Monolayer transition-metal dichalcogenides (ML-TMDs) offer exciting opportunities to test the manifestations of many-body interactions through changes in the charge density. The two-dimensional character and reduced screening in ML-TMDs lead to the formation of neutral and charged excitons with binding energies orders of magnitude larger than those in conventional bulk semiconductors. Tuning the charge density by a gate voltage leads to profound changes in the optical spectra of excitons in ML-TMDs. On the one hand, the increased screening at large charge densities should result in a blueshift of the exciton spectral lines due to reduction in the binding energy. On the other hand, exchange and correlation effects that shrink the band-gap energy at elevated charge densities (band-gap renormalization) should result in a redshift of the exciton spectral lines. While these competing effects can be captured through various approximations that model long-wavelength charge excitations in the Bethe–Salpeter equation, we show that a novel coupling between excitons and shortwave charge excitations is essential to resolve several experimental puzzles. Unlike ubiquitous and well-studied plasmons, driven by collective oscillations of the background charge density in the long-wavelength limit, we discuss the emergence of shortwave plasmons that originate from the short-range Coulomb interaction through which electrons transition between the and valleys. The shortwave plasmons have a finite energy-gap because of the removal of spin-degeneracy in both the valence- and conduction-band valleys (a consequence of breaking of inversion symmetry in combination with strong spin–orbit coupling in ML-TMDs). We study the coupling between the shortwave plasmons and the neutral exciton through the self-energy of the latter. We then elucidate how this coupling as well as the spin ordering in the conduction band give rise to an experimentally observed optical sideband in electron-doped W-based MLs, conspicuously absent in electron-doped Mo-based MLs or any hole-doped ML-TMDs. While the focus of this review is on the optical manifestations of many-body effects in ML-TMDs, a systematic description of the dynamical screening and its various approximations allow one to revisit other phenomena, such as nonequilibrium transport or superconducting pairing, where the use of the Bethe–Salpeter equation or the emergence of shortwave plasmons can play an important role.

Monolayers of semiconducting transition metal dichalcogenides (TMDCs) with unique spin-valley contrasting properties and remarkably strong excitonic effects continue to be a subject of intense research interests. These model 2D semiconductors feature two fundamental intravalley excitons species–optically accessible ‘bright’ excitons with anti-parallel spins and optically inactive ‘dark’ excitons with parallel spins. For applications exploiting radiative recombination of bright excitons or long lifetime dark excitons, it is essential to understand the radiative character of the exciton ground state and establish the energy separation between the lowest energy bright and dark excitons. Here, we report a direct spectroscopic measure of dark excitons in monolayer MoSe ₂ encapsulated in hexagonal boron nitride. By applying strong in-plane magnetic field, we induce mixing and splitting of bright and dark exciton branches, which enables an accurate spectroscopic determination of their energies. We confirm the bright character of the exciton ground state separated by a 1.5 meV gap from the higher energy dark exciton state, much smaller compared to the previous theoretical expectations. These findings provide critical information for further improvement of the accurate theoretical description of TMDCs electronic structure.

We present photoluminescence measurements in monolayer ${\mathrm{WSe}}_2$, which point to the importance of the interaction between charged particles and excitonic complexes. The theoretical analysis highlights the key role played by exchange scattering, referring to cases wherein the particle composition of the complex changes after the interaction. For example, exchange scattering renders bright excitonic complexes dark in monolayer ${\mathrm{WSe}}_2$ on accounts of the unique valley-spin configuration in this material. In addition to the ultrafast energy relaxation of hot excitonic complexes following their interaction with electrons or holes, our analysis sheds light on several key features that are commonly seen in the photoluminescence of this monolayer semiconductor. In particular, we can understand why the photoluminescence intensity of the neutral bright exciton is strongest when the monolayer is hole doped rather than charge neutral or electron doped. Similarly, we can understand the reason for the dramatic increase of the photoluminescence intensity of negatively charged excitons (trions) as soon as electrons are added to the monolayer. To self-consistently explain the findings, we further study the photoluminescence spectra at different excitation energies and analyze the behavior of the elusive indirect exciton.

Just as photons are the quanta of light, plasmons are the quanta of orchestrated charge-density oscillations in conducting media. Plasmon phenomena in normal metals, superconductors, and doped semiconductors are often driven by long-wavelength Coulomb interactions. However, in crystals whose Fermi surface is comprised of disconnected pockets in the Brillouin zone, collective electron excitations can also attain a shortwave component when electrons transition between these pockets. In this work, we show that the band structure of monolayer transition-metal dichalcogenides gives rise to an intriguing mechanism through which shortwave plasmons are paired up with excitons. The coupling elucidates the origin for the optical sideband that is observed repeatedly in monolayers of ${\mathrm{WSe}}_2$ and ${\mathrm{WS}}_2$ but not understood. The theory makes it clear why exciton-plasmon coupling has the right conditions to manifest itself distinctly only in the optical spectra of electron-doped tungsten-based monolayers.

In the archetypal monolayer semiconductor ${\mathrm{WSe}}_2$, the distinct ordering of spin-polarized valleys (low-energy pockets) in the conduction band allows for studies of not only simple neutral excitons and charged excitons (i.e., trions), but also more complex many-body states that are predicted at higher electron densities. We discuss magneto-optical measurements of electron-rich ${\mathrm{WSe}}_2$ monolayers and interpret the spectral lines that emerge at high electron doping as optical transitions of six-body exciton states (“hexcitons”) and eight-body exciton states (“oxcitons”). These many-body states emerge when a photoexcited electron-hole pair interacts simultaneously with multiple Fermi seas, each having distinguishable spin and valley quantum numbers. In addition, we explain the relations between dark trions and satellite optical transitions of hexcitons in the photoluminescence spectrum.

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 intervalley 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 $g_{c1}=0.86\pm 0.1$, $g_{c2}=3.84\pm 0.1$ for the bottom (top) conduction bands and $g_v=6.1\pm 0.1$ for the valence band of monolayer ${\mathrm{WSe}}_2$. 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.