arXiv subjects

M. Belli

Publications and source records attributed to M. Belli.

7 recordsLinked to original sources

arXiv2025

Transition Metal Dichalcogenide 1T$'$-MoTe$_2$ Nanoscale Films as Spin Pumping Platforms

Transition metal dichalcogenides (TMDs) have emerged as a promising class of materials for spintronics, with the aim of promoting efficient spin-charge conversion (SCC) in TMD/ferromagnet (FM)-based devices. The MoTe$_2$ semimetal with distorted orthorhombic crystal structure in the 1T$'$ phase has gathered particular attention due to its high spin-orbit coupling and reconfigurability as a type-II Weyl semimetal close to room temperature. Here, we report on the role of chemically grown 1T$'$-MoTe$_2$ thin films in inducing SCC in 1T$'$-MoTe$_2$/FM heterostructures as measured at room temperature. Ferromagnetic resonance (FMR) and electrically detected spin-pumping FMR measurements performed on 1T$'$-MoTe$_2$/Co/Au and 1T$'$-MoTe$_2$/Au/Co/Au heterostructures reveal a spin-mixing conductance value of up to $\sim1.6 \times 10^{20}~\mathrm{m^{-2}}$ and a spin Hall angle of $1.7\%$. These findings position MoTe$_2$ thin films as a competitive spin-charge conversion option compared to other functional materials (e.g., heavy metals, topological insulators), highlighting their potential for future applications in spintronic devices.

cond-mat.mtrl-sci↗

arXiv2025

Magnetic properties of Ge, Re and Cr substituted Fe$_5$SiB$_2$

One of the possible approaches to decrease the demand for critical elements such as rare earths is to develop new sustainable magnets. Iron-based materials are suitable for gap magnets applications since iron is the most abundant ferromagnetic element on Earth. Fe$_5$SiB$_2$ is a candidate as gap magnet thanks to its high Curie temperature (T$_{\text{C}} \sim$ 800 K) and saturation magnetization (M$_{\text{S}}\sim$ 140 Am$^2$kg$^{-1}$). However its anisotropy field is too low for applications (H$_{\text{A}} \sim$ 0.8 T). In order to increase the anisotropy value, we synthesized a series of Ge, Re and Cr substituted Fe$_5$SiB$_2$ samples and studied their magnetic properties. They all crystallize in the Cr$_5$B$_3$-type tetragonal structure with the $I4/mcm$ space group. Curie temperature (T$_{\text{C}}$ = 803 K) and saturation magnetization (M$_{\text{S}}$ = 138 Am$^2$kg$^{-1}$) are slightly decreased by elemental substitution with Re having the largest effect. Despite being reduced, T$_{\text{C}}$ and M$_{\text{S}}$ still maintain significant values (T$_{\text{C}}>$ 750 K and M$_{\text{S}}$ = 118 Am$^2$kg$^{-1}$). The room temperature anisotropy field has been measured by Singular Point Detection (SPD) and increases by about 15% upon Re substitution, reaching 0.92 T for Fe$_{4.75}$Re$_{0.25}$SiB$_2$. We have also used Nuclear Magnetic Resonance and SPD measurements to study the spin reorientation transition which takes place at 172 K and we have found that it is partially suppressed by substitution of Ge from 172 K to 140 K and completely suppressed upon Cr and Re substitution.

cond-mat.mtrl-sci↗

arXiv2023

Giant spin-charge conversion in ultrathin films of the MnPtSb half-Heusler compound

Half-metallic half-Heusler compounds with strong spin-orbit-coupling and broken inversion symmetry in their crystal structure are promising materials for generating and absorbing spin-currents, thus enabling the electric manipulation of magnetization in energy-efficient spintronic devices. In this work, we report the spin-to-charge conversion in sputtered ultrathin films of the half-Heusler compound MnPtSb with thickness (t) in the range from 1 to 6 nm. A combination of X-ray and transmission electron microscopy measurements evidence the epitaxial nature of these ultrathin non-centrosymmetric MnPtSb films, with a clear (111)-orientation obtained on top of (0001) single-crystal sapphire substrates. The study of the thickness (t)-dependent magnetization dynamics of the MnPtSb(t)/Co(5nm)/Au(5nm) heterostructure revealed that the MnPtSb compound can be used as an efficient spin current generator, even at film thicknesses as low as 1 nm. By making use of spin pumping FMR, we measure a remarkable t-dependent spin-charge conversion in the MnPtSb layers, which clearly demonstrate the interfacial origin of the conversion. When interpreted as arising from the inverse Edelstein effect (IEE), the spin-charge conversion efficiency extracted at room temperature for the thinnest MnPtSb layer reaches {\lambda}IEE~3 nm, representing an extremely high spin-charge conversion efficiency at room temperature. The still never explored ultrathin regime of the MnPtSb films studied in this work and the discover of their outstanding functionality are two ingredients which demonstrate the potentiality of such materials for future applications in spintronics.

cond-mat.mtrl-sci↗

arXiv2019

Probing two-level systems with electron spin inversion recovery of defects at the Si/SiO$_2$ interface

The main feature of amorphous materials is the presence of excess vibrational modes at low energies, giving rise to the so called "boson peak" in neutron and optical spectroscopy. These same modes manifest themselves as two level systems (TLSs) causing noise and decoherence in qubits and other sensitive devices. Here we present an experiment that uses the spin relaxation of dangling bonds at the Si/(amorphous)SiO$_2$ interface as a probe of TLSs. We introduce a model that is able to explain the observed non-exponential electron spin inversion recovery and provides a measure of the degree of spatial localization and concentration of the TLSs close to the interface, their maximum energy and its temperature dependence.

cond-mat.mes-hall↗

arXiv2012

Charge dynamics of a single donor coupled to a few electrons quantum dot in silicon

We study the charge transfer dynamics between a silicon quantum dot and an individual phosphorous donor using the conduction through the quantum dot as a probe for the donor ionization state. We use a silicon n-MOSFET (metal oxide field effect transistor) biased near threshold in the SET regime with two side gates to control both the device conductance and the donor charge. Temperature and magnetic field independent tunneling time is measured. We measure the statistics of the transfer of electrons observed when the ground state D0 of the donor is aligned with the SET states.

cond-mat.mes-hall↗

arXiv2007

Recovering Metallicity in A4C60: The Case of Monomeric Li4C60

The restoration of metallicity in the high-temperature, cubic phase of Li4C60 represents a remarkable feature for a member of the A4C60 family (A = alkali metal), invariably found to be insulators. Structural and resonance technique investigations on Li4C60 at T > 600 K, show that its fcc structure is associated with a complete (4e) charge transfer to C60 and a sparsely populated Fermi level. These findings not only emphasize the crucial role played by lattice symmetry in fulleride transport properties, but also re-dimension the role of Jahn-Teller effects in band structure determination. Moreover, they suggest the present system as a potential precursor to a new class of superconducting fullerides.

cond-mat.str-el↗

arXiv2005

Unusual polymerization in the Li4C60 fulleride

Li4C60, one of the best representatives of lithium intercalated fullerides, features a novel type of 2D polymerization. Extensive investigations, including laboratory x-ray and synchrotron radiation diffraction, 13C NMR, MAS and Raman spectroscopy, show a monoclinic I2/m structure, characterized by chains of [2+2]-cycloaddicted fullerenes, sideways connected by single C-C bonds. This leads to the formation of polymeric layers, whose insulating nature, deduced from the NMR and Raman spectra, denotes the complete localization of the electrons involved in the covalent bonds.

cond-mat.mtrl-sci↗