arXiv subjects

M. Cinchetti

Publications and source records attributed to M. Cinchetti.

18 recordsLinked to original sources

arXiv2024

Anomalous hardening of spin waves in cobalt/molecular-semiconductor heterostructures reveals strongly anisotropic spinterface magnetism

The interface between a ferromagnetic metal and an organic molecular semiconductor, commonly referred to as a spinterface, is an important component for advancing spintronic technologies. Hybridization of the ferromagnetic-metal surface d orbitals with the molecular-semiconductor p orbitals induces profound modifications not only in the interfacial molecular layer, but also in the surface ferromagnetic-metal atomic layer. These effects are particularly pronounced at low temperatures, manifesting as substantial modifications in the magnetic properties of thin-film magnetic-metal/organic heterostructures. Despite extensive research and interest, the magnetic-ordering and magnetic-properties of the spinterface remain poorly understood. Using ultrafast time-resolved magneto-optical spectroscopy, to investigate the magnetic dynamics in such heterostructures, we unveil the unique spinterface-magnetism and its universality for a broad variety of cobalt/molecular-semiconductor interfaces. In particular, our findings demonstrate the presence of highly anisotropic low-temperature superparamagnetism at the cobalt/molecular-semiconductor spinterface. This anisotropic interfacial superparamagnetism is likely driven by strong chemical modifications in the cobalt interfacial layer caused by the chemisorbed molecular layer. These results highlight the pivotal role of molecular chemisorption in tuning the magnetic properties at spinterfaces, paving the way for future spintronic applications.

cond-mat.mtrl-sci↗

arXiv2024

Temperature Dependence of Relativistic Valence Band Splitting Induced by an Altermagnetic Phase Transition

Altermagnetic (AM) materials exhibit non-relativistic, momentum-dependent spin-split states, ushering in new opportunities for spin electronic devices. While the characteristics of spin-splitting have been documented within the framework of the non-relativistic spin group symmetry, there has been limited exploration of the inclusion of relativistic symmetry and its impact on the emergence of a novel spin-splitting in the band structure. This study delves into the intricate relativistic electronic structure of an AM material, alpha-MnTe. Employing temperature-dependent angle-resolved photoelectron spectroscopy across the AM phase transition, we elucidate the emergence of a relativistic valence band splitting concurrent with the establishment of magnetic order. This discovery is validated through disordered local moment calculations, modeling the influence of magnetic order on the electronic structure and confirming the magnetic origin of the observed splitting. The temperature-dependent splitting is ascribed to the advent of relativistic spin-splitting resulting from the strengthening of AM order in alpha-MnTe as the temperature decreases. This sheds light on a previously unexplored facet of this intriguing material.

cond-mat.mtrl-sci↗

arXiv2023

Laser-induced Demagnetization in van der Waals $XY$- and Ising-like Antiferromagnets NiPS$_3$ and FePS$_3$

The critical behaviour of laser-induced changes in magnetic ordering is studied experimentally in two-dimensional zigzag antiferromagnets $XY$-like NiPS$_3$ and Ising-like FePS$_3$. To examine laser-induced dynamics in flakes of these compounds, we employ time-resolved exchange linear dichroism effect sensitive to zigzag magnetic ordering and independent of the orientation of the antiferromagnetic vector. In both compounds laser excitation in the vicinity of the absorption edge induces partial quenching of the antiferromagnetic ordering manifested by exchange linear dichroism reduction. The amplitude of the effect varies with temperature as the derivative of the antiferromagnetic vector and exhibits a critical behaviour with the exponents corresponding to $XY$- and Ising-models for NiPS$_3$ and FePS$_3$, respectively. Critical slowing down of the demagnetization in the vicinity of N\'eel temperature is found, however, only in FePS$_3$. In contrast, the increase of the demagnetization time near the ordering temperature in NiPS$_3$ is minor. We show that the difference in the demagnetization times correlates well with the spin specific heat in both compounds. Beyond the range of slowing down, the demagnetization times in NiPS$_3$ and FePS$_3$ are comparable, about 5 - 10 ps, and are longer than those reported earlier for CoPS$_3$ and considerably shorter than for MnPS$_3$. This points to the importance of the unquenched angular momentum of transition-metal ions in laser-induced demagnetization process.

