首页> 外文OA文献 >Temperature dependent photoluminescence of erbium doped YAG, zinc nitride and manganese-doped cadmium selenide optical materials.
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Temperature dependent photoluminescence of erbium doped YAG, zinc nitride and manganese-doped cadmium selenide optical materials.

机译:掺Y YAG,氮化锌和掺锰硒化镉光学材料的温度依赖性光致发光。

摘要

Temperature dependent studies of a selection of materials including erbium-doped yttrium aluminum garnet (Er:YAG), zinc nitride nanocrystals(NCs) and manganese-doped cadmium selenide (CdMnSe) NCS have been undertaken in order to determine their fundamental optical properties. The study is based upon the measurement of their photoluminescence (PL) and PL transient decay transient over the temperature range of 300K to 5K.ududFor the Er:YAG samples, two different sample types are studied as a function of erbium concentration that are a fast-cooled (mono-phase) and a slow-cooled (bi-phasic) polycrystalline material. Due to the presence of emission upconversion in these materials the emission dependence on excitation power is also studied. It is found that for high Er concentrations (40-50%) energy transfer upconversion (ETU) occurs that may be of use for assisting population inversion at the 4I11/2 level for the laser 3µm emission. Generally it is confirmed that the single phase and bi-phasic materials possess slightly different optical properties and that the material production must therefore be carefully controlled in order to realize optimized materials for optical applications.ududZinc nitride NC materials are studied for the first time with four samples representing a range of NC diameters characterized. These materials were highly susceptible to oxidation which presented a significant challenge in their handling and study. Strong emission was observed across the visible spectral region though the origin of this it was found probably included trap state emission and for the smallest NC samples organic ligand emission. The PL was found to shifting to higher energies as the size of the NC is decreased as expected due to increased quantum confinement and in line with the Brus equation. Two of the samples (8.9nm and 2.7nm diameter NCs) display a temperature dependence of the optical properties in line that seen in other semiconductor NCs such as PbS. The other samples displayed anomalous behavior that could be due to ligand emission (2.5nm NC sample) or higher energy trap states caused by localized oxidation (3.8nm NCs). ududA study of temperature dependent optical properties of CdMnSe NCs was focused around the role of NC shape and type. Core only, core/shell and dot-in-rod samples were studied and all found to display a blue shift as temperature is reduced from 300K to ~5K of between ~24meV to 58meV. The core only NCs display a different luminescent behavior to that of the core-shell and dot-in-a-rod samples. The PL is related to the recombination of confined excitons within the NC, together with a contribution from what are most probably trap states located at the surface of the NC. In these samples no contribution from the Mn2+ ion is found suggesting that the dopant ions are not fully incorporated into the NC but may reside on the surface.
机译:为了确定它们的基本光学性能,已经对包括-掺杂钇铝石榴石(Er:YAG),氮化锌纳米晶体(NCs)和锰掺杂硒化镉(CdMnSe)NCS在内的多种材料进行了温度依赖性研究。这项研究基于在300K至5K的温度范围内对它们的光致发光(PL)和PL瞬态衰减瞬变的测量。 ud ud对于Er:YAG样品,研究了两种不同样品类型作为as浓度的函数,是一种快冷(单相)和慢冷(双相)多晶材料。由于这些材料中存在发射上转换,因此还研究了发射对激励功率的依赖性。已经发现,对于高浓度的Er(40-50%),会发生能量转移上转换(ETU),可用于协助4μl1/ 2级激光3μm发射的粒子反转。通常,已确认单相和双相材料的光学性能略有不同,因此必须仔细控制材料的生产,以实现用于光学应用的优化材料。 ud ud氮化锌NC材料首先被研究用四个代表一系列NC直径的样品进行时间分析。这些材料极易被氧化,这对它们的处理和研究提出了重大挑战。在可见光谱范围内观察到强发射,尽管其起源可能是陷阱态发射和最小的NC样品有机配体发射。人们发现,随着量子限制的增加,NC尺寸减小,并且符合Brus方程,PL转移到更高的能量。其中两个样品(直径为8.9nm和2.7nm的NC)显示出光学特性的温度依赖性,这与其他半导体NC(如PbS)中看到的一致。其他样品显示出异常行为,这可能是由于配体发射(2.5nm NC样品)或局部氧化(3.8nm NCs)引起的更高的能量陷阱状态所致。 ud udCdMnSe NCs的依赖温度的光学特性研究集中在NC形状和类型的作用上。研究了仅核心,核心/壳和棒中点的样本,并且发现它们都随温度从300K降低到〜5K,从〜24meV降低到58meV而显示出蓝移。仅核心的NC显示出与核心壳和棒中样品不同的发光行为。 PL与NC内部受限激子的重组有关,并与NC表面最可能的陷阱态有关。在这些样品中,未发现Mn2 +离子的贡献,表明掺杂剂离子未完全掺入NC中,但可能残留在表面上。

著录项

  • 作者

    Norhashim Nurhakimah;

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  • 年度 2017
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  • 原文格式 PDF
  • 正文语种 en
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