Light Harvesting Molecular Assemblies in the Design of Highly Luminescent Sol-Gel Derived Glasses

1990 ◽  
Vol 180 ◽  
Author(s):  
Joel I. Dulebohn ◽  
Béatrice Van Vlierberge ◽  
Kris A. Berglund ◽  
Ronald B. Lessard ◽  
Jeong-a Yu ◽  
...  

ABSTRACTSol-gel derived molecular composites exhibiting intense luminescence, induced from efficient energy transduction processes, have been prepared. The composites are comprised of an Eu3+⊂ 2.2.1 cryptate complex or native Eu3+ ion embedded in sol-gel derived titania glass films. The titania glasses contain interconnected porous networks that permit the diffusion of exogenous substrates, such as the salts of benzoic and 4-tert-butylbenzoic acids, through the film. Interaction of the substrate with the embedded lanthanide complex is indicated by enhanced luminescence from the lanthanide ion. The carboxylic acid salts whose electronic excited states are produced upon capture of incident photons, undergo facile transfer of their electronic energy to the lanthanide ion. By monitoring europium ion luminescence, the diffusion constants of the benzoate and 4-tert-butylbenzoate salts have been measured. Although the diffusion of the 4-tert-butylbenzoate is slower than that of benzoate, the overall higher sensitivity of the former is consistent with hydrophobic guest-host interactions. These new molecular composites relying on the immobilization of an absorption-energytransfer- emission molecular assembly in porous, optically transparent ceramic glasses may be useful in the design of practical sensing devices.

1989 ◽  
Vol 155 ◽  
Author(s):  
Ronald B. Lessard ◽  
Kris A. Berglundl ◽  
Daniel G. Nocera

ABSTRACTMolecular composites that possess unique emission properties have been prepared by introducing luminescent molecules into sol-gel based silica glasses. The lumophores chosen for study are terbium(III) and europium(III) ions whose emissions are quenched in aqueous and sol-gel environments owing to coordination of water molecules to the lanthanide ion. To overcome the quenching process the ions have been encapsulated within cryptands. The resulting terbium(IU) and europium(III) cryptates possess long-lived excited states in both aqueous solution and solgel glassy matrices. Measurements of the excited state dynamics of these molecularly engineered composites demonstrate the feasibility of tailoring molecules to retain their excited state properties in sol-gel derived glasses.


2007 ◽  
Vol 2007 ◽  
pp. 1-8 ◽  
Author(s):  
Iko Hyppänen ◽  
Jorma Hölsä ◽  
Jouko Kankare ◽  
Mika Lastusaari ◽  
Laura Pihlgren

Combustion and sol-gel methods were used to prepare the upconverting nanocrystallineZrO2:Yb3+,Er3+phosphors. The crystal structure was studied by X-ray powder diffraction and the crystallite sizes were estimated with the Scherrer formula. Impurities and nanomaterials' thermal degradation were analyzed with FT-IR spectroscopy and thermal analysis, respectively. Upconversion luminescence and luminescence decays were studied with IR-laser excitation at 977 nm. All nanomaterials possessed the cubicZrO2fluorite-type structure except for a small monoclinic impurity obtained with the sol-gel method. The conventionalNO3−andOH−impurities were observed for the combustion synthesis products. TheZrO2:Yb3,Er3+nanomaterials showed red (630–710 nm) and green (510–570 nm) upconversion luminescence due to the4F9/2→4I15/2and(2H11/2,4S3/2)→4I15/2transitions ofEr3+, respectively. The products of the combustion synthesis exhibited the most intense luminescence intensity and showed considerable afterglow. It was concluded that excitation energy is partially trapped in the system and subsequently bleached thermally to the luminescentEr3+center to yield “persistent upconversion”.


2021 ◽  
Vol 2021 ◽  
pp. 1-21
Author(s):  
Dmitry Bokov ◽  
Abduladheem Turki Jalil ◽  
Supat Chupradit ◽  
Wanich Suksatan ◽  
Mohammad Javed Ansari ◽  
...  

