Ultrafast atomic-scale scanning tunnelling spectroscopy of a single vacancy in a monolayer crystal
Carmen Roelcke, Lukas Z. Kastner, Maximilian Graml, Andreas Biereder, Jan Wilhelm, Jascha Repp, R. Huber, Yaroslav A. Gerasimenko
Abstract
Abstract Defects in atomically thin semiconductors and their moiré heterostructures have emerged as a unique testbed for quantum science. Strong light–matter coupling, large spin–orbit interaction and enhanced Coulomb correlations facilitate a spin–photon interface for future qubit operations and efficient single-photon quantum emitters. Yet, directly observing the relevant interplay of the electronic structure of a single defect with other microscopic elementary excitations on their intrinsic length, time and energy scales remained a long-held dream. Here we directly resolve in space, time and energy how a spin–orbit-split energy level of an isolated selenium vacancy in a moiré-distorted WSe 2 monolayer evolves under the controlled excitation of lattice vibrations, using lightwave scanning tunnelling microscopy and spectroscopy. By locally launching a phonon oscillation and taking ultrafast energy-resolved snapshots of the vacancy’s states faster than the vibration period, we directly measure the impact of electron–phonon coupling in an isolated single-atom defect. The combination of atomic spatial, sub-picosecond temporal and millielectronvolt energy resolution marks a disruptive development towards a comprehensive understanding of complex quantum materials, where the key microscopic elementary interactions can now be disentangled, one by one.