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.