Time resolved photoluminescence is a powerful technique to study the collective dynamics of excitons and polaritons in semiconductor nanostructures. We present a two excitation pulses technique to induce the ultrafast and controlled quenching of the exciton emission in a quantum well. The depth of the dip is given by the magnitude of the warming of the carriers induced by the arrival of a laser pulse when an exciton population is already present in the sample. We use this technique to study the relaxation mechanisms of polaritons in semiconductor microcavities, which are of great importance to enhance the conditions for their condensation under non-resonant excitation. We also explore the dynamics of polariton fluids resonantly created in the lower polariton branch in a triggered optical parametric oscillator configuration, showing evidence of polariton superfluidity, and opening up the way to the real-time study of quantum fluids.
Deep Dive into Collective dynamics of excitons and polaritons in semiconductor nanostructures.
Time resolved photoluminescence is a powerful technique to study the collective dynamics of excitons and polaritons in semiconductor nanostructures. We present a two excitation pulses technique to induce the ultrafast and controlled quenching of the exciton emission in a quantum well. The depth of the dip is given by the magnitude of the warming of the carriers induced by the arrival of a laser pulse when an exciton population is already present in the sample. We use this technique to study the relaxation mechanisms of polaritons in semiconductor microcavities, which are of great importance to enhance the conditions for their condensation under non-resonant excitation. We also explore the dynamics of polariton fluids resonantly created in the lower polariton branch in a triggered optical parametric oscillator configuration, showing evidence of polariton superfluidity, and opening up the way to the real-time study of quantum fluids.
arXiv:0912.1937v1 [cond-mat.mes-hall] 10 Dec 2009
Collective dynamics of excitons and polaritons in
semiconductor nanostructures
A Amo‡, D Sanvitto and L Vi˜na
Departamento de F´ısica de Materiales, Universidad Auton´oma de Madrid, 28049
Madrid, Spain
E-mail: alberto.amo@spectro.jussieu.fr
Abstract.
Time
resolved
photoluminescence
is
a
powerful
technique
to
study the collective dynamics of excitons and polaritons in semiconductor
nanostructures.
We present a two excitation pulses technique to induce the
ultrafast and controlled quenching of the exciton emission in a quantum well. The
depth of the dip is given by the magnitude of the warming of the carriers induced
by the arrival of a laser pulse when an exciton population is already present in the
sample. We use this technique to study the relaxation mechanisms of polaritons
in semiconductor microcavities, which are of great importance to enhance the
conditions for their condensation under non-resonant excitation. We also explore
the dynamics of polariton fluids resonantly created in the lower polariton branch
in a triggered optical parametric oscillator configuration, showing evidence of
polariton superfluidity, and opening up the way to the real-time study of quantum
fluids.
1. Introduction
Semiconductor nanostructures offer a privileged workbench for the study of many
fundamental properties of the light-matter interaction and of the collective excitations
in solids. Due to single atomic monolayer resolution achieved with epitaxial growth
techniques, semiconductor devices can be designed into heterostructures in which the
dimensionality of the excitations, the strength of the light-matter interaction and
the particle character according to its statistics (bosonic or fermionic) can be finely
controlled. Additionally, if the materials of choice in the structure present a direct gap,
excitations in its basic form of electrons promoted from the valence to the conduction
band can be easily created and detected by optical means.
In quantum wells (QWs), optical excitation leads to the formation of two types
of populations: free electrons and holes, and exciton complexes. The two types of
populations coexist in quasi thermal equilibrium (Szczytko et al. 2004, Chatterjee
et al. 2004, Bajoni et al. unpublished), with a temperature which decreases in time
towards the lattice temperature when the excitation is pulsed (von der Linde &
Lambrich 1979, Capizzi et al. 1984, Leo et al. 1988a, Yoon et al. 1996, Bajoni
et al. unpublished). By varying the lattice temperature and density of the photoexcited
carriers it is possible to control the ratio between the two populations, allowing
for the observation of a transition from an exciton dominated phase (insulating
‡ Present address: Laboratoire Kastler Brossel, Universit´e Pierre et Marie Curie, Ecole Normale
Sup´erieure et CNRS, UPMC Case 74, 4 place Jussieu, 75252 Paris Cedex 05, France
Collective dynamics of excitons and polaritons in semiconductor nanostructures
2
due to the neutral character of these quasiparticles) to a free carrier phase (i.
e.
conducting) (Kaindl et al. 2003, Kappei et al. 2005, Amo et al. 2006, Stern
et al. 2008).
Additionally, the energy separation of the exciton and free carrier
recombination enables the detailed study of phase-space filling effects associated to
the fermionic character of the free electron-hole populations (Kappei et al. 2005).
For instance, Pauli blockade is one of the typical effects in a fermionic degenerate
system (Warburton et al. 1997, Kalevich et al. 2001, Ono et al. 2002), and has
been shown to greatly alter the electron spin-flip dynamics in semiconductors and,
consequently, the polarisation dynamics of the light emitted by the system (Potemski
et al. 1999, Dzhioev et al. 2002, Nemec et al. 2005, Amo et al. 2007).
Semiconductor nanostructures allow also for the study of the many body
properties of boson ensembles.
In particular, microcavities consitute an excellent
playground.
In these systems the fundamental excitations are polaritons: bosons
formed from the linear combination of quantum well excitons embedded in a cavity,
and the photon modes confined by Bragg mirrors. Due to their partially photonic
nature, polaritons have a very small mass, (∼10−5 me, the free electron mass)
and, consequently, a very high critical temperature for Bose-Einstein condensation
(BEC) (Kasprzak et al. 2006, Christopoulos et al. 2007, Christmann et al. 2008).
Additionally, the properties of the ensemble can be easily probed through the
light escaping from the cavity, which arises from the annihilation of polaritons and
contains all the energy, coherence and density information of the polariton ensemble
inside the cavity.
Recent experiments have shown the achievement of polariton
condensates in CdTe and GaAs based microcavities at temperatures of the order
of ∼10 K (Kasprzak et al. 2006, Balili et al. 2007, Wertz et al. 2009).
Despite
their out of equilibrium character (their lifetimes range up to ∼
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