Ag-sensitized Tb3+/Yb3+ codoped silica-zirconia glasses and glass-ceramics: Systematic and detailed investigation of the broadband energy-transfer and downconversion processes

Abstract Various studies report that Tb3+/Yb3+ co-doped materials can split one UV or 488 nm (visible) photon in two near infrared (NIR) photons at 980 nm by an energy-transfer process involving one Tb3+ and two Yb3+ ions. Additionally, it was demonstrated that Ag multimers can provide an efficient optical sensitizing effect for rare earth ions (RE3+ ions), resulting in a broadband enhanced excitation, which could have a significant technological impact, overcoming their limited spectral absorptions and small excitation cross sections. However, a systematic and detailed investigation of the down-conversion process enhanced by Ag nanoaggregates is still lacking, which is the focus of this paper. Specifically, a step by step analysis of the energy-transfer quantum-cutting chain in Ag-exchanged Tb3+/Yb3+ co-doped glasses and glass-ceramics is presented. Moreover, the direct Ag-Yb3+ energy-transfer is also considered. Results of structural, compositional, and optical characterizations are given, providing quantitative data for the efficient broadband Ag-sensitization of Tb3+/Yb3+ quantum cutting. A deeper understanding of the physical processes beneath the optical properties of the developed materials will allow a wiser realization of more efficient energy-related devices, such as spectral converters for silicon solar cells and light-emitting devices (LEDs) in the visible and NIR spectral regions

Theoretical and Experimental Analysis for Cleaning Ice Cores from EstisolTM 140 Drill Liquid

Featured ApplicationThis work gives indications for cleaning and preservation of ice cores, which will be drilled in Antarctica during the EU project Beyond EPICA Oldest Ice and provides general guidelines for ice drilling activities and preservation of ice cores.To reconstruct climate history of the past 1.5 Million years, the project: Beyond EPICA Oldest Ice (BEOI) will drill about 2700 m of ice core in East Antarctica (2021-2025). As drilling fluid, an aliphatic ester fluid, Estisol(TM) 140, will be used. Newly drilled ice cores will be retrieved from the drill soaked in fluid, and this fluid should be removed from the cores. Most of it will be vacuum-cleaned off in a Fluid Extraction Device and wiped off with paper towels. Based on our experiences in Greenland deep ice coring, most of the residual fluid can be removed by storing the cores openly on shelves in a ventilated room. After a week of "drying", the cores have a dry feel, handling them do not give "wet" gloves and they can easily be marked with lead pencils. This paper presents a theoretical investigation and some simple testing on the "drying" process. The rates of sublimation of ice and evaporation of fluid have been calculated at different temperatures. The calculations show that sublimation of the ice core should not occur, and that evaporation of fluid should be almost negligible. Our test results support these calculations, but also revealed significant fluid run-off and dripping, resulting in the removal of most of the fluid in a couple of days, independent of temperature and ventilation conditions. Finally, we discuss crucial factors that ensure optimal long-term ice core preservation in storage, such as temperature stability, defrosting cycles of freezers and open core storage versus storage of cores in insulated crates

Rare-earth doped glasses and light managing in solar cells

Glasses doped with rare earth elements possess unique photoluminescence properties. They find application in several devices, such as lasers, optical amplifiers, and sensors. More recently, rare-earth doped glass thin films have been the subject of investigation for the development of frequency-converting layers able to increase the efficiency of silicon solar cells. Another approach to the improvement of the performance of a solar cell is based on the capture of a larger flux of light by the detector, which can be obtained by surface texture, plasmonics, or waveguide structures. Here, the recent advances in this area will be briefly reviewed

Impact of oxalate ligand in co-precipitation route on morphological properties and phase constitution of undoped and Rh-Doped BaTiO3 nanoparticles

In order to design and tailor materials for a specific application like gas sensors, the synthesis route is of great importance. Undoped and rhodium-doped barium titanate powders were successfully synthesized by two routes; oxalate route and classic route (a modified conventional route where solid-state reactions and thermal evaporation induced precipitation takes place). Both powders were calcined at different temperatures. X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), energy-dispersive x-ray spectroscopy (EDX) and Brunauer-Emmet-Teller (BET) analyses are employed to identify the phases and polymorphs, to determine the morphology, the chemical composition and the specific surface area of the synthesized materials, respectively. The so-called oxalate route yields pure BaTiO3 phase for undoped samples at 700?C and 900?C (containing both cubic and tetragonal structures), while the classic route-synthesized powder contains additional phases such as BaCO3, TiO2 and BaTi2O5. Samples of both synthesis routes prepared by the addition of Rh contain no metallic or oxide phase of rhodium. Instead, it was observed that Ti was substituted by Rh at temperatures 700 °C and 900 °C and there was some change in the composition of BaTiO3 polymorph (increase of tetragonal structure). Heat-treatments above these temperatures show that rhodium saturates out of the perovskite lattice at 1000 °C, yielding other secondary phases such as Ba3RhTi2O9 behind. Well-defined and less agglomerated spherical nanoparticles are obtained by the oxalic route, while the classic route yields particles with an undefined morphology forming very large block-like agglomerates. The surface area of the synthesized materials is higher with the oxalate route than with the classic route (4 times at 900 °C). The presence of the oxalate ligand with its steric hindrance that promotes the uniform distribution and the homogeneity of reactants could be responsible for the great difference observed between the powders prepared by two preparation routes