cond-mat.mes-hall↗

arXiv2021

Femtosecond phononic coupling to both spins and charges in a room temperature antiferromagnetic semiconductor

Spintronics is postulated on the possibility to employ the magnetic degree of freedom of electrons for computation and couple it to charges. In this view, the combination of the high-frequency of spin manipulations offered by antiferromagnets, with the wide tunability of the electronic properties peculiar of semiconductors provides a promising and intriguing platform. Here we explore this scenario in $\alpha$-MnTe, which is a semiconductor antiferromagnetically ordered at room temperature. Relying on a Raman mechanism and femtosecond laser pulses, we drive degenerate modes of coherent optical phonons, which modulate the chemical bonds involved in the super-exchange interaction. The spectrally-resolved measurements of the transient reflectivity reveal a coherent modulation of the band-gap at the frequency of 5.3 THz. The detection of the rotation of the polarisation, typically associated with magneto-optical effects, shows coherent and incoherent contributions. Modelling how the ionic motion induced by the phonons affects the exchange interaction in the material, we calculate the photoinduced THz spin dynamics: the results predict both a coherent and incoherent response, the latter of which is consistent with the experimental observation. Our work demonstrates that the same phonon modes modulate both the charge and magnetic degree of freedom, suggesting the resonant pumping of phonons as a viable way to link spin and charge dynamics even in nonlinear regimes.

physics.optics↗

arXiv2021

Positive magnetoresistance and chiral anomaly in exfoliated type-II Weyl semimetal $T_\mathrm{d}$-WTe$_{2}$

Layered van der Waals semimetallic $T_\mathrm{d}$-WTe$_{2}$, exhibiting intriguing properties which include non-saturating extreme positive magnetoresistance (MR) and tunable chiral anomaly, has emerged as model topological type-II Weyl semimetal system. Here, $\sim$45 nm thick mechanically exfoliated flakes of $T_\mathrm{d}$-WTe$_{2}$ are studied $via$ atomic force microscopy, Raman spectroscopy, low-$T$/high-$μ_{0}H$ magnetotransport measurements and optical reflectivity. The contribution of anisotropy of the Fermi liquid state to the origin of the large positive transverse $\mathrm{MR}_\perp$ and the signature of chiral anomaly of the type-II Weyl fermions are reported. The samples are found to be stable in air and no oxidation or degradation of the electronic properties are observed. A transverse $\mathrm{MR}_\perp$ $\sim$1200\,\% and an average carrier mobility of $5000$\, cm$^{2}$V$^{-1}$s$^{-1}$ at $T=5\,\mathrm{K}$ for an applied perpendicular field $μ_{0}H_{\perp} = 7\,\mathrm{T}$ are established. The system follows a Fermi liquid model for $T\leq50\,\mathrm{K}$ and the anisotropy of the Fermi surface is concluded to be at the origin of the observed positive MR. The anisotropy of the electronic behaviour is also confirmed by optical reflectivity measurements. The relative orientation of the crystal axes and of the applied electric and magnetic fields is proven to give rise to the observed chiral anomaly in the in-plane magnetotransport.

cond-mat.mes-hall↗

arXiv2021

Ultrafast amplification and non-linear magneto-elastic coupling of coherent magnon modes in an antiferromagnet

