T. Moeller

Bio: T. Moeller is an academic researcher from University of Illinois at Urbana–Champaign. The author has contributed to research in topics: Stability constants of complexes & Chloride. The author has an hindex of 13, co-authored 23 publications receiving 574 citations. Previous affiliations of T. Moeller include University of São Paulo.

Organic light emitting diodes: Energy saving lighting technology—A review

Abstract: This paper reflects the achievements and the challenges ahead in the field of organic light emitting diodes (OLEDs). The primary intention of this paper is to study different organic materials synthesized so far and the OLEDs fabricated for solid-state lighting. After deep review of literature we have synthesized and characterized rare earth based europium organic complexes Eu(TTA)3Phen, Eu(x)Y(1−x)(TTA)3Phen, and Eu(x)Tb(1−x)(TTA)3Phen, where x = 0.4 and 0.5 by solution technique maintaining stoichiometric ratio. Blended films of pure and doped Eu complexes that are molecularly doped into polymer resins namely polymethylmethacrylate (PMMA) and polystyrene (PS) are prepared according to weight percentage. Concentration effect on absorption and emission spectra of the blended films was studied for different weight percentages (10, 25, 50, 60%). All the complexes doped in PMMA showed an excellent transparency of 90–97% while the complexes doped in polystyrene showed a transparency of 85–90%, bit less than in PMMA. Energy gap of the synthesized complexes have been determined in PMMA and PS. Considering the facts that these complexes have good solubility in most of the organic solvents, the absorption spectra of Eu(TTA)3Phen, Eu0.5Y0.5(TTA)3Phen and Eu0.5Tb0.5(TTA)3Phen complexes are studied, and OLED devices having the structure ITO/m-MTDATA/α-NPD/TPBi:Eu(x)Y(1−x)(TTA)3Phen/Alq3/LiF:Al (where x = 0.4, 0.5) were fabricated and characterized. Significant red emission was observed from fabricated OLED devices at 612 nm when operated in a range of 10–18 V. Thus the synthesized rare earth based organic complexes are the best suitable candidates for fabrication of red OLED devices. The extensive review on OLEDS concludes that our present lighting system can be replaced with white OLEDS, recently developed energy saving lighting technology.

Review Article: A Review of the Development and Operational Characteristics of the TALSPEAK Process

Abstract: The separation of trivalent transplutonium actinides from fission product lanthanide ions represents arguably the most challenging aspect of advanced nuclear fuel partitioning schemes. A considerable amount of effort has been dedicated to the development of effective methods for accomplishing this separation, essential for transmutation of the actinides heavier than Pu. Among the methods currently considered to be ready for technological deployment is the TALSPEAK (Trivalent Actinide ‐ Lanthanide Separation by Phosphorus reagent Extraction from Aqueous Komplexes) Process, developed in the late 1960s at Oak Ridge National Laboratory. This process is based on the partitioning of lanthanides and actinides between an acidic organophosphorus extractant ((RO)2PO2H) solution and an aqueous phase containing a high concentration of a carboxylic acid buffer and a polyaminopolycarboxylate complexant. The latter reagent is principally responsible for holding back the trivalent actinides, allowing the selecti...

DTPA-coupled antibodies labeled with yttrium-90.

Abstract: Yttrium-90 has been described as one of the best radionuclides for tumor therapy when chelated to tumor-associated antibodies. This evaluation is based on the superior properties of this radionuclide (suitable half-life, pure beta-ray emitter of intermediate energy, stable daughter, and suitable chemical properties) and because it is available as a radionuclide generator product by decay of its 28-yr parent 90Sr. We have determined that 90Y obtained from one such generator is suitable for labeling antibodies coupled with DTPA. Furthermore, we have shown that the dissociation rate of [90Y]DTPA-IgG in serum at 37 degrees C is similar to that of [111In]DTPA-IgG at about 8-9%/day. Biodistribution studies of 111In- and 90Y-labeled to DTPA-coupled IgG show that the labels distribute nearly identically at 1 hr postadministration, although differences in distribution are apparent at 24 hr. It is possible that these differences reflect the redistribution of the labels following catabolism at the site of localization.