Organic/Inorganic Hybrid Silicate Materials for Optical Applications; Highly Fluorinated Hybrid Glasses Doped with (Erbium-ions/CdSe nanoparticles) for Laser Amplifier Material

2004 ◽  
Vol 846 ◽  
Author(s):  
Kyung M. Choi ◽  
John A. Rogers

A new family of organic/inorganic hybrid silicate materials, bridged polysilsesquioxanes, was designed and synthesized through a molecular-level mixing technique. Since hybrid materials in the molecular-composite level, whose domain sizes are in the nanometer-scale, and whose constituents often lose individual identities and thus create new properties, we obtained a set of improved properties from those organically modified glasses. By modifying the Si-O-Si polymeric network, in this study, we produced controllable, porous hybrid glasses for facile and uniform doping of various ions, metals or semiconductor particles. By taking advantage of void volume created in those molecularly modified silicate systems, novel optical materials with designed properties can thus be achieved. Via a chemical strategy, we designed hexylene- or fluoroalkylene-bridged hybrid glasses doped with both Er+3 ions and CdSe nano-particles for the development of new laser amplifier materials. In photoluminescence experiments, a significant enhancement in fluorescence intensity at 1540 nm has been obtained from the fluoroalkylene-bridged glass. The presence of CdSe nano-particles, by virtue of their low phonon energy, also appears to significantly influence the nature of the surrounding environment of Er+3 ions in those modified silicate systems, resulting in the increased fluorescence intensity.

2007 ◽  
Vol 1015 ◽  
Author(s):  
Kyung Choi

AbstractHybrid organic/inorganic silicate materials are employed to incorporate rare-earth metal ions for laser amplification applications. Performance of laser amplifiers doped with rare-earth ions significantly relies on glassy hosts. We thus designed and synthesized highly fluorinated glassy hosts doped with biphase of Er3+/CdSe nano-particles. Fluoroalkylene-bridged xerogels containing Er3+-ions show low absorptions at the 1540 nm in this study. The presence of CdSe nano-particles also significantly influences the fluorescence environment of Er3+-ions in the fluorinated glassy matrices.


Author(s):  
Marieli Oliveira Rodrigues ◽  
Victória Goulart Isoppo ◽  
Angélica Venturini Moro ◽  
Fabiano Severo Rodembusch

2018 ◽  
Vol 5 (12) ◽  
pp. 1916-1927 ◽  
Author(s):  
Pedro Bosch ◽  
David Sucunza ◽  
Francisco Mendicuti ◽  
Alberto Domingo ◽  
Juan J. Vaquero

A new family of weakly fluorescent azonia cations with DNA-binding ability by intercalation whose fluorescence intensity increases significantly upon DNA addition is reported. A live-cell staining cells analysis showed the capacity of these new compounds for active uptake and accumulation by living cells.


2021 ◽  
Vol 21 (2) ◽  
pp. 895-902
Author(s):  
Lei Wei ◽  
Feng Yu ◽  
Ying Meng

In this experiment, the advantages of both liposomes and polymer nanoparticles were used to synthesize adriamycin-loaded liposome-polymer nanoparticles and conjugate them with PD-L 1 antibody (referred to as PD-L 1 antibody nano particles). The nanoparticles were encapsulated with doxorubicin hydrochloride and the near-infrared dye DIR, and small animal imaging methods were used in animal experiments to evaluate the targeting and therapeutic effects. The results showed that the red fluorescence of doxorubicin hydrochloride entered the cells, and the red fluorescence of the PD-L1 antibody nanoparticles in the 4h group was better than that in the 2h group. The intracellular red fluorescence of PD-L1 antibody nanoparticles 4h group was stronger than that of free doxorubicin 4h group. Flow cytometry and confocal experiments showed that A549 cells took up more PD-L1 antibody nanoparticles. The results showed that the fluorescence intensity of the PD-L1 antibody nanoparticle group was significantly stronger than that of the nanoparticle group, and the tumor outline was clear, and the fluorescence intensity became stronger and stronger over time, indicating that the PD-L1 antibody nanoparticles were targeted. Has certain targeting capabilities. The PD-L1 antibody nanoparticles synthesized in this study are a good drug carrier targeting lung cancer tumor cells, which can be better taken up by A549 lung cancer cells, and can more effectively kill tumor cells, inhibit tumor growth, and wrap near-infrared dyes are more conducive to in vivo imaging of animals and are useful for observing the effects of targeted treatment of lung cancer.


1996 ◽  
Vol 435 ◽  
Author(s):  
A. Sarkar ◽  
Y. Yan ◽  
Z. Duan ◽  
Y. Hoshino ◽  
S. Ray Chaudhuri

RSC Advances ◽  
2016 ◽  
Vol 6 (89) ◽  
pp. 86012-86018 ◽  
Author(s):  
Mengmeng Li ◽  
Xiaoyan Song ◽  
Tingbin Zhang ◽  
Lintao Zeng ◽  
Jinfeng Xing

The fluorescence intensity change of TPE encapsulated in POSS–PNIPAM with a particular LCST (37.5 °C) with the temperature change.


2015 ◽  
Vol 1769 ◽  
Author(s):  
A. Crespo-Sosa ◽  
P.E. Mota-Santiago ◽  
J.L. Jiménez-Hernández ◽  
H.G. Silva-Pereyra ◽  
E.V. García-Ramírez ◽  
...  

ABSTRACTSapphire is best known for its hardness that makes it ideal for many mechanical and optical applications, but its resistance to radiation damage and its optical properties, combined with metallic nano-particles, make it promising for future opto-electronic and plasmonic devices. In this paper, we present an overview of our work on the fabrication of metallic nano-particles embedded in synthetic sapphire by means of ion implantation, thermal annealing and high energy ion irradiation. We show that we can have control over the amount and size of the nano particles formed inside the matrix by carefully choosing the parameters during the preparation process. Furthermore, we show that anisotropic nano particles can be obtained by an adequate high energy ion irradiation of the originally spherical nano particles. We also have studied the linear and non-linear optical properties of these nano-composites and have confirmed that they are large enough for future applications.


Sign in / Sign up

Export Citation Format

Share Document