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Register a new userFermi polaron-polaritons in charge-tunable atomically thin semiconductors
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The dynamics of a mobile quantum impurity in a degenerate Fermi system is a fundamental problem in many-body physics. The interest in this field has been renewed due to recent ground-breaking experiments with ultra-cold Fermi gases. Optical creation of an exciton or a polariton in a two-dimensional electron system embedded in a microcavity constitutes a new frontier for this field due to an interplay between cavity-coupling favoring ultra-low mass polariton formation and exciton-electron interactions leading to polaron or trion formation. Here, we present cavity spectroscopy of gate-tunable monolayer MoSe$_2$ exhibiting strongly bound trion and polaron resonances, as well as non-perturbative coupling to a single microcavity mode. As the electron density is increased, the oscillator strength determined from the polariton splitting is gradually transferred from the higher-energy repulsive-exciton-polaron resonance to the lower-energy attractive-polaron manifold. Simultaneous observation of polariton formation in both attractive and repulsive branches indicate a new regime of polaron physics where the polariton impurity mass is much smaller than that of the electrons. Our findings shed new light on optical response of semiconductors in the presence of free carriers by identifying the Fermi polaron nature of excitonic resonances and constitute a first step in investigation of a new class of degenerate Bose-Fermi mixtures.
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While conventional semiconductor technology relies on the manipulation of electrical charge for the implementation of computational logic, additional degrees of freedom such as spin and valley offer alternative avenues for the encoding of information. In transition metal dichalcogenide (TMD) monolayers, where spin-valley locking is present, strong retention of valley chirality has been reported for MoS$_2$, WSe$_2$ and WS$_2$ while MoSe$_2$ shows anomalously low valley polarisation retention. In this work, chiral selectivity of MoSe$_2$ cavity polaritons under helical excitation is reported with a polarisation degree that can be controlled by the exciton-cavity detuning. In contrast to the very low circular polarisation degrees seen in MoSe$_2$ exciton and trion resonances, we observe a significant enhancement of up to 7 times when in the polaritonic regime. Here, polaritons introduce a fast decay mechanism which inhibits full valley pseudospin relaxation and thus allows for increased retention of injected polarisation in the emitted light. A dynamical model applicable to cavity-polaritons in any TMD semiconductor, reproduces the detuning dependence through the incorporation of the cavity-modified exciton relaxation, allowing an estimate of the spin relaxation time in MoSe$_2$ which is an order of magnitude faster than those reported in other TMDs. The valley addressable exciton-polaritons reported here offer robust valley polarised states demonstrating the prospect of valleytronic devices based upon TMDs embedded in photonic structures, with significant potential for valley-dependent nonlinear polariton-polariton interactions.
Transition metal dichalcogenide (TMD) monolayers are direct bandgap semiconductors that feature tightly bound excitons, strong spin-orbit coupling, and spin-valley degrees of freedom. Depending on the spin configuration of the electron-hole pairs, intra-valley excitons of TMD monolayers can be either optically bright or dark. Dark excitons involve nominally spin-forbidden optical transitions with zero in-plane transition dipole moment, making their detection with conventional far-field optical techniques challenging. Here, we introduce a new method for probing the optical properties of two-dimensional (2D) materials via near-field coupling to surface plasmon polaritons (SPPs), which selectively enhances optical transitions with dipole moments normal to the 2D plane. We utilize this method to directly detect dark excitons in monolayer TMDs. When a WSe2 monolayer is placed on top of a single-crystal silver film, its emission into near-field-coupled SPPs displays new spectral features whose energies and dipole orientations are consistent with dark neutral and charged excitons. The SPP-based near-field spectroscopy significantly enhances experimental capabilities for probing and manipulating exciton dynamics of atomically thin materials.
Electronic states in two-dimensional layered materials can exhibit a remarkable variety of correlated phases including Wigner-crystals, Mott insulators, charge density waves, and superconductivity. Recent experimental and theoretical research has indicated that ferromagnetic phases can exist in electronically-doped transition metal dichalcogenide (TMD) semiconductors, but a stable magnetic state at zero magnetic field has eluded detection. Here, we experimentally demonstrate that mesoscopic ferromagnetic order can be generated and controlled by local optical pumping in monolayer WSe2 at zero applied magnetic field. In a spatially resolved pump-probe experiment, we use polarization-resolved reflectivity from excitonic states as a probe of charge-carrier spin polarization. When the sample is electron-doped at density $n_e = 10^{12} cm^{-2}$, we observe that a local, circularly-polarized, microwatt-power optical pump breaks the symmetry between equivalent ferromagnetic spin configurations and creates magnetic order which extends over mesoscopic regions as large as 8 um x 5 um, bounded by sample edges and folds in the 2D semiconductor. The experimental signature of magnetic order is circular dichroism (CD) in reflectivity from the excitonic states, with magnitude exceeding 20% at resonant wavelengths. The helicity of the pump determines the orientation of the magnetic state, which can be aligned along the two principle out-of-plane axes. In contrast to previous studies in 2D materials that have required non-local, slowly varying magnetic fields to manipulate magnetic phases, the demonstrated capability to control long-range magnetism and corresponding strong CD with local and tunable optical pumps is highly versatile. This discovery will unlock new TMD-based spin and optical technologies and enable sophisticated control of correlated electron phases in two-dimensional electron gases (2DEGs).
We show that a transition metal dichalcogenide monolayer with a radiatively broadened exciton resonance would exhibit perfect extinction of a transmitted field. This result holds for s- or p-polarized weak resonant light fields at any incidence angle, due to the conservation of in-plane momentum of excitons and photons in a flat defect-free two dimensional crystal. In contrast to extinction experiments with single quantum emitters, exciton-exciton interactions lead to an enhancement of reflection with increasing power for incident fields that are blue detuned with respect to the exciton resonance. We show that the interactions limit the maximum reflection that can be achieved by depleting the incoming coherent state into an outgoing two-mode squeezed state.
The ability to modulate light at high speeds is of paramount importance for telecommunications, information processing, and medical imaging technologies. This has stimulated intense efforts to master optoelectronic switching at visible and near-infrared frequencies, although coping with current computer speeds in integrated architectures still remains a major challenge. As a partial success, midinfrared light modulation has been recently achieved through gating patterned graphene. Here we show that atomically thin noble metal nanoislands can extend optical modulation to the visible and near-infrared spectral range. We find plasmons in thin metal nanodisks to produce similar absorption cross-sections as spherical particles of the same diameter. Using realistic levels of electrical doping, plasmons are shifted by about half their width, thus leading to a factor-of-two change in light absorption. These results, which we substantiate on microscopic quantum theory of the optical response, hold great potential for the development of electrical visible and near-infrared light modulation in integrable, nanoscale devices.
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