2 research outputs found

    Effect of the Thermal Conductivity on Resistive Switching in GeTe and Ge<sub>2</sub>Sb<sub>2</sub>Te<sub>5</sub> Nanowires

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    The thermal conduction characteristics of GeTe and Ge<sub>2</sub>Sb<sub>2</sub>Te<sub>5</sub>(GST) nanowires were investigated using an optical method to determine the local temperature by Raman spectroscopy. Since the localization of surface charge in a single-crystalline nanostructure can enhance charge-phonon scattering, the thermal conductivity value (κ) of single crystalline GeTe and GST nanowires was decreased significantly to 1.44 Wm<sup>–1</sup> K<sup>–1</sup> for GeTe and 1.13 Wm<sup>–1</sup> K<sup>–1</sup> for GST, compared to reported values for polycrystalline structures. The SET-to-RESET state in single-crystalline GeTe and GST nanowires are characteristic of a memory device. Unlike previous reports using GeTe and GST nanowires, the SET-to-RESET characteristics showed a bipolar switching shape and no unipolar switching. In addition, after multiple cycles of operation, a significant change in morphology and composition was observed without any structural phase transition, indicating that atoms migrate toward the cathode or anode, depending on their electronegativities. This change caused by a field effect indicates that the structural phase transition does not occur in the case of GeTe and GST nanowires with a significantly lowered thermal conductivity and stable crystalline structure. Finally, the formation of voids and hillocks as the result of the electromigration critically degrades device reliability

    Characterization of Rotational Stacking Layers in Large-Area MoSe<sub>2</sub> Film Grown by Molecular Beam Epitaxy and Interaction with Photon

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    Transition metal dichalcogenides (TMDCs) are promising next-generation materials for optoelectronic devices because, at subnanometer thicknesses, they have a transparency, flexibility, and band gap in the near-infrared to visible light range. In this study, we examined continuous, large-area MoSe<sub>2</sub> film, grown by molecular beam epitaxy on an amorphous SiO<sub>2</sub>/Si substrate, which facilitated direct device fabrication without exfoliation. Spectroscopic measurements were implemented to verify the formation of a homogeneous MoSe<sub>2</sub> film by performing mapping on the micrometer scale and measurements at multiple positions. The crystalline structure of the film showed hexagonal (2H) rotationally stacked layers. The local strain at the grain boundaries was mapped using a geometric phase analysis, which showed a higher strain for a 30° twist angle compared to a 13° angle. Furthermore, the photon–matter interaction for the rotational stacking structures was investigated as a function of the number of layers using spectroscopic ellipsometry. The optical band gap for the grown MoSe<sub>2</sub> was in the near-infrared range, 1.24–1.39 eV. As the film thickness increased, the band gap energy decreased. The atomically controlled thin MoSe<sub>2</sub> showed promise for application to nanoelectronics, photodetectors, light emitting diodes, and valleytronics
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