材料科学
尖晶石
发光
俘获
兴奋剂
化学物理
纳米技术
光电子学
冶金
化学
生态学
生物
作者
Zhihao Zhou,Shuai Zhang,Yakun Le,Hong Ming,Yang Li,Shi Ye,Mingying Peng,Jianrong Qiu,Guoping Dong
标识
DOI:10.1002/adom.202101669
摘要
Abstract Spinel configuration is a kind of broadly considered host candidate when designing persistent luminescence (PersL) materials due to the easy generation of vacancies and anti‐site defects. Here, a new strategy of defect enrichment for the activation of PersL is proposed, and in contrast to the spinel configuration, it is demonstrated that the crystal structure of near inverse spinel ensures more numerous defects to activate the near‐infrared (NIR) PersL of Fe 3+ . Fe 3+ ‐doped MgGa 2 O 4 displays the PersL band in the range of 600 to 900 nm and possesses a super‐long PersL duration time >15 h. The optical analysis and the calculation of density functional theory unravel that the near inverse spinel structure can lower the carrier transfer barriers to accelerate the formation of carrier trap states within the bandgap. Therefore, more numerous defects in this structure may participate in the trapping and de‐trapping process by comparison with the normal spinel configuration. These findings are expected to accelerate the development of new PersL materials through Fe 3+ doping toward versatile biological applications in NIR window.
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