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Hot-Electron Transfer from Semiconductor Nanocrystals
by
Timp, Brooke A
, Williams, Kenrick J
, Tisdale, William A
, Norris, David J
, Aydil, Eray S
, Zhu, X.-Y
in
Atoms & subatomic particles
/ Charge
/ Charge carriers
/ chemical elements
/ Chemical treatment
/ Conduction bands
/ cooling
/ Devices
/ electric field
/ Electric fields
/ Electron transfer
/ Electrons
/ Energy
/ Lead selenides
/ Nanocrystals
/ Phonons
/ photons
/ photovoltaic cells
/ Quantum dots
/ Semiconductors
/ Solar cells
/ Titanium dioxide
/ Vibration
2010
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Hot-Electron Transfer from Semiconductor Nanocrystals
by
Timp, Brooke A
, Williams, Kenrick J
, Tisdale, William A
, Norris, David J
, Aydil, Eray S
, Zhu, X.-Y
in
Atoms & subatomic particles
/ Charge
/ Charge carriers
/ chemical elements
/ Chemical treatment
/ Conduction bands
/ cooling
/ Devices
/ electric field
/ Electric fields
/ Electron transfer
/ Electrons
/ Energy
/ Lead selenides
/ Nanocrystals
/ Phonons
/ photons
/ photovoltaic cells
/ Quantum dots
/ Semiconductors
/ Solar cells
/ Titanium dioxide
/ Vibration
2010
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Hot-Electron Transfer from Semiconductor Nanocrystals
by
Timp, Brooke A
, Williams, Kenrick J
, Tisdale, William A
, Norris, David J
, Aydil, Eray S
, Zhu, X.-Y
in
Atoms & subatomic particles
/ Charge
/ Charge carriers
/ chemical elements
/ Chemical treatment
/ Conduction bands
/ cooling
/ Devices
/ electric field
/ Electric fields
/ Electron transfer
/ Electrons
/ Energy
/ Lead selenides
/ Nanocrystals
/ Phonons
/ photons
/ photovoltaic cells
/ Quantum dots
/ Semiconductors
/ Solar cells
/ Titanium dioxide
/ Vibration
2010
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Journal Article
Hot-Electron Transfer from Semiconductor Nanocrystals
2010
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Overview
In typical semiconductor solar cells, photons with energies above the semiconductor bandgap generate hot charge carriers that quickly cool before all of their energy can be captured, a process that limits device efficiency. Although fabricating the semiconductor in a nanocrystalline morphology can slow this cooling, the transfer of hot carriers to electron and hole acceptors has not yet been thoroughly demonstrated. We used time-resolved optical second harmonic generation to observe hot-electron transfer from colloidal lead selenide (PbSe) nanocrystals to a titanium dioxide (TiO₂) electron acceptor. With appropriate chemical treatment of the nanocrystal surface, this transfer occurred much faster than expected. Moreover, the electric field resulting from sub-50-femtosecond charge separation across the PbSe-TiO₂ interface excited coherent vibrations of the TiO₂ surface atoms, whose motions could be followed in real time.
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