Excitation-Dependent Anisotropic Raman Response of Atomically Thin Pentagonal PdSe₂.

ABSTRACT: The group-10 noble-metal dichalcogenides have recently emerged as a promising group of two-dimensional materials due to their unique crystal structures and fascinating physical properties. In this work, the resonance enhancement of the interlayer breathing mode (B1) and intralayer A_g ¹ and A_g ³ modes in atomically thin pentagonal PdSe₂ were studied using angle-resolved polarized Raman spectroscopy with 13 excitation wavelengths. Under the excitation energies of 2.33, 2.38, and 2.41 eV, the Raman intensities of both the low-frequency breathing mode B1 and high-frequency mode A_g ¹ of all the thicknesses are the strongest when the incident polarization is parallel to the a axis of PdSe₂, serving as a fast identification of the crystal orientation of few-layer PdSe₂. We demonstrated that the intensities of B1, A_g ¹, and A_g ³ modes are the strongest with the excitation energies between 2.18 and 2.38 eV when the incident polarization is parallel to PdSe₂ a axis, which arises from the resonance enhancement caused by the absorption. Our investigation reveals the underlying interplay of the anisotropic electron-phonon and electron-photon interactions in the Raman scattering process of atomically thin PdSe₂. It paves the way for future applications on PdSe₂-based optoelectronics.

SUBMITTER: Luo W 

PROVIDER: S-EPMC9706783 | biostudies-literature | 2022 Nov

REPOSITORIES: biostudies-literature