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Photoinduced Enhancement of Photoluminescence of Colloidal II-VI Nanocrystals in Polymer Matrices

机译:聚合物基质中胶体II-VI纳米晶体光致发光的光突出

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摘要

The environment strongly affects both the fundamental physical properties of semiconductor nanocrystals (NCs) and their functionality. Embedding NCs in polymer matrices is an efficient way to create a desirable NC environment needed for tailoring the NC properties and protecting NCs from adverse environmental factors. Luminescent NCs in optically transparent polymers have been investigated due to their perspective applications in photonics and bio-imaging. Here, we report on the manifestations of photo-induced enhancement of photoluminescence (PL) of aqueous colloidal NCs embedded in water-soluble polymers. Based on the comparison of results obtained on bare and core/shell NCs, NCs of different compounds (CdSe, CdTe, ZnO) as well as different embedding polymers, we conclude on the most probable mechanism of the photoenhancement for these sorts of systems. Contrary to photoenhancement observed earlier as a result of surface photocorrosion, we do not observe any change in peak position and width of the excitonic PL. Therefore, we suggest that the saturation of trap states by accumulated photo-excited charges plays a key role in the observed enhancement of the radiative recombination. This suggestion is supported by the unique temperature dependence of the trap PL band as well as by power-dependent PL measurement.
机译:环境强烈影响半导体纳米晶体(NCS)的基本物理性质及其功能。在聚合物矩阵中嵌入NCS是一种有效的方法,可以创建剪裁NC性能并保护NCS免受不利环境因素所需的理想NC环境。由于其在光子学和生物成像中的透视应用,已经研究了光学透明聚合物中的发光NC。在这里,我们报告了嵌入水溶性聚合物中的水性胶体NCs的光致发光(PL)的光致发光(PL)的表现。基于在裸核/壳NCS上获得的结果的比较,不同化合物(CDSE,CDTE,ZnO)以及不同的嵌入聚合物的NCS,我们得出了这些系统的光敏机制的结论。与表面光腐蚀的结果相反,由于表面光腐蚀而观察到的光敏性,我们不会观察Excitonic PL的峰值位置和宽度的任何变化。因此,我们建议通过积累的照片激发电荷占陷阱状态的饱和在观察到的辐射重组的增强中起着关键作用。该建议是通过陷阱PL频带以及通过依赖性PL测量的独特温度依赖来支持。

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