We investigate the coherent exciton spin dynamics in a single InAlAs/AlGaAs quantum dot using time-resolved quantum state tomography. Under two-LO-phonon quasi-resonant excitation of neutral exciton, we observe pronounced quantum beats in the circular and diagonal polarization components, reflecting the fine-structure splitting (
Δ≈19.6 μeV). By employing a global fitting procedure across three orthogonal polarization bases, we demonstrate that the spin evolution is consistently described by a unified Hamiltonian dominated by the anisotropic exchange interaction. While the initial degree of circular polarization is limited to
≈0.28 due to fast relaxation processes during carrier cooling, the subsequent dynamics reveal a long-lived spin coherence (
1.1±0.2 ns) that exceeds the exciton lifetime (
∼767 ps). Our analysis reveals that the spin-formation time is significantly shorter than the instrument response function, and the absence of a discernible Overhauser shift confirms a negligible influence from the local nuclear environment under the present conditions. These results provide a quantitative benchmark for the three-dimensional reconstruction of spin trajectories using differential polarization signals, demonstrating the feasibility of using quasi-resonant excitation for stable spin initialization in semiconductor nanostructures.
We report the single-photon Fourier spectroscopy of exciton and exciton complexes in single self-assembled InAlAs∕AlGaAs quantum dots. A Michelson interferometer was inserted in the photoluminescence path for measuring the coherence length of the time-averaged emission of neutral excitons and their complexes. The effects of exchange interactions and fluctuations in the surrounding excess charges were estimated by comparing the coherence times and the excitation energies of the excitons and their complexes.