Publication date: 15th July 2022
Ligand exchange performed during or after material synthesis provides an efficient route for the electronic functionalization of colloidal nanomaterials for electronic and optoelectronic devices. Herein, we develop a simple post-synthetic process that can produce electronic-active films of all-inorganic and hybrid lead halide perovskite nanocrystals (NCs), namely green-emitting CsPbBr3 NCs and infrared-emitting FAPbI3 NCs. We focus on the impact of such functionalization on the morphological, optical, and electrical properties of the treated NC solids while adjusting parameters of the reaction such as the ligand washing exposure time and the processing atmosphere conditions.
Microscopy and spectroscopy unravel the evolution of morphology and photophysics from the nano- to the mesoscopic regime and from isolated NC excitons to electronic and defect transitions of sintered NCs, respectively. As the ligand removal reaction time increases electronic communication improves and the obtained photo-current in simple lateral photoconductive devices increases by up to ~90% and ~60% for the case of FAPbI3 NCs and CsPbBr3 NCs respectively. THz spectroscopy further supports the photoconductivity findings and produces consistent trends with treatment reaction time in transport and recombination figures of merit such as the real and imaginary conductivity, carrier mobility and auger coefficient.
This work was financially supported by the Research and Innovation Foundation of Cyprus, under the "NEW STRATEGIC INFRASTRUCTURE UNITS-YOUNG SCIENTISTS" Program.