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  • 2020-2024  (3)
  • Chemistry/Pharmacy  (3)
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  • 2020-2024  (3)
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  • Chemistry/Pharmacy  (3)
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  • 1
    Online Resource
    Online Resource
    Wiley ; 2020
    In:  Journal of the American Ceramic Society Vol. 103, No. 2 ( 2020-02), p. 1174-1186
    In: Journal of the American Ceramic Society, Wiley, Vol. 103, No. 2 ( 2020-02), p. 1174-1186
    Abstract: Er 3+ ‐activated NaSrLa(MoO 4 )O 3 phosphors were synthesized by a traditional solid‐state reaction technique, which exhibited bright green emissions ascribing to the ( 2 H 11/2 , 4 S 3/2 ) →  4 I 15/2 transitions of Er 3+ ions under 377 nm excitation. The luminescence intensity increased with increasing the Er 3+ ion concentration and achieved its maximum value when the doping concentration was 4 mol%. Moreover, the critical distance was estimated to be 25.32 Å, and the dipole‐dipole interaction played a significant role in NR energy transfer between Er 3+ ions in NaSrLa(MoO 4 )O 3 host lattices. At a forward bias current of 100 mA, the Light Emitting Diode (LED) device emitted a bright green emission with the color coordinate of (0.2547, 0.5996) that can be observed by the naked eye. Besides, based on the thermally coupled levels of 2 H 11/2 and 4 S 3/2 , the temperature sensing performances of the prepared phosphors in the temperature range of 303‐483 K were studied using the fluorescence intensity ratio technique. The maximum sensor sensitivity was about 0.0150 K −1 when the temperature was 483 K, and the Er 3+ ion concentration largely influenced the sensor sensitivity of studied samples. Furthermore, the prepared phosphors exhibited excellent water resistance and thermal stability behavior. These characteristics demonstrated that the Er 3+ activated NaSrLa(MoO 4 )O 3 phosphors were dual‐functional materials for solid‐state illumination and non‐contact temperature measurement.
    Type of Medium: Online Resource
    ISSN: 0002-7820 , 1551-2916
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2008170-4
    detail.hit.zdb_id: 219232-9
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  • 2
    In: Journal of the American Ceramic Society, Wiley, Vol. 104, No. 10 ( 2021-10), p. 5086-5098
    Abstract: Ce 3+ /Tb 3+ co‐doped NaMgBO 3 phosphors were successfully synthesized by solid‐state method. Under 381 nm excitation, the cyan emission owing to the 5d → 4f of Ce 3+ ions and green emissions arising from the 5 D 4  →  7 F J (J = 6, 5, 4, and 3) transitions of Tb 3+ ions were seen in all the phosphors. Through theoretical analysis, one knows that the energy transfer from Ce 3+ to Tb 3+ ions with high efficiency of 83.74% was contributed by dipole–dipole transition. Furthermore, the internal quantum efficiency of NaMgBO 3 :0.01Ce 3+ ,0.03Tb 3+ phosphor was 54.28%. Compared with that of at 303 K, the emission intensity of the developed products at 423 K still kept 73%, revealing the splendid thermal stability of the studied phosphors. Through utilizing the resultant phosphors as cyan‐green components, the fabricated white‐LED device exhibited an excellent correlated color temperature of 2785 K, high color‐rendering index of 85.73, suitable luminance efficiency of 25.00 lm/W, and appropriate color coordinate of (0.4279, 0.3617). Aside from the superior photoluminescence, the synthesized phosphors also exhibited excellent cathode‐luminescence properties which were sensitive to the current and accelerating voltage. Furthermore, the NaMgBO 3 :0.01Ce 3+ ,0.03Tb 3+ phosphors with multi‐mode emissions were promising candidates for optical anti‐counterfeiting. All the results indicated that the Ce 3+ /Tb 3+ co‐doped NaMgBO 3 phosphors were potential multi‐platforms toward white‐LED, field emission displays, and optical anti‐counterfeiting applications.
    Type of Medium: Online Resource
    ISSN: 0002-7820 , 1551-2916
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2008170-4
    detail.hit.zdb_id: 219232-9
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  • 3
    In: Catalysis Today, Elsevier BV, Vol. 388-389 ( 2022-04), p. 323-328
    Type of Medium: Online Resource
    ISSN: 0920-5861
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2022
    detail.hit.zdb_id: 2012626-8
    detail.hit.zdb_id: 56797-8
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