首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Novel heterometal-organic complexes as first single source precursors for up-converting NaY(Ln)F _4 (Ln = Yb, Er, Tm) nanomaterials
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Novel heterometal-organic complexes as first single source precursors for up-converting NaY(Ln)F _4 (Ln = Yb, Er, Tm) nanomaterials

机译:新型杂金属-有机配合物作为上转换NaY(Ln)F _4(Ln = Yb,Er,Tm)纳米材料的第一个单一来源前体

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摘要

First heterometal-organic single source precursors for NaYF _4 nanomaterials as a host matrix for up-conversion emission are reported. These novel heterobimetallic derivatives NaY(TFA) _4(diglyme) (1), [Na(triglyme) _2][Y _2(TFA) _7(THF) _2] (2) and Na _2Y(TFA) _5(tetraglyme) (3) (TFA = trifluoroacetate), which were fully characterized by elemental analysis, FT-IR and ~1H NMR spectroscopy, TG-DTA data as well as single crystal X-ray structures, are advantageous in terms of being anhydrous and having lower decomposition temperatures in comparison to the homometallic precursor Y(TFA) _3(H _2O) _3. In addition, they also contain chelating glyme ligands, which act as capping reagents during decomposition to control the NaYF _4 particle size and render them monodisperse in organic solvents. On decomposition in 1-octadecene, the molecular derivatives 1 and 3 are converted, in the absence of any surfactant or capping reagent, to cubic NaYF _4 nanocrystals at significantly lower temperatures (below 250 °C). At higher temperature, a mixture of the cubic and hexagonal phases was obtained, the relative ratio of the two phases depending on the reaction temperature. A pure hexagonal phase, which is many folds more efficient for UC emission than the cubic phase, was obtained by calcining nanocrystals of mixed phase at 400°C. In order to co-dope this host matrix with up-converting lanthanide cations, analogous complexes NaLn(TFA) _4(diglyme) [Ln = Er (4), Tm (5), Yb (6)] and Na _2Ln(TFA) _5(tetraglyme) [Ln = Er (7), Yb (8)] were also prepared and characterized. The decomposition in 1-octadecene of suitable combinations and appropriate molar ratios of these yttrium, ytterbium and erbium/thulium derivatives gave cubic and/or hexagonal NaYF _4: Yb ~(3+), Er ~(3+)/Tm ~(3+) nanocrystals (NCs) capped by diglyme or tetraglyme ligands, which were characterized by IR, TG-DTA data, EDX analysis and TEM studies. Surface modification of these NCs by ligand exchange reactions with poly acrylic acid (PAA) and polyethyleneglycol (PEG) diacid 600 was also carried out to render them water soluble. The THF solutions of suitable combinations of the diglyme derivatives were also used to elaborate the thin films of NaYF _4:Yb ~(3+), Er ~(3+)/Tm ~(3+) on a glass or Si wafer substrate by spin coating. The multicolour up-conversion fluorescence was successfully realized in the Yb ~(3+)/Er ~(3+) (green/red) and Yb ~(3+)/Tm ~(3+) (blue/violet) co-doped NaYF _4 nanoparticles and thin films, which demonstrates that they are promising UC nanophosphors of immense practical interest. The up-conversion excitation pathways for the Er ~(3+)/Yb ~(3+) and Tm ~(3+)/Yb ~(3+) co-doped materials are discussed.
机译:报告了NaYF _4纳米材料的第一个杂金属-有机单源前驱体,作为上转换发射的基质。这些新型的异双金属衍生物NaY(TFA)_4(diglyme)(1),[Na(triglyme)_2] [Y _2(TFA)_7(THF)_2](2)和Na _2Y(TFA)_5(tetraglyme)(3) )(TFA =三氟乙酸盐),通过元素分析,FT-IR和〜1H NMR光谱,TG-DTA数据以及单晶X射线结构进行了充分表征,在无水且分解温度较低方面具有优势与同金属前体Y(TFA)_3(H _2O)_3相比。此外,它们还含有螯合的甘醇二甲醚配体,这些配体在分解过程中用作封端剂,以控制NaYF _4粒径并使它们单分散在有机溶剂中。在1-十八碳烯中分解时,在没有任何表面活性剂或封端剂的情况下,分子衍生物1和3在明显较低的温度(低于250°C)下转化为立方NaYF _4纳米晶体。在更高的温度下,获得了立方相和六方相的混合物,两相的相对比例取决于反应温度。通过在400°C下煅烧混合相的纳米晶体,获得了纯六方相,它的UC发射效率比立方相高出许多倍。为了用上转换的镧系元素阳离子共掺杂该基质,类似的配合物NaLn(TFA)_4(diglyme)[Ln = Er(4),Tm(5),Yb(6)]和Na _2Ln(TFA)还制备并表征了_5(四甘醇二甲醚)[Ln = Er(7),Yb(8)]。这些钇、,和and / th衍生物的合适组合和合适的摩尔比在1-十八碳烯中分解得到立方和/或六角形的NaYF _4:Yb〜(3+),Er〜(3 +)/ Tm〜(3 +)被二甘醇二甲醚或四甘醇二甲醚配体封端的纳米晶体(NC),其特征在于IR,TG-DTA数据,EDX分析和TEM研究。还通过与聚丙烯酸(PAA)和聚乙二醇(PEG)二酸600进行配体交换反应对这些NC进行了表面改性,以使其水溶性。合适的二甘醇二甲醚衍生物组合的THF溶液也可用于通过以下方法在玻璃或Si晶片基板上制备NaYF _4:Yb〜(3 +),Er〜(3 +)/ Tm〜(3+)的薄膜。旋涂。在Yb〜(3 +)/ Er〜(3+)(绿色/红色)和Yb〜(3 +)/ Tm〜(3+)(蓝色/紫色)共-色中成功实现了多色上转换荧光掺杂的NaYF _4纳米粒子和薄膜,表明它们是有前途的UC纳米磷光体,具有巨大的实际应用价值。讨论了Er〜(3 +)/ Yb〜(3+)和Tm〜(3 +)/ Yb〜(3+)共掺杂材料的上转换激发途径。

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