The sol-gel process is a more chemical method (wet chemical method) for the synthesis of various nanostructures, especially metal oxide nanoparticles. In this method, the molecular precursor (usually metal alkoxide) is dissolved in water or alcohol and converted to gel by heating and stirring by hydrolysis/alcoholysis. Since the gel obtained from the hydrolysis/alcoholysis process is wet or damp, it should be dried using appropriate methods depending on the desired properties and application of the gel. For example, if it is an alcoholic solution, the drying process is done by burning alcohol. After the drying stage, the produced gels are powdered and then calcined. The sol-gel method is a cost-effective method and due to the low reaction temperature there is good control over the chemical composition of the products. The sol-gel method can be used in the process of making ceramics as a molding material and can be used as an intermediate between thin films of metal oxides in various applications. The materials obtained from the sol-gel method are used in various optical, electronic, energy, surface engineering, biosensors, and pharmaceutical and separation technologies (such as chromatography). The sol-gel method is a conventional and industrial method for the synthesis of nanoparticles with different chemical composition. The basis of the sol-gel method is the production of a homogeneous sol from the precursors and its conversion into a gel. The solvent in the gel is then removed from the gel structure and the remaining gel is dried. The properties of the dried gel depend significantly on the drying method. In other words, the “removing solvent method” is selected according to the application in which the gel will be used. Dried gels in various ways are used in industries such as surface coating, building insulation, and the production of special clothing. It is worth mentioning that, by grinding the gel by special mills, it is possible to achieve nanoparticles.


Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1955 ◽  
Author(s):  
Mohammad Wehbi ◽  
Ahmad Mehdi ◽  
Ali Alaaeddine ◽  
Nada Jaber ◽  
Bruno Ameduri

Novel triethoxysilane and dimethyl phosphonate functional vinylidene fluoride (VDF)-containing terpolymers, for potential applications in Eu ion extraction from water, were produced by conventional radical terpolymerization of VDF with vinyltriethoxylsilane (VTEOS) and vinyldimethylphosphonate (VDMP). Although initial attempts for the copolymerization of VTEOS and VDMP failed, the successful terpolymerization was initiated by peroxide to lead to multiple poly(VDF-ter-VDMP-ter-VTEOS) terpolymers, that had different molar percentages of VDF (70–90 mol.%), VTEOS (5–20 mol.%) and VDMP (10 mol.%) in 50–80% yields. The obtained terpolymers were characterized by 1H, 19F, 29Si and 31P NMR spectroscopies. The crosslinking of such resulting poly(VDF-ter-VDMP-ter-VTEOS) terpolymers was achieved by hydrolysis and condensation (sol–gel process) of the triethoxysilane groups in acidic media, to obtain a 3D network, which was analyzed by solid state 29Si and 31P NMR spectroscopies, TGA and DSC. The thermal stability of the terpolymers was moderately high (up to 300 °C under air), whereas they display a slight increase in their crystallinity-rate from 9.7% to 12.1% after crosslinking. Finally, the dimethyl phosphonate functions were hydrolyzed into phosphonic acid successfully, and the europium ion extraction capacity of terpolymer was studied. The results demonstrated a very high removal capacity of Eu(III) ions from water, up to a total removal at low concentrations.


2004 ◽  
Vol 41 (9) ◽  
pp. 981-1000 ◽  
Author(s):  
Hongliu Sun ◽  
James E. Mark ◽  
Narayanan Venkatasubramanian ◽  
Marlene D. Houtz ◽  
Seng C. Tan ◽  
...  

1993 ◽  
Vol 316 ◽  
Author(s):  
Timothy E. Levine ◽  
Emmanuel P. Giannelis ◽  
Padma Kodali ◽  
Joseph Tesmer ◽  
Michael Nastasi ◽  
...  

ABSTRACTWe have investigated the densification behavior of sol-gel zirconia films resulting from ion irradiation. Three sets of films were implanted with neon, krypton, or xenon. The ion energies were chosen to yield approximately constant energy loss through the film and the doses were chosen to yield similar nuclear energy deposition. Ion irradiation of the sol-gel films resulted in carbon and hydrogen loss as indicated by Rutherford backscattering spectrometry and forward recoil energy spectroscopy. Although the densification was hypothesized to result from target atom displacement, the observed densification exhibits a stronger dependence on electronic energy deposition.


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