Excitation Dependence of Dipole-Dipole Broadening in Selective Reflection Spectroscopy

We investigate the dipole-dipole broadened selective reflection spectrum with the Cs atomic aensity of 10^14- 10^15 cm^-3. The dipole-dipole broadening is reduced and the hyperfine splitting is well resolved when the ground state atoms are excited by a detuned pump beam. The dependences of dipoleMipole broadening of Cs atoms in the 6S1/2（F= 3） → 6P3/2（F＇= 4） hyperfine transition line on atomic density and the excitation factor are studied. It is found that the reduction of the dipole-dipole broadening is dependent on the pump beam power and is independent of the atomic density in this density range. These results are useful for understanding of the dynamical process in this range of atomic density.

A Versatile Tetraphenylethene Derivative Bearing Excitation Wavelength Dependent Emission,Multistate Mechanochromism,Reversible Photochromism,and Circularly Polarized Luminescence and Its Applications in Multimodal Anticounterfeiting

Multimodal anticounterfeiting has become increasingly challenging in modern society to guarantee information security and the safety of property.In this study,a versatile cholesterol-containing tetraphenylethene derivative is shown to have multiple optical properties,including stimuli-responsive fluorescence,reversible photochromism,excitation wavelength dependent luminescence,and circularly polarized luminescence.After the application of diverse processing methods(writing,screen painting,drawing,and pyrography),we found that this molecule can serve as an anticounterfeiting toolbox to provide rich anticounterfeiting effects through the synergistical use of multiple optical properties.This work offers important insight for designing novel small organic molecules for advanced multimodal anticounterfeiting technology.

White light emission in 0D halide perovskite[(CH_(3))_(3)S]_(2)SnCl_(6)·H_(2)O crystals through variation of doping ns^(2) ions

With the rapid development of white LEDs,the research of new and efficient white light emitting materials has attracted increasing attention.Zero dimensional(0D)organic–inorganic hybrid metal halide perovskites with superior luminescent property are promising candidates for LED application,due to their abundant and tailorable structure.Herein,[(CH_(3))_(3)S]_(2)SnCl_(6)・H_(2)O is synthesized as a host for dopant ions Bi^(3+)and Sb^(3+).The Sb^(3+)doped,or Bi^(3+)/Sb^(3+)co-doped,[(CH_(3))3S]_(2)SnCl_(6)・H_(2)O has a tunable optical emission spectrum by means of varying dopant ratio and excitation wavelength.As a result,we can achieve single-phase materials suitable for emission ranging from cold white light to warm white light.The intrinsic mechanism is examined in this work,to clarify the dopant effect on the optical properties.The high stability of title crystalline material,against water,oxygen and heat,makes it promising for further application.

Color-tunable ultralong organic phosphorescence materials for visual UV-light detection

Ultralong organic phosphorescence(UOP)materials have roused considerable attention in the field of photonics and optoelectronics owing to the feature of long-lived emission lifetimes.However,to develop UOP materials with color-tunability is still a formidable challenge.Here,we report a class of UOP materials containing carbonyl,amino or amide groups,exhibiting colortunable persistent luminescence ranging from blue(458 nm)to yellow-green(508 nm)under different UV wavelength excitation.Taken theoretical and experimental results together,we conclude that the excitation dependent color-tunable UOP emission is ascribed to multiple emission centers from single molecular and aggregated states in crystal.Given color-tunable UOP feature,these materials are used to successfully realize visual UV-light detection.This finding not only provides a strategy to design new organic phosphorescent molecules with colorful emission,but also extends the scope of the applications of purely organic phosphorescent materials.

Remarkable fluorescence enhancement of upconversion composite film and its application on mercury sensing

To achieve a stable, sensitive, and high-efficiency biological probe, a novel NaYF4：Yb,Er nanocrystals/TiO2 inverse opal composite film was designed by self-assembly and solvent evaporation methods. 32-fold enhanced upconversion（UC） emission was investigated under 980 nm excitation. According to size-dependency, excitation power density-dependency as well as photonic stop band（PSB）-dependency upconversion spectra, the enhancement mechanism of the composite film was put down to the stochastical diffraction of IOPCs multi-layered structure to the excitation laser. On the basis of the enhancement effect of the composite film, energy transfer between upconversion nanoparticles（UCNPs） and quantum dots（QDs）, and the sensitive sensing of CdTe QDs on mercury, the UC composite film was used for sensing of Hg^2＋ in serum. The solid sensor as a mercury detector owns lots of superiorities such as feasible operation, good linear relationship（R=0.997）, low limit of detection（70.5 nmol/L） and thus may have broad prospects in the biosensing field.