Lead halide perovskites have emerged as promising materials
for
light-emitting devices. Here, we report the preparation of colloidal
CsPbBr3 nanoplatelets (3 × 4 × 23 nm3) experiencing a strong quasi-one-dimensional quantum confinement.
Ultrafast transient absorption and broadband fluorescence up-conversion
spectroscopies were employed to scrutinize the carrier and quasiparticle
dynamics and to obtain a full description of the spectroscopic properties
of the material. An exciton binding energy of 350 meV, an absorption
cross section at 3.2 eV of 5.0 ± 0.3 × 10–15 cm–2, an efficient biexciton Auger recombination
lifetime of 9 ± 1 ps, and a biexciton binding energy of 74 ±
4 meV were determined. Moreover, a short-lived emission from hot excitons
was observed, which is related to the formation of band-edge excitons.
The time constant of both processes is 300 ± 50 fs. These results
show that CsPbBr3 nanoplatelets are indeed quite promising
for light-emitting technological applications.
We investigate systematically the influence of the nature of thiol-type capping ligands on the optical and structural properties of highly luminescent CdTe quantum dots synthesized in aqueous media, comparing mercaptopropionic acid (MPA), thioglycolic acid (TGA), 1-thioglycerol (TGH), and glutathione (GSH). The growth rate, size distribution, and quantum yield strongly depend on the type of surface ligand used. While TGH binds too strongly to the nanocrystal surface inhibiting growth, the use of GSH results in the fastest growth kinetics. TGA and MPA show intermediate growth kinetics, but MPA yields a much lower initial size distribution than TGA. The obtained fluorescence quantum yields range from 38% to 73%. XPS studies unambiguously put into evidence the formation of a CdS shell on the CdTe core due to the thermal decomposition of the capping ligands. This shell is thicker when GSH is used as ligand, as compared with TGA ligands.
Homogeneous silicon boron oxycarbide (Si-B-O-C) glasses based on SiOx C 4 -x and BO y C 3-y mixed environments were obtained by pyrolysis under inert atmosphere of sol-gelderived precursors. Their high-temperature structural evolution from 1000°to 1500°C was followed using XRD, 29 Si and 11 B MAS NMR, and chemical analysis and compared with the behavior of the parent boron-free Si-O-C glasses. The XRD study revealed that, for the Si-O-C and the Si-B-O-C systems, high-temperature annealing led to the crystallization of nanosized -SiC into an amorphous SiO 2 -based matrix. NMR analysis suggested that the -SiC crystallization occurred with a consumption of the mixed silicon and boron oxycarbide units. Finally, by comparing the behavior of the Si-O-C and Si-B-O-C glasses, it was shown that the presence of boron increased the crystallization kinetics of -SiC.
A new analytical expression for the size-dependent bandgap of colloidal semiconductor nanocrystals is proposed within the framework of the finite-depth square-well effective mass approximation in order to provide a quantitative description of the quantum confinement effect. This allows one to convert optical spectroscopic data (photoluminescence spectrum and absorbance edge) into accurate estimates for the particle size distributions of colloidal systems even if the traditional effective mass model is expected to fail, which occurs typically for very small particles belonging to the so-called strong confinement limit. By applying the reported theoretical methodologies to CdTe nanocrystals synthesized through wet chemical routes, size distributions are inferred and compared directly to those obtained from atomic force microscopy and transmission electron microscopy. This analysis can be used as a complementary tool for the characterization of nanocrystal samples of many other systems such as the II-VI and III-V semiconductor materials.
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.