arXiv subjects

Laëtitia Marty

Publications and source records attributed to Laëtitia Marty.

9 recordsLinked to original sources

arXiv2026

Emergent gold-induced interfacial magnetism in monolayer FePS$_3$

Owing to their atomically clean interfaces and extreme thinness, two-dimensional (2D) materials are ideal hosts for strong proximity effects, whereby contact with an adjacent material reshapes their ground state. Here, we demonstrate such an effect within a hybrid heterostructure, between the 2D antiferromagnet FePS$_3$ and an ultrathin gold film. Rather than a passive support, the latter profoundly changes the nature of the magnetism in the 2D magnet, inducing a sizeable interfacial moment. Large-area flakes from Au-assisted exfoliation, combined with element-selective X-ray absorption mapping, enable a layer-by-layer study from monolayer to bulk, benchmarked against an inert SiO$_2$ substrate reference. At 9 T and 5 K, the monolayer on gold shows a three-fold enhanced X-ray magnetic circular dichroism relative to SiO$_2$, with a $\sim$40% reduction of the orbital-to-spin moment ratio. Resonant inelastic X-ray scattering reveals a collapse of the crystal-field (d-d) excitations and a massive spectral-weight transfer to the charge-transfer region, unveiling the microscopic mechanism behind this change. Supported by atomic multiplet calculations, we identify interfacial charge transfer and Fe 3d-Au hybridization as the origin of these effects, which decay over the first three layers and vanish at the pentalayer, establishing layer number combined with substrate engineering as an atomically precise handle.

cond-mat.mtrl-sci↗

arXiv2025

Strain and doping transfer between suspended and supported bilayer graphene

Due to their unique dimensionality, the physical properties of two-dimensional materials are deeply impacted by their surroundings, calling for a thorough understanding and control of these effects. We investigated the influence of the substrate and the pressure transmitting medium on bilayer graphene in a unique high-pressure environment where the sample is partially suspended and partially supported. By employing Raman spectroscopy with a sub-micron spatial resolution, we explored the evolution of strain and doping, and demonstrated that they are both similarly induced in the suspended and supported regions of the bilayer graphene within the studied pressure range. Almost full strain and doping transfer between the supported and suspended regions is concluded. We observed that charge carrier density saturates quickly at low pressures (2 GPa) while biaxial strain continuously increases with pressure. Additionally, Raman spatial mapping highlights a rather uniform doping and strain distribution, yet with significant local variations revealing a more complex scenario than previously documented by single-point studies at high pressure.

cond-mat.mes-hall↗

arXiv2025

Laser patterning of the room temperature van der Waals ferromagnet 1$T$-CrTe$_2$

Lamellar crystalline materials, whose layers are bond by van der Waals forces, can be stacked to form ultrathin artificial heterostructures, and in particular vertical magnetic junctions when some of the stacked materials are (ferro)magnetic. Here, using the room temperature van der Waals ferromagnet 1$T$-CrTe$_2$, we report a method for patterning lateral magnetic junctions. Exploiting the heat-induced phase transformation of the material into Cr$_x$Te$_y$ compounds ($x/y>1/2$), we use local laser heating to imprint patterns at the micron-scale. Optimizing laser heat dissipation, we further demonstrate the crucial role of the substrate to control the phase transformation. If plain, unstructured poorly heat-conducting substrates allow for direct writing of magnetic patterns, structured $h$-BN layers can serve as heat stencils to draw potentially thinner patterns. Besides, $h$-BN encapsulation turns out to be heat-protective (in addition from protecting against oxidation as it is generally used for), allowing the demonstration of room temperature ferromagnetism in $<$7~nm-thick 1$T$-CrTe$_2$.

cond-mat.mtrl-sci↗

arXiv2023

Stability of the In-Plane Room Temperature van der Waals Ferromagnet Chromium Ditelluride and Its Conversion to Chromium-Interleaved CrTe$_2$ Compounds

Van der Waals magnetic materials are building blocks for novel kinds of spintronic devices and playgrounds for exploring collective magnetic phenomena down to the two-dimensional limit. Chromium-tellurium compounds are relevant in this perspective. In particular, the 1$T$ phase of CrTe$_2$ has been argued to have a Curie temperature above 300~K, a rare and desirable property in the class of lamellar materials, making it a candidate for practical applications. However, recent literature reveals a strong variability in the reported properties, including magnetic ones. Using electron microscopy, diffraction and spectroscopy techniques, together with local and macroscopic magnetometry approaches, our work sheds new light on the structural, chemical and magnetic properties of bulk 1$T$-CrTe$_2$ exfoliated in the form of flakes having a thickness ranging from few to several tens of nanometers. We unambiguously establish that 1$T$-CrTe$_2$ flakes are ferromagnetic above room temperature, have an in-plane easy axis of magnetization, low coercivity, and we confirm that their Raman spectroscopy signatures are two modes, $E_{2\text{g}}$ (103.5~cm$^{-1}$) and $A_{1\text{g}}$ (136.5~cm$^{-1}$). We also prove that thermal annealing causes a phase transformation to monoclinic Cr$_5$Te$_8$ and, to a lesser extent, to trigonal Cr$_5$Te$_8$. In sharp contrast with 1$T$-CrTe$_2$, none of these compounds have a Curie temperature above room temperature, and they both have perpendicular magnetic anisotropy. Our findings reconcile the apparently conflicting reports in the literature and open opportunities for phase-engineered magnetic properties.

cond-mat.mtrl-sci↗

arXiv2020

Fermi resonance in the Raman spectrum of graphene

We report the observation of an intense anomalous peak at 1608 cm$^{-1}$ in the Raman spectrum of graphene associated to the presence of chromium nanoparticles in contact with graphene. Bombardment with an electron beam demonstrates that this peak is distinct from the well studied D$'$ peak appearing as defects are created in graphene; the new peak is found non dispersive. We argue that the bonding of chromium atoms with carbon atoms softens the out-of-plane optical (ZO) phonon mode, in such a way that the frequency of its overtone decreases to $2ω_{\rm ZO}\simω_{\rm G}$, where $ω_{\rm G}$=1585~cm$^{-1}$ is the frequency of the Raman-active E$_{\rm 2g}$ mode. Thus, the observed new peak is attributed to the 2ZO mode which becomes Raman-active following a mechanism known as Fermi resonance. First-principles calculations on vibrational and anharmonic properties of the graphene/Cr interface support this scenario.

cond-mat.mes-hall↗

arXiv2018

Coherence and density dynamics of excitons in a single-layer MoS$_2$ reaching the homogeneous limit

We measure the coherent nonlinear response of excitons in a single-layer of molybdenum disulphide embedded in hexagonal boron nitride, forming a $h$-BN/MoS$_2$/$h$-BN heterostructure. Using four-wave mixing microscopy and imaging, we correlate the exciton homogeneous and inhomogeneous broadenings. We find that the exciton dynamics is governed by microscopic disorder on top of the ideal crystal properties. Analyzing the exciton ultra-fast density dynamics using amplitude and phase of the response, we investigate the relaxation pathways of the resonantly driven exciton population. The surface protection via encapsulation provides stable monolayer samples with low disorder, avoiding surface contaminations and the resulting exciton broadening and modifications of the dynamics. We identify areas localized to a few microns where the optical response is totally dominated by homogeneous broadening. Across the sample of tens of micrometers, weak inhomogeneous broadening and strain effects are observed, attributed to the remaining interaction with the $h$-BN and imperfections in the encapsulation process.

cond-mat.mes-hall↗

arXiv2018

Weakly Trapped, Charged, and Free Excitons in Single-Layer MoS2 in the Presence of Defects, Strain, and Charged Impurities

Few- and single-layer MoS2 host substantial densities of defects. They are thought to influence the doping level, the crystal structure, and the binding of electron-hole pairs. We disentangle the concomitant spectroscopic expression of all three effects and identify to what extent they are intrinsic to the material or extrinsic to it, i.e., related to its local environment. We do so by using different sources of MoS2 -- a natural one and one prepared at high pressure and high temperature -- and different substrates bringing varying amounts of charged impurities and by separating the contributions of internal strain and doping in Raman spectra. Photoluminescence unveils various optically active excitonic complexes. We discover a defect-bound state having a low binding energy of 20 meV that does not appear sensitive to strain and doping, unlike charged excitons. Conversely, the defect does not significantly dope or strain MoS2. Scanning tunneling microscopy and density functional theory simulations point to substitutional atoms, presumably individual nitrogen atoms at the sulfur site. Our work shows the way to a systematic understanding of the effect of external and internal fields on the optical properties of two-dimensional materials.

cond-mat.mtrl-sci↗

arXiv2016

Deviation from the normal mode expansion in a coupled graphene-nanomechanical system

We optomechanically measure the vibrations of a nanomechanical system made of a graphene membrane suspended on a silicon nitride nanoresonator. When probing the thermal noise of the coupled nanomechanical device, we observe a significant deviation from the normal mode expansion. It originates from the heterogeneous character of mechanical dissipation over the spatial extension of coupled eigenmodes, which violates one of the fundamental prerequisite for employing this commonly used description of the nanoresonators' thermal noise. We subsequently measure the local mechanical susceptibility and demonstrate that the fluctuation-dissipation theorem still holds and permits a proper evaluation of the thermal noise of the nanomechanical system. Since it naturally becomes delicate to ensure a good spatial homogeneity at the nanoscale, this approach is fundamental to correctly describe the thermal noise of nanomechanical systems which ultimately impact their sensing capacity.

cond-mat.mes-hall↗

arXiv2011

First order $0/π$ quantum phase transition in the Kondo regime of a superconducting carbon nanotube quantum dot

We study a carbon nanotube quantum dot embedded into a SQUID loop in order to investigate the competition of strong electron correlations with proximity effect. Depending whether local pairing or local magnetism prevails, a superconducting quantum dot will respectively exhibit positive or negative supercurrent, referred to as a 0 or $π$ Josephson junction. In the regime of strong Coulomb blockade, the 0 to $π$ transition is typically controlled by a change in the discrete charge state of the dot, from even to odd. In contrast, at larger tunneling amplitude the Kondo effect develops for an odd charge (magnetic) dot in the normal state, and quenches magnetism. In this situation, we find that a first order 0 to $π$ quantum phase transition can be triggered at fixed valence when superconductivity is brought in, due to the competition of the superconducting gap and the Kondo temperature. The SQUID geometry together with the tunability of our device allows the exploration of the associated phase diagram predicted by recent theories. We also report on the observation of anharmonic behavior of the current-phase relation in the transition regime, that we associate with the two different accessible superconducting states. Our results ultimately reveal the spin singlet nature of the Kondo ground state, which is the key process in allowing the stability of the 0-phase far from the mixed valence regime.

cond-mat.mes-hall↗