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Valley Zeeman effect and Landau levels in Two-Dimensional Transition Metal Dichalcogenides

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 Added by Fengyuan Xuan
 Publication date 2020
  fields Physics
and research's language is English




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This paper presents a theoretical description of both the valley Zeeman effect (g-factors) and Landau levels in two-dimensional H-phase transition metal dichalcogenides (TMDs) using the Luttinger-Kohn approximation with spin-orbit coupling. At the valley extrema in TMDs, energy bands split into Landau levels with a Zeeman shift in the presence of a uniform out-of-plane external magnetic field. The Landau level indices are symmetric in the $K$ and $K$ valleys. We develop a numerical approach to compute the single band g-factors from first principles without the need for a sum over unoccupied bands. Many-body effects are included perturbatively within the GW approximation. Non-local exchange and correlation self-energy effects in the GW calculations increase the magnitude of single band g-factors compared to those obtained from density functional theory. Our first principles results give spin- and valley-split Landau levels, in agreement with recent optical experiments. The exciton g-factors deduced in this work are also in good agreement with experiment for the bright and dark excitons in monolayer WSe$_2$, as well as the lowest-energy bright excitons in MoSe$_2$-WSe$_2$ heterobilayers with different twist angles.



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Transition metal dichalcogenides (TMDCs) have emerged as a new two dimensional materials field since the monolayer and few-layer limits show different properties when compared to each other and to their respective bulk materials. For example, in some cases when the bulk material is exfoliated down to a monolayer, an indirect-to-direct band gap in the visible range is observed. The number of layers $N$ ($N$ even or odd) drives changes in space group symmetry that are reflected in the optical properties. The understanding of the space group symmetry as a function of the number of layers is therefore important for the correct interpretation of the experimental data. Here we present a thorough group theory study of the symmetry aspects relevant to optical and spectroscopic analysis, for the most common polytypes of TMDCs, i.e. $2Ha$, $2Hc$ and $1T$, as a function of the number of layers. Real space symmetries, the group of the wave vectors, the relevance of inversion symmetry, irreducible representations of the vibrational modes, optical selection rules and Raman tensors are discussed.
We present a many-body formalism for the simulation of time-resolved nonlinear spectroscopy and apply it to study the coherent interaction between excitons and trions in doped transition-metal dichalcogenides. Although the formalism can be straightforwardly applied in a first-principles manner, for simplicity we use a parameterized band structure and a static model dielectric function, both of which can be obtained from a calculation using the $GW$ approximation. Our simulation results shed light on the interplay between singlet and triplet trions in molybdenum- and tungsten-based compounds. Our two-dimensional electronic spectra are in excellent agreement with recent experiments and we accurately reproduce the beating of a cross-peak signal indicative of quantum coherence between excitons and trions. Although we confirm that the quantum beats in molybdenum-based monolayers unambigously reflect the exciton-trion coherence time, they are shown here to provide a lower-bound to the coherence time of tungsten analogues due to a destructive interference emerging from coexisting singlet and triplet trions.
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