Abstract
The integration of trivalent europium ion (Eu3+)-doped zinc molybdate (ZnMoO4) as red phosphors in next-generation solid-state lighting (SSL) is impeded by their extended electron lifetime and suboptimal thermal stability. To overcome these limitations, we propose a co-doping approach by incorporating Mn2+ and Eu3+ in ZnMoO4, aiming to improve thermal reversibility and reduce the lifetime of electron transitions. A series of Eu3+-doped ZnMoO4 and Mn2+/Eu3+-co-doped ZnMoO4 phosphor materials were synthesized via the conventional sol-gel method, and their photoluminescence properties were compared under high-temperature conditions. Experimental results indicate that the introduction of Mn2+ into Eu3+-doped ZnMoO4 leads to a decrease in quantum efficiency and electron lifetime, primarily attributed to defects within the crystal lattice and energy transfer from Eu3+ to Mn2+, resulting in enhanced non-radiative transitions. However, the addition of a small quantity of Mn2+ remarkably improves the thermal stability and reversibility of the phosphors. Consequently, this co-doping strategy presents a promising avenue for expanding the application possibilities of phosphor materials, particularly for high-power SSL applications subjected to elevated temperatures. Hence, Eu3+-only doped samples are well-suited for lighting applications due to their high IQE and excellent thermal stability. Conversely, Eu3+/Mn2+-co-doped samples show promise in applications that require a shorter electron lifetime and good reversibility.
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