Absorption and luminescence of the surface states in ZnS nanoparticles

A broad absorption band around 500 nm is observed in ZnS nanoparticles. The absorption becomes more intensive and shifts to the blue as the particle size is decreased. The absorption energy is lower than the band gap of the particles and is considered to be caused by the surface states. This assignment is supported by the results of the fluorescence and of the thermoluminescence of the surface states. Both the absorption and the fluorescence reveal that the surface states are size dependent. The glow peak of the semiconductor particles is not varied as much upon decreasing size, indicating the trap depth of the surface states is not sensitive to the particle size. Considering these results, a new model on the size dependence of the surface states is proposed, which may explain our observations reasonably. (C) 1997 American Institute of Physics.

Thermoluminescence of ZnS nanoparticles

The thermoluminescence (TL) of ZnS nanoparticles is reported. The TL intensity increases as the particle size is decreased. The consistency of the size dependence of the TL with that of the surface fluorescence indicates that the TL may be related to the surface states. TL may be caused by the recombination of carriers released from the surface states or defect sites by heating. Smaller particles have higher surface/volume ratio and more surface states, therefore contain more accessible carriers for TL. Besides, the carrier recombination rate increases upon decreasing size due to the increase of the overlap between the electron and hole wave functions. These two effects may make the TL increase upon decreasing size of the particles. The appearance of TL prior to any radiation reveals that trapped carriers have pre-existed. The investigation of TL may provide some useful information about the surface states that may explain the size dependence of the surface fluorescence. (C) 1997 American Institute of Physics.

ZnS中Te等电子中心的时间分辨光谱研究

用时间分辨光谱研究了很大的Te组分范围内的ZnS1-xTex(x=0.005-0.85)合金的发光动力学特性,结果表明:不同形态的Te等电子中心具有不同的辐射复合寿命,从几个ns到几十个ns的范围内变化,当x=0.15左右时,寿命达到最大值(约40 ns).其物理机理源于不同的Te等电子中心具有不同的局域化特性.当Te组分较小时,等电子中心从Te1逐渐演变到Te2,Te3或Te4时,相应发光寿命增加,表现出不断增强的激子发光局域化特性;而当Te组分较大时,Te原子团变得较大,其局域势与基体原子势的相互作用增强,等电子中心的局域化特性减弱,而基体价带扩展态特征变得明显起来,相应发光寿命逐渐减小.还研究了激子束缚能随Te组分的变化以及发光强度随温度的变化关系,所得结果进一步支持了时间分辨光谱研究所得到的结论.

不同尺寸ZnS:Mn纳米粒子的静压光致发光研究

测量了ZnS:Mn纳米粒子以及相应体材料在不同压力下的光致发光谱.随压力增大,来源于Mn2+离子的4T1-6A1跃迁的桔黄色发光明显红移.体材料和10,4.5,3.5,3 nm的ZnS:Mn纳米粒子中Mn2+发光的压力系数分别是-29.4±0.3和-30.1±0.3,-33.3±0.6,-34.6±0.8,-39±1 meV/GPa,压力系数的绝对值随粒子尺寸减小而增大,该种尺寸关系由晶体场场强Dq和Racah参数B值的尺寸依赖性引起.1nm样品的Mn2+发光的特殊压力行为是因为样品的粒子尺寸比较小,另外,分布在Y型沸石中的纳米粒子的表面状况也不同于其它样品.

静压下ZnS∶Te中Te等电子陷阱的发光

研究了4块ZnS∶Te薄膜样品(Te组分从0.5%到3.1%)的光致发光谱在常压下的温度特性.对于Te组分较小的2块样品观察到2个发光峰,分别来自Te1和Te2等电子陷阱;而对Te组分较大的2块样品则只观察到1个来自Te2等电子陷阱的发光.我们还研究了这些发光峰在低温15K下的流体静压压力行为.观察到与Te1有关的发光峰压力系数比ZnS带边的要大很多,而与Te2有关的发光峰压力系数则比带边小.根据Koster-Slater模型,价带态密度半宽随压力的增加是Te1中心有较大压力系数的主要原因,而Te1和Te2中心的不同压力行为则是由于压力对两者缺陷势增强的不同效果引起的.

稀土掺杂ZnS纳米晶中稀土离子与纳米基质之间的能量传递

以甲基丙烯酸为表面包覆剂在水/醇溶液中合成了ZnS:Eu~3+, ZnS:Tb~3+纳米晶，用傅里叶变换红外光谱和X射线粉末衍射谱表征了样品的表面与晶型，样品均为立方闪锌矿型，没有出现与稀土离子相关的相；用光致发光和激发谱研究了样品中的发光过程，其中ZnS:Tb~3+纳米晶中存在纳米基质与Tb~3+之间的能量传递，并引起Tb~3+的特征发射。

Al_xGa_(1-x)As/GaAs太阳电池MgF_2/ZnS双层减反射膜的研究

介绍了在AlGaAs/GaAs太阳电池上制备MgF_2/ZnS双层减反射膜的研究工作。引入了有效反射率R_e，并通过使R_e极小来实现减反射膜的优化设计，考虑了MgF_2/ZnS双层减反射膜与窗口层的耦合。实验上获得了良好的减反射膜，提高了AlGaAs/GaAs太阳电池的短路电流和效率，表明用R_e极小化来设计减反射膜是合理的。

静压下ZnS（0.02）Te（0.98）混晶的共振喇螺散射研究

于2010-11-23批量导入

Formation of ZnS clusters in xeolite-Y

于2010-11-23批量导入

Synthesis and luminescence of CdS/ZnS core/shell nanocrystals

CdS/ZnS core/shell nanocrystals were prepared from an aqueous/alcohol medium. A red shift of the absorption spectrum and an increase of the room temperature photoluminescence intensity accompanied shell growth.