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Sökning: WFRF:(Aeschlimann M.)

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1.
  • Frisoni, G. B., et al. (författare)
  • Dementia prevention in memory clinics: recommendations from the European task force for brain health services
  • 2023
  • Ingår i: Lancet Regional Health-Europe. - : Elsevier BV. - 2666-7762. ; 26
  • Tidskriftsartikel (refereegranskat)abstract
    • Observational population studies indicate that prevention of dementia and cognitive decline is being accomplished, possibly as an unintended result of better vascular prevention and healthier lifestyles. Population aging in the coming decades requires deliberate efforts to further decrease its prevalence and societal burden. Increasing evidence sup-ports the efficacy of preventive interventions on persons with intact cognition and high dementia risk. We report recommendations for the deployment of second-generation memory clinics (Brain Health Services) whose mission is evidence-based and ethical dementia prevention in at-risk individuals. The cornerstone interventions consist of (i) assessment of genetic and potentially modifiable risk factors including brain pathology, and risk stratification, (ii) risk communication with ad-hoc protocols, (iii) risk reduction with multi-domain interventions, and (iv) cognitive enhancement with cognitive and physical training. A roadmap is proposed for concept validation and ensuing clinical deployment.
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2.
  • Lloyd-Hughes, J., et al. (författare)
  • The 2021 ultrafast spectroscopic probes of condensed matter roadmap
  • 2021
  • Ingår i: Journal of Physics. - : Institute of Physics Publishing (IOPP). - 0953-8984 .- 1361-648X. ; 33:35
  • Forskningsöversikt (refereegranskat)abstract
    • In the 60 years since the invention of the laser, the scientific community has developed numerous fields of research based on these bright, coherent light sources, including the areas of imaging, spectroscopy, materials processing and communications. Ultrafast spectroscopy and imaging techniques are at the forefront of research into the light-matter interaction at the shortest times accessible to experiments, ranging from a few attoseconds to nanoseconds. Light pulses provide a crucial probe of the dynamical motion of charges, spins, and atoms on picosecond, femtosecond, and down to attosecond timescales, none of which are accessible even with the fastest electronic devices. Furthermore, strong light pulses can drive materials into unusual phases, with exotic properties. In this roadmap we describe the current state-of-the-art in experimental and theoretical studies of condensed matter using ultrafast probes. In each contribution, the authors also use their extensive knowledge to highlight challenges and predict future trends.
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3.
  • Hofherr, M., et al. (författare)
  • Speed and efficiency of femtosecond spin current injection into a nonmagnetic material
  • 2017
  • Ingår i: Physical Review B. - : AMER PHYSICAL SOC. - 2469-9950 .- 2469-9969. ; 96:10
  • Tidskriftsartikel (refereegranskat)abstract
    • We investigate femtosecond spin injection from an optically excited Ni top layer into an Au bottom layer using time-resolved complex magneto-optical Kerr effect (C-MOKE) measurements. Employing the C-MOKE formalism, we are able to follow layer-resolved demagnetization in Ni and the simultaneous spin injection into the adjacent Au film, both occurring within similar to 40 fs. We confirm the ballistic to diffusive propagation of the spin transfer process with ab initio theory and superdiffusive transport calculations. In particular, our combined experimental-theoretical effort does allow us to quantify the so far elusive amount of spin injection, and therefore the spin injection efficiency at the interface.
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4.
  • Rudolf, Dennis, et al. (författare)
  • Element Selective Investigation of Spin Dynamics in Magnetic Multilayers
  • 2015
  • Ingår i: Ultrafast Magnetism I. - Cham : Springer International Publishing. - 9783319077437 - 9783319077420 ; , s. 307-309
  • Konferensbidrag (refereegranskat)abstract
    • Our understanding of ultrafast switching processes in novel spin-based electronics depends on our detailed knowledge of interactions between spin, charge and phonons in magnetic structures. We present element-selective studies, using extreme ultraviolet (XUV) light, to gain insight into spin dynamics in exchange coupled magnetic multilayers on the femtosecond time scale.
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5.
