having a Cr moment μ C r I C = ( 2.20 ± 0.03 ) μ B . It is suggested that the C-AFM and IC-AFM modulations have two different electronic origins, being due to itinerant and localized contributions to the magnetic moment respectively. Finally, the direct measurement of the magnetic order parameter for the C-AFM structure provided a value of the critical exponent β = 0.245 ≈ 1 4 , suggesting a non conventional critical behavior for the magnetic phase transition in NaCr2O4
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| 15. |
- Nocerino, Elisabetta, et al.
(författare)
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Unusually large magnetic moment and tricritical behavior of the CMR compound NaCr2O4 revealed with high resolution neutron diffraction and mu(+) SR
- 2023
-
Ingår i: Journal of Physics. - : IOP Publishing. - 2515-7639. ; 6:3
-
Tidskriftsartikel (refereegranskat)abstract
- The mixed valence Cr3+/Cr4+ compound NaCr2O4, hosts a plethora of unconventional electronic properties. In the present study, muon spin rotation/relaxation (mu(+) SR) and high-resolution time-of-flight neutron powder diffraction measurements were carried out on high-quality samples to clarify the complex magnetic ground state of this unique material. We identified a commensurate canted antiferromagnetic order (C-AFM) with a canting angle of the Cr spin axial vector equal to theta
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| 16. |
- Rizell, Josef, 1996, et al.
(författare)
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Neutron Reflectometry Study of Solid Electrolyte Interphase Formation in Highly Concentrated Electrolytes
- 2023
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Ingår i: Small Structures. - : WILEY. - 2688-4062. ; 4:11
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Tidskriftsartikel (refereegranskat)abstract
- Highly concentrated electrolytes have been found to improve the cycle life and Coulombic efficiency of lithium metal anodes, as well as to suppress dendrite growth. However, the mechanism for these improvements is not well understood. Partly, this can be linked to the difficulty of accurately characterizing the solid electrolyte interphase (SEI), known to play an important role for anode stability and stripping/plating efficiency. Herein, in situ neutron reflectometry is used to obtain information about SEI formation in a highly concentrated ether-based electrolyte. With neutron reflectometry, the thickness, scattering length density (SLD), and roughness of the SEI layer formed on a Cu working electrode are nondestructively probed. The reflectivity data point to the formation of a thin (5 nm) SEI in the highly concentrated electrolyte (salt:solvent ratio 1:2.2), while a considerably thicker (13 nm) SEI is formed in an electrolyte at lower salt concentration (salt:solvent ratio 1:13.7). Further, the SEI formed in the electrolyte with high salt concentration has a higher SLD, suggesting that the chemical composition of the SEI changes. The results from neutron reflectometry correlate well with the electrochemical data from SEI formation.
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| 17. |
- Stendahl, Sjoerd, et al.
(författare)
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Material design optimization for large-m 11B4C-based Ni/Ti supermirror neutron optics
- 2024
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Ingår i: Materials & design. - : Elsevier. - 0264-1275 .- 1873-4197. ; 243
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Tidskriftsartikel (refereegranskat)abstract
- State-of-the-art Ni/Ti supermirror neutron optics have limited reflected intensity and a restricted neutron energy range due to the interface width. Incorporating low-neutron-absorbing 11B4C enhances reflectivity and allows for thinner layers to be deposited, with which more efficient supermirrors with higher m-values can be realized. However, incorporating 11B4C reduces the optical contrast, limiting the attainable reflectivity at low scattering vectors, making this approach infeasible. This study explores various approaches to optimize the material design of 11B4C-containing Ni/Ti supermirrors to maintain high reflectivity at low scattering vectors and achieve low interface widths at large scattering vectors. The scattering length density contrast versus interface width is investigated for multilayer periods of 30 Å, 48 Å, and 84 Å, for designs involving pure Ni/Ti multilayers, multilayers with 11B4C co-deposited in Ni and Ti layers, multilayers with 11B4C co-deposited only in Ni layers, and multilayers with 11B4C as thin interlayers between Ni and Ti layers. Our results suggest that a depth-graded hybrid material design by incorporating 11B4C inside the Ni and Ti layers, below approximately 26 Å, and introducing 1.5 Å 11B4C interlayers between the thicker Ni and Ti layers can achieve a higher reflectivity than state-of-the-art Ni/Ti multilayers over the entire scattering vector range.
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| 18. |
- Stendahl, Sjoerd, et al.
