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Luminescence properties of Eu~(3+) doped CaMoO_4 nanoparticles

机译:Eu〜(3+)掺杂CaMoO_4纳米粒子的发光特性

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摘要

When Eu~(3+) ions occupy Ca~(2+) sites of CaMoO _4, which has a body centered tetragonal structure with inversion symmetry, only the magnetic dipole transition (~5D_0→ ~7F_1) should be allowed according to Judd-Ofelt theory. Even if there are a few distortions in the Eu~(3+) environment, its intensity should be more than that of the electric dipole transition (~5D_0→~7F_2). We report here the opposite effect experimentally and ascribe this to the polarizability effect of the MoO4 tetrahedron, which is neighboring to EuO_8 (symmetric environment). The contribution of the energy transfer process from the Mo-O charge transfer band to Eu~(3+) and the role of Eu~(3+) over the surface of the particle could be distinguished when luminescence decay processes were measured at two different excitations (250 and 398 nm). Further, the luminescence intensities and lifetimes increase significantly with increasing heat-treatment temperature of the doped samples. This is attributed to the reduction of H_2O from the surface of the particles and a non-radiative process after heat treatment.
机译:当Eu〜(3+)离子占据CaMoO _4的Ca〜(2+)位点时,CaMoO _4具有体心四方结构且具有反转对称性,根据Judd-,仅应允许磁偶极跃迁(〜5D_0→〜7F_1)。 Ofelt理论。即使在Eu〜(3+)环境中出现少量畸变,其强度也应大于电偶极跃迁的强度(〜5D_0→〜7F_2)。我们在这里通过实验报道了相反的效应,并将其归因于MoO4四面体的极化作用,该四面体与EuO_8(对称环境)相邻。当在两个不同的位置测量发光衰减过程时,可以区分出Mo-O电荷转移带对Eu〜(3+)的能量转移过程的贡献以及Eu〜(3+)在粒子表面上的作用。激发(250和398 nm)。此外,发光强度和寿命随着掺杂样品的热处理温度升高而显着增加。这归因于来自颗粒表面的H_2O的减少和热处理后的非辐射过程。

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