Journal
ACS NANO
Volume 2, Issue 11, Pages 2206-2212Publisher
AMER CHEMICAL SOC
DOI: 10.1021/nn800336b
Keywords
PbS QDs; near-infrared; electron transfer time; titanium dioxide; solar cells; cyclic voltammetry; k center dot P theory; electron affinity; fluorescence lifetime
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Funding
- Center for Nanoscale Systems through National Science Foundation [EEC-0646547]
- NYSTAR
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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.
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