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作 者:翟永清[1] 王蒙[1] 李璇[1] 杨红蕾[1] 丁皇慧 余佳宝
机构地区:[1]河北大学化学与环境科学学院,保定071002
出 处:《人工晶体学报》2015年第6期1523-1528,共6页Journal of Synthetic Crystals
基 金:国家自然科学基金(21301046);河北大学实验室开放项目基金(sy 2015033)
摘 要:采用水热法经过煅烧热处理成功制备了ZnWO4∶Sm3+白色荧光粉。通过X射线粉末衍射仪,扫描电子显微镜及荧光分光光度计对样品的物相结构、形貌粒度及发光性能进行了分析和表征。结果表明:在pH值为6和7下,所合成的Zn WO4∶Sm3+晶体结构与Zn WO4相似,为单斜晶系结构,样品颗粒为类球形,颗粒尺寸范围为100~220nm。Sm3+的摩尔掺杂量为0.5%时,发射峰强度达到最大值;继续增加Sm3+浓度,其发射峰强度反而减弱,出现了浓度猝灭效应。在254 nm波长激发下,ZnWO4∶Sm3+的色坐标集中在冷白光区。ZnWO4∶ Sm3+ white phosphors were prepared via hydrothermal process with further heat treatment. The phase structure,morphology and luminescent properties of the samples were characterized by X-ray diffraction( XRD),scanning electron microscope( SEM) and fluorescence spectrophotometer,respectively. The results indicate that the crystal structure of as-synthesized ZnWO4∶ Sm3 +is similar to the pure monoclinic Zn WO4 under the p H value of 6 and 7. These samples are approximately spherical particles with the particles size from 100 to 220 nm. When the concentration of Sm3 +is 0. 5%,the intensity of emission peak reaches the maximum. The concentration quenching occurs when Sm3 +concentration is beyond 0. 5%. Under 254 nm excitation,the chromaticity coordinates are located in cold white light zone.
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