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首页> 外文期刊>Journal of Physics. Condensed Matter >Photoluminescence mechanism of self-activated titanate phosphors investigated by x-ray absorption spectroscopy under UV irradiation
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Photoluminescence mechanism of self-activated titanate phosphors investigated by x-ray absorption spectroscopy under UV irradiation

机译:紫外线辐射下X射线吸收光谱研究的自激钛酸磷光体的光致发光机理

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摘要

The electronic states of self-activated titanate phosphors (Ba2TiSi2O8, Sr2TiSi2O8, and Na2TiSiO5) were investigated by Ti K-edge x-ray absorption spectroscopy under ultraviolet (UV) irradiation in order to unveil the photoluminescence mechanism in the absence of particular atomic color centers. The overall spectral features of all samples were identical, main edges and large pre-edges corresponding to the Ti 4p and Ti 3d states, respectively. The pre-edge peak of Sr2TiSi2O8 shifted toward lower energy by 0.2 eV compared with the other two samples, corresponding to a red shift of the photoluminescence spectrum. In the region between these features, a small hump was observed for each sample, which gradually diminishes as a function of UV power. The hump can be attributed to the Ti 4p state based on the calculated electron density of states determined by multiple scattering theory, and this hump serves as a trap for UV-excited electrons.
机译:通过Ti K-Edge X射线吸收光谱法在紫外(UV)照射下研究了自激活钛酸磷光体(Ba2Tisi2O8,Sr2Tisi2O8和Na2TisiO5)的电子状态,以在不存在特定原子色中心的情况下揭示光致发光机制 。 所有样品的整体光谱特征是分别与TI 4P和TI 3D状态相同的,主边缘和大的预平面。 与其他两个样品相比,SR2TISI2O8的预先边缘峰值通过0.2eV移动到较低的能量,对应于光致发光光谱的红色偏移。 在这些特征之间的区域中,针对每个样品观察到小驼峰,这逐渐减小为UV功率的函数。 基于多个散射理论确定的所计算的电子密度,驼峰可以归因于TI 4P状态,并且该驼峰用作用于UV激发电子的陷阱。

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