Determinants of a traditional agricultural landscape

The study aim was to define the landscape determinants as certificates of natural and cultural heritage which identify the young glacial landscape under traditional agricultural management. These studies were conducted in the upper Parsęta basin (Pomerania, Poland) covered by the many annual environmental monitoring programs since 1994. The aim of this monitoring is to observe changes in geoecosystems of the temperate climate zone. The parameters of the abiotic landscape subsystem have been monitored in a wide range of terms, whereas biotic elements and cultural resources only in a very limited way. This was the reason for undertaking complementary studies. The paper presents the so-called “zero-state” for 2014, which will be a reference point from which to track the direction of landscape changes in the future. The abiotic, geobotanical, and cultural determinants of this state chosen have been characterized on the basis of field mapping data and the available literature. They were chosen based on the methodology of landscape audit to define the specificity of the traditional agricultural landscape. They were selected on the basis of assessment criteria for landscape structure: complexity (diversification of land use and cover), naturalness (syngenesis of plant communities, hydrochemical properties of surface waters), coherence of composition with natural conditions, stewardship (intensity of use, crop weeds, ecological succession, fallows, anthropogenic denudation), aesthetic and visual perception, historicity (continuity of natural landscape elements, continuation of traditional agricultural use, architectural objects), and disharmonious elements

Energy transfer study on Tb3+/Eu3+ Co-activated sol-gel glass-ceramic materials containing MF3 (M = Y, La) nanocrystals for NUV optoelectronic devices

In the present work, the Tb3+/Eu3+ co-activated sol-gel glass-ceramic materials (GCs) containing MF3 (M = Y, La) nanocrystals were fabricated during controlled heat-treatment of silicate xerogels at 350 C. The studies of Tb3+ ! Eu3+ energy transfer process (ET) were performed by excitation and emission spectra along with luminescence decay analysis. The co-activated xerogels and GCs exhibit multicolor emission originated from 4fn–4fn optical transitions of Tb3+ (5D4 !7FJ, J = 6–3) as well as Eu3+ ions (5D0 ! 7FJ, J = 0–4). Based on recorded decay curves, it was found that there is a significant prolongation in luminescence lifetimes of the 5D4 (Tb3+) and the 5D0 (Eu3+) levels after the controlled heat-treatment of xerogels. Moreover, for both types of prepared GCs, an increase in ET e ciency was also observed (from ET 16% for xerogels up to ET = 37.3% for SiO2-YF3 GCs and ET = 60.8% for SiO2-LaF3 GCs). The changes in photoluminescence behavior of rare-earth (RE3+) dopants clearly evidenced their partial segregation inside low-phonon energy fluoride environment. The obtained results suggest that prepared SiO2-MF3:Tb3+, Eu3+ GC materials could be considered for use as optical elements in RGB-lighting optoelectronic devices operating under near-ultraviolet (NUV) excitation

Aerogel insulation materials for industrial installation : properties and structure of new factory-made products

In this article the comparisons of two new factory-made Chinese aerogel products with the Pyrogel® product, all available on the market, are presented. The aerogel products are in a flexible blanket form and all products are dedicated for high temperature applications. The properties of the samples such as their dimension stability, water vapour transmission and water absorption are also described. Additionally the microstructure and chemical composition of the products are analysed using SEM/ EDS (scanning electron microscopy coupled with X-ray energy-dispersive spectroscopy). The differences in the maximum service temperature are presented. The internal self-heating of the aerogel samples is described and is compared to a similar effect observed in mineral wool samples. The results in the change of the thermal properties in a wide range of temperatures (+ 10–600°C) are shown. The obtained results are correlated with the mineral wool data. The correlation shows an advantage in a highefficiency thermal performance of aerogel products compared to other insulation materials at high temperatures

Reddish-Orange Luminescence from BaF2:Eu3+ Fluