RESUMO
Doping Cd element into perovskite materials is an effective strategy to improve the photoelectric property. However, the further discussion for carrier dynamic behavior in perovskites affected by Cd element remains not sufficient. In this research letter, based on steady and transient spectroscopy, it is found that adding Cd element into CsPbBr3 nanocrystals can enhance the activity of photo-generated carriers and accompany with the optimization of crystal structure. The former improves the carrier heating effect, which makes carrier keep high temperature for a long time and accelerate the bimolecular and the Auger recombination simultaneously. The latter can restrict the monomolecular recombination through passivating the defect states. Finally, they together improve the photoluminescence characteristics of the Cd doped CsPbBr3 nanocrystals and make them exhibit a huge potential in the fields of optoelectronics or photo-catalysis.
RESUMO
Quasi-2D halide perovskites have potential in lasing due to their amplified spontaneous emission (ASE) properties. The ASE of (PBA)2MAn-1PbnBr3n+1 thin films has been confirmed by photoluminescence (PL) testing using stripe light excitation (SLE). The ASE threshold decreases with decreasing environmental temperature (TE) or increasing number of inorganic layers (n). Using the transient absorption technique, the Auger recombination and the cooling process of the high-activity carrier are accelerated with the decrease of n or TE. A new ASE mechanism is proposed where high-activity carriers directly emit photons under photon perturbation from adjacent sites, leading to the accumulation and amplification of emitted photons only in the SLE region for ASE to occur. In addition, the reduction of n promotes light scattering between nano-thin layers, which supports a rapid increase in the ASE signal after the ASE threshold is crossed.
RESUMO
A series of molecules 1-5 containing the same fluorophore and different alkyl chains are synthesized to reveal the significant effect of molecular conformations on the emission properties. In crystalline state, molecules 1-3 exhibit strong orange emissions with maxima (λem) of about 600 nm and quantum yields (ΦF) of around 60%, while molecules 4 and 5 display much longer emissions to the deep red/near-infrared (NIR) region as well as even higher efficiencies (λem = 693 nm, ΦF = 73% for 4; λem = 654 nm, ΦF = 93% for 5). The largely red-shifted emissions of 4 and 5 as well as the significantly improved ΦF are very unusual. Furthermore, the ΦF of 4 and 5 represent the highest values among organic solids with similar deep red/NIR emission wavelengths. On the basis of the experimental measurements and theoretical calculations, the new molecular design of conformation engineering, the impressive emission properties, and the potential NIR fluorescence sensing and lasing applications are comprehensively investigated.