Eu3+ doped-CdTe(CdTe:Eu3+)nanocrystals were prepared via a facile hydrothermal method,and Eu3+ was successfully incorporated into the crystal lattice of CdTe and measured by X-ray powder diffraction(XRD),transmission ...Eu3+ doped-CdTe(CdTe:Eu3+)nanocrystals were prepared via a facile hydrothermal method,and Eu3+ was successfully incorporated into the crystal lattice of CdTe and measured by X-ray powder diffraction(XRD),transmission electron microscopy(TEM),ultraviolet-visible(UV-Vis) absorption spectroscopy and fluorescence emission.The CdTe:Eu^3+ nanocrystals still have a cubic crystal structure,and the corresponding XRD peaks of CdTe:Eu3+nanocrystals shift to larger angles compared with those of pure CdTe.The CdTe:Eu3+ nanocrystals are monodisperse and the particles size is about 2-4 nm.Compared with pure CdTe,the CdTe:Eu^3+ nanocrystals have larger band gap and thus exhibit blueshift in the emission spectra,which could be accounted for by the energy transfer between Eu^3+ and CdTe.To enhance the stability and functionality of CdTe:Eu3+nanocrystals,the CdTe:Eu3+nanocrystals were coated with SiO2 and the core-shell SiO2-coated CdTe:Eu3+nanocrystals(CdTe:Eu^3+@SiO2) were prepared via microemulsion method.TEM results show that CdTe:Eu3+nanocrystals are uniformly dispersed in the shell,and CdTe:Eu3+@SiO2 nanospheres are uniformly spherical with an average diameter of about 75 nm.The fluorescence emission of CdTe:Eu3+@SiO2(567 nm) shows a blueshift compared with that of CdTe:Eu^3+nanocrystals(632 nm),possibly because of altered surface properties after SiO2 coating.CdTe:Eu^3+and CdTe:Eu^3+@SiO2 with tunable photoluminescence are potentially useful in fabricating optical and bioimaging devices.展开更多
In this study,the preparation of a new kind of magnetic and luminescent Fe3O4/CdTe nanocomposites was demonstrated. Superparamagnetic Fe3O4 nanoparticles were first synthesized by hydrothermal coprecipitation of ferri...In this study,the preparation of a new kind of magnetic and luminescent Fe3O4/CdTe nanocomposites was demonstrated. Superparamagnetic Fe3O4 nanoparticles were first synthesized by hydrothermal coprecipitation of ferric and ferrous ions,followed by the modification of their surfaces with tetramethylammonium hydroxide（TMAOH） and the chemical activation with aspartic acid.The surface-modified Fe3O4 nanoparticles were then covalently coated with CdTe quantum dots（QDs）,which were modified with mercaptoacetic acid（MPA）,to form the Fe3O4/CdTe magnetic and luminescent nanocomposites through the coordination of the amino groups on the surfaces of Fe3O4 and the carboxyl groups on CdTe QDs.The structure and properties of as-synthesized nanocomposites were characterized.It was indicated that the nanocomposites possessed structure with an average diameter of 40- 50 nm,yellow-green emission feature and room temperature ferro-magnetism.Both the fluorescence and UV-vis absorption spectra of the nanocomposites showed a blue shift comparing with those of CdTe QDs.The mechanism of the blue shift was presented.The nanocomposites retained the ferromagnetic property with a saturation magnetization of 8.9 emu/g.展开更多
基金financially supported by the National Natural Science Foundation of China (No.21364007)the Natural Science Foundation of Inner Mongolia (No.2016MS0201)the Program for Young Talents of Science and Technology of Baotou Teachers College (No.01135003)
文摘Eu3+ doped-CdTe(CdTe:Eu3+)nanocrystals were prepared via a facile hydrothermal method,and Eu3+ was successfully incorporated into the crystal lattice of CdTe and measured by X-ray powder diffraction(XRD),transmission electron microscopy(TEM),ultraviolet-visible(UV-Vis) absorption spectroscopy and fluorescence emission.The CdTe:Eu^3+ nanocrystals still have a cubic crystal structure,and the corresponding XRD peaks of CdTe:Eu3+nanocrystals shift to larger angles compared with those of pure CdTe.The CdTe:Eu3+ nanocrystals are monodisperse and the particles size is about 2-4 nm.Compared with pure CdTe,the CdTe:Eu^3+ nanocrystals have larger band gap and thus exhibit blueshift in the emission spectra,which could be accounted for by the energy transfer between Eu^3+ and CdTe.To enhance the stability and functionality of CdTe:Eu3+nanocrystals,the CdTe:Eu3+nanocrystals were coated with SiO2 and the core-shell SiO2-coated CdTe:Eu3+nanocrystals(CdTe:Eu^3+@SiO2) were prepared via microemulsion method.TEM results show that CdTe:Eu3+nanocrystals are uniformly dispersed in the shell,and CdTe:Eu3+@SiO2 nanospheres are uniformly spherical with an average diameter of about 75 nm.The fluorescence emission of CdTe:Eu3+@SiO2(567 nm) shows a blueshift compared with that of CdTe:Eu^3+nanocrystals(632 nm),possibly because of altered surface properties after SiO2 coating.CdTe:Eu^3+and CdTe:Eu^3+@SiO2 with tunable photoluminescence are potentially useful in fabricating optical and bioimaging devices.
基金supported by the National Natural Science Foundation of China(Nos.20345006 and 20575043)
文摘In this study,the preparation of a new kind of magnetic and luminescent Fe3O4/CdTe nanocomposites was demonstrated. Superparamagnetic Fe3O4 nanoparticles were first synthesized by hydrothermal coprecipitation of ferric and ferrous ions,followed by the modification of their surfaces with tetramethylammonium hydroxide（TMAOH） and the chemical activation with aspartic acid.The surface-modified Fe3O4 nanoparticles were then covalently coated with CdTe quantum dots（QDs）,which were modified with mercaptoacetic acid（MPA）,to form the Fe3O4/CdTe magnetic and luminescent nanocomposites through the coordination of the amino groups on the surfaces of Fe3O4 and the carboxyl groups on CdTe QDs.The structure and properties of as-synthesized nanocomposites were characterized.It was indicated that the nanocomposites possessed structure with an average diameter of 40- 50 nm,yellow-green emission feature and room temperature ferro-magnetism.Both the fluorescence and UV-vis absorption spectra of the nanocomposites showed a blue shift comparing with those of CdTe QDs.The mechanism of the blue shift was presented.The nanocomposites retained the ferromagnetic property with a saturation magnetization of 8.9 emu/g.