Correction: Unexpected optical activity of cerium in Y2O3:Ce3+, Yb3+, Er3+ up and down-conversion system

Correction for 'Unexpected optical activity of cerium in Y2O3:Ce3+, Yb3+, Er3+ up and down-conversion system' by Riccardo Marin et al., Dalton Trans., 2013, 42, 16837–16845

Tuning ZnO nanorods photoluminescence through atmospheric plasma treatments

Room temperature atmospheric plasma treatments are widely used to activate and control chemical functionalities at surfaces. Here, we investigated the effect of atmospheric pressure plasma jet (APPJ) treatments in reducing atmosphere (Ar/1 parts per thousand H-2 mixture) on the photoluminescence (PL) properties of single crystal ZnO nanorods (NRs) grown through hydrothermal synthesis on fluorine-doped tin oxide glass substrates. The results were compared with a standard annealing process in air at 300 degrees C. Steady-state photoluminescence showed strong suppression of the defect emission in ZnO NRs for both plasma and thermal treatments. On the other side, the APPJ process induced an increase in PL quantum efficiency (QE), while the annealing does not show any improvement. The QE in the plasma treated samples was mainly determined by the near band-edge emission, which increased 5-6 fold compared to the as-prepared samples. This behavior suggests that the quenching of the defect emission is related to the substitution of hydrogen probably in zinc vacancies (V-Zn), while the enhancement of UV emission is due to doping originated by interstitial hydrogen (H-i), which diffuses out during annealing. Our results demonstrate that atmospheric pressure plasma can induce a similar hydrogen doping as ordinarily used vacuum processes and highlight that the APPJ treatments are not limited to the surfaces but can lead to subsurface modifications. APPJ processes at room temperature and under ambient air conditions are stable, convenient, and efficient methods, compared to thermal treatments to improve the optical and surface properties of ZnO NRs, and remarkably increase the efficiency of UV emission. (c) 2019 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)

Ultra-small dye-doped silica nanoparticles via modified sol-gel technique

In modern biosensing and imaging, fluorescence-based methods constitute the most diffused approach to achieve optimal detection of analytes, both in solution and on the single-particle level. Despite the huge progresses made in recent decades in the development of plasmonic biosensors and label-free sensing techniques, fluorescent molecules remain the most commonly used contrast agents to date for commercial imaging and detection methods. However, they exhibit low stability, can be difficult to functionalise, and often result in a low signal-to-noise ratio. Thus, embedding fluorescent probes into robust and bio-compatible materials, such as silica nanoparticles, can substantially enhance the detection limit and dramatically increase the sensitivity. In this work, ultra-small fluorescent silica nanoparticles (NPs) for optical biosensing applications were doped with a fluorescent dye, using simple water-based sol-gel approaches based on the classical Stober procedure. By systematically modulating reaction parameters, controllable size tuning of particle diameters as low as 10 nm was achieved. Particles morphology and optical response were evaluated showing a possible single-molecule behaviour, without employing microemulsion methods to achieve similar results

Comparison of energy transfer between Terbium and Ytterbium ions in glass and glass ceramic: Application in photovoltaic

