首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Generation of Multiple Excitons in PbSe and CdSe Quantum Dots by Direct Photoexcitation: First-Principles Calculations on Small PbSe and CdSe Clusters
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Generation of Multiple Excitons in PbSe and CdSe Quantum Dots by Direct Photoexcitation: First-Principles Calculations on Small PbSe and CdSe Clusters

机译:通过直接光激发在PbSe和CdSe量子点中生成多个激子:小PbSe和CdSe团簇的第一性原理计算

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We demonstrate for the first time using a combination of the Hartree—Fock approximation and the symmetry adapted cluster theory with configuration interaction (SAC-CI) that multiple excitons (ME) in PbSe and CdSe quantum dots (QD) can be generated directly upon photoexcitation. At energies 2.5—3 times the lowest excitation, almost all optically excited states in Pb4Se4 become MEs, while both single excitons and MEs are seen in Cd6Se6. We analyze the high-level SAC-CI results of the small clusters based on the band structure and then extend our band structure analysis to Pb_(68)Se_(68), Pb_(180)Se_(180), Cd_(33)Se_(33), and Cd_(111)Se_(111). Our results explain the ultrafast generation of MEs without the need for a phonon relaxation bottleneck and clarify why PbSe is particularly suitable for generation of MEs. Efficient exciton multiplication can be used to considerably increase the efficiency of QD-based solar cells.
机译:我们首次证明了结合使用Hartree-Fock近似和具有结构相互作用的对称适应簇理论(SAC-CI),可以在光激发时直接生成PbSe和CdSe量子点(QD)中的多个激子(ME) 。在最低激发能量的2.5到3倍的能量下,Pb4Se4中几乎所有的光学激发态都变成了ME,而Cd6Se6中同时出现了单激子和ME。我们基于能带结构分析了小型集群的高级SAC-CI结果,然后将能带结构分析扩展到Pb_(68)Se_(68),Pb_(180)Se_(180),Cd_(33)Se_ (33)和Cd_(111)Se_(111)。我们的结果解释了不需要声子弛豫瓶颈的超快生成MEs,并阐明了为什么PbSe特别适合生成MEs。可以使用有效的激子倍增来显着提高基于QD的太阳能电池的效率。

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