Abstract
A deep understanding of the effect of the A-site cation cross-exchange on the hot-carrier relaxation dynamics in perovskite quantum dots (PQDs) has profound implications on the further development of disruptive photovoltaic technologies. In this study, we investigated the hot carrier cooling kinetics of pure FAPbI3 , MAPbI3 , CsPbI3 and alloyed FA0.5 MA0.5 PbI3 , FA0.5 Cs0.5 PbI3 , and MA0.5 Cs0.5 PbI3 QDs using ultrafast transient absorption (TA) spectroscopy. The lifetimes of the initial fast cooling stage (<1ps) of all the organic cation-containing PQDs were shorter than those of the CsPbI3 QDs, as verified by the electron-phonon coupling strength extracted from the temperature-dependent photoluminescence spectra. The lifetimes of the slow cooling stage of the alloyed PQDs were longer under illumination greater than 1 sun, which was ascribed to the introduction of co-vibrational optical phonon modes in the alloyed PQDs. This facilitated efficient acoustic phonon upconversion and enhanced the hot-phonon bottleneck effect, as demonstrated by first-principles calculations. This article is protected by copyright. All rights reserved.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