The structural and optical properties of thin layers based on 70%SiO 2 –30%HfO 2 doped with different concentra- tion of rare earth ions (terbium and ytterbium) have been studied with a view to integrating them in a photovoltaic cell as a spectral conversion layer in order to improve its efficiency, by using down-conversion process. These thin films were synthesized by using sol gel technique and deposited on the pure silica substrate by dip-coating method. The DC layer can be placed on the front side of a solar cell and can enhance the current by converting ultraviolet (UV) photons into a large number of visible photons. In present study two series of samples are compared, the first series corresponds to samples treated at 900 °C (glass- S) while the second series concerns samples treated at 1000 °C (glass-ceramic- SC). These series are based on 70SiO 2 –30HfO 2 activated by different molar concentrations of rare earths [Tb + Yb]/[Si + Hf] = 7%, 9%, 12%, 15%, 17%, 19% and 21%. Photoluminescence results of reference samples (without Yb 3 + ) showed an emission from 5 D 4 to 7 F J ( J = 3, 4, 5, 6) level characteristic transitions of Tb 3 + , with a maximum peak in the green centered at 543.5 nm cor- responding to the 5 D 4 →7 F 5 transition. For the co-doped samples a clear NIR PL emission around 980 nm was detected, due to the 2 F 5/2 →2 F 7/2 transition of Yb 3 + ions. From luminescence decay curves of Tb 3 + maximum emission peak ( 7 F 5 →5 D 4 transition at 543.5 nm) we have identified the energy transfer efficiency. The quantum efficiency increases by increasing the total [Tb + Yb] concentration. The most significant yield was achieved with [Tb + Yb] = 19%, the maximum quantum transfer efficiency obtained was 190% for glass-ceramic samples and 161% for glassy one

Investigation on the Luminescence Properties of InMO4 (M = V5+, Nb5+, Ta5+) Crystals Doped with Tb3+ or Yb3+ Rare Earth Ions

We explore the potential of Tb- and Yb-doped InVO4, InTaO4, and InNbO4 for applications as phosphors for light-emitting sources. Doping below 0.2% barely change the crystal structure and Raman spectrum but provide optical excitation and emission properties in the visible and near-infrared (NIR) spectral regions. From optical measurements, the energy of the first/second direct band gaps was determined to be 3.7/4.1 eV in InVO4, 4.7/5.3 in InNbO4, and 5.6/6.1 eV in InTaO4. In the last two cases, these band gaps are larger than the fundamental band gap (being indirect gap materials), while for InVO4, a direct band gap semiconductor, the fundamental band gap is at 3.7 eV. As a consequence, this material shows a strong self-activated photoluminescence centered at 2.2 eV. The other two materials have a weak self-activated signal at 2.2 and 2.9 eV. We provide an explanation for the origin of these signals taking into account the analysis of the polyhedral coordination around the pentavalent cations (V, Nb, and Ta). Finally, the characteristic green (D-5(4) -> F-7(J)) and NIR (F-2(5/2) -> F-2(7/2)) emissions of Tb3+ and Yb3+ have been analyzed and explained

Investigation on the Luminescence Properties of InMO4 (M = V5+, Nb5+, Ta5+) Crystals Doped with Tb3+ or Yb3+ Rare Earths Ions

[EN] We explore the potential of Tb- and Yb-doped InVO4, InTaO4, and InNbO4 for applications as phosphors for light-emitting sources. Doping below 0.2% barely change the crystal structure and Raman spectrum but provide optical excitation and emission properties in the visible and near-infrared (NIR) spectral regions. From optical measurements, the energy of the first/second direct band gaps was determined to be 3.7/4.1 eV in InVO4, 4.7/5.3 in InNbO4, and 5.6/6.1 eV in InTaO4. In the last two cases, these band gaps are larger than the fundamental band gap (being indirect gap materials), while for InVO4, a direct band gap semiconductor, the fundamental band gap is at 3.7 eV. As a consequence, this material shows a strong self-activated photoluminescence centered at 2.2 eV. The other two materials have a weak self-activated signal at 2.2 and 2.9 eV. We provide an explanation for the origin of these signals taking into account the analysis of the polyhedral coordination around the pentavalent cations (V, Nb, and Ta). Finally, the characteristic green (D-5(4) -> F-7(J)) and NIR (F-2(5/2) -> F-2(7/2)) emissions of Tb3+ and Yb3+ have been analyzed and explained.The authors thank the financial support from the Spanish Ministerio de Ciencia, Innovacion y Universidades, Spanish ́ Research Agency (AEI), Generalitat Valenciana, and European Fund for Regional Development (ERDF, FEDER) under grants no. MAT2016-75586-C4-1/2-P, RTI2018-101020-BI00, RED2018-102612-T (MALTA Consolier Team), and Prometeo/2018/123 (EFIMAT). P.B. acknowledges financial support from the Kempe Foundation and the Knut & Alice Wallenberg Foundation via a doctoral studentship. A.B.G. thanks the support provided by Universitat de Valencia to perform a research stay (Atraccióde Talent, VLC-CAMPUS)Botella, P.; Enrichi, F.; Vomiero, A.; Muñoz-Santiuste, JE.; Garg, AB.; Arvind, A.; Manjón, F.... (2020). Investigation on the Luminescence Properties of InMO4 (M = V5+, Nb5+, Ta5+) Crystals Doped with Tb3+ or Yb3+ Rare Earths Ions. ACS Omega. 5(5):2148-2158. https://doi.org/10.1021/acsomega.9b02862S214821585