Hydrothermal synthesis of 4ZnO•B2O3•H2O:Ln3+ (Ln = Eu, Tb) phosphors: Morphology-tunable and luminescence properties

被引:12
作者
Cao, Shiwei [1 ]
Jiao, Yang [1 ]
Han, Weifang [1 ]
Ge, Chunhua [1 ]
Song, Bo [1 ]
Wang, Jie [1 ]
Zhang, Xiangdong [1 ]
机构
[1] Liaoning Univ, Coll Chem, Shenyang 110036, Liaoning, Peoples R China
关键词
Hydrothermal; Zinc borate; Luminescence; Eu3+ and Tb3+ co-doped; RARE-EARTH IONS; FLAME-RETARDANT PROPERTIES; LIGHT-EMITTING-DIODES; ENERGY-TRANSFER; CONTROLLABLE SYNTHESIS; EMISSION PROPERTIES; OPTICAL-ABSORPTION; HYBRID PRECURSORS; RED PHOSPHOR; PHOTOLUMINESCENCE;
D O I
10.1016/j.saa.2017.09.040
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
4ZnO center dot B2O3 center dot H2O:Ln(3+) (Ln = Eu, Tb) phosphors with different morphologies have been successfully synthesized via one-step hydrothermal method through regulating the molar amount of Eu3+ and Tb3+. Comprehensive scanning electron microscopy (SEM), X-ray diffraction (XRD) Fourier transform infrared spectrum (FT-IR) and inductively coupled plasma atomic emission spectrometer (ICP-AES) characterizations all confirm that obtained products are 4ZnO center dot B2O3 center dot H2O:Ln(3) (Ln = Eu, Tb). The experimental results displayed that the morphology and photoluminescence of compounds is regularly changed with increased the molar amount of rare earth ions. For the Eu3+-doped, Tb3+-doped and Eu3+/Tb3+ co-doped 4ZnO center dot B2O3 center dot H2O phosphors of morphologies, the rodlike structures gradually changed to flower-like structures, fine wire-like structure and hybrid structure, respectively. To their photoluminescence, the Eu3+ shows a red emission (615 nm); the Tb3+ shows a green emission (545 nm); for the Eu3+/Tb3+ co-doped 4ZnO center dot B2O3 center dot H2O phosphors, a combination of blue (5d-4f of Eu2+), green (D-5(4)-F-7(5) of Tb3+) and red (D-5(0) -F-7(2) of Eu3+) emissions emerges to achieve white emission. In addition, the energy transfer among Eu3+, Eu2+ and Tb3+ ions was also discussed. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:231 / 238
页数:8
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