Спектрально-люминесцентные свойства кристаллов ZrO-=SUB=-2-=/SUB=--Sc-=SUB=-2-=/SUB=-O-=SUB=-3-=/SUB=--Tb-=SUB=-2-=/SUB=-O-=SUB=-3-=/SUB=-

Crystals of the concentration series ZrO2- (8-10) mol.% Sc2O3- (1-2) mol.% Tb2O3 were grown by the method of directional crystallization of the melt from a cold container. Analysis of the spectral-luminescence characteristics of these crystals after growth and after annealing processing in a vacuum revealed the presence of both Tb3 + and Tb4 + ions in them. In crystals ZrO2- (8-10) mol.% Sc2O3- (1-2) mol.% Tb2O3, the presence of a process of non-radiative energy transfer from Tb4 + ions to Tb3 + ions was revealed.

Highly luminescent hetero-ligand MOF nanocrystals with engineered massive Stokes shift for photonic applications.

A high efficiency emission with a massive Stokes shift is obtained by fluorescent conjugated acene building blocks arranged in nanocrystals. The two ligands of equal molecular length and connectivity, yet complementary electronic properties, are co-assembled by zirconium oxy-hydroxy clusters, generating highly crystalline hetero-MOF nanoparticles The fast diffusion of singlet molecular excitons in the framework, coupled with the fine matching of ligands absorption and emission properties, enables to achieve an ultrafast activation of the low energy emission by diffusion-mediated non-radiative energy transfer in the 100 ps time scale, by using a low amount of co-ligands. This allow to obtain MOF nanocrystals with a fluorescence quantum efficiency of ̴ 70% and an actual Stokes shift as large as 750 meV. This large Stokes shift suppresses the reabsorption of fast emission issues in bulk devices, pivotal for a plethora of applications in photonics and photon managing spacing from solar technologies, imaging, and detection of high energy radiation. These features allowed to realize a prototypal fast nanocomposite scintillator that shows an enhanced performance with respect to the homo-ligand nanocrystals, achieving benchmark. values which compete with those of some inorganic and organic commercial systems.

A Cocktail Approach Toward Tunable Organic Afterglow Systems

In this work, a cocktail approach toward tunable organic long-lived luminescence materials in solid, solution, and gel states is proposed. The tunable long-lived luminescence (τ > 0.7 s) is realized by controlling the energy transfer via manipulating the photo-induced isomerization of the energy acceptor (5). The afterglow can be regulated between blue and yellow emission upon irradiation of UV or visible light. And the “apparent lifetime” for the long-lived fluorescence is the same as the lifetime of the energy donor. The function is relying on the simple radiative energy transfer (reabsorption) between a long-lived phosphorescence and a highly efficient fluorescent isomer (5b), rather than the complicated communication between the excited state of the molecules such as Förster resonance energy transfer or Dexter energy transfer. The simple working principle endows this strategy with huge universality, flexibility, and operability. This work offers an extremely simple, feasible, and universal way to construct tunable afterglow materials in solid, solution, and gel states.

Challenges in 3D Live Cell Imaging

A short overview on 3D live cell imaging is given. Relevant samples are described and various problems and challenges—including 3D imaging by optical sectioning, light scattering and phototoxicity—are addressed. Furthermore, enhanced methods of wide-field or laser scanning microscopy together with some relevant examples and applications are summarized. In the future one may profit from a continuous increase in microscopic resolution, but also from molecular sensing techniques in the nanometer range using e.g., non-radiative energy transfer (FRET).