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Träfflista för sökning "WFRF:(Rafie Zinedine Safi) "

Search: WFRF:(Rafie Zinedine Safi)

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1.
  • Alqedra, Mohammed K., et al. (author)
  • Optical coherence properties of Kramers' rare-earth ions at the nanoscale for quantum applications
  • 2023
  • In: Physical Review B. - 2469-9950. ; 108:7
  • Journal article (peer-reviewed)abstract
    • Rare Earth (RE) ion doped nanomaterials are promising candidates for a range of quantum technology applications. Among RE ions, the so-called Kramers' ions possess spin transitions in the GHz range at low magnetic fields, which allows for high-bandwidth multimode quantum storage, fast qubit operations as well as interfacing with superconducting circuits. They also present relevant optical transitions in the infrared. In particular, Er3+ has an optical transition in the telecom band, while Nd3+ presents a high-emission-rate transition close to 890 nm. In this paper, we measure spectroscopic properties that are of relevance to using these materials in quantum technology applications. We find the inhomogeneous linewidth to be 10.7 GHz for Er3+ and 8.2 GHz for Nd3+, and the excited state lifetime T1 to be 13.68 ms for Er3+ and 540μs for Nd3+. We study the dependence of homogeneous linewidth on temperature for both samples, with the narrowest linewidth being 379 kHz (T2=839 ns) for Er3+ measured at 3 K, and 62 kHz (T2=5.14μs) for Nd3+ measured at 1.6 K. Further, we investigate time-dependent homogeneous linewidth broadening due to spectral diffusion and the dependence of the homogeneous linewidth on magnetic field to get additional clarity of mechanisms that can influence the coherence time. In light of our results, we discuss two applications: single qubit-state readout and a Fourier-limited single photon source.
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2.
  • Shi, Juanzi, et al. (author)
  • Photoluminescence Polarization of MAPbBr3 Perovskite Nanostructures. Can the Dielectric Contrast Effect Explain It?
  • 2022
  • In: ACS Photonics. - : American Chemical Society (ACS). - 2330-4022. ; 9:12, s. 3888-3898
  • Journal article (peer-reviewed)abstract
    • The dielectric contrast effect is usually evoked to explain anisotropy of optical properties of elongated nanoobjects, for example, semiconductor nanowires. We applied two-dimensional polarization imaging microscopy to measure the polarization of photoluminescence (PL) excitation and PL intensity of nanoaggregates of in-situ formed MAPbBr3perovskite nanoparticles in a stretched polymeric matrix. Scanning electron microscopy images of these objects were also acquired to characterize their sizes and shapes. We find that individual perovskite aggregates with sizes of 100-300 nm often possess a PL excitation polarization degree as high as 0.5-0.9, which is up to three times higher than the polarization degree of absorption predicted by the dielectric contrast effect. Small aggregates of nanoparticles possess an emission polarization degree substantially higher than that of excitation. Computer simulations of many possible scenarios show that the dielectric contrast alone cannot quantitatively explain the polarization properties of the studied objects. We propose energy transfer to localized emitting sites and the dependence of PL yield on excitation power density as possible factors strongly influencing the polarization properties of PL emission and PL excitation, respectively.
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