Ref HAL: hal-01306898_v1
DOI: 10.1103/PhysRevB.93.115202
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The dynamics of the free-exciton capture by boron acceptors and phosphorus donors in diamond is observed in the picosecond range by time-resolved photoluminescence experiments at low temperature. The formation of boron-bound excitons is observed with a delay of 410 ps after the formation of free excitons. For phosphorus, this delay is 120 ps. This is the result of the free-exciton capture by B° and P° impurities. The lifetimes of boron- and phosphorus-bound excitons are measured and found to be equal to 270 and 70 ps, respectively. These values are about four orders of magnitude shorter than for the same impurities in silicon. Ei being the ionization energy of dopants, these results scale well with the Ei4 dependence of the Auger recombination rate expected for bound excitons in indirect band-gap semiconductors.

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Commentaires: Ecole Internationale. Cours présenté par Masha Vladimirova.

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An indirect exciton (IX) is a quasiparticle consisting of an electron and a hole spatially separated in two different planes of a quantum nanostructure, thus exhibiting a strongly dipolar character. Current research on transport properties of IXs is opening a pathway to the development of novel optoelectronic devices, which have already been demonstrated in GaAs-based heterostructures [1-3]. Applying the same ideas to IXs in wide-band gap polar quantum wells (QWs) is particularly promising because of much larger exciton binding energies and natural dipoles induced by strong built-in electric fields. We have recently studied the transport of IXs in GaN/AlGaN QWs grown on sapphire substrates, at temperatures up to 80 K [4], by mapping the micro-photoluminescence (µ-PL) signal obtained under intense, point excitation. The low-temperature PL recorded at long distances from the excitation spot (30 < r < 100µm) turned out to be a secondary PL, excited by the light emitted at the central spot, guided along the plane, due to the refractive index contrast between the layer and the substrate. At higher temperatures, this signal is rapidly quenched and the distance reached by the measurable PL is limited by recombination of excitons at non-radiative defects. Using GaN substrates instead of sapphire should both suppress the secondary emission and the nonradiative recombination, by reducing dislocation densities by 3-4 orders of magnitude. In this work, we compare exciton propagations in two GaN/Al0.19Ga0.81N QWs of identical structures, except for the substrates, respectively of GaN and sapphire. For the GaN substrate, we indeed observe the mere propagation of excitons up to 35 µm away from the excitation spot and up to 250 K (see below). We propose a drift/diffusion modelling of exciton transport, accounting for dipole-dipole repulsion in high-density regions and for disorder along the sample plane.[1]Y. Y. Kuznetsova, M. Remeika, A. A. High, A. T. Hammack, L. V. Butov, M. Hanson, and A. C. Gossard. Optics Letters 35 (10), 1587 (2010).[2]A.A. High, E.E. Novitskaya, L.V. Butov, and A.C. Gossard. Science 321, 229 (2008).[3]A.A. High, A.T. Hammack, L.V. Butov, and A.C. Gossard. Optics Letters 32, 2466 (2007).[4]F. Fedichkin, P. Andreakou, B. Jouault, M. Vladimirova, T. Guillet, C. Brimont, P. Valvin, T. Bretagnon, A. Dussaigne, N. Grandjean, P. Lefebvre. Phys. Rev. B 91, 205424 (2015).

Ref HAL: hal-01305086_v1
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This lecture will present the specific features of GaN- and ZnO-based quantum wells that make them interesting candidates for the creation and manipulation of dipolar, indirect excitons. Conceived as a comparison with what is currently obtained in biased GaAs-based structures, the presentation will emphasize the consequences of a number of properties such as: (i) much larger exciton binding, (ii) much larger Mott densities, (iii) built-in electric fields larger by one order of magnitude, (iv) the subsequent radiative lifetimes that can easily reach several tens of µs… Actual material properties that can be considered detrimental, at present, will also be discussed, like the current crystalline quality of the materials, inducing high densities of nonradiative defects.Theoretical and experimental results will be commented, in order to illustrate the current understanding of the physics of the dipolar excitons that appear naturally in these systems, with no need of an externally applied electric field. In particular, the change of exciton energies under high-density conditions will be discussed. The complex recombination dynamics, measured by time-resolved spectroscopy, will be explained. Recent results on the in-plane propagation of those dipolar excitons will be shown.

