Electron Injection from Colloidal PbS Quantum Dots into Titanium Dioxide Nanoparticles

被引:529
作者
Hyun, Byung-Ryool [1 ]
Zhong, Yu-Wu. [2 ]
Bartnik, Adam C. [1 ]
Sun, Liangfeng [1 ]
Abruna, Hector D. [2 ]
Wise, Frank W. [1 ]
Goodreau, Jason D. [3 ]
Matthews, James R. [3 ]
Leslie, Thomas M. [3 ]
Borrelli, Nicholas F. [3 ]
机构
[1] Cornell Univ, Dept Appl Phys, Ithaca, NY 14850 USA
[2] Cornell Univ, Dept Chem & Biol Chem, Ithaca, NY 14850 USA
[3] Corning Inc, Corning, NY 14831 USA
基金
美国国家科学基金会;
关键词
PbS QDs; near-infrared; electron transfer time; titanium dioxide; solar cells; cyclic voltammetry; k center dot P theory; electron affinity; fluorescence lifetime;
D O I
10.1021/nn800336b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Injection of photoexcited electrons from colloidal PbS quantum dots into TiO2 nanoparticles is investigated. The electron affinity and ionization potential of PbS quantum dots, inferred from cyclic voltammetry measurements, show strong size dependence due to quantum confinement. On the basis of the measured energy levels, photoexcited electrons should transfer efficiently from the quantum dots into TiO2 only for quantum-dot diameter below similar to 4.3 nm. Continuous-wave fluorescence spectra and fluorescence transients of PbS quantum dots coupled to titanium dioxide nanoparticles are consistent with electron transfer for small quantum dots. The measured electron transfer time is surprisingly slow (similar to 100 ns), and implications of this for future photovoltaics will be discussed. Initial results obtained from solar cells sensitized with PbS quantum dots are presented.
引用
收藏
页码:2206 / 2212
页数:7
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