M. Den Hertog
Centre national de la recherche scientifique
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Featured researches published by M. Den Hertog.
Nano Letters | 2012
F. González-Posada; R. Songmuang; M. Den Hertog; E. Monroy
We report on the photocurrent behavior of single GaN n-i-n nanowires (NWs) grown by plasma-assisted molecular-beam epitaxy on Si(111). These structures present a photoconductive gain in the range of 10(5)-10(8) and an ultraviolet (350 nm) to visible (450 nm) responsivity ratio larger than 6 orders of magnitude. Polarized light couples with the NW geometry with a maximum photoresponse for polarization along the NW axis. The photocurrent scales sublinearly with optical power, following a I ~ P(β) law (β < 1) in the measured range with β increasing with the measuring frequency. The photocurrent time response remains in the millisecond range, which is in contrast to the persistent (hours) photoconductivity effects observed in two-dimensional photoconductors. The photocurrent is independent of the measuring atmosphere, either in the air or in vacuum. Results are interpreted taking into account the effect of surface states and the total depletion of the NW intrinsic region.
Nanotechnology | 2011
Gabriel Tourbot; Catherine Bougerol; A Grenier; M. Den Hertog; D Sam-Giao; David Neil Cooper; P Gilet; B. Gayral; B. Daudin
The structural and optical properties of InGaN/GaN nanowire heterostructures grown by plasma-assisted molecular beam epitaxy have been studied using a combination of transmission electron microscopy, electron tomography and photoluminescence spectroscopy. It is found that, depending on In content, the strain relaxation of InGaN may be elastic or plastic. Elastic relaxation results in a pronounced radial In content gradient. Plastic relaxation is associated with the formation of misfit dislocations at the InGaN/GaN interface or with cracks in the InGaN nanowire section. In all cases, a GaN shell was formed around the InGaN core, which is assigned to differences in In and Ga diffusion mean free paths.
Nanotechnology | 2012
Pascal Gentile; A Solanki; Nicolas Pauc; Fabrice Oehler; B. Salem; G Rosaz; T. Baron; M. Den Hertog; V Calvo
The introduction of hydrogen chloride during the in situ doping of silicon nanowires (SiNWs) grown using the vapor-liquid-solid (VLS) mechanism was investigated. Compared with non-chlorinated atmospheres, the use of HCl with dopant gases considerably improves the surface morphology of the SiNWs, leading to extremely smooth surfaces and a greatly reduced tapering. Variations in the wire diameter are massively reduced for boron doping, and cannot be measured at 600 °C for phosphorous over several tens of micrometers. This remarkable feature is accompanied by a frozen gold migration from the catalyst, with no noticeable levels of gold clusters observed using scanning electron microscopy. A detailed study of the apparent resistivity of the NWs reveals that the dopant incorporation is effective for both types of doping. A graph linking the apparent resistivity to the dopant to silane dilution ratio is built for both types of doping and discussed in the frame of the previous results.
Nano Letters | 2012
M. Den Hertog; F. González-Posada; R. Songmuang; Jean-Luc Rouvière; T. Fournier; B. Fernandez; E. Monroy
GaN nanowires (NWs) with an AlN insertion were studied by correlated optoelectronic and aberration-corrected scanning transmission electron microscopy (STEM) characterization on the same single NW. Using aberration-corrected annular bright field and high angle annular dark field STEM, we identify the NW growth axis to be the N-polar [000-1] direction. The electrical transport characteristics of the NWs are explained by the polarization-induced asymmetric potential profile and by the presence of an AlN/GaN shell around the GaN base of the wire. The AlN insertion blocks the electron flow through the GaN core, confining the current to the radial GaN outer shell, close to the NW sidewalls, which increases the sensitivity of the photocurrent to the environment and in particular to the presence of oxygen. The desorption of oxygen adatoms in vacuum leads to a reduction of the nonradiative surface trap density, increasing both dark current and photocurrent.
Nano Letters | 2012
S. Bounouar; M. Elouneg-Jamroz; M. Den Hertog; C. Morchutt; E. Bellet-Amalric; R. André; Catherine Bougerol; Y. Genuist; J.-Ph. Poizat; S. Tatarenko; K. Kheng
Epitaxial semiconductor quantum dots are particularly promising as realistic single-photon sources for their compatibility with manufacturing techniques and possibility to be implemented in compact devices. Here, we demonstrate for the first time single-photon emission up to room temperature from an epitaxial quantum dot inserted in a nanowire, namely a CdSe slice in a ZnSe nanowire. The exciton and biexciton lines can still be resolved at room temperature and the biexciton turns out to be the most appropriate transition for single-photon emission due to a large nonradiative decay of the bright exciton to dark exciton states. With an intrinsically short radiative decay time (≈300 ps) this system is the fastest room temperature single-photon emitter, allowing potentially gigahertz repetition rates.
Nano Letters | 2010
Fabrice Oehler; Pascal Gentile; T. Baron; Pierre Ferret; M. Den Hertog; Jean-Luc Rouvière
The state of the lateral surface plays a great role in the physics of silicon nanowires. Surprisingly, little is known about the phenomena that occur during growth on the facets of the wires. We demonstrate here that the size and shape of the facets evolve with the exposure time and the radial growth speed. Depending on the chemistry of the surface, either passivated by chlorine or decorated by gold clusters, the radial growth speed varies and the evolution of the facets is enhanced or impeded. If the radial growth speed is high enough, the faceting of the wire can change from top to bottom due to the exposure time difference. Three types of faceting are exposed, dodecagonal, hexagonal, and triangular. An evolution model is introduced to link the different faceting structures and the possible transitions.
Applied Physics Letters | 2011
R. Songmuang; D. Kalita; P. Sinha; M. Den Hertog; R. André; T. Ben; D. González; H. Mariette; E. Monroy
Photoluminescence (PL) studies of GaN/Al(x)Ga(1-x)N quantum dots (QDs) in nanowires demonstrate an efficient carrier confinement, resulting in thermally stable decay times up to 300 K. The evolution of the PL transition energy as a function of both the QD height and the Al mole fraction in the barriers, as well as the evolution of the decay time as a function of the QD height, point out that a built-in electric field is significantly smaller than the value expected from the spontaneous polarization discontinuity. This is explained by the uniaxial compressive strain resulting from the spontaneously formed Al-rich shell that envelops the QD stack
Applied Physics Letters | 2013
A. Artioli; P. Rueda-Fonseca; P. Stepanov; E. Bellet-Amalric; M. Den Hertog; Catherine Bougerol; Y. Genuist; Fabrice Donatini; R. André; Gilles Nogues; K. Kheng; S. Tatarenko; D. Ferrand; J. Cibert
Optically active gold-catalyzed ZnTe nanowires have been grown by molecular beam epitaxy, on a ZnTe(111) buffer layer, at low temperature 350°C under Te rich conditions, and at ultra-low density (from 1 to 5 nanowires per micrometer²). The crystalline structure is zinc blende as identified by transmission electron microscopy. All nanowires are tapered and the majority of them are oriented. Low temperature micro-photoluminescence and cathodoluminescence experiments have been performed on single nanowires. We observe a narrow emission line with a blue-shift of 2 or 3 meV with respect to the exciton energy in bulk ZnTe. This shift is attributed to the strain induced by a 5 nm-thick oxide layer covering the nanowires, and this assumption is supported by a quantitative estimation of the strain in the nanowires.
Applied Physics Letters | 2013
F. González-Posada; R. Songmuang; M. Den Hertog; E. Monroy
In this work, we compare the photodetector performance of single nearly defect-free undoped and n-i-n GaN nanowires (NWs). Undoped NWs present a dark current three orders of magnitude lower than n-i-n structures, about ten times lower gain, and a strong dependence of the measurement environment. In vacuum, undoped NWs react with an increase of their responsivity, accompanied by stronger nonlinearities and persistent photoconductivity effects. This behavior is attributed to the unpinned Fermi level at the m-plane NW sidewalls, which enhances the role of surface states in the photodetection dynamics. In the air, adsorbed oxygen accelerates the carrier dynamics at the price of reducing the photoresponse. In contrast, in n-i-n NWs, the Fermi level pinning at the contact regions limits the photoinduced sweep of the surface band bending, hence reducing the environment sensitivity and preventing persistent effects even in vacuum.
Nano Letters | 2016
R. Songmuang; Le Thuy Thanh Giang; Joël Bleuse; M. Den Hertog; Yann-Michel Niquet; Le Si Dang; H. Mariette
We present a set of experimental results showing a combination of various effects, that is, surface recombination velocity, surface charge traps, strain, and structural defects, that govern the carrier dynamics of self-catalyzed GaAs/AlGaAs core-shell nanowires (NWs) grown on a Si(111) substrate by molecular beam epitaxy. Time-resolved photoluminescence of NW ensemble and spatially resolved cathodoluminescence of single NWs reveal that emission intensity, decay time, and carrier diffusion length of the GaAs NW core strongly depend on the AlGaAs shell thickness but in a nonmonotonic fashion. Although 7 nm AlGaAs shell can efficiently suppress the surface recombination velocity of the GaAs NW core, the influence of the surface charge traps and the strain between the core and the shell that redshift the luminescence of the GaAs NW core remain observable in the whole range of the shell thickness. In addition, the band bending effect induced by the surface charge traps can alter the scattering of the excess carriers inside the GaAs NW core at the core/shell interface. If the AlGaAs shell thickness is larger than 50 nm, the luminescence efficiency of the GaAs NW cores deteriorates, ascribed to defect formation inside the AlGaAs shell evidenced by transmission electron microscopy.