Luther Joseph M, Beard Matthew C, Song Qing, Law Matt, Ellingson Randy J, Nozik Arthur J
Chemical and Biosciences Center, National Renewable Energy Laboratory, Golden, Colorado 80401, USA.
Nano Lett. 2007 Jun;7(6):1779-84. doi: 10.1021/nl0708617. Epub 2007 May 27.
We study multiple exciton generation (MEG) in electronically coupled films of PbSe quantum dots (QDs) employing ultrafast time-resolved transient absorption spectroscopy. We demonstrate that the MEG efficiency in PbSe does not decrease when the QDs are treated with hydrazine, which has been shown to greatly enhance carrier transport in PbSe QD films by decreasing the interdot distance. The quantum yield is measured and compared to previously reported values for electronically isolated QDs suspended in organic solvents at approximately 4 and 4.5 times the effective band gap. A slightly modified analysis is applied to extract the MEG efficiency and the absorption cross section of each sample at the pump wavelength. We compare the absorption cross sections of our samples to that of bulk PbSe. We find that both the biexciton lifetime and the absorption cross section increase in films relative to isolated QDs in solution.
我们采用超快时间分辨瞬态吸收光谱法研究了电子耦合的PbSe量子点(QD)薄膜中的多激子产生(MEG)。我们证明,当量子点用肼处理时,PbSe中的MEG效率不会降低,肼已被证明可通过减小量子点间距离大大增强PbSe量子点薄膜中的载流子传输。测量了量子产率,并将其与先前报道的悬浮在有机溶剂中的电子隔离量子点在有效带隙约4倍和4.5倍时的值进行了比较。应用了一种略有修改的分析方法来提取每个样品在泵浦波长下的MEG效率和吸收截面。我们将样品的吸收截面与块状PbSe的吸收截面进行了比较。我们发现,相对于溶液中分离的量子点,薄膜中的双激子寿命和吸收截面均增加。