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Bernardo R. A. Neves

Publications and source records attributed to Bernardo R. A. Neves.

7 recordsLinked to original sources

Magnetic permeability and zone-folded phonons in layered NiPS$_3$

Nickel phosphorus trisulfide (NiPS$_3$) stands out as a Mott insulator exhibiting XY-type antiferromagnetic order. In this work, we investigate the electrodynamic response of single-crystalline NiPS$_3$ using Terahertz Time-Domain Spectroscopy (THz-TDS) as a function of temperature. In cases where the magnetic permeability cannot be approximated to unity, conventional THz transmission analysis is often restricted to the complex refractive index, hindering the distinction between magnetic and dielectric contributions. To overcome this limitation, we demonstrate an extraction methodology capable of decoupling the magnetic permeability from the electric permittivity. Assuming that the dielectric contribution remains invariant below the N'eel temperature (TN), we used data from the paramagnetic phase to isolate the intrinsic magnetic component at 13 K. The angular and thermal dependence of the spectra revealed a magnon mode near 1 THz (for 0$^\circ$ orientation) and, distinctively, a zone-folded phonon activated by symmetry breaking (at 90$^\circ$). The isolated magnetic permeability was successfully modeled using Drude-Lorentz oscillators, enabling the extraction of fundamental spin dynamics parameters in this material.

cond-mat.mtrl-sci↗

Resonance-Enhanced Four-Wave Mixing Imaging for Mapping Defect Regions in Vanadium-Doped WS2 Monolayers

Defect engineering is crucial for tuning 2D transition metal dichalcogenide properties for quantum and optoelectronic applications. While conventional photoluminescence (PL) and Raman spectroscopies are important characterization tools, their mapping in large area samples can be time-consuming and lacks direct sensitivity for comprehensive defect characterization. Here, we introduce resonance-enhanced four-wave mixing (FWM) imaging for precise imaging and characterization of vanadium-induced defect states in WS2 monolayers. Our multi-modal investigation, integrating hyperspectral PL, Raman, and supported by density functional calculations, reveals nanoscale doping inhomogeneities, their influence on excitonic and vibrational properties. We observe resonance-enhanced FWM signals correlating with vanadium-induced defect regions, evidencing their unique nonlinear optical response. This work establishes FWM as an essential platform for high-resolution, defect-sensitive imaging, advancing defect-engineered excitonic devices and enabling novel nonlinear quantum photonics.

cond-mat.mes-hall↗

Nano-Raman Spectroscopy Analysis of Nanoprotuberances in MoSe2

Contaminations in the formation of two-dimensional heterostructures can hinder or generate desired properties. Recent advancements have highlighted the potential of tip-enhanced Raman spectroscopy (TERS) for studying materials in the 2D semiconductor class. In this work, we investigate the influence of 50-200nm sized nanoprotuberances within a monolayer of MoSe$_2$ deposited on hBN using nano-Raman spectroscopy, establishing correlations between the presence of localized contaminations and the observed hyperspectral variations. A figure of merit is established for the identification of surface impurities, based on MoSe$_2$ peaks ratio. Notably, new spectral peaks were identified, which are associated with the presence of nanoprotuberances and may indicate contamination and oxidation.

physics.optics↗

Nano-optical investigation of grain boundaries, strain and edges in CVD grown MoS$_{2}$ monolayers