  • Rudolf, Dennis, et al. (författare)
  • Ultrafast magnetization enhancement in metallic multilayers driven by superdiffusive spin current
  • 2012
  • Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 3, s. 1037-
  • Tidskriftsartikel (refereegranskat)abstract
    • Uncovering the physical mechanisms that govern ultrafast charge and spin dynamics is crucial for understanding correlated matter as well as the fundamental limits of ultrafast spin-based electronics. Spin dynamics in magnetic materials can be driven by ultrashort light pulses, resulting in a transient drop in magnetization within a few hundred femtoseconds. However, a full understanding of femtosecond spin dynamics remains elusive. Here we spatially separate the spin dynamics using Ni/Ru/Fe magnetic trilayers, where the Ni and Fe layers can be ferroor antiferromagnetically coupled. By exciting the layers with a laser pulse and probing the magnetization response simultaneously but separately in Ni and Fe, we surprisingly find that optically induced demagnetization of the Ni layer transiently enhances the magnetization of the Fe layer when the two layer magnetizations are initially aligned parallel. Our observations are explained by a laser-generated superdiffusive spin current between the layers.
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6.
  • Chylarecka, D., et al. (författare)
  • Indirect Magnetic Coupling of Manganese Porphyrin to a Ferromagnetic Cobalt Substrate
  • 2011
  • Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 115:4, s. 1295-1301
  • Tidskriftsartikel (refereegranskat)abstract
    • The coupling mechanism of magnetic molecules to ferromagnetic surfaces is of scientific interest to design and tune molecular spintronic interfaces utilizing their molecular and surface architecture. Indirect magnetic coupling has been proposed earlier on the basis of density functional theory +U (DFT+U) calculations, for the magnetic coupling of manganese(II) porphyrin (MnP) molecules to thin Co films. Here we provide an experimental X-ray magnetic circular dichroism (XMCD) spectroscopy and scanning tunneling microscopy (STM) study of manganese(III) tetraphenylporphyrin chloride (MnTPPCl) on rough (exhibiting a high density of monatomic steps) and smooth (exhibiting a low density of monatomic steps) thin Co films grown on a Cu(001) single crystal toward the assessment of the magnetic coupling mechanism. After deposition onto the surface, MnTPPCl molecules were found to couple ferromagnetically to both rough and smooth Co substrates. For high molecular coverage, we observed higher XMCD signals at the Mn L-edges on the smooth Co substrate than on the rough Co substrate, as expected for the proposed indirect magnetic coupling mechanism on the basis of its predominance on the flat surface areas. In particular, DFT+U calculations predict a weak ferromagnetic molecule-substrate coupling only if the chloride ion of the MnTPPCl molecule orients away (Co-Mn-Cl) from the Co surface.
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7.
  • Turgut, Emrah, et al. (författare)
  • Stoner versus Heisenberg : Ultrafast exchange reduction and magnon generation during laser-induced demagnetization
  • 2016
  • Ingår i: PHYSICAL REVIEW B. - 2469-9950. ; 94:22
  • Tidskriftsartikel (refereegranskat)abstract
    • Understanding how the electronic band structure of a ferromagnetic material is modified during laser-induced demagnetization on femtosecond time scales has been a long-standing question in condensed matter physics. Here, we use ultrafast high harmonics to measure time-, energy-, and angle-resolved M-edge magnetic asymmetry spectra for Co films after optical pumping to induce ultrafast demagnetization. This provides a complete data set that we can compare with advanced ab initio magneto-optical calculations. Our analysis identifies that the dominant mechanisms contributing to ultrafast demagnetization on time scales up to several picoseconds are a transient reduction in the exchange splitting and the excitation of ultrafast magnons. Surprisingly, we find that the magnon contribution to ultrafast demagnetization is already strong on subpicosecond time scales, while the reduction in exchange splitting persists to several picoseconds.
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8.
