材料科学
发光
兴奋剂
能量转移
电子转移
电子
持续发光
竞赛(生物学)
分析化学(期刊)
化学物理
原子物理学
纳米技术
光化学
光电子学
核物理学
物理
环境化学
化学
生态学
热释光
生物
作者
Ying Lv,Chaofeng Li,Ning Zhao,Rujun Yang,Jiang Zhu,Yu Liu,Chunlai Huang,Shihai You,Jumpei Ueda
标识
DOI:10.1002/adfm.202511845
摘要
Abstract Exploring efficient strategies to enhance persistent luminescence (PersL) is highly demanded to facilitate advanced applications of inorganic PersL phosphors. In this work, a remarkable enhancement of Mn 2+ PersL in LiYGeO 4 (LYGO) with tunable wavelengths is achieved through Bi 3+ codoping. The Mn 2+ emission can be tuned from 600 to 664 nm by increasing the doping concentration, attributed to site‐selective occupation of different crystallographic sites. The pronounced enhancement in the PersL of Mn 2+ is achieved through the synergistic interplay of energy transfer from Bi 3+ to Mn 2+ and electron‐capture competition between the two hole‐trapped ions. Specifically, the PersL intensity of LYGO:0.5%Mn 2+ ,0.125%Bi 3+ at 30 s increased by 444 times compared to that of LYGO:0.5%Mn 2+ after 254 nm excitation. Thermoluminescence measurement reveals that introduction of Bi 3+ creates an additional trap center with depth of 0.60 eV. Moreover, LYGO:Mn 2+ ,Bi 3+ exhibits excellent water resistance and shows great potential for applications in information storage and X‐ray detection. This work not only demonstrates an intense red PersL phosphor, but also provides an efficient strategy to enhance PersL in inorganic materials via energy transfer and electron‐capture competition.
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