(författare)
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Morphology of Buried Interfaces in Ion-Assisted Magnetron Sputter-Deposited 11B4C-Containing Ni/Ti Multilayer Neutron Optics Investigated by Grazing-Incidence Small-Angle Scattering
- 2024
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Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 16:17, s. 22665-22675
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Tidskriftsartikel (refereegranskat)abstract
- Multilayer neutron optics require precise control of interface morphology for optimal performance. In this work, we investigate the effects of different growth conditions on the interface morphology of Ni/Ti-based multilayers, with a focus on incorporating low-neutron-absorbing (B4C)-B-11 and using different ion assistance schemes. Grazing-incidence small-angle X-ray scattering was used to probe the structural and morphological details of buried interfaces, revealing that the layers become more strongly correlated and the interfaces form mounds with increasing amounts of (B4C)-B-11. Applying high flux ion assistance during growth can reduce mound formation but lead to interface mixing, while a high flux modulated ion assistance scheme with an initial buffer layer grown at low ion energy and the top layer at higher ion energy prevents intermixing. The optimal condition was found to be adding 26.0 atom % (B4C)-B-11 combined with high flux modulated ion assistance. A multilayer with a period of 48.2 & Aring; and 100 periods was grown under these conditions, and coupled fitting to neutron and X-ray reflectivity data revealed an average interface width of only 2.7 & Aring;, a significant improvement over the current state-of-the-art commercial Ni/Ti multilayers. Overall, our study demonstrates that the addition of (B4C)-B-11 and the use of high flux modulated ion assistance during growth can significantly improve the interface morphology of Ni/Ti multilayers, leading to improved neutron optics performance.
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| 19. |
- Zubayer, Anton, 1995-
(författare)
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Enhanced Polarizing Neutron Optics with 11B4C Incorporation : SLD Tunability, Interface Refinement, and Elimination of Magnetic Coercivity
- 2023
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- This thesis explores novel strategies for improving Fe-based polarizing neutron optics, a critical part for improving neutron scattering methods to study materials science, physics, biology, medicine, chemistry and cultural heritage. Polarization analysis is important in uncovering data on magnetic domains, protein structures, molecular composition and orientation in biological systems, and ion-diffusion mechanisms that would otherwise be inaccessible. However, conventional methods, particularly state-of-the-art multilayer polarizing neutron optics, are hindered by low specular reflectivity, low polarization at higher scattering vectors/angles, high diffuse scattering and the need for high external magnetic fields for polarizer magnetization. The outcomes leading to this thesis, introduces the concept of scattering length density tuning, strategies to decrease the interface width, the diminishing of lateral correlation and magnetic coercivity. All improvements realized by introducing 11B4C in clever ways.The multilayers were deposited using ion-assisted DC magnetron sputter deposition (DCMS). Our improvement of Fe-based multilayer mirrors all revolves around the use of 11B4C. 11B4C in various concentrations can be used together with other materials to tune the scattering length density contrasts. It can amorphize the interfaces and layers to achieve smaller interface width, diminish lateral correlations and eliminate magnetic coercivity. In other words, increase reflectivity, increase polarization, decrease diffuse scattering and saturate at lower fields. The multilayers were mainly characterized using X-ray reflectivity (XRR), X-ray diffraction (XRD), grazing incidence small/wide angle X-ray scattering (GISAXS/GIWAXS), elastic recoil detection analysis (ERDA), magneto-optical Kerr effect (MOKE), vibrating sample magnetometry (VSM), transmission electron microscopy (TEM) and polarized neutron reflectivity (PNR). All results prove the benefit of using 11B4C in Fe-based polarizing neutron optics.
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| 20. |
- Zubayer, Anton, et al.
(författare)
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Reflective, polarizing, and magnetically soft amorphous neutron optics with 11B-enriched B4C
- 2024
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Ingår i: Science Advances. - : AMER ASSOC ADVANCEMENT SCIENCE. - 2375-2548. ; 10:7
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Tidskriftsartikel (refereegranskat)abstract
- The utilization of polarized neutrons is of great importance in scientific disciplines spanning materials science, physics, biology, and chemistry. However, state-of-the-art multilayer polarizing neutron optics have limitations, particularly low specular reflectivity and polarization at higher scattering vectors/angles, and the requirement of high external magnetic fields to saturate the polarizer magnetization. Here, we show that, by incorporating (B4C)-B-11 into Fe/Si multilayers, amorphization and smooth interfaces can be achieved, yielding higher neutron reflectivity, less diffuse scattering, and higher polarization. Magnetic coercivity is eliminated, and magnetic saturation can be reached at low external fields (>2 militesla). This approach offers prospects for substantial improvement in polarizing neutron optics with nonintrusive positioning of the polarizer, enhanced flux, increased data accuracy, and further polarizing/analyzing methods at neutron scattering facilities.
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