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Synthesis and Luminescence Properties of Water Soluble α-NaGdF4/β-NaYF4:YbEr Core–Shell Nanoparticles

机译:水溶性α-NaGdF4/β-NaYF4:YbEr核壳纳米粒子的合成及发光性质

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摘要

Hexagonal phase (β) sodium rare earth tetrafluorides (NaREF4, RE = Y, Gd, Lu, et al.) are considered the ideal matrices for lanthanide (Ln) ions doped upconversion (UC) luminescence materials, because they can provide favorable crystal lattice structures for the doped luminescent Ln ions to make intensive emissions. However, the cubic phase (α) NaREF4 always preferentially forms at low reaction temperature in short time as it is dynamically stable. Therefore, it is hard to obtain small sized β-NaREF4 via the traditional solvothermal method. In this paper, small sized β-NaYF4:Yb,Er nanoparticles were synthesized by a heterogeneous-core-induced method via the solvothermal reaction. The heterogeneous α-NaGdF4/β-NaYF4: Yb, Er core–shell structure was confirmed by the local elemental mapping. The formation mechanism of β-NaYF4:Yb,Er shell on the surface of α-NaGdF4 core was explained in detail. We reasoned that a hetero interface with a lower lattice symmetric structure was produced by cation exchanges between the core and shell, which caused the preferential growth of anisotropic hexagonal phase shell. The existence of this hetero interface has also been proven by observation of Gd3+ UC emission.
机译:六方相(β)稀土四氟化钠(NaREF4,RE == Y,Gd,Lu等)被认为是镧系元素(Ln)离子掺杂上转换(UC)发光材料的理想基质,因为它们可以提供良好的晶格掺杂的发光Ln离子的结构,可产生高强度发射。但是,立方晶相(Na)NaREF4由于动态稳定,总是优先在短时间内在低反应温度下形成。因此,难以通过传统的溶剂热法获得小尺寸的β-NaREF4。本文通过溶剂热反应通过异质核诱导法合成了小尺寸的β-NaYF4:Yb,Er纳米粒子。 α-NaGdF4/β-NaYF4:Yb,Er核-壳结构的异质性通过局部元素映射得到证实。详细解释了α-NaGdF4核表面β-NaYF4:Yb,Er壳的形成机理。我们认为,核与壳之间的阳离子交换产生了具有较低晶格对称结构的异质界面,从而导致各向异性六角相壳的优先生长。观察到Gd 3 + UC的发射也证明了该异质界面的存在。

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