In the field of novel applications involving upconverting processes, the determination of new strategies for realizing emission-tunable nanomaterials is a challenge. In this work the design of Y and Er codoped bismuth oxide-based upconverting nanoparticles is presented, evidencing that the active role of the matrix allows for the emission selectivity with chromaticity control. The bandgap of the bismuth oxide-based host can be manipulated in the range of 0.65 eV, consequently leading to upconversion emission color tunability from red to yellow-greenish. The resulting fine control of the nanoparticle chromaticity through accurate host bandgap engineering reveals a novel concept for the development of a new generation of upconverting nanophosphors.
The enhancement of the low absorption cross section and widening of the absorption range of the RE ions in the UV-blue region is still a challenge to develop optical systems with high performance. In this work we synthesized Bi- and Er-codoped Y2O3 nanocrystals by means of Pechini type sol-gel process. X-ray powder diffraction (XRPD) and transmission electron microscopy (TEM) were performed to evaluate the nanocrystalline particle size and phase. Photoluminescence investigation in the UV–vis and IR regions showed that the presence of Bi3+ ions promotes the strengthening of Er3+ emitter properties. In particular, an Er3+ sensitization process based on a broadband energy transfer mediated by the Bi3+ ions in the C2 site was evaluated, resulting in a wavelength spread for the photostimulation of the rare earth emissions in the visible and NIR range. We pointed out a resonant type via a dipole-dipole interaction as the most probable mechanism of energy transfer. Moreover, the critical distance between the Bi3+ and Er3+ ions was estimated to be of about 8.5 Å
In this work we synthesized rare earth-doped yttria nanocrystals via the Pechini method. We used Ce(3+), Yb(3+) and Er(3+) as dopant ions and studied their behavior when they are simultaneously embedded in the yttrium oxide lattice. The tri-doped system exhibits both downshifting and up-converting properties, due to the presence of, respectively, cerium-erbium and ytterbium-erbium couples. Efforts were put into determination of the effects of the presence of increasing content of cerium. We synthesized a series of samples having the general formula (Y0.88-xCexYb0.1Er0.02)2O3, where x = 0.01, 0.02, 0.10, 0.20, and 0.40. The structural properties of the samples were analyzed by the X-ray powder diffraction (XRPD) technique and the morphological features were disclosed using transmission electron microscope (TEM) observations. Photoluminescence properties were tested by carrying out photoluminescence (PL) emission, photoluminescence excitation (PLE) and lifetime (LT) measurements.
Correction for 'Unexpected optical activity of cerium in Y 2 O 3 :Ce 3+ , Yb 3+ , Er 3+ up and down-conversion system' by Riccardo Marin et al., Dalton Trans., 2013, 42, 16837-16845. b NanoFab -Nanofabrication facility, Parco Scientifico e Tecnologico Vega -Torre Hammon, Via delle Industrie 5, 30175 Marghera, VE, Italy 7066 | Dalton Trans., 2015, 44, 7066-7067 This journal is
Ab initio in silico design of proteins and enzymes has emerged as a powerful tool to design application-tailored proteins and catalysts for a wide range of applications. Several enzymes exploit the unique features of metal cofactors to achieve catalytic activity otherwise unattainable through the use of only natural amino acid residues. One of the major bottlenecks in ab initio design of novel proteins relies on long-range and epistatic effects that severely limit the possibility of a rational design. Within this framework there is an ongoing effort to reduce protein length and complexity to unlock the full potential of in silico protein design. In this work we specifically address this problem designing and investigating the dynamic features of 10 in silico designed minimal metallo-proteins. In particular, in this paper we investigate whether and to what extent it is possible to design a minimal metallo-enzyme made of only residues involved in metal binding. In this research we address these questions by investigating the ability of 10 different "mini-proteins" with a length shorter than 15 residues. Molecular dynamics studies clearly show that it is possible to design a minimal protein able to bind a metal atom with the correct geometry. It is noteworthy that designed mini-proteins cannot achieve the formation of a canonical hydrophobic core, rather the metal ion provides a "metal core" around which the entire protein is organized. This opens the possibility of designing synthetic enzymes composed of only functional residues organized around a "metal core" which acts as both structural and functional determinat.
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