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作 者:李宏 XIA Mengling LUO Kaifei WANG Paul W
机构地区:[1]State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology [2]Department of Physics, Bradley University
出 处:《Journal of Wuhan University of Technology(Materials Science)》2015年第1期16-21,共6页武汉理工大学学报(材料科学英文版)
基 金:Funded by the Science and Technology Planning Project of Wuhan City(No.2013010501010135);the Science and Technology Planning Project of Hubei Province(Nos.2013BAA095,2014BAA136);National Natural Science Foundation of China(No.51372179)
摘 要:Pr3+ doped ZnO quantum dots (QDs) were successfully synthesized by sol-gel process. X-ray diffraction (XRD) and X-ray Phtoelectron spectroscopy (XPS) were used to analyze the microstructure variation of ZnO QDs and the chemical environment of Pr3+ with increasing Pr3+ doping concentrations. Most of Pr3+ ions distribute on the surface ofZnO QDs while a few of them penetrate into the ZnO lattice to substitute Zn2+ which causes the lattice distortion and the change of the crystal size. With increasing concentration of Pr3+ ions, the crystal size of ZnO QDs firstly increases and then decreases meanwhile the amorphization gradually increases. New Pr-O-Zn bonds formed after Pr3+ doping and Pr3+ ions have at least two chemical bonding environments: one is Pr-O-Zn bond and the other is Pr-O bond surrounded by oxygen vacancies.Pr3+ doped ZnO quantum dots (QDs) were successfully synthesized by sol-gel process. X-ray diffraction (XRD) and X-ray Phtoelectron spectroscopy (XPS) were used to analyze the microstructure variation of ZnO QDs and the chemical environment of Pr3+ with increasing Pr3+ doping concentrations. Most of Pr3+ ions distribute on the surface ofZnO QDs while a few of them penetrate into the ZnO lattice to substitute Zn2+ which causes the lattice distortion and the change of the crystal size. With increasing concentration of Pr3+ ions, the crystal size of ZnO QDs firstly increases and then decreases meanwhile the amorphization gradually increases. New Pr-O-Zn bonds formed after Pr3+ doping and Pr3+ ions have at least two chemical bonding environments: one is Pr-O-Zn bond and the other is Pr-O bond surrounded by oxygen vacancies.
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