  • Aeschlimann, S., et al. (författare)
  • Ultrafast momentum imaging of pseudospin-flip excitations in graphene
  • 2017
  • Ingår i: Physical Review B. - 2469-9969 .- 2469-9950. ; 96:2
  • Tidskriftsartikel (refereegranskat)abstract
    • The pseudospin of Dirac electrons in graphene manifests itself in a peculiar momentum anisotropy for photoexcited electron-hole pairs. These interband excitations are in fact forbidden along the direction of the light polarization and are maximum perpendicular to it. Here, we use time-and angle-resolved photoemission spectroscopy to investigate the resulting unconventional hot carrier dynamics, sampling carrier distributions as a function of energy, and in-plane momentum. We first show that the rapidly-established quasithermal electron distribution initially exhibits an azimuth-dependent temperature, consistent with relaxation through collinear electron-electron scattering. Azimuthal thermalization is found to occur only at longer time delays, at a rate that depends on the substrate and the static doping level. Further, we observe pronounced differences in the electron and hole dynamics in n-doped samples. By simulating the Coulomb-and phonon-mediated carrier dynamics we are able to disentangle the influence of excitation fluence, screening, and doping, and develop a microscopic picture of the carrier dynamics in photoexcited graphene. Our results clarify new aspects of hot carrier dynamics that are unique to Dirac materials, with relevance for photocontrol experiments and optoelectronic device applications.
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9.
  • Chen, Cong, et al. (författare)
  • Distinguishing attosecond electron-electron scattering and screening in transition metals
  • 2017
  • Ingår i: Proceedings of the National Academy of Sciences of the United States of America. - : National Academy of Sciences. - 0027-8424 .- 1091-6490. ; 114:27, s. E5300-E5307
  • Tidskriftsartikel (refereegranskat)abstract
    • Electron-electron interactions are the fastest processes in materials, occurring on femtosecond to attosecond timescales, depending on the electronic band structure of the material and the excitation energy. Such interactions can play a dominant role in light-induced processes such as nano-enhanced plasmonics and catalysis, light harvesting, or phase transitions. However, to date it has not been possible to experimentally distinguish fundamental electron interactions such as scattering and screening. Here, we use sequences of attosecond pulses to directly measure electron-electron interactions in different bands of different materials with both simple and complex Fermi surfaces. By extracting the time delays associated with photoemission we show that the lifetime of photoelectrons from the d band of Cu are longer by similar to 100 as compared with those from the same band of Ni. We attribute this to the enhanced electron-electron scattering in the unfilled d band of Ni. Using theoretical modeling, we can extract the contributions of electron-electron scattering and screening in different bands of different materials with both simple and complex Fermi surfaces. Our results also show that screening influences high-energy photoelectrons (approximate to 20 eV) significantly less than low-energy photoelectrons. As a result, high-energy photoelectrons can serve as a direct probe of spin-dependent electron-electron scattering by neglecting screening. This can then be applied to quantifying the contribution of electron interactions and screening to low-energy excitations near the Fermi level. The information derived here provides valuable and unique information for a host of quantum materials.
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10.
  • Krause, R., et al. (författare)
  • Microscopic Understanding of Ultrafast Charge Transfer in van der Waals Heterostructures
  • 2021
  • Ingår i: Physical Review Letters. - 1079-7114 .- 0031-9007. ; 127:27
  • Tidskriftsartikel (refereegranskat)abstract
    • Van der Waals heterostructures show many intriguing phenomena including ultrafast charge separation following strong excitonic absorption in the visible spectral range. However, despite the enormous potential for future applications in the field of optoelectronics, the underlying microscopic mechanism remains controversial. Here we use time- and angle-resolved photoemission spectroscopy combined with microscopic many-particle theory to reveal the relevant microscopic charge transfer channels in epitaxial WS2/graphene heterostructures. We find that the timescale for efficient ultrafast charge separation in the material is determined by direct tunneling at those points in the Brillouin zone where WS2 and graphene bands cross, while the lifetime of the charge separated transient state is set by defect-assisted tunneling through localized sulphur vacancies. The subtle interplay of intrinsic and defect-related charge transfer channels revealed in the present work can be exploited for the design of highly efficient light harvesting and detecting devices.
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11.
