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Synthesis and photoluminescence properties of Eu~(3+)-doped silica@coordination polymer core-shell structures and their calcinated silica@Gd_2O_3:Eu and hollow Gd_2O_3:Eu microsphere products

机译:Eu〜(3+)掺杂二氧化硅@配位聚合物核-壳结构及其煅烧二氧化硅@ Gd_2O_3:Eu和中空Gd_2O_3:Eu微球产物的合成与光致发光性质

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摘要

The conjugation of Eu~(3+)-doped coordination polymers constructed from Gd~(3+) and isophthalic acid (H_2IPA) with silica particles is investigated for the production of luminescent microspheres. A series of doping ratio-controlled silica@coordination polymer core-shell spheres is easily synthesized by altering the amounts of metal nodes used in the reactions, where the ratios of Gd~(3+) and Eu~(3+) are 10:0 (1a), 9:1 (1b), 8:2 (1c), 7:3 (1d), 5:5 (1e), and 0:10 (1f). The formation of monodisperse uniform core-shell structures is achieved throughout the entirety of a series. Investigations of the photoluminescence property of the resulting series of silica@coordination polymer core-shell spheres reveal that 20% Eu ~(3+)-doped product (1c) has the strongest emission intensity. The subsequent calcination process on the silica@coordination polymer core-shell structures (1a-f) results in the formation of a series of doping ratio-controlled silica@Gd_2O_3:Eu core-shell microspheres (2a-f) with uniform shell thickness. During the calcination step, the coordination polymers within silica@coordination polymer core-shells are transformed into metal oxides, resulting in silica@Gd_2O _3:Eu core-shell structures. The final etching process on the silica@Gd_2O_3:Eu core-shell microspheres (2a-f) produces a series of hollow Gd_2O_3:Eu microspheres (3a-f) as a result of the elimination of silica cores. The luminescence intensities of silica@Gd_2O_3:Eu core-shell (2a-f) and hollow Gd _2O_3:Eu microspheres (3a-f) also vary depending upon the doping ratio of Eu~(3+) ions. A series of monodisperse Eu ~(3+)-doped luminescent silica@coordination polymer core-shell microspheres is synthesized through the growth of coordination polymers on silica surfaces. The doping ratio is controlled by altering the amounts of metal ions used in the reactions. The subsequent calcination and etching processes result in the formation of doping ratio-controlled luminescent silica@Gd _2O_3:Eu core-shell and hollow Gd_2O _3:Eu microspheres.
机译:研究了由Gd〜(3+)和间苯二甲酸(H_2IPA)构成的Eu〜(3+)掺杂配位聚合物与二氧化硅颗粒的共轭结构,用于制备发光微球。通过改变反应中所用金属节点的数量即可轻松合成一系列掺杂比例可控的二氧化硅@配位聚合物核-壳球,其中Gd〜(3+)和Eu〜(3+)的比例为10: 0(1a),9:1(1b),8:2(1c),7:3(1d),5:5(1e)和0:10(1f)。在整个系列的整个过程中均形成了单分散均匀的核-壳结构。对所得的一系列二氧化硅@配位聚合物核-壳球的光致发光性能的研究表明,掺杂20%Eu〜(3+)的产物(1c)具有最强的发射强度。二氧化硅@配位聚合物核-壳结构(1a-f)上的后续煅烧过程导致形成一系列具有均匀壳厚度的掺杂比控制的二氧化硅@ Gd_2O_3:Eu核-壳微球(2a-f)。在煅烧步骤中,二氧化硅@配位聚合物核-壳内的配位聚合物被转化为金属氧化物,从而形成二氧化硅@ Gd_2O_3:Eu核-壳结构。由于消除了二氧化硅核,对silica @ Gd_2O_3:Eu核-壳微球(2a-f)的最终蚀刻过程产生了一系列空心的Gd_2O_3:Eu微球(3a-f)。二氧化硅@ Gd_2O_3:Eu核壳(2a-f)和空心Gd_2O_3:Eu微球(3a-f)的发光强度也随Eu〜(3+)离子的掺杂比而变化。通过配位聚合物在二氧化硅表面的生长,合成了一系列单分散的Eu〜(3+)掺杂的发光硅@配位聚合物核-壳微球。通过改变反应中使用的金属离子的量来控制掺杂率。随后的煅烧和蚀刻过程导致形成掺杂比例控制的发光二氧化硅@Gd _2O_3:Eu核壳和中空的Gd_2O _3:Eu微球。

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