We investigate the role of domain walls in the ultrafast magnon dynamics of an antiferromagnetic NiO single crystal in a pump-probe experiment with variable pump photon energy. Analysing the amplitude of the energy-dependent photo-induced ultrafast spin dynamics, we detect a yet unreported coupling between the material's characteristic THz- and a GHz-magnon modes. We explain this unexpected coupling between two orthogonal eigenstates of the corresponding Hamiltonian by modelling the magneto-elastic interaction between spins in different domains. We find that such interaction, in the non-linear regime, couples the two different magnon modes via the domain walls and it can be optically exploited via the exciton-magnon resonance.

cond-mat.other↗

arXiv2021

Temperature dependence of the interface spin Seebeck effect

We performed temperature-dependent optical pump - THz emission measurements in Y3Fe5O12 (YIG)|Pt from 5 K to room temperature in the presence of an externally applied magnetic field. We study the temperature dependence of the spin Seebeck effect and observe a continuous increase as temperature is decreased, opposite to what is observed in electrical measurements where the spin Seebeck effect is suppressed as 0K is approached. By quantitatively analysing the different contributions we isolate the temperature dependence of the spin-mixing conductance and observe features that are correlated to the bands of magnon spectrum in YIG.

cond-mat.mtrl-sci↗

arXiv2019

Enhancing Light Emission in Interface Engineered Spin-OLEDs Through Spin-Polarized Injection at High Voltages

The quest for a spin-polarized organic light emitting diode (spin-OLED) is a common goal in the emerging fields of molecular electronics and spintronics. In this device two ferromagnetic electrodes are used to enhance the electroluminescence intensity of the OLED through a magnetic control of the spin polarization of the injected carriers. The major difficulty is that the driving voltage of an OLED device exceeds of a few volts, while spin injection in organic materials is only efficient at low voltages. We report here the fabrication of a spin-OLED that uses a conjugated polymer as bipolar spin collector layer and ferromagnetic electrodes. Through a careful engineering of the organic/inorganic interfaces we have succeeded in obtaining a light-emitting device showing spin-valve effects at high voltages (up to 14 V). This has allowed us to detect a magneto-electroluminescence enhancement on the order of a 2.4 % at 9 V for the antiparallel configuration of the magnetic electrodes. This observation provides evidence for the long-standing fundamental issue of injecting spins from magnetic electrodes into the frontier levels of a molecular semiconductor. Our finding opens the way for the design of multifunctional devices coupling the light and the spin degrees of freedom.

cond-mat.mes-hall↗

arXiv2019

Adsorption induced pyramidal distortion of the tri-metallic nitride core inside the endohedral fullerene Sc$_3$N@C$_{80}$ on the Ag(111) surface

Our ability to understand and tailor metal-organic interfaces is mandatory to functionalize organic complexes for next generation electronic and spintronic devices. For magnetic data storage applications, metal-carrying organic molecules, so called single molecular magnets (SMM) are of particular interest as they yield the possibility to store information on the molecular scale. In this work, we focus on the adsorption properties of the prototypical SMM Sc3N@C80 grown in a monolayer film on the Ag(111) substrate. We provide clear evidence of a pyramidal distortion of the otherwise planar Sc3N core inside the carbon cage upon the adsorption on the Ag(111) surface. This adsorption induced structural change of the Sc3N@C80 molecule can be correlated to a charge transfer from the substrate into the lowest unoccupied molecular orbital of Sc3N@C80, which significantly alters the charge density of the fullerene core. Our comprehensive characterization of the Sc3N@C80-Ag(111) interface hence reveals an indirect coupling mechanism between the Sc3N core of the fullerene molecule and the noble metal surface mediated via an interfacial charge transfer. Our work shows that such an indirect coupling between the encapsulated metal centers of SMM and metal surfaces can strongly affect the geometric structure of the metallic centers and thereby potentially also alters the magnetic properties of SMMs on surfaces.

cond-mat.mtrl-sci↗

arXiv2019

Structure and electronic properties of the ($\sqrt{3}\times \sqrt{3}$)$R30^{\circ}$ SnAu$_2$/Au(111) surface alloy

