2024/06/05 by Bethany R. de Roulet, Lorenz Drescher, de Roulet, Bethany R. +5 · 2 citations
Biochemistry, Genetics and Molecular Biology · Engineering · Materials Science · #Advanced Electron Microscopy Techniques and Applications #Advanced Materials Characterization Techniques #Chemical Physics (physics.chem-ph) #Electron and X-Ray Spectroscopy Techniques #FOS: Physical sciences #Materials Science (cond-mat.mtrl-sci) #Optics (physics.optics)
paper · pdf · doi:10.48550/arxiv.2406.03567
openalex publication_date 2024/06/05 · openalex created_date 2024/06/08 · openalex updated_date 2026/08/01
Understanding initial electron thermalization has relevance to both fundamental scientific knowledge and application to the construction of novel devices. In this study, attosecond transient absorption is used to directly measure initial electron thermalization times of 38 ± 8 fs, 15 ± 3 fs, 4.2 ± 1 fs, and 2.0 ± 0.3 fs for Mg, Pt, Fe, and Co, respectively. Through time dependent density function theory calculations, it is shown that the fast electron thermalization observed in Fe and Co is correlated with a strong local field effect. We find that a simple analytical model can be used to calculate the initial electron thermalization time measured by the transient extreme ultraviolet absorption spectroscopy method performed here. Our results suggest that the most significant contributions to the initial electron thermalization times are the basic metal properties of the density of states volume available for scattering and screened electron interaction. Many-body effects contribute less, but still significantly to the initial electron thermalization time. Ultimately the information gained through this study shows the unique view that attosecond transient absorption spectroscopy contributes to unraveling and monitoring electron dynamics and its connection to many-body effects in metals and beyond.