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Ricardo Javier Peña Román

Publications and source records attributed to Ricardo Javier Peña Román.

5 recordsLinked to original sources

Nanoscale magnetometry of a synthetic three-dimensional spin texture

Multilayered synthetic antiferromagnets (SAFs) are artificial three-dimensional (3D) architectures engineered to create novel, complex, and stable spin textures. Non-invasive and quantitative nanoscale magnetic imaging of the two-dimensional stray field profile at the sample surface is essential for understanding the fundamental properties of the spin-structure and being able to tailor them to achieve new functionalities. However, the deterministic detection of spin textures and their quantitative characterization at the nanoscale remain challenging. Here, we use nitrogen-vacancy scanning probe microscopy (NV-SPM) under ambient conditions to perform the first quantitative vector-field magnetometry measurements in the multilayered SAF [(Co/Pt)$_5$/Co/Ru]$_3$/(Co/Pt)$_6$. We investigate nanoscale static and dynamic properties of antiferromagnetic domains with boundaries hosting ``one-dimensional'' ferromagnetic stripes with ~ 100 nm of width and periodic modulation of the magnetization. By employing NV-SPM measurements in different imaging modes and involving NV-probes with various crystallographic orientations, we demonstrated distinct fingerprints emerging from GHz-range spin noise and constant stray fields on the order of several mT. This provides quantitative insights into the structure of domains and domain walls, as well as, into magnetic noise associated with thermal spin-waves. Our work opens up new opportunities for quantitative vector-field magnetometry of modern magnetic materials with tailored 3D spin textures and stray field profiles, and potentially novel spin-wave dispersions--in a quantitative and non-invasive manner, with exceptional magnetic sensitivity and nanometer scale spatial resolution.

cond-mat.mes-hall↗

Sub-diffraction-resolved spatial distribution of emitting excitons in STM-induced luminescence of 2D semiconductors via Richardson-Lucy deconvolution

Using scanning tunneling microscopy-induced luminescence (STML), the optical properties of two-dimensional (2D) semiconductors may be investigated at the nanoscale. This is possible because the tunneling current under the tip is an extremely localized electrical excitation source. However, in most STML applications, the spatial distribution of the emission relative to the excitation point is unresolved. Yet this distribution contains key information about how the interaction of excitons with injected charge carriers affects the luminescence of these materials, and about exciton transport. Resolving this spatial distribution at the nanoscale is relevant both for a fundamental understanding of exciton physics and for device applications; yet it remains a significant challenge. In this work, we resolve the spatial distribution of the emission beyond the diffraction limit of light by deconvolving real-space optical microscopy images of the STML using an iterative algorithm, i.e., Richardson-Lucy (RL) deconvolution. To showcase this technique, we apply it to the STML of monolayer tungsten diselenide ($\mathrm{WSe_2}$) and tungsten disulfide ($\mathrm{WS_2}$). Thus, we highlight hitherto ignored or misunderstood aspects of STML on 2D semiconductors related to exciton and charge carrier transport, namely the dependence of the spatial distribution of emission on the tunnel current setpoint and the origin of the emission from hot spots located micrometers from the excitation source.

cond-mat.mes-hall↗

Design and implementation of a device based on an off-axis parabolic mirror to perform luminescence experiments in a scanning tunneling microscope

We present the design, implementation, and illustrative results of a light collection/injection strategy based on an off-axis parabolic mirror collector for a low-temperature Scanning Tunneling Microscope (STM). This device allows us to perform STM induced Light Emission (STM-LE) and Cathodoluminescence (STM-CL) experiments and in situ Photoluminescence (PL) and Raman spectroscopy as complementary techniques. Considering the Étendue conservation and using an off-axis parabolic mirror, it is possible to design a light collection and injection system that displays 72% of collection efficiency (considering the hemisphere above the sample surface) while maintaining high spectral resolution and minimizing signal loss. The performance of the STM is tested by atomically resolved images and scanning tunneling spectroscopy results on standard sample surfaces. The capabilities of our system are demonstrated by performing STM-LE on metallic surfaces and two-dimensional semiconducting samples, observing both plasmonic and excitonic emissions. In addition, we carried out in situ PL measurements on semiconducting monolayers and quantum dots and in situ Raman on graphite and hexagonal boron nitride (h-BN) samples. Additionally, STM-CL and PL were obtained on monolayer h-BN gathering luminescence spectra that are typically associated with intragap states related to carbon defects. The results show that the flexible and efficient light injection and collection device based on an off-axis parabolic mirror is a powerful tool to study several types of nanostructures with multiple spectroscopic techniques in correlation with their morphology at the atomic scale and electronic structure.

physics.ins-det↗

Tunneling-current-induced local excitonic luminescence in p-doped WSe$_2$ monolayers

We have studied the excitonic properties of exfoliated tungsten diselenide (WSe$_2$) monolayers transferred to gold substrates using the tunneling current in a Scanning Tunneling Microscope (STM) operated in air to excite the light emission locally. In obtained spectra, emission energies are independent of the applied bias voltage and resemble photoluminescence (PL) results, indicating that, in both cases, the light emission is due to neutral and charged exciton recombination. Interestingly, the electron injection rate, that is, the tunneling current, can be used to control the ratio of charged to neutral exciton emission. The obtained quantum yield in the transition metal dichalcogenide (TMD) is $~5x10^{-7}$ photons per electron. The proposed excitation mechanism is the direct injection of carriers into the conduction band. The monolayer WSe$_2$ presents bright and dark defects spotted by STM images performed under UHV. STS confirms the sample as p-doped, possibly as a net result of the observed defects. The presence of an interfacial water layer decouples the monolayer from the gold support and allows excitonic emission from the WSe$_2$ monolayer. The creation of a water layer is an inherent feature of the sample transferring process due to the ubiquitous air moisture. Consequently, vacuum thermal annealing, which removes the water layer, quenches excitonic luminescence from the TMD. The tunneling current can locally displace water molecules leading to excitonic emission quenching and to plasmonic emission due to the gold substrate. The present findings extend the use and the understanding of STM induced light emission (STM-LE) on semiconducting TMDs to probe exciton emission and dynamics with high spatial resolution.

physics.optics↗

Band gap measurements of monolayer h-BN and insights into carbon-related point defects

Being a flexible wide band gap semiconductor, hexagonal boron nitride (h-BN) has great potential for technological applications like efficient deep ultraviolet light sources, building block for two-dimensional heterostructures and room temperature single photon emitters in the ultraviolet and visible spectral range. To enable such applications, it is mandatory to reach a better understanding of the electronic and optical properties of h-BN and the impact of various structural defects. Despite the large efforts in the last years, aspects such as the electronic band gap value, the exciton binding energy and the effect of point defects remained elusive, particularly when considering a single monolayer. Here, we directly measured the density of states of a single monolayer of h-BN epitaxially grown on highly oriented pyrolytic graphite, by performing low temperature scanning tunneling microscopy (STM) and spectroscopy (STS). The observed h-BN electronic band gap on defect-free regions is $(6.8\pm0.2)$ eV. Using optical spectroscopy to obtain the h-BN optical band gap, the exciton binding energy is determined as being of $(0.7\pm0.2)$ eV. In addition, the locally excited cathodoluminescence and photoluminescence show complex spectra that are typically associated to intragap states related to carbon defects. Moreover, in some regions of the monolayer h-BN we identify, using STM, point defects which have intragap electronic levels around 2.0 eV below the Fermi level.

cond-mat.mes-hall↗