Attosecond All-Optical Retrieval of Valley Polarization via Circular Dichroism in Transient Absorption
arXiv:2412.19612 · doi:10.1103/7n3p-cq9f
Abstract
We propose a scheme for retrieving the ultrafast valley polarization (VP) dynamics in two-dimensional hexagonal materials via attosecond circular dichroism (CD) transient absorption spectroscopy. This approach builds on the CD transition between the first and higher conduction bands induced by the circularly polarized probe pulses. The population imbalance at nonequivalent valleys in the first conduction band is proportionally mapped onto the difference in absorption coefficients of two probe pulses with opposite helicities, supporting an unprecedented quantitative retrieval of the corresponding VP dynamics with subfemtosecond time resolution. We theoretically demonstrate the scheme for h-BN and MoS2 through ab initio calculations, achieving an accurate retrieval of the VP dynamics, particularly the transient VP switching processes, with a time resolution of 250 as.
References in corpus (8)
- Valley polarization in MoS2 monolayers by optical pumping
- High harmonic generation from Bloch electrons in solids
- Light-Induced Valleytronics in Pristine Graphene
- Temperature Dependent Valley Relaxation Dynamics in Single Layer WS2 Measured Using Ultrafast Spectroscopy
- All-Optical Ultrafast Valley Switching in Two-Dimensional Materials
- Graphene valley polarization as a function of carrier-envelope phase in few-cycle laser pulses and its footprints in harmonic signals
- First-principles calculations for transient absorption of laser-excited magnetic materials
- Simulating strong-field electron-hole dynamics in solids probed by attosecond transient absorption spectroscopy