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Tb3+ and Ce3+ as a functional couple for enhanced luminescence in YAG ceramics for X-ray imaging and high-power white LEDs and laser diodes

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F25%3A00641700" target="_blank" >RIV/68378271:_____/25:00641700 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://hdl.handle.net/11104/0372128" target="_blank" >https://hdl.handle.net/11104/0372128</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d5ma00464k" target="_blank" >10.1039/d5ma00464k</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Tb3+ and Ce3+ as a functional couple for enhanced luminescence in YAG ceramics for X-ray imaging and high-power white LEDs and laser diodes

  • Popis výsledku v původním jazyce

    The exposure of luminescent materials to X-ray radiation and high-power laser excitation results in significant heating, leading to thermal quenching and a corresponding reduction in phosphor efficiency. This study aimed to address this limitation by enhancing material efficiency while maintaining high thermal stability. YAG:Ce,Tb transparent ceramics were successfully fabricated via vacuum reactive sintering method, with moderate concentrations of Tb3+ ions (1, 5 and 10 at%) codopants. These ceramics exhibited a dense microstructure without micropores, achieving high transparency of 77–80% at 900 nm. The incorporation of Tb3+ ions, is evidenced by the systematic increase in lattice constants from 12.608 Å (YAG:Ce) to 12.615 Å (YAG:Ce,Tb10%) in accordance with Vegard's law. The phonon-assisted Ce3+ ↔ Tb3+ bidirectional resonance mechanism, which facilitated energy transfer between Ce3+ and Tb3+ ions, was observed. The optimal transfer rate was observed at approximately 480 K. Beyond this temperature, the rate progressively accelerated, leading to accelerated decay times. Notably, YAG:Ce,Tb10% ceramics demonstrated a two-fold increase in radioluminescence intensity compared to uncodoped YAG:Ce ceramics. This substantial improvement in luminescence performance highlights the potential of YAG:Ce,Tb ceramics as highly efficient phosphors for X-ray imaging applications, offering enhanced brightness and energy transfer efficiency under high-temperature operating conditions. The Tb3+ codoping also enhanced Ce3+ emission, allowing for tuning of the correlated color temperature to a maximum of 6013 K, while maintaining a stable color rendering index of 69–73 and luminous efficacy of ∼123 lm W−1. It was shown that the luminous efficacy was not a constant parameter, but depended on the excitation laser power, initially increasing with power up to 0.5 W and then saturating. These results establish YAG:Ce,Tb transparent ceramics as highly promising materials for white LEDs due to their good thermal stability, tunable optical properties, and enhanced luminescence performance.n

  • Název v anglickém jazyce

    Tb3+ and Ce3+ as a functional couple for enhanced luminescence in YAG ceramics for X-ray imaging and high-power white LEDs and laser diodes

  • Popis výsledku anglicky

    The exposure of luminescent materials to X-ray radiation and high-power laser excitation results in significant heating, leading to thermal quenching and a corresponding reduction in phosphor efficiency. This study aimed to address this limitation by enhancing material efficiency while maintaining high thermal stability. YAG:Ce,Tb transparent ceramics were successfully fabricated via vacuum reactive sintering method, with moderate concentrations of Tb3+ ions (1, 5 and 10 at%) codopants. These ceramics exhibited a dense microstructure without micropores, achieving high transparency of 77–80% at 900 nm. The incorporation of Tb3+ ions, is evidenced by the systematic increase in lattice constants from 12.608 Å (YAG:Ce) to 12.615 Å (YAG:Ce,Tb10%) in accordance with Vegard's law. The phonon-assisted Ce3+ ↔ Tb3+ bidirectional resonance mechanism, which facilitated energy transfer between Ce3+ and Tb3+ ions, was observed. The optimal transfer rate was observed at approximately 480 K. Beyond this temperature, the rate progressively accelerated, leading to accelerated decay times. Notably, YAG:Ce,Tb10% ceramics demonstrated a two-fold increase in radioluminescence intensity compared to uncodoped YAG:Ce ceramics. This substantial improvement in luminescence performance highlights the potential of YAG:Ce,Tb ceramics as highly efficient phosphors for X-ray imaging applications, offering enhanced brightness and energy transfer efficiency under high-temperature operating conditions. The Tb3+ codoping also enhanced Ce3+ emission, allowing for tuning of the correlated color temperature to a maximum of 6013 K, while maintaining a stable color rendering index of 69–73 and luminous efficacy of ∼123 lm W−1. It was shown that the luminous efficacy was not a constant parameter, but depended on the excitation laser power, initially increasing with power up to 0.5 W and then saturating. These results establish YAG:Ce,Tb transparent ceramics as highly promising materials for white LEDs due to their good thermal stability, tunable optical properties, and enhanced luminescence performance.n

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10306 - Optics (including laser optics and quantum optics)

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Materials Advances

  • ISSN

    2633-5409

  • e-ISSN

    2633-5409

  • Svazek periodika

    6

  • Číslo periodika v rámci svazku

    22

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    15

  • Strana od-do

    8464-8478

  • Kód UT WoS článku

    001593356700001

  • EID výsledku v databázi Scopus

    2-s2.0-105025966463