首页 | 本学科首页   官方微博 | 高级检索  
     


Effects of argon sintering atmosphere on luminescence characteristics of Ca6BaP4O17:Sm3+ phosphors
Authors:Chung-Hao Chiang  Hsiu-Hsien Su  Ying-Chien Fang  Sheng-Yuan Chu
Affiliation:1. Department of Electrical Engineering, National Cheng Kung University, 1 University Rd., Tainan 70101, Taiwan;2. Department of Materials Science and Engineering, National Cheng Kung University, Tainan 70101, Taiwan;3. Center for Micro/Nano Science and Technology, National Cheng Kung University, Tainan 70101, Taiwan
Abstract:In this paper, Ca6BaP4O17:Sm3+ and Li+ co-doped Ca6BaP4O17:Sm3+ phosphors were synthesized in air and argon atmospheres using a solid-state reaction method. The phosphor morphologies and crystal structure were studied using scanning electron microscopy and X-ray diffraction, respectively. The emission and absorption characteristics were investigated using photoluminescence emission spectroscopy and diffuse reflectance spectroscopy. The surface states and composition of phosphor were investigated using X-ray photoelectron spectroscopy. The emission integrated intensities of the phosphors sintered in an argon atmosphere increased 3.5 fold than the ones sintered in air atmosphere, with Li+ ions becoming embedded in the lattice of the Ca6BaP4O17:Sm3+ phosphor. This occurs because there are fewer defect/oxygen vacancies and less of the secondary phase forms, leading to better Sm3+ emission. The results suggest that sintering a mixture of the raw materials of a phosphor in an argon atmosphere is a good approach for synthesizing Ca6BaP4O17:Sm3+ phosphor powders. The color purity and CIE values of an optimized phosphor sample sintered in an argon atmosphere with an Li+ ion compensator were calculated to be ~ 99.6% and (0.612,0.386) in the orange–red region under 405-nm excitation, respectively. Moreover, the solid solubility of Sm3+ ions in the Ca6BaP4O17 host can be enhanced by using an argon atmosphere in the synthesis process.
Keywords:Argon atmosphere  Charge compensator  Solid solubility
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号