We have investigated the atomic and electronic structure of the ($\sqrt{3}\times \sqrt{3}$)$R30^{\circ}$ SnAu$_2$/Au(111) surface alloy. Low energy electron diffraction and scanning tunneling microscopy measurements show that the native herringbone reconstruction of bare Au(111) surface remains intact after formation of a long range ordered ($\sqrt{3}\times \sqrt{3}$)$R30^{\circ}$ SnAu$_2$2/Au(111) surface alloy. Angle-resolved photoemission and two-photon photoemission spectroscopy techniques reveal Rashba-type spin-split bands in the occupied valence band with comparable momentum space splitting as observed for the Au(111) surface state, but with a hole-like parabolic dispersion. Our experimental findings are compared with density functional theory (DFT) calculation that fully support our experimental findings. Taking advantage of the good agreement between our DFT calculations and the experimental results, we are able to extract that the occupied Sn-Au hybrid band is of (s, d)-orbital character while the unoccupied Sn-Au hybrid bands are of (p, d)-orbital character. Hence, we can conclude that the Rashba-type spin splitting of the hole-like Sn-Au hybrid surface state is caused by the significant mixing of Au d- to Sn s-states in conjunction with the strong atomic spin-orbit coupling of Au, i.e., of the substrate.

cond-mat.mtrl-sci↗

arXiv2014

All-optical control of ferromagnetic thin films and nanostructures

The interplay of light and magnetism has been a topic of interest since the original observations of Faraday and Kerr where magnetic materials affect the light polarization. While these effects have historically been exploited to use light as a probe of magnetic materials there is increasing research on using polarized light to alter or manipulate magnetism. For instance deterministic magnetic switching without any applied magnetic fields using laser pulses of the circular polarized light has been observed for specific ferrimagnetic materials. Here we demonstrate, for the first time, optical control of ferromagnetic materials ranging from magnetic thin films to multilayers and even granular films being explored for ultra-high-density magnetic recording. Our finding shows that optical control of magnetic materials is a much more general phenomenon than previously assumed. These results challenge the current theoretical understanding and will have a major impact on data memory and storage industries via the integration of optical control of ferromagnetic bits.

cond-mat.mtrl-sci↗

arXiv2011

Driving Force of Ultrafast Magnetization Dynamics

Irradiating a ferromagnetic material with an ultrashort laser pulse leads to demagnetization on a femtosecond timescale. We implement Elliott-Yafet type spin-flip scattering, mediated by electron-electron and electron-phonon collisions, into the framework of a spin-resolved Boltzmann equation. Considering three mutually coupled reservoirs, (i) spin-up electrons, (ii) spin-down electrons and (iii) phonons, we trace non-equilibrium electron distributions during and after laser excitation. We identify the driving force for ultrafast magnetization dynamics as the equilibration of temperatures and chemical potentials between the electronic subsystems. This principle can be used to easily predict the maximum quenching of magnetization upon ultrashort laser irradiation in any material, as we show for the example of 3d-ferromagnetic nickel.

cond-mat.mtrl-sci↗

arXiv2006

Spin-flip processes and ultrafast magnetization dynamics in Co - unifying the microscopic and macroscopic view of femtosecond magnetism

The femtosecond magnetization dynamics of a thin cobalt film excited with ultrashort laser pulses has been studied using two complementary pump-probe techniques, namely spin-, energy- and time-resolved photoemission and time-resolved magneto-optical Kerr effect. Combining the two methods it is possible to identify the microscopic electron spin-flip mechanisms responsible for the ultrafast macroscopic magnetization dynamics of the cobalt film. In particular, we show that electron-magnon excitation does not affect the overall magnetization even though it is an efficient spin-flip channel on the sub-200 fs timescale. Instead we find experimental evidence for the relevance of Elliott-Yafet type spin-flip processes for the ultrafast demagnetization taking place on a time scale of 300 fs.

cond-mat.other↗

arXiv2006

Towards a full Heusler alloy showing room temperature half-metallicity at the surface

