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Photoionization Cross‐Section in Tetrapod Quantum Dots: Impact of Pressure, Temperature, and Polarization Direction

A. Ed‐DahmounyScience and Engineering Research Laboratory (LaRSI) Faculty of Sciences and Technology Sidi Mohamed Ben Abdellah University Fez 2202 MoroccoHind AlthibDepartment of Physics College of Science Imam Abdulrahman Bin Faisal University P.O. Box 1982 Dammam 31441 Saudi ArabiaAli H. AlkhaldiDepartment of Physics College of Science Imam Abdulrahman Bin Faisal University P.O. Box 1982 Dammam 31441 Saudi ArabiaAbderrahman El KharrimEnergy, Materials, and Computing Physics Research team Abdelmalek Essaadi University Ecole Normale Supérieure (ENS) Martil 93150 MoroccoM. JaouaneLPS Laboratory Department of Physics Faculty of Science Dhar El Mahraz Sidi Mohamed Ben Abdellah University Fez 1796 MoroccoR. ArraouiLPS Laboratory Department of Physics Faculty of Science Dhar El Mahraz Sidi Mohamed Ben Abdellah University Fez 1796 MoroccoA. FakkahiLPS Laboratory Department of Physics Faculty of Science Dhar El Mahraz Sidi Mohamed Ben Abdellah University Fez 1796 MoroccoN. ZeiriCondensed Matter and Nanosciences Laboratory Department of Physics Faculty of Sciences of Monastir Monastir 5019 TunisiaA. SaliLPS Laboratory Department of Physics Faculty of Science Dhar El Mahraz Sidi Mohamed Ben Abdellah University Fez 1796 MoroccoC.A. DuqueGMC‐UdeA Instituto de Física Facultad de Ciencias Exactas y Naturales Universidad de Antioquia UdeA Medellín Calle 70 No. 52‐21 Colombia
2025en
ABI

Аннотация

Abstract This study investigates the photoionization cross‐section (PCS) in GaAs‐Ga 0.7 Al 0.3 As core–shell tetrapod quantum dot (CSTQD), elucidating its dependence on temperature, hydrostatic pressure, and polarization direction of incoming light. The intrinsic asymmetry of these nanostructures breaks rotational symmetry, rendering polarization dependence a critical parameter. Utilizing a theoretical framework rooted in the effective mass approximation (EMA) and numerical simulations performed with the finite element method (FEM), the electronic states are rigorously analyzed. The analysis extends to their influence on the binding energies (BEs) of the ground and first excited states, alongside the spatial distribution of electron probability densities within the nanostructure. Subsequently, the PCS variation across a range of pressures, temperatures, polarization directions, and impurity positions is systematically examined. The findings reveal that elevated temperature and pressure profoundly impact both the energy levels and the PCS for the two transitions under investigation. Specifically, the PCS undergoes a discernible blue shift (toward higher energies) with increasing pressure. Crucially, the PCS exhibits pronounced anisotropy concerning the polarization angle. This directional sensitivity underscores promising applications in polarization‐selective optoelectronic devices and provides fundamental insights for the precise tuning of quantum dot‐based photodetectors and sensors.

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