Coherent Exciton-Lattice Dynamics in a 2D Metal Organochalcogenolate Semiconductor

Abstract

Hybrid organic-inorganic nanomaterials can exhibit transitional behavior that deviates from models developed for all-organic or all-inorganic materials systems. Here, we reveal the complexity of exciton-phonon interactions in a recently discovered 2D layered hybrid organic-inorganic semiconductor, silver phenylselenolate (AgSePh). Using femtosecond resonant impulsive vibrational spectroscopy and non-resonant Raman scattering, we measure multiple hybrid organic-inorganic vibrational modes and identify a subset of these modes that strongly couple to the electronic excited state. Calculations by density functional perturbation theory show that these strongly coupled modes exhibit large out-of-plane silver atomic motions and silver-selenium spacing displacements. Moreover, analysis of photoluminescence fine-structure splitting and temperature-dependent peak-shifting/linewidth-broadening suggests that light emission in AgSePh is most strongly affected by a compound 100 cm-1 mode involving the wagging motion of phenylselenolate ligands and accompanying metal-chalcogen stretching. Finally, red-shifting of vibrational modes with increasing temperature reveals a high degree of anharmonicity arising from non-covalent interactions between phenyl rings. These findings reveal the unique effects of hybrid vibrational modes in organic-inorganic semiconductors and motivate future work aimed at specifically engineering such interactions through chemical and structural modification.