arXiv subjects

Emmanuel Courtade

Publications and source records attributed to Emmanuel Courtade.

8 recordsLinked to original sources

arXiv2020

Measurement of Conduction and Valence Bands g-factors in a Transition Metal Dichalcogenide Monolayer

The electron valley and spin degree of freedom in monolayer transition-metal dichalcogenides can be manipulated in optical and transport measurements performed in magnetic fields. The key parameter for determining the Zeeman splitting, namely the separate contribution of the electron and hole g-factor, is inaccessible in most measurements. Here we present an original method that gives access to the respective contribution of the conduction and valence band to the measured Zeeman splitting. It exploits the optical selection rules of exciton complexes, in particular the ones involving inter-valley phonons, avoiding strong renormalization effects that compromise single particle g-factor determination in transport experiments. These studies yield a direct determination of single band g factors. We measure gc1= 0.86, gc2=3.84 for the bottom (top) conduction bands and gv=6.1 for the valence band of monolayer WSe2. These measurements are helpful for quantitative interpretation of optical and transport measurements performed in magnetic fields. In addition the measured g-factors are valuable input parameters for optimizing band structure calculations of these 2D materials.

cond-mat.mtrl-sci↗

arXiv2019

Perfect absorption by an atomically thin crystal

Optical absorption is one of fundamental light-matter interactions. In most materials, optical absorption is a weak perturbation to the light. In this regime, absorption and emission are irreversible, incoherent processes due to strong damping. Excitons in monolayer transition metal dichalcogenides, however, interact strongly with light, leading to optical absorption in the non-perturbative regime where coherent re-emission of the light has to be considered. Between the incoherent and coherent limits, we show that a robust critical coupling condition exists, leading to perfect optical absorption. Up to 99.6% absorption is measured in a sub-nanometer thick MoSe2 monolayer placed in front of a mirror. The perfect absorption is controlled by tuning the exciton-phonon, exciton-exciton, and exciton-photon interactions by temperature, pulsed laser excitation, and a movable mirror, respectively. Our work suggests unprecedented opportunities for engineering exciton-light interactions using two-dimensional atomically thin crystals, enabling novel photonic applications including ultrafast light modulators and sensitive optical sensing.

cond-mat.mtrl-sci↗

arXiv2018

Interlayer excitons in bilayer MoS2 with strong oscillator strength up to room temperature

Coulomb bound electron-hole pairs, excitons, govern the optical properties of semi-conducting transition metal dichalcogenides like MoS$_2$ and WSe$_2$. We study optical transitions at the K-point for 2H homobilayer MoS$_2$ in Density Functional Theory (DFT) including excitonic effects and compare with reflectivity measurements in high quality samples encapsulated in hexagonal BN. In both calculated and measured spectra we find a strong interlayer exciton transition in energy between A and B intralayer excitons, observable for T$=4 -300$ K, whereas no such transition is observed for the monolayer in the same structure in this energy range. The interlayer excitons consist of an electron localized in one layer and a hole state delocalized over the bilayer, which results in the unusual combination of high oscillator strength and a static dipole moment. We also find signatures of interlayer excitons involving the second highest valence band (B) and compare absorption calculations for different bilayer stackings. For homotrilayer MoS$_2$ we also observe interlayer excitons and an energy splitting between different intralayer A-excitons originating from the middle and outer layers, respectively.

cond-mat.mtrl-sci↗

arXiv2017

Identifying optical signatures of momentum-dark excitons in transition metal dichalcogenide monolayers

Transition metal dichalcogenide (TMD) monolayers (MLs) exhibit rich photoluminescence spectra associated with interband optical transitions of direct-gap semiconductors. Upon absorption of photons, direct excitons with zero center-of-mass momentum are formed by photo-excited electrons in the conduction band and the respective unoccupied states in the valence band of the same valley. Different spin configurations of such momentum-direct excitons as well as their charged counterparts provide a powerful platform for spin-valley and microcavity physics in two-dimensional materials. The corresponding spectral signatures, however, are insufficient to explain the main characteristic peaks observed in the photoluminescence spectra of ML TMDs on the basis of momentum-\textit{direct} excitons alone. Here, we show that the notion of momentum-\textit{indirect} excitons is important for the understanding of the versatile photoluminescence features. Taking into account phonon-assisted radiative recombination pathways for electrons and holes from dissimilar valleys, we interpret unidentified peaks in the emission spectra as acoustic and optical phonon sidebands of momentum-dark excitons. Our approach will facilitate the interpretation of optical, valley and spin phenomena in TMDs arising from bright and dark exciton manifolds.

