arXiv subjects

J. A. Davis

Publications and source records attributed to J. A. Davis.

3 recordsLinked to original sources

arXiv2026

Tuning the low-energy band structure in twisted bilayer WSe2

Tuning the electronic structures of two-dimensional (2D) material-based heterostructures is of crucial importance for their use in functional next-generation electronics. Here, through angle-resolved photoemission spectroscopy with nanoscale spatial resolution (nano-ARPES), we systematically track the evolution of the near-Fermi-level electronic structure of bilayer WSe2 over a large range of twist angle. While the momentum positioning of the valence band maxima is independent of twist angle, we find that the energetic separation between the hole bands at the K point of the Brillouin zone and the higher binding-energy hole band at Γ can be varied in excess of 100 meV. We explore the mechanisms underpinning this evolution and discuss the implications for tuning both the size of the band gaps, and the efficiency of the spin-dependent electron-phonon coupling channels in homobilayer transition metal dichalcogenide devices.

cond-mat.mtrl-sci↗

arXiv2021

Coherent Dynamics of Floquet-Bloch States in Monolayer WS2 Reveals Fast Adiabatic Switching

Floquet engineering offers a path to optically-controlled materials, but experimental implementations have frequently relied on femtosecond pulses to achieve the high peak fields required to maximise interactions and obtain a measurable response. The Floquet formalism, however, is based on a continuous, periodic drive. Here we use femtosecond laser pulses to drive the optical Stark effect, a simple realization of Floquet engineering, in monolayer WS2. By monitoring the coherent evolution of the free-induction decay, we show that the system evolves adiabatically, and that the finite duration of the pulses does not introduce any effects beyond Floquet theory. Furthermore, we demonstrate that the induced energy shift follows a linear dependence on instantaneous intensity, even for ultrafast driving fields of fewer than 15 optical cycles.

physics.optics↗

arXiv2021

Motional narrowing, ballistic transport, and trapping of room-temperature exciton polaritons in an atomically-thin semiconductor

Atomically-thin transition metal dichalcogenide crystals (TMDCs) hold great promise for future semiconductor optoelectronics due to their unique electronic and optical properties. In particular, electron-hole pairs (excitons) in TMDCs are stable at room temperature and interact strongly with light. When TMDCs are embedded in an optical microcavity, the excitons can hybridise with cavity photons to form exciton polaritons (polaritons herein), which display both ultrafast velocities and strong interactions. The ability to manipulate and trap polaritons on a microchip is critical for future applications. Here, we create a potential landscape for room-temperature polaritons in monolayer WS$_2$, and demonstrate their free propagation and trapping. We show that the effect of dielectric disorder, which restricts the diffusion of WS$_2$ excitons and broadens their spectral resonance, is dramatically reduced in the strong exciton-photon coupling regime leading to motional narrowing. This enables the ballistic transport of WS$_2$ polaritons across tens of micrometers with an extended range of partial first-order coherence. Moreover, the dephasing of trapped polaritons is dramatically suppressed compared to both WS$_2$ excitons and free polaritons. Our results demonstrate the possibility of long-range transport and efficient trapping of TMDC polaritons in ambient conditions.

cond-mat.mes-hall↗