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Pedro L. Gastelois

Publications and source records attributed to Pedro L. Gastelois.

2 recordsLinked to original sources

Strong magneto-optical responses of an ensemble of defect-bound excitons in ambient exposed WS$_{2}$ and WSe$_{2}$ monolayers

Transition metal dichalcogenide (TMD) monolayers present a singular coupling in their spin and valley degrees of freedom. Moreover, by applying an external magnetic field it is possible to break the energy degeneracy between their K and $-$K valleys. This valley Zeeman effect opens the possibility of controlling and distinguishing the spin and valley characters of charge carriers in TMDs by their optical transition energies, making these materials promising for the next generation of spintronic and photonic devices. However, the free excitons of pristine TMD monolayers present a moderate valley Zeeman splitting of $\approx 0.23$ meV/T. Therefore, alternative excitonic states with higher magnetic responses are mandatory for application purposes. Here, we investigate the magneto-optical properties of ambient exposed WS$_2$ and WSe$_2$ monolayers by circularly polarized magneto-photoluminescence experiments at cryogenic temperatures. A broad lower energy photoluminescence emission related to an ensemble of defects is observed, presenting remarkable valley-related splittings of $\approx 1.45$ meV/T and $\approx 1.11$ meV/T for WS$_2$ and WSe$_2$ monolayers, respectively. In addition, we report a significant valley polarization of charge carriers in the defect mid-gap states induced by the external magnetic field. We explain this valley-polarized population and enhanced valley-related splitting in terms of imbalanced intervalley relaxations, leading to a magnetic field-dependent distribution of charge carriers in multiple defect levels. This effect, together with the individual Zeeman shiftings of the mid-gap states, explains the strong magneto-optical responses observed. Our work uncovers the singular potential of manipulating the light emission of ambient exposed TMD monolayers by an external magnetic field.

cond-mat.mes-hall↗

Structural, morphological, and magnetic characterizations of (Fe0.25Mn0.75)2O3 nanocrystals: a comprehensive stoichiometric determination

Iron manganese trioxide (Fe0.25Mn0.75)2O3 nanocrystals were synthesized by the sol-gel method. The 80 K Mossbauer spectrum was well-fitted using two doublets representing the 8b and 24d crystallographic sites of the (FexMn1-x)2O3 phase and two weak extra sextets which were attributed to crystalline and amorphous hematite. Our findings showed formation of a bixbyite primary phase. The Raman spectrum exhibits six Raman active modes, typical of (Fe,Mn)2O3, and two extra Raman modes associated with the secondary hematite phase. X-ray photoelectron spectroscopy analysis confirmed the presence of oxygen vacancy onto the (FexMn1-x)2O3 particle surface, with varying oxidation states. X-band magnetic resonance data revealed a single broad resonance line in the whole temperature range (3.8 K - 300 K). The temperature dependence of both resonance field and resonance linewidth shows a remarkable change in the range of 40 - 50 K, herein credited to surface spin glass behavior. The model picture used assumes (FexMn1-x)2O3 nanoparticles with a core-shell structure. Results indicate that below about 50 K the spin system of shell reveals a paramagnetic to spin glass-like transition upon cooling, with a critical temperature estimated at 43 K. In the higher temperature range, the superparamagnetic hematite (secondary) phase contributes remarkably to the temperature dependence of the resonance linewidth. Zero-field-cooled (ZFC) and fieldcooled (FC) data show strong irreversibility and a peak in the ZFC curve at 33 K, attributed to a paramagnetic-ferrimagnetic transition of the main phase. Hysteresis curve at 5 K shows a low coercive field of 4 kOe, with the magnetization not reaching saturation at 70 kOe, suggesting the occurrence of a ferrimagnetic core with a magnetic disorder at surface, characteristic of core-shell spin-glass-like behavior.

cond-mat.mtrl-sci↗