Publications
Electrically tunable single- and few-layer MoS2 nanoelectromechanical systems with broad dynamic range
Atomically thin semiconducting crystals [such as molybdenum disulfide (MoS2)] have outstanding electrical, optical, and mechanical properties, thus making them excellent constitutive materials for innovating new two-dimensional (2D) nanoelectromechanical systems (NEMS). Although prototype structures have recently been demonstrated toward functional devices such as ultralow-power, high-frequency tunable oscillators and ultrasensitive resonant transducers, both electrical tunability and large dynamic range (DR) are critical and desirable.
Strongly Interaction-Enhanced Valley Magnetic Response in Monolayer WSe2
We measure the doping dependence of the valley Zeeman splitting of the fundamental optical transitions in monolayer WSe2 under an out-of-plane magnetic field by optical reflection contrast and photoluminescence spectroscopy. A nonlinear valley Zeeman effect, correlated with an over fourfold enhancement in the g factor, is observed. The effect occurs when the Fermi level crosses the spin-split upper conduction band, corresponding to a change of the spin-valley degeneracy from two to four. The enhancement increases and shows no sign of saturation as the sample temperature decreases.
Electrical Tuning of Interlayer Exciton Gases in WSe2 Bilayers
van der Waals heterostructures formed by stacking two-dimensional atomic crystals are a unique platform for exploring new phenomena and functionalities. Interlayer excitons, bound states of spatially separated electron-hole pairs in van der Waals heterostructures, have demonstrated potential for rich valley physics and optoelectronics applications and been proposed to facilitate high-temperature superfluidity. Here, we demonstrate highly tunable interlayer excitons by an out-of-plane electric field in homobilayers of transition metal dichalcogenides.
Valley magnetoelectricity in single-layer MoS 2
The magnetoelectric (ME) effect, the phenomenon of inducing magnetization by application of an electric field or vice versa, holds great promise for magnetic sensing and switching applications. Studies of the ME effect have so far focused on the control of the electron spin degree of freedom (DOF) in materials such as multiferroics and conventional semiconductors. Here, we report a new form of the ME effect based on the valley DOF in two-dimensional Dirac materials.
The role of electron-phonon interactions on the coherence lifetime of monolayer transition metal dichalcogenides
We investigate the excitonic dephasing of transition metal dichalcogenides, namely MoS2, MoSe2 and WSe2 atomic monolayer thick and bulk crystals, in order to understand the factors that determine the optical coherence in these materials. Coherent nonlinear optical spectroscopy, temperature dependent absorption combined with theoretical calculations of the phonon spectra, reveal the important role electron-phonon interactions plat in dephasing process.
Vapor–liquid–solid synthesis of ZnSnN2
A series of experiments was carried out to explore the conditions under which ZnSnN2 would form by vapor–liquid–solid synthesis from a Zn–Sn melt exposed to a nitrogen plasma. ZnSnN2 precipitated at melt temperatures between 455 and 560 °C for melt compositions between 1.5 and 15 at.% Zn. Sn3N4 formed for temperatures between 440 and 560 °C for melt compositions below 1 at.% Zn. Zn3N2 apparently grew only in the vapor phase, and only at melt temperatures between 409 and 463 °C. Each of the materials was identified by its characteristic Raman spectrum and by Auger chemical analysis.
Characterization and control of ZnGeN2 cation lattice ordering
ZnGeN2 and other heterovalent ternary semiconductors have important potential applications in optoelectronics, but ordering of the cation sublattice, which can affect the band gap, lattice parameters, and phonons, is not yet well understood. Here the effects of growth and processing conditions on the ordering of the ZnGeN2 cation sublattice were investigated using x-ray diffraction and Raman spectroscopy. Polycrystalline ZnGeN2 was grown by exposing solid Ge to Zn and NH3 vapors at temperatures between 758 °C and 914 °C.
Probing the Spin-Polarized Electronic Band Structure in Monolayer Transition Metal Dichalcogenides by Optical Spectroscopy
We study the electronic band structure in the K/K′ valleys of the Brillouin zone of monolayer WSe2 and MoSe2 by optical reflection and photoluminescence spectroscopy on dual-gated field-effect devices. Our experiment reveals the distinct spin polarization in the conduction bands of these compounds by a systematic study of the doping dependence of the A and B excitonic resonances. Electrons in the highest-energy valence band and the lowest-energy conduction band have antiparallel spins in monolayer WSe2 and parallel spins in monolayer MoSe2.
Raman study of the vibrational modes in ZnGeN2 (0001)
A Raman spectroscopy study was carried out on ZnGeN2 hexagonal single crystal (0001)-oriented platelets obtained by reaction of gaseous ammonia with a Zn-Ge-Sn liquid alloy at 758 °C. The sample geometry allowed measurement of the A2 and A1 Raman modes. First-principles calculations of the spectra were carried out using an improved pseudopotential. Measurements with crossed polarizers yielded spectra that agreed well with first-principles calculations of the A2 modes. Measurements with parallel polarizers should in principle provide the A1L modes.
Valley- and spin-polarized Landau levels in monolayer WSe2
Electrons in monolayer transition metal dichalcogenides are characterized by valley and spin quantum degrees of freedom, making it possible to explore new physical phenomena and to foresee novel applications in the fields of electronics and optoelectronics. Theoretical proposals further suggest that Berry curvature effects, together with strong spin-orbit interactions, can generate unconventional Landau levels (LLs) under a perpendicular magnetic field. In particular, these would support valley- and spin-polarized chiral edge states in the quantum Hall regime.