Multiple Exciton Dissociation in CdSe Quantum Dots by Ultrafast Electron Transfer to Adsorbed Methylene Blue

被引:208
作者
Huang, Jier [1 ]
Huang, Zhuangqun [1 ]
Yang, Ye [1 ]
Zhu, Haiming [1 ]
Lian, Tianquan [1 ]
机构
[1] Emory Univ, Dept Chem, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
EFFICIENCY CARRIER MULTIPLICATION; PHOTOINDUCED CHARGE-TRANSFER; SEMICONDUCTOR NANOCRYSTALS; IMPACT IONIZATION; COLLOIDAL CDS; HOLE TRANSFER; PBSE; SIZE; NANOPARTICLES; GENERATION;
D O I
10.1021/ja100106z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multiexciton generation in quantum dots (QDs) may provide a new approach for improving the solar-to-electric power conversion efficiency in QD-based solar cells. However, it remains unclear how to extract these excitons before the ultrafast exciton-exciton annihilation process. In this study we investigate multiexciton dissociation dynamics in CdSe QDs adsorbed with methylene blue (MB+) molecules by transient absorption spectroscopy. We show that excitons in QDs dissociate by ultrafast electron transfer to MB+ with an average time constant of similar to 2 ps. The charge separated state is long-lived (>1 ns), and the charge recombination rate increases with the number of dissociated excitons. Up to three MB+ molecules per QD can be reduced by exciton dissociation. Our result demonstrates that ultrafast interfacial charge separation can effectively compete with exciton-exciton annihilation, providing a viable approach for utilizing short-lived multiple excitons in QDs.
引用
收藏
页码:4858 / 4864
页数:7
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