Excited-state charge-carrier dynamics governs the performance of organometal trihalide perovskites (OTPs) and is strongly influenced by the crystal structure. Characterizing the excited-state charge-carrier dynamics in OTPs under high pressure is imperative for providing crucial insights into structure-property relations. Here, we conduct in situ high-pressure femtosecond transient absorption spectroscopy experiments to study the excited-state carrier dynamics of CH3NH3PbBr3 (MAPbBr3) under hydrostatic pressure. The results indicate that compression is an effective approach to modulate the carrier dynamics of MAPbBr3. Across each pressure-induced phase, carrier relaxation, phonon scattering, and Auger recombination present different pressure-dependent properties under compression. Responsiveness is attributed to the pressure-induced variation in the lattice structure, which also changes the electronic band structure. Specifically, simultaneous prolongation of carrier relaxation and Auger recombination is achieved in the ambient phase, which is very valuable for excess energy harvesting. Our discussion provides clues for optimizing the photovoltaic performance of OTPs.
We have proposed a new technique to obtain highly polarized atoms for improving the sensitivity of the all-optical Cs atomic magnetometer. In a Bell–Bloom magnetometer, the resonance pumping from the ground state F g = 3 to the excited state F e = 4 at the D1 line is used to polarize the Cs atoms and populate the sublevels of the | F g = 4 , m F = 4 ⟩ partly as the transition F g = 4 → F e = 3 remains leaking. Here we utilize a modulation technique to generate a sideband frequency to pump both transitions simultaneously, which drives more atoms to the target state | F g = 4 , m F = 4 ⟩ . This improvement significantly increases the magnetic resonance signal but with little effect on its linewidth. It is very suitable for the miniaturization of the atomic magnetometer in the future.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.