2006
DOI: 10.1088/0268-1242/21/9/010
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Carrier transfer in coupled asymmetric GaAs/AlGaAs double quantum wells after ultrafast intersubband excitation

Abstract: Intersubband scattering processes are investigated in selectively doped asymmetric tunnel-coupled GaAs/AlGaAs quantum wells by infrared pump probe spectroscopy. Various subbands are excited by resonant absorption of a mid-infrared pump pulse and the carrier relaxation is observed via timeand frequency-resolved absorption changes monitored by a subsequent infrared probe pulse. The experimental data show that most of the carriers remain in the quantum well in which the excitation process mainly takes place. Only… Show more

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Cited by 8 publications
(7 citation statements)
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“…From [12] it can be deduced that times t 12 , t 13 and t 23 at the liquid nitrogen temperature remain close to their room temperature estimates of 0.1 ps. Times T 13 and T 23 also remain approximately the same, but T 21 grows by several times due to the non-resonant nature of longitudinal optical (LO) phonon emission at THz-range transition 2 ↔ 1 [40]. Time τ l at the liquid nitrogen temperature is 7 times larger than its value at room temperature [21] whereas time τ is 4 times smaller [51].…”
Section: Optimal Active Region and Waveguide Designmentioning
confidence: 97%
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“…From [12] it can be deduced that times t 12 , t 13 and t 23 at the liquid nitrogen temperature remain close to their room temperature estimates of 0.1 ps. Times T 13 and T 23 also remain approximately the same, but T 21 grows by several times due to the non-resonant nature of longitudinal optical (LO) phonon emission at THz-range transition 2 ↔ 1 [40]. Time τ l at the liquid nitrogen temperature is 7 times larger than its value at room temperature [21] whereas time τ is 4 times smaller [51].…”
Section: Optimal Active Region and Waveguide Designmentioning
confidence: 97%
“…Due to intrasubband electronphonon and electron-electron scattering, they relax to the Fermi distributions ρ jj e determined by quasi-equilibrium chemical potentials μ j which, in turn, are determined by the instantaneous subband electron sheet densities N j ≡ +∞ 0 ρ jj 2πp dp/(2πh) 2 (the upper integration limit is put to infinity here due to the rapid exponential decrease of the integrand for large p) through the relation N j = +∞ 0 ρ jj e 2πp dp/(2πh) 2 . As the times of the intrasubband relaxation are typically much shorter than the times of intersubband relaxation [23,[32][33][34][35][36][37][38][39][40], it will be assumed for estimates below that ρ jj = ρ jj e .…”
Section: Modelmentioning
confidence: 99%
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“…Due to intrasubband electronphonon and electron-electron scattering, they relax to the Fermi distributions ρ jj e determined by quasi-equilibrium chemical potentials μ j which, in turn, are determined by the instantaneous subband electron sheet densities N j ≡ +∞ 0 ρ jj 2πp dp/(2π h) 2 (the upper integration limit is put to infinity here due to the rapid exponential decrease of the integrand for large p) through the relation N j = +∞ 0 ρ jj e 2πp dp/(2π h) 2 . As the times of the intrasubband relaxation are typically much shorter than the times of intersubband relaxation [23,[32][33][34][35][36][37][38][39][40], it will be assumed for estimates below that ρ jj = ρ jj e .…”
Section: Modelmentioning
confidence: 99%
“…4,5 But also coherent aspects of the dynamics, many-body effects, and the identification of relevant relaxation mechanisms have been issues of interest. [6][7][8][9][10][11][12][13][14][15][16] For intersubband experiments, where the carriers in the conduction bands are provided by doping, the available spin orientations are initially equally occupied. With these initial conditions optical spin orientation can be achieved in intersubband transitions that are driven by circularly polarized in-plane fields.…”
Section: Introductionmentioning
confidence: 99%