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作 者:徐春祥[1] 娄志东[2] 马龙 刘行仁[3] 徐叙瑢[4]
机构地区:[1]东南大学分子与生物分子电子学开放实验室 [2]天津大学应用物理系 [3]中国科学院长春物理研究所 [4]北方交通大学光电子技术研究所
出 处:《中国稀土学报》1998年第2期121-125,共5页Journal of the Chinese Society of Rare Earths
基 金:国家自然科学基金
摘 要:研究了Ga3+在SrS∶Ce和SrGa2S4∶Ce薄膜电致发光(TFEL)材料中的作用及其对Ce3+发光特性的影响。在SrS中掺入Ga2S3并烧结,发现Ga3+的浓度增加时,Ce3+的发光显著向短波方向移动,激发谱中对应于SrS带间吸收的激发峰相对减弱,而对应于Ce3+的基态到激发态跃迁的激发效率相对提高,并出现逐渐增强的SrGa2S4的带间吸收。Ga3+的引入使Ce3+周围的配位场发生变化,相应的能级分布有所改变,Sr2+离子性的增强和Ce3+-Ce3+相互作用的减弱对Ce3+发光特性有显著影响。The electrooptical characteristics of SrS∶Ce and SrGa_2S_4∶Ce as two kinds of hopeful blue TFEL phosphor have been intensively investigated. The color purity of SrGa_2S_4∶Ce is better than that of SrS∶Ce. In this paper, the influence of Ga^3+ on PL characteristics is first reported. Ga_2S_3 was doped into SrS, then sintered. The emission spectra shift obviously towards short wavelength range with increase of Ga^3+ concentration. At the same time, the relative intensity of the excitation peaks corresponding to the interband absorption of SrS reduces, and the exciting efficiency corresponding to the transition from the ground states to the excited states of Ce^3+ ions increases. The ligand field around Ce^3+ is changed by doping Ga^3+. After occupied by Ce^3+ the ionicity of Sr^2+ becomes stronger and Ce^3+-Ce^3+ interaction becomes weaker. These factors are advantegeous for blue emission.
分 类 号:TN383.104[电子电信—物理电子学] TN383.204
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