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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Ultrafast Exciton Dynamics in CdSe Quantum Dots Studied from Bleaching Recovery and Fluorescence Transients
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Ultrafast Exciton Dynamics in CdSe Quantum Dots Studied from Bleaching Recovery and Fluorescence Transients

机译:从漂白回收和荧光瞬变研究CdSe量子点中的超快激子动力学

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We have performed ultrafast absorption bleach recovery and fluorescence upconversion measurements (approx 100 fs time resolution) for three CdSe samples,with nanoparticle diameters of 2.7,2.9,and 4.3 nm.The two types of experiments provide complementary information regarding the contributions of the different processes involved in the fast relaxation of electrons and holes in the CdSe quantum dots.Transient absorption and emission experiments were conducted for the 1S [1S(e) - 1S_(3/2)(h)] transition,lS(e) and 1S_(3/2)(h) representing the lowest electron (e) and hole (h) levels.The bleach recovery of the 1S transition shows a approx 400-500 fs initial rise,which is followed by a size-dependent approx 10-90 ps decay and finally a long-lived (approx ns) decay.The fluorescence upconversion signal for the 1S transition shows quite different temporal behavior: a two times slower rise time (approx 700-1000 fs) and,when the fluorescence upconversion signal has risen to about 20% of its maximum intensity,the signal displays a slight leveling off (bend),followed by a continued rise until the maximum intensity is reached.This bend is well reproducible and power and concentration independent.Simulations show that the bend in the rise is caused by a very fast decay component with a typical time of about 230-430 fs.Considering that the 1S quantum dot excitation is comprised of five exciton substates (F = +-2,+- 1~L,0~L,+- 1~U,and 0~U),we attribute the disparity in the rise of the bleaching and emission transients to the results from the dynamics of the different excitons involved in respectively the bleaching and fluorescence experiments.More specifically,in transient absorption,population changes of the F = +-1~U excitons are probed,in emission population effects for the F = +-2 ("dark") and the F=+-1~L ("bright") exciton states are monitored.It is discussed that the fast (approx 400-500 fs) rise of the bleach recovery is representative of the feeding of the F = +-1~U exciton (by filling of the 1S(e) electron level) and that the slower (approx 700-1000 fs) feeding of the emissive +-2,+-1~L excitons is determined by the relaxation of the hole levels within the 1S_(3/2) fine structure.Finally,the approx 230-430 fs component,typical of the bend in the fluorescence transient,is attributed to the thermalization of the close-lying +-2 ("dark") and +-1~L ("bright") excitons.
机译:我们对三种CdSe样品进行了超快吸收漂白回收和荧光上转换测量(约100 fs时间分辨率),样品的纳米粒径分别为2.7、2.9和4.3 nm。这两种类型的实验提供了有关不同过程贡献的补充信息1S [1S(e)-1S_(3/2)(h)]跃迁,1S(e)和1S_( 3/2)(h)代表最低的电子(e)和空穴(h)含量.1S过渡态的漂白度恢复显示出约400-500 fs的初始上升,其后随尺寸变化约10-90 ps衰减,最后是长寿命(约ns)衰减.1S跃迁的荧光上转换信号显示出截然不同的时间行为:上升时间慢两倍(约700-1000 fs),并且当荧光上转换信号上升时大约是其最大值的20%在强度上,信号显示出轻微的水平变化(弯曲),然后持续上升直到达到最大强度。此弯曲具有良好的重现性,并且功率和浓度无关。模拟表明,上升的弯曲是由快速衰减分量的典型时间约为230-430 fs。考虑到1S量子点激发由五个激子子态(F = + -2,+ 1-L,0-L,+ 1-U,和0〜U),我们将漂白和发射瞬态上升的差异归因于分别参与漂白和荧光实验的不同激子的动力学结果。更具体地说,在F的瞬态吸收,种群变化中探测= + -1〜U激子,在F = + -2(“暗”)和F = +-1〜L(“亮”)激子的发射总体效应中进行监测。漂白剂恢复迅速(约400-500 fs)上升代表F = + -1〜U激子的进料(通过填充1S(e)电子能级)和发射+ -2,+-1〜L激子的较慢(大约700-1000 fs)进料取决于1S_(3 / 2)精细的结构。最后,大约230-430 fs的分量(通常是荧光瞬变中的弯曲)归因于紧密的+ -2(“暗”)和+ -1〜L( “明亮”)激子。

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