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In situ co-precipitation synthesis and photoluminescence of Y_xGd_(1-x)VO_4: Tm~(3+) microcrystalline phosphors by hybrid precursors

机译:杂化前驱体原位共沉淀合成Y_xGd_(1-x)VO_4:Tm〜(3+)微晶荧光粉

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摘要

Y_xGd_(1-x)VO_4: Tm~(3+) (5 mol%) phosphors were prepared by in situ co-precipitation technology with the different content ratio of Y/Gd (x = 0.2,0.3,0.4,0.5,0.6,0.8, respectively). During the process, rare earth coordination polymers with o-hydroxylbenzoate were used as precursors, composing with polyethylene glycol (PEG) as dispersing media. After heat-treatment of the resulting multicomponent hybrid precursors at 900 ℃, the samples were obtained. SEM indicated the particles present good crystalline state, whose crystalline grain sizes were about 0.2-2 μm. Under the excitation of 257 nm, all the materials show the characteristic emission of Tm~(3+) which is the strong blue emission centered at 475 nm originating from ~1G_4 → ~3H_6 of Tm~(3+). Besides this, concentration quenching appears in the system of YVO_4: Tm~(3+) and GdVO_4: Tm~(3+). And when x reaches 0.5, the system of Y_xGd_(1-x)VO_4: Tm~(3+) shows the strongest blue emission.
机译:Y_xGd_(1-x)VO_4:采用原位共沉淀技术制备了具有不同含量的Y / Gd(x = 0.2,0.3,0.4,0.5,0.6)的Tm〜(3+)(5 mol%)荧光粉,分别为0.8)。在此过程中,将具有邻羟基苯甲酸酯的稀土配位聚合物用作前体,并与聚乙二醇(PEG)组成分散介质。在900℃下对所得的多组分杂化前体进行热处理后,获得了样品。 SEM表明颗粒呈现良好的晶态,其晶粒尺寸为约0.2-2μm。在257nm的激发下,所有材料均表现出Tm〜(3+)的特征发射,这是强的蓝色发射,中心在475nm,起源于Tm〜(3+)的〜1G_4→〜3H_6。除此之外,浓度猝灭出现在YVO_4:Tm〜(3+)和GdVO_4:Tm〜(3+)的体系中。当x达到0.5时,Y_xGd_(1-x)VO_4:Tm〜(3+)的系统显示出最强的蓝色发射。

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