Hot Exciton Effect in Photoluminescence of Monolayer Transition Metal Dichalcogenide
Ke Xiao1, Ruihuan Duan2, Zheng Liu2, Kenji Watanabe3, Takashi Taniguchi4, Wang Yao1, Xiaodong Cui1, *
1 Department of Physics, University of Hong Kong, Hong Kong SAR
2 School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore
3 Research Center for Functional Materials, National Institute for Materials Science, 1-1 Namiki, Tsukuba 305-0044, Japan
4 International Center for Materials Nanoarchitectonics, National Institute for Materials Science, 1-1 Namiki, Tsukuba 305-0044, Japan
* e-mail: xdcui@hku.hk
Abstract
Hot excitons are usually neglected in optical spectroscopy in 2D semiconductors for the sake of momentum conservation, as the majority of hot excitons are out of light cones. In this letter, we elaborate the contribution of hot excitons to optical properties of monolayer MoSe2 with photoluminescence (PL) and photoluminescence excitation (PLE) spectroscopy. With the excitation-intensity-dependent PL, temperature-dependent PL and PLE experiments combined with the simulations, we experimentally distinguish the influences of the exciton temperature and the lattice temperature in the PL spectrum. It is concluded that the acoustic phonon assisted photoluminescence accounts for the non-Lorentzian high energy tail in the PL spectrum and the hot exciton effect is significant to linear optical properties of TMDs. Besides, the effective exciton temperature is found to be several tens of Kelvin higher than the lattice temperature at non-resonant optical excitation. It indicates that the exciton temperature needs to be carefully taken into account when considering the exciton related quantum phase phenomena such as exciton condensation. It is experimentally demonstrated that the effective exciton temperature can be tuned by excitation energy.
Introduction:
Monolayer transition metal dichalcogenides (TMDs) has been recognized as one of superior playgrounds for two-dimensional (2D) physics, particularly 2D exciton study. The weak Coulomb screening and 2D nature lead to prominent excitons with a giant binding energy dominating monolayer TMDs’ optical properties1, 2, 3, 4, 5, 6. The attributes of excitons in monolayer TMDs featuring strong oscillator strength, richness of degrees of freedom, i.e. spin and valley, and spin-valley locking7, 8 have been stimulating intriguing experiments in many-body physics.9, 10Especially, the strong spin-orbit coupling of the transition metal atoms gives rise to the large spin splitting in valence band, resulting in the two families of optical accessible bright excitons, namely A excitons (lower energy) and B excitons (higher energy).11, 12As yet not much attention has been paid to the influence of hot excitons whose kinetic energy is significantly higher than lattice temperature. Unlike hot electrons which affect physics properties in many aspects13, 14, 15, hot excitons are usually neglected in optical spectroscopy except in dynamics study16 for the sake of momentum conservation, as the majority of hot excitons are out of light cone. Figure 1 depicts the photoluminescence (PL) process in TMDs. The excited electrons and holes immediately form excitons in a highly non-equilibrium state once pumped as the Fig.1(a) elaborates. After a time\(\tau_{\text{th}}\)(~sub-100fs ),17, 18 a thermalization among excitons themselves is reached and excitons follow the Boson/Boltzmann distribution characterized with the exciton temperature \(T_{\text{exciton}}\) (Fig.1(b)). Note that the exciton temperature is still much higher than the lattice temperature\(T_{\text{lattice}}\) at this time. The excitons further cool down accompanying with an energy transfer to lattice via exciton-phonon scattering or some other process19, 20, 21 until achieving thermal equilibrium (\(T_{\text{exciton}}=T_{\text{lattice}}\)), characterized by a time scale \(\tau_{ex-ph}\) (~tens of picosecond).16, 22, 23, 24, 25.
It is widely assumed that excitons and lattice share the same temperature in optical spectroscopy. Given that the excitons’ radiative lifetime of sub-picosecond 26 is much shorter than\(\tau_{ex-ph}\), the excitons could radiate before thermalizing with the lattice. Meanwhile, only the excitons inside the light cone can realize direct radiative recombination for the requirement of in-plane momentum conservation (Fig.1(d)). Intuitively, the temperature of excitons seems not as important as that of electrons since these radiation-active excitons are much less influenced by the exciton temperature. The homogeneous linewidth broadening (~several meV ) can also relax to some extent the energy-momentum conservation requirement in exciton’s light emission27. We calculate the PL spectra at various exciton temperatures (\(T_{\text{exciton}}\)) and conclude this homogeneous linewidth broadening effect is considerably minor and has a negligible contribution to the PL linewidth (more specifically in SI). The other mechanism accounting for the linewidth broadening is the acoustic phonon assisted exciton photoluminescence28, 29, 30. The hot excitons (green circle in Fig.1(d)) could be scattered into the light cone by absorbing or emitting acoustic phonons.