The role of defects in two-dimensional semiconductors and how they affect the intrinsic properties of these materials have been a wide researched topic over the past decades. Optical characterization such as photoluminescence and Raman spectroscopies are important tools to probe their physical properties and the impact of defects. However, conventional optical techniques present a spatial resolution limitation lying in a $μ$m-scale, which can be overcomed by the use of near-field optical measurements. Here, we use tip-enhanced photoluminescence and Raman spectroscopies to unveil nanoscale optical heterogeneities at grain boundaries, local strain fields and edges in grown MoS$_{2}$ monolayers. A noticeable enhancement of the exciton peak intensity corresponding to a trion emission quenching is observed at narrow regions down to 47 nm of width at grain boundaries related to doping effects. Besides, localized strain fields inside the sample lead to non-uniformities in the intensity and energy position of photoluminescence peaks. Finally, distinct samples present different nano-optical responses at their edges due to strain and passivation defects. The passivated defective edges show a photoluminescence intensity enhancement and energy blueshift as well as a frequency blueshift of the 2LA Raman mode. On the other hand, the strained edges display a photoluminescence energy redshift and frequency redshifts for E$_{2g}$ and 2LA Raman modes. Our work shows that different defect features can be only probed by using optical spectroscopies with a nanometric resolution, thus revealing hindered local impact of different nanoscale defects in two-dimensional materials.

cond-mat.mtrl-sci↗

Phyllosilicates as earth-abundant layered materials for electronics and optoelectronics: Prospects and challenges in their ultrathin limit

Phyllosilicate minerals are an emerging class of naturally occurring layered insulators with large bandgap energy that have gained attention from the scientific community. This class of lamellar materials has been recently explored at the ultrathin two-dimensional level due to their specific mechanical, electrical, magnetic, and optoelectronic properties, which are crucial for engineering novel devices (including heterostructures). Due to these properties, phyllosilicates minerals can be considered promising low-cost nanomaterials for future applications. In this Perspective article, we will present relevant features of these materials for their use in potential 2D-based electronic and optoelectronic applications, also discussing some of the major challenges in working with them.

physics.app-ph↗

Photoluminescence and charge transfer in the prototypical 2D/3D semiconductor heterostructure MoS$_2$/GaAs

The new generation of two-dimensional (2D) materials has shown a broad range of applications for optical and electronic devices. Understanding the properties of these materials when integrated with the more traditional three-dimensional (3D) semiconductors is an important challenge for the implementation of ultra-thin electronic devices. Recent observations have shown that by combining MoS$_2$ with GaAs it is possible to develop high quality photodetectors and solar cells. Here, we present a study of the effects of intrinsic GaAs, p-doped GaAs, and n-doped GaAs substrates on the photoluminescence of monolayer MoS$_2$. We observe a decrease of an order of magnitude in the emission intensity of MoS$_2$ in all MoS$_2$/GaAs heterojunctions, when compared to a control sample consisting of a MoS$_2$ monolayer isolated from GaAs by a few layers of hexagonal boron nitride. We also see a dependence of the trion to A-exciton emission ratio in the photoluminescence spectra on the type of substrate, a dependence that we relate to the static charge exchange between MoS$_2$ and the substrates when the junction is formed. Scanning Kelvin probe microscopy measurements of the heterojunctions suggest type-I band alignments, so that excitons generated on the MoS$_2$ monolayer will be transferred to the GaAs substrate. Our results shed light on the charge exchange leading to band offsets in 2D/3D heterojunctions which play a central role in the understanding and further improvement of electronic devices.

cond-mat.mes-hall↗

Center of mass acceleration in coupled nanowaveguides due to transverse optical beating force

Eigenmode optical forces arising in symmetrically coupled waveguides have opposite sign on opposite waveguides and thus can deform the waveguides by changing their relative separation, but cannot change any other degree of freedom on their own. It would be extremely desirable to have a way to act on the center of mass of such a system. In this work we show that it is possible to do so by injecting a superposition of eigenmodes that are degenerate in frequency and have opposite parity along the desired direction, resulting in beating forces that have the same sign on opposite waveguides and therefore act on the center of mass. We have used both the Maxwell Stress Tensor formalism and the induced dipole force equation to numerically calculate this transverse beating force and have found its magnitude to be comparable to the eigenmode forces. We also show that the longitudinal variation caused by the spatial beating pattern on the time-averaged quantities used in the calculations must be taken into account in order to properly employ the divergence theorem and obtain the correct magnitudes. We then propose a heuristic model that shows good quantitative agreement with the numerical results and may be used as a prototyping tool for accurate and fast computation without relying on expensive numerical computation.

physics.optics↗