Floriana Morabito1,2,Charles Sayers1,Valeria Nicolosi3,Christoph Gadermaier1
Politecnico di Milano1,Istituto Italiano di Tecnologia2,Trinity College Dublin, The University of Dublin3
Floriana Morabito1,2,Charles Sayers1,Valeria Nicolosi3,Christoph Gadermaier1
Politecnico di Milano1,Istituto Italiano di Tecnologia2,Trinity College Dublin, The University of Dublin3
MoS<sub>2</sub> is a bidimensional material, belonging to the class of transition metal dichalcogenides (TMDs). Its semiconducting 2H phase has unique optoelectronic properties, due to its strong light-matter interaction and chemical stability in both mono- or few-layer form. As a result, it is an excellent candidate for light harvesting applications, which rely on the photogeneration of sufficiently long-lived charge carriers.<br/>Liquid phase exfoliation (LPE) is a high yield and industrially scalable technique to produce high quality nanosheet colloidal dispersions that can be easily processed and incorporated into device fabrication processes.<br/>In this study, we investigate LPE MoS<sub>2 </sub>samples using time-resolved optical spectroscopy. The transient response of this material is dictated by the formation and recombination of bound states, e.g. excitons and trions. Using a specially designed pump-probe setup, we measured the lifetime of these photoexcited states from the femtosecond to microsecond range. We observe spectral features related to charge carriers with lifetimes up to ~ 100 ns. A comparison between different exfoliation techniques aims at understanding the role of the different thicknesses and details of the nanosheet morphology on the photo-generated charge carrier dynamics.