In this article we investigate the surface spin polarization in a 100 nm Co2Cr0.6Fe0.4Al (CCFA) film grown ex situ epitaxially on MgO(100) with a 10 nm Fe buffer layer by means of spin resolved photoemission. We show that a careful in situ preparation of the sample surface leads to values for the room temperature spin polarization up to 45% at the Fermi level. To our knowledge, this is the highest value measured so far at the surface region of a full Heusler alloy at room temperature.

cond-mat.mtrl-sci↗

arXiv2006

Epitaxial film growth and magnetic properties of Co_2FeSi

We have grown thin films of the Heusler compound Co_2FeSi by RF magnetron sputtering. On (100)-oriented MgO substrates we find fully epitaxial (100)-oriented and L2_1 ordered growth. On Al_2O_3 (11-20) substrates, the film growth is (110)-oriented, and several in-plane epitaxial domains are observed. The temperature dependence of the electrical resistivity shows a power law with an exponent of 7/2 at low temperatures. Investigation of the bulk magnetic properties reveals an extrapolated saturation magnetization of 5.0 mu_B/fu at 0 K. The films on Al_2O_3 show an in-plane uniaxial anisotropy, while the epitaxial films are magnetically isotropic in the plane. Measurements of the X-ray magnetic circular dichroism of the films allowed us to determine element specific magnetic moments. Finally we have measured the spin polarization at the surface region by spin-resolved near-threshold photoemission and found it strongly reduced in contrast to the expected bulk value of 100%. Possible reasons for the reduced magnetization are discussed.

cond-mat.mtrl-sci↗

arXiv2006

Spin- and time-resolved photoemission studies of thin Co2FeSi Heusler alloy films

We have studied the possibly half metallic Co2FeSi full Heusler alloy by means of spin- and time-resolved photoemission spectroscopy. For excitation, the second and fourth harmonic of femtosecond Ti:sapphire lasers were used, with photon energies of 3.1 eV and 5.9 eV, respectively. We compare the dependence of the measured surface spin polarization on the particular photoemission mechanism, i.e. 1-photon-photoemission (1PPE) or 2-photon photoemission (2PPE). The observed differences in the spin polarization can be explained by a spin-dependent lifetime effect occurring in the 2-photon absorption process. The difference in escape depth of the two methods in this context suggests that the observed reduction of spin polarization (compared to the bulk) cannot be attributed just to the outermost surface layer but takes place at least 4-6 nm away from the surface.

cond-mat.mtrl-sci↗

arXiv2005

Photoemission Electron Microscopy as a tool for the investigation of optical near fields

Photoemission electron microscopy was used to image the electrons photoemitted from specially tailored Ag nanoparticles deposited on a Si substrate (with its native oxide SiO$_{x}$). Photoemission was induced by illumination with a Hg UV-lamp (photon energy cutoff $\hbarω_{UV}=5.0$ eV, wavelength $λ_{UV}=250$ nm) and with a Ti:Sapphire femtosecond laser ($\hbarω_{l}=3.1$ eV, $λ_{l}=400$ nm, pulse width below 200 fs), respectively. While homogeneous photoelectron emission from the metal is observed upon illumination at energies above the silver plasmon frequency, at lower photon energies the emission is localized at tips of the structure. This is interpreted as a signature of the local electrical field therefore providing a tool to map the optical near field with the resolution of emission electron microscopy.

physics.optics↗

arXiv1999

Phase covariant quantum cloning

We consider an N -> M quantum cloning transformation acting on pure two-level states lying on the equator of the Bloch sphere. An upper bound for its fidelity is presented, by establishing a connection between optimal phase covariant cloning and phase estimation. We give the explicit form of a cloning transformation that achieves the bound for the case N=1, M=2, and find a link between this case and optimal eavesdropping in the quantum cryptographic scheme BB84.

quant-ph↗