Structure-Dependent Electronic Relaxation Dynamics of Two-Dimensional Silver Monolayers
Matthew W-J Liu1, Kanchan Ajit Ulman2, Boyang Zheng3
1Department of Materials Science and Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Abstract:
The electronic relaxation dynamics of two-dimensional silver polar metal heterostructures (2D-PMets), isolated with two different Ag lattice structures, were studied with femtosecond transient absorption (fs-TA) spectroscopy. The two 2D Ag phases, called Ag(1) and Ag(2), differ in atomic packing density, which leads to phase-specific ultralow frequency (ULF) phonon modes and visible electronic absorption transitions. Time-resolved kinetic traces for both phases were fit to a biexponential decay function, with the first decay component pertaining to ultrafast electronic relaxation and the second corresponding to carrier-phonon scattering. The first decay time constant τ1 is <400 fs for both phases. In contrast, carrier-phonon scattering exhibited lattice-specific and excitation wavelength-independent relaxation time constants; τ2 ∼ 2 ps for Ag(1) and ∼ 1 ps for Ag(2). The shorter τ2 in Ag(2) is attributed to increased carrier-phonon scattering probability in more close-packed lateral structures. The results indicate that atomic-level structure controls energy flow in spatially confined 2D materials.
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