  • Lindblom, Anders, et al. (författare)
  • The intrinsic factor-vitamin B12 receptor, cubilin, is assembled into trimers via a coiled-coil alpha-helix
  • 1999
  • Ingår i: Journal of Biological Chemistry. - 1083-351X. ; 274:10, s. 6374-6380
  • Tidskriftsartikel (refereegranskat)abstract
    • A large protein was purified from bovine kidney, using selective extraction with EDTA to solubilize proteins anchored by divalent cation-dependent interactions. An antiserum raised against the purified protein labeled the apical cell surface of the epithelial cells in proximal tubules and the luminal surface of small intestine. Ten peptide sequences, derived from the protein, all matched the recently published sequences for rat (Moestrup, S. K., Kozyraki, R., Kristiansen, M., Kaysen, J. H., Holm Rasmussen, H., Brault, D., Pontillon, F., Goda, F. O., Christensen, E. I., Hammond, T. G., and Verroust, P. J. (1998) J. Biol. Chem. 273, 5235-5242) and human cubilin, a receptor for intrinsic factor-vitamin B12 complexes, identifying the protein as bovine cubilin. In electron microscopy, a three-armed structure was seen, indicating an oligomerization of three identical subunits. This model was supported by the Mr values of about 1,500,000 for the intact protein and 440,000 for its subunits obtained by analytical ultracentrifugation. In a search for a potential assembly domain, we identified a region of heptad repeats in the N-terminal part of the cubilin sequence. Computer-assisted analysis supported the presence of a coiled-coil alpha-helix between amino acids 103 and 132 of the human cubilin sequence and predicted the formation of a triple coiled-coil. We therefore conclude that cubilin forms a noncovalent trimer of identical subunits connected by an N-terminal coiled-coil alpha-helix.
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12.
  • Stiehl, Martin, et al. (författare)
  • All-optical switching in Cr- and Mn-doped L10 FePt thin films
  • 2024
  • Ingår i: Physical Review Applied. - : American Physical Society. - 2331-7019. ; 21:5
  • Tidskriftsartikel (refereegranskat)abstract
    • Optical manipulation of the magnetization of thin films opens up exciting possibilities for ever-faster magnetic storage applications. In this context, ?⁢10 chemically ordered Fe⁢Pt thin films are of particular interest due to their high perpendicular magnetic anisotropy and their use as a storage material for heat-assisted magnetic recording devices. However, these materials are difficult to manipulate with external fields due to their high coercivity field. Thus, we want to explore the possibility of tailoring the properties of these materials to enable switching using all-optical techniques. While stochastic all-optical switching between partially magnetized states has been reported for undoped Fe⁢Pt thin films, we have investigated to what extent doping with third elements can influence the switching behavior. Reducing the saturation magnetization may be one way to facilitate all-optical switching. While this is expected with the introduction of additional elements, we also want to highlight the role of the inverse Faraday effect and the magnetic circular dichroism in stochastic all-optical switching. In this study, Cr was found to be a promising dopant, which can almost double the relative magnetization change of the partially magnetized states compared to pure Fe⁢Pt.
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13.
  • Tengdin, Phoebe, et al. (författare)
  • Direct light–induced spin transfer between different elements in a spintronic Heusler material via femtosecond laser excitation
  • 2020
  • Ingår i: Science Advances. - : American Association for the Advancement of Science. - 2375-2548. ; 6:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Heusler compounds are exciting materials for future spintronics applications because they display a wide range of tunable electronic and magnetic interactions. Here, we use a femtosecond laser to directly transfer spin polarization from one element to another in a half-metallic Heusler material, Co2MnGe. This spin transfer initiates as soon as light is incident on the material, demonstrating spatial transfer of angular momentum between neighboring atomic sites on time scales < 10 fs. Using ultrafast high harmonic pulses to simultaneously and independently probe the magnetic state of two elements during laser excitation, we find that the magnetization of Co is enhanced, while that of Mn rapidly quenches. Density functional theory calculations show that the optical excitation directly transfers spin from one magnetic sublattice to another through preferred spin-polarized excitation pathways. This direct manipulation of spins via light provides a path toward spintronic devices that can operate on few-femtosecond or faster time scales.
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  • Resultat 1-14 av 14

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