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DOI: 10.1364/OL.40.003667
WoS: 000358802800059
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12 Citations
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We report on spatially- and time-resolved emission measurements and observation of transport of indirect excitons in ZnO/MgZnO wide single quantum wells.

Ref HAL: hal-01154792_v1
DOI: 10.1103/PhysRevB.91.205424
WoS: 000354972700012
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19 Citations
Résumé:

We investigate the transport of dipolar indirect excitons along the growth plane of polar (Al,Ga)N/GaN quantum well structures by means of spatially and time-resolved photoluminescence spectroscopy. The transport in these strongly disordered quantum wells is activated by dipole-dipole repulsion. The latter induces an emission blue shift that increases linearly with exciton density, whereas the radiative recombination rate increases exponentially. Under continuous, localized excitation, we observe continuously decreasing emission energy, as excitons propagate away from the excitation spot. This corresponds to a steady-state gradient of exciton density,measured over several tens of micrometers. Time-resolved microphotoluminescence experiments provide information on the dynamics of recombination and transport of dipolar excitons.We account for the ensemble of experimental results by solving the nonlinear drift-diffusion equation. Quantitative analysis suggests that in such structures, exciton propagation on the scale of 10 to 20 μm is mainly driven by diffusion, rather than by drift, due to the strong disorder and the presence of nonradiative defects. Secondary exciton creation, most probably by the intense higher-energy luminescence, guided along the sample plane, is shown to contribute to the excitonemission pattern on the scale up to 100 μm. The exciton propagation length is strongly temperature dependent, the emission being quenched beyond a critical distance governed by nonradiative recombination.

Résumé:

GaN/AlGaN polar single quantum wells have attracted particular attention due to their large binding energies and the presence of strong internal electric fields that naturally induce long-lived excitons. In this case, the exciton transport is driven by the potential landscape caused by the local alteration of the built-in electric field, which results from the exciton accumulation at the same point. We study by spatially- and time-resolved PL experiments AlGaN/GaN coupled quantum wells (QW). The active zone of studied sample consists of a 30 nm thick Al0.20Ga0.80N barrier, a 4.4 nm (17 atomic monolayers) GaN QW followed by 1 monolayer of Al0.20Ga0.80N and a 1.6 nm (6 atomic monolayers) GaN QW and 30 nm thick Al0.20Ga0.80N cap layer. By solving Schroedinger-Poisson equation, we illustrate the two regimes of strongly screened electric field and the totally un-screened QW system. We show that the screening of the build-in electric field enhances the electron-hole wave-function overlap and increases the optical recombination energy. In other words, dipoledipole repulsion between excitons raises their potential energy and drastically increases their radiative recombination rate. A blue-shift of 0.3 eV under continues wave, localized excitation and a quasi-continuous red-shift of the emission as excitons are drifted away from the excitation spot up to distances of 90 μm are observed experimentally. Strong LO-phonon replica are also noticed, as a result of the strongly dipolar character of excitons [1]. These replicas follow the same position dependence as the zerophonon line. Using our Schroedinger-Poisson equation solver, we can extract from the measured blue-shift the position-dependent exciton density. Last, we present simulations of the observed transport features, namely the exciton densities and luminescence intensities by solving the nonlinear drift-diffusion equation. We establish that the long-range excitonic transport is mainly dominated by drift caused by repulsive dipole-dipole interaction between excitons in combination with their long lifetimes. [1] S. Kalliakos, X. B. Zhang, T. Taliercio, P. Lefebvre, B. Gil, N. Grandjean, B. Damilano, and J. Massies. Applied Physics Letters 80, 428 (2002).