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Ln3+ (Ln = Eu,Dy) - doped Sr2CeO4 fine phosphor particles: Wet chemical preparation,energy transfer and tunable luminescence
Affiliation:1. Key Laboratory of Inorganic Nanomaterials of Hebei Province, College of Chemistry and Materials Science, Hebei Normal University, Shijiazhuang 050024, China;2. Physics Department and CICECO - Aveiro Institute of Materials, University of Aveiro, 3810-193, Aveiro, Portugal;1. School of Chemistry and Materials Engineering, Changzhou Vocational Institute of Engineering, Changzhou 213164, PR China;2. School of Mechanical and Electrical Engineering, Henan Institute of Science and Technology, Xinxiang 453003, PR China;3. Department of Chemical & Materials Engineering, The University of Auckland, Auckland 1142, New Zealand;1. Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Key Laboratory of Chemical Biology of Hebei Province, College of Chemistry and Environmental Science, Hebei University, Baoding 071002, PR China;2. Hebei United University Qian?an College, Qian?an 064400, PR China;1. Department of Optoelectronics, Xiamen University of Technology, Xiamen 361024, China;2. Fujian Provincial Key Laboratory of Optoelectronic Technologies and Devices, Xiamen University of Technology, Xiamen 361024, China;3. Department of Materials Science and Engineering, DaYue University, Taiwan
Abstract:The Sr2CeO4:Ln3+ (Ln = Eu, Dy) fine phosphor particles were prepared by a facile wet chemical approach, in which the consecutive hydrothermal-combustion reaction was performed. The doping of Ln3+ into Sr2CeO4 has little influence on the structure of host, and the as-prepared samples display well-crystallized spherical or elliptical shape with an average particle size at about 100–200 nm. For Eu3+ ions-doped Sr2CeO4, with the increase of Eu3+-doping concentration, the blue light emission band with the maximum at 468 nm originating from a Ce4+ → O2? charge transfer of the host decreases obviously and the characteristic red light emission of Eu3+ (5D07F2 transition at 618 nm) is enhanced gradually. Simultaneously, the fluorescent lifetime of the broadband emission of Sr2CeO4 decreases with the doping of Eu3+, indicating an efficient energy transfer from the host to the doping Eu3+ ions. The energy transfer efficiency from the host to Eu3+ was investigated in detail, and the emitting color of Sr2CeO4:Eu3+ can be easily tuned from blue to red by varying the doping concentration of Eu3+ ions. Moreover, the luminescence of Dy3+-doped Sr2CeO4 was also studied. Similar energy transfer phenomenon can be observed, and the incorporation of Dy3+ into Sr2CeO4 host leads to the characteristic emission of 4F9/2 → 6H15/2 (488 nm, blue light) and 4F9/2 → 6H13/2 (574 nm, yellow light) of Dy3+. The Sr2CeO4:Ln3+ fine particles with tunable luminescence are quite beneficial for its potential applications in the optoelectronic fields.
Keywords:Wet chemistry preparation  Phosphor  Luminescence  Energy transfer
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