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Robin Salvatore

Publications and source records attributed to Robin Salvatore.

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Doping-controlled topological superconducting transition in misfit layer compounds

Achieving topological superconductivity is a key goal in quantum physics, offering a path to fault-tolerant quantum computers. A central challenge in this field is to continuously drive a material through a topological quantum phase transition to directly observe the evolution from trivial to topological superconductivity. However, finding a robust platform that allows such extreme and precise tuning remains a challenge. Here, we demonstrate a doping-controlled phase transition from a conventional to a topological superconducting state in the bulk misfit layer compound (LaxPb1-xSe)1.14(NbSe2)2. We reveal a non-monotonic phase diagram characterized by two distinct superconducting regimes separated by a non-superconducting phase at a precise doping. In the highly doped regime, the superconducting phase becomes remarkably sensitive to non-magnetic disorder, and orientation-selective in-gap modes emerge at atomic step edges. Supported by Bogoliubov-de Gennes calculations, these emergent spatial signatures are consistent with a time-reversal-symmetric crystalline-topological order parameter. Our results establish misfit compounds as a platform to engineering topological superconductivity.

cond-mat.supr-con

Doping tunable charge density waves in misfit layer compounds

The ability to tune charge density waves (CDWs) through external control knobs, such as doping, pressure or strain is crucial for exploring the phase diagram of two dimensional (2D) or quasi-2D materials. Yet, controlling CDWs critical temperature and ordering vector remains a challenge for current experimental techniques. In this work, we establish misfit layer compound heterostructures as a reliable platform to manipulate CDWs in transition metal dichalcogenides. By combining ab initio calculations with low-temperature scanning tunneling microscopy, we show how to achieve doping tunable control over NbSe2 CDW by chemically alloying in the rocksalt subunit. Crucially, we prove that tuning the La Pb ratio in the misfit family (LaxPb1xSe)1.14(NbSe2)2 enables stabilization of different CDW orders, such as 2x2 or 3x3 patterns, and even coexisting phases. This work paves the way for engineering transition metal dichalcogenides with tailored charge density waves within misfit heterostructures.

cond-mat.mtrl-sci

Tuning the Charge Transfer of Transition Metal Dichalcogenides via Misfit Layer Compounds

Misfit layer compounds (MLCs) are a versatile platform for exploring the electronic phase diagram of two dimensional (2D) materials beyond the limits of conventional gating techniques. This work demonstrates the precise tunability of electron doping in NbSe2 monolayers through chemical alloying within the rocksalt layer of (LaxPb1xSe)1.14(NbSe2)2 heterostructures. By combining first principles density functional theory (DFT) calculations with angle resolved photoemission spectroscopy (ARPES), we prove that the rocksalt unit acts as an universal electron donor. We show that varying the La Pb ratio results in a rigid Fermi level shift, still preserving the NbSe2 electronic structure. Crucially, photon energy dependent ARPES confirms that the NbSe2 layers nearly maintain their intrinsic 2D character and orbital identity within the three dimensional misfit. This study establishes MLCs as a reliable platform for engineering emergent states in 2D transition metal dichalcogenides through precise stoichiometric control.

cond-mat.mtrl-sci

Near complete laser-induced modulation of the ferromagnetic-antiferromagnetic phase fraction in FeRh films

With its huge entropy change and a strong interplay between magnetic order, structural and electrical properties, the first-order antiferromagnetic/ferromagnetic phase transition is a paradigmatic example of the multicaloric effect. The unraveling of the physics underlying the phase transition needs a better understanding of the thermal hysteresis of FeRh within the AF-FM phase coexistence region. In this work, we compare the effect of two very different types of thermal cycling on the hysteresis of the magnetic order: quasi-static heating, and cooling of the entire 195 nm thick film, and a f =100 kHz modulated heating driven by a laser focused down to a spot of about ten microns squared at the film surface. Taking advantage of the reflectivity difference between both phases to probe optically their respective fraction, we show that whereas only temperature-driven reflectivity variations ($dR/dT$, thermoreflectance) are detected in the pure phases, a huge modulation of the phase-dependent reflectance at the driving frequency $f$ is detected in the phase coexistence temperature range. This is quantitatively described as resulting from a substantial modulation of the FM fraction (up to 90% with increasing laser power. A simplified rate-independent hysteresis model with return-point-memory (RPM), represented in terms of bistable units that undergo a temperature excursion corresponding to a given laser power, reproduces very well the optically measured FM phase modulation characteristics for a broad range of temperature excursions. This offers an insight into the leading role of quenched disorder in defining thermal hysteresis in FeRh under high excitation frequency, when the material is periodically driven out-of-equilibrium.

cond-mat.mtrl-sci