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Mohammed El Amine Miloudi

Publications and source records attributed to Mohammed El Amine Miloudi.

5 recordsLinked to original sources

Mismatch between Raman shear modes and ferroelectric polarization in 3R-MoS$_{2}$

Sliding ferroelectricity in parallel-stacked two-dimensional van der Waals materials enables a broad range of novel device concepts, but exploiting it requires reliable, non-destructive assignment of the underlying stacking order and polarization state. Here, we combine Kelvin-probe force microscopy (KPFM) with low-frequency Raman spectroscopy to probe the polarization domains and stacking configurations of a exfoliated trilayer 3R-MoS$_{2}$ flake on a hBN substrate. We find that ABA and BAB - both stackings with zero net polarization - are indistinguishable in KPFM, yet show drastically different low-frequency shear modes. This observation is reproduced across multiple flakes and is corroborated by low-temperature photoluminescence. Notably, the standard bond-polarizability model does not account for the difference in shear-mode activity between the ABA and BAB configurations, indicating that the interlayer Raman response of these stackings is governed by physics beyond a simple polarizability picture. Our results show that none of the here-used individual techniques alone is sufficient to assign sliding-ferroelectric stacking order and motivate a combined spectroscopic-scanning-probe approach.

cond-mat.mes-hall↗

Stacking-Directed Polarization and Excitonic Engineering in MoS$_2$/MoSe$_2$ van der Waals Heterostructures

The stacking-dependent polarization and excitonic response of MoS$_2$/MoSe$_2$ heterostructures were investigated using GW+BSE many-body perturbation theory. While homobilayer MoS$_2$ exhibited a switchable interlayer dipole driven by registry-induced symmetry breaking, the MoS$_2$/MoSe$_2$ hetero-interface remained pinned by the intrinsic chemical potential mismatch between sulfur and selenium. In 2L-MoS$_2$/MoSe$_2$ trilayers, the stacking sequence enabled a deterministic control of photogenerated electrons between the central and bottom MoS$_2$ layers, governed by internal electric fields and quasiparticle band-edge shifts of 60--70~meV. Our calculations predicted a 36~meV interlayer excitonic shift, in remarkable agreement with recent experiments. These results elucidate the microscopic link between atomic registry and many-body interactions, establishing transition metal dichalcogenide trilayers as a potential platform for sliding ferroelectricity and programmable optoelectronic functionalities.

cond-mat.mtrl-sci↗

Ferroelectric Control of Interlayer Excitons in 3R-MoS$_{2}$ / MoSe$_{2}$ Heterostructures

We investigate the interaction between interlayer excitons and ferroelectric domains in hBN-encapsulated 3R-MoS$_2$/MoSe$_2$ heterostructures, combining photoluminescence experiments with density functional theory and many-body Green's function calculations. Low-temperature photoluminescence spectroscopy reveals a strong redshift of the interlayer exciton energy with increasing MoS$_2$ layer thickness, attributed to band renormalization and dielectric effects. We observe local variations in exciton energy that correlate with local ferroelectric domain polarization of the 3R-MoS$_2$ layer, showcasing distinct domain-dependent interlayer exciton transition energies. Gate voltage experiments demonstrate that the interlayer exciton energy can be tuned by electrically induced domain switching. These results highlight the potential for interlayer exciton control by local ferroelectric order and establish a foundation for future ferroelectric optoelectronic devices based on van der Waals heterostructures.

cond-mat.mtrl-sci↗

Chemical Control of Mechanical Anisotropy and Band Alignment in Perylene-based Two-dimensional MoS$_2$-Organic Hybrids

This study presents a comprehensive investigation of hybrid interfaces formed by monolayer MoS$_2$ coupled with the organic molecules perylene (P), perylene diimide (PDI), and perylene orange (PO). Using density functional theory, we demonstrate the extent to which the mechanical and electronic properties of a hybrid system can be altered by the chemical modification of a given chromophore. The three systems exhibit distinct differences due to their chemical composition and van der Waals contact enabled by their geometry. All systems are structurally stable. The binding energies follow the order PD$>$P$>$PO due to the large $π$-system (PD) and strong structural distortion (PO). Young's modulus and Poisson's ratio exhibit pronounced anisotropy in all cases. PO exhibits the greatest anisotropy due to steric effects and a permanent dipole, which introduce directionality to the molecule-surface interaction. Physisorption is accompanied by net charge transfer in the same order as the binding energies. The associated interfacial polarization results in a change in the work function compared to pristine MoS$_2$ in the order P$>$PO$>$PD. Finally, the presence of organic molecules introduces states into the MoS$_2$ energy gap, with the band alignment being either type II (P, PO) or type I (PD).

cond-mat.mtrl-sci↗

From Structural Stability to Electronic Flexibility: Unveiling Strain-induced Effects in a MoS$_2$/Perylene Orange Hybrid System

This study delves into the interaction between a monolayer of molybdenum disulfide (MoS$_2$) and a single Perylene Orange (PO) molecule, representative of inorganic and organic semiconductor materials, respectively. Investigation of the amalgamation of these materials under mechanical strains reveals significant alterations in the electronic properties of the MoS$_2$/PO interface. Tensile strain induces a reduction in the bandgap, while compressive strain initially engenders an increase, followed by a subsequent decrease. Notably, MoS$_2$ undergoes a transition from a direct to an indirect bandgap under both stretching and compression conditions. These alterations stem from shifts in the density of states and band structure adjustments resulting from lattice deformations induced by applied strain. Remarkably, under specific compression conditions, the MoS$_2$/PO system manifests a transition between type II and type I band alignments. The detailed analysis of a range of strain magnitudes yields profound insights into the behavior of MoS$_2$ and MoS$_2$/PO systems under mechanical strain, with potential implications for nano- and optoelectronics applications.

cond-mat.mtrl-sci↗