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Inverse-Tunable Red Luminescence and Electronic Properties of Nitridoberylloaluminates Sr_2-x Ba_x [BeAl₃ N₅ ]:Eu²⁺ (x=0-2).

ABSTRACT: The nitridoberylloaluminate Ba₂ [BeAl₃ N₅ ]:Eu²⁺ and solid solutions Sr_2-x Ba_x [BeAl₃ N₅ ]:Eu²⁺ (x=0.5, 1.0, 1.5) were synthesized in a hot isostatic press (HIP) under 50 MPa N₂ atmosphere at 1200 °C. Ba₂ [BeAl₃ N₅ ]:Eu²⁺ crystallizes in triclinic space group P1‾ (no. 2) (Z=2, a=6.1869(10), b=7.1736(13), c=8.0391(14) Å, α=102.754(8), β=112.032(6), γ=104.765(7)°), which was determined from single-crystal X-ray diffraction data. The lattice parameters of the solid solution series have been obtained from Rietveld refinements and show a nearly linear dependence on the atomic ratio Sr : Ba. The electronic properties and the band gaps of M₂ [BeAl₃ N₅ ] (M=Sr, Ba) have been investigated by a combination of soft X-ray spectroscopy and density functional theory (DFT) calculations. Upon irradiation with blue light (440-450 nm), the nitridoberylloaluminates exhibit intense orange to red luminescence, which can be tuned between 610 and 656 nm (fwhm=1922-2025 cm^-1 (72-87 nm)). In contrast to the usual trend, the substitution of the smaller Sr²⁺ by larger Ba²⁺ leads to an inverse-tunable luminescence to higher wavelengths. Low-temperature luminescence measurements have been performed to exclude anomalous emission.

SUBMITTER: Elzer E

PROVIDER: S-EPMC9303288 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Eu3+-activated Ba2Y5B5O17 (Ba2Y5-x Eu x B5O17; x = 0.1-1) red-emitting phosphors were synthesized by the conventional high temperature solid-state reaction method in an air atmosphere. Powder X-ray diffraction (XRD) analysis confirmed the pure phase formation of the as-synthesized phosphors. Morphological studies were performed using field emission-scanning electron microscopy (FE-SEM). The photoluminescence spectra, lifetimes, color coordinates and internal quantum efficiency (IQE) as well as the temperature-dependent emission spectra were investigated systematically. Upon 396 nm excitation, Ba2Y5-x Eu x B5O17 showed red emission peaking at 616 nm which was attributed to the 5D0 → 7F2 electric dipole transition of Eu3+ ions. Meanwhile, the influences of different concentrations of Eu3+ ions on the PL intensity were also discussed. The optimum concentration of Eu3+ ions in the Ba2Y5-x Eu x B5O17 phosphors was found to be x = 0.8. The concentration quenching mechanism was attributed to the dipole-dipole interaction and the critical distance (R c) for energy transfer among Eu3+ ions was determined to be 5.64 Å. The asymmetry ratio [(5D0 → 7F2)/(5D0 → 7F1)] of Ba2Y4.2Eu0.8B5O17 phosphors was calculated to be 3.82. The fluorescence decay lifetimes were also determined for Ba2Y5-x Eu x B5O17 phosphors. In addition, the CIE color coordinates of the Ba2Y4.2Eu0.8B5O17 phosphors (x = 0.653, y = 0.345) were found to be very close to the National Television System Committee (NTSC) standard values (x = 0.670, y = 0.330) of red emission and also showed high color purity (∼94.3%). The corresponding internal quantum efficiency of the Ba2Y4.2Eu0.8B5O17 sample was measured to be 47.2%. Furthermore, the as-synthesized phosphors exhibited good thermal stability with an activation energy of 0.282 eV. The above results revealed that the red emitting Ba2Y4.2Eu0.8B5O17 phosphors could be potential candidates for application in near-UV excited white light emitting diodes.

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Inverse-Tunable Red Luminescence and Electronic Properties of Nitridoberylloaluminates Sr_2-x Ba_x [BeAl₃ N₅ ]:Eu²⁺ (x=0-2).

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Inverse-Tunable Red Luminescence and Electronic Properties of Nitridoberylloaluminates Sr2-x Bax [BeAl3 N5 ]:Eu2+ (x=0-2).

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Inverse-Tunable Red Luminescence and Electronic Properties of Nitridoberylloaluminates Sr_2-x Ba_x [BeAl₃ N₅ ]:Eu²⁺ (x=0-2).