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arXiv 0902.1068cond-mat.mtrl-scicond-mat.str-el
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强光激发下SrTiO3的蓝色发光

Blue luminescence of SrTiO3 under intense optical excitation

A. Rubano, D. Paparo, F. Miletto, U. Scotti di Uccio, L. Marrucci

摘要:

实验研究了纯钛酸锶和电子掺杂钛酸锶在强脉冲近紫外光激发下的蓝绿色光致发光,其发光强度与激发强度和温度的关系。发射光谱和时间分辨的发射衰减测量和分析的框架内简单的唯象模型。我们发现一个有趣的蓝到绿的转变发生在纯样品中的温度增加,而不是在掺杂材料中不存在。作为温度的函数测量的发光产率和衰减速率可以建模以及作为标准的激活行为。领先的电子空穴复合过程中发生的初始衰变被确定为二阶,或双分子,在最近的报道中,有利于三阶解释为俄歇过程。发光的时间衰减可以很好地描述的模型的基础上的两个相互作用的人口的激发,分别确定与相互作用的缺陷捕获(可能形成激子)和移动电荷。最后,从测量的掺杂和样品依赖的发光产率,我们得出结论,负责发光的辐射中心可能是本征结构缺陷以外的体氧空位。

英文摘要:

The blue-green photoluminescence emitted by pure and electron-doped strontium titanate under intense pulsed near-ultraviolet excitation is studied experimentally, as a function of excitation intensity and temperature. Both emission spectra and time-resolved decays of the emission are measured and analyzed in the framework of simple phenomenological models. We find an interesting blue-to-green transition occurring for increasing temperatures in pure samples, which is instead absent in doped materials. The luminescence yield and decay rate measured as a function of temperature can be modeled well as standard activated behaviors. The leading electron-hole recombination process taking place in the initial decay is established to be second-order, or bimolecular, in contrast to recent reports favoring a third-order interpretation as an Auger process. The temporal decay of the luminescence can be described well by a model based on two interacting populations of excitations, respectively identified with interacting defect-trapped (possibly forming excitons) and mobile charges. Finally, from the measured doping and sample dependence of the luminescence yield, we conclude that the radiative centers responsible for the luminescence are probably intrinsic structural defects other than bulk oxygen vacancies.

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