cond-mat.mes-hall↗

arXiv2017

Fine Structure and Lifetime of Dark Excitons in Transition Metal Dichalcogenide Monolayers

The intricate interplay between optically dark and bright excitons governs the light-matter interaction in transition metal dichalcogenide monolayers. We have performed a detailed investigation of the "spin-forbidden" dark excitons in WSe2 monolayers by optical spectroscopy in an out-of-plane magnetic field Bz. In agreement with the theoretical predictions deduced from group theory analysis, magneto-photoluminescence experiments reveal a zero field splitting $\delta=0.6 \pm 0.1$ meV between two dark exciton states. The low energy state being strictly dipole forbidden (perfectly dark) at Bz=0 while the upper state is partially coupled to light with z polarization ("grey" exciton). The first determination of the dark neutral exciton lifetime $\tau_D$ in a transition metal dichalcogenide monolayer is obtained by time-resolved photoluminescence. We measure $\tau_D \sim 110 \pm 10$ ps for the grey exciton state, i.e. two orders of magnitude longer than the radiative lifetime of the bright neutral exciton at T=12 K.

cond-mat.mtrl-sci↗

arXiv2015

A minimal titration modelization of the mammalian dynamical heat shock response

Environmental stress, such as oxidative or heat stress, induces the activation of the Heat Shock Response (HSR) which leads to an increase in the heat shock proteins (HSPs) level. These HSPs act as molecular chaperones to maintain proteostasis. Even if the main heat shock response partners are well known, a detailed description of the dynamical properties of the HSR network is still missing. In this study, we derive a minimal mathematical model of cellular response to heat shock that reproduces available experimental data sets both on transcription factor activity and cell viability. This simplistic model highlights the key mechanistic processes that rule the HSR network and reveals (i) the titration of Heat Shock Factor 1 (HSF1) by chaperones as the guiding line of the network, (ii) that protein triage governs the fate of damaged proteins and (iii) three different temperature regimes describing normal, acute or chronic stress.

physics.bio-ph↗

arXiv2006

Dark Optical Lattice of Ring Traps for Cold Atoms

We propose a new geometry of optical lattice for cold atoms, namely a lattice made of a 1D stack of dark ring traps. It is obtained through the interference pattern of a standard Gaussian beam with a counter-propagating hollow beam obtained using a setup with two conical lenses. The traps of the resulting lattice are characterized by a high confinement and a filling rate much larger than unity, even if loaded with cold atoms from a MOT. We have implemented this system experimentally, and obtained a lattice of ring traps populated with typically 40 atoms per site with a life time of 30 ms. Applications in statistical physics, quantum computing and Bose-Einstein condensate dynamics are conceivable.

physics.atom-ph↗

arXiv2004

A broadband Ytterbium-doped tunable fiber laser for 3He optical pumping at 1083 nm

Large amounts of hyperpolarized 3He gas with high nuclear polarization rates are required for use in neutron spin filters or nuclear magnetic resonance imaging of human lung. Very high efficiency can be obtained by metastability exchange optical pumping using multimode lasers to excite the 23S-23P transition at 1083 nm. Broadband Ytterbium-doped tunable fiber lasers have been designed for that particular application. Different options for the architecture of the fiber oscillator are presented and compared. Emphasis is given to a linear cavity configuration that includes a high reflectivity fiber mirror and a low reflectivity tunable fiber Bragg grating. Optical measurements are performed to finely characterize the spectral behavior of the lasers. Atomic response is also quantitatively probed to assess the optimal design of the oscillator for optical pumping. Multimode operation matching the 2 GHz Doppler-broadened helium resonance line and tunability over more than 200 GHz are demonstrated. Boosting the output of this fiber laser with a Yb-doped fiber power amplifier, all-fiber devices are built to provide robust, high power turn-key sources at 1083 nm for improved production of laser polarized 3He.

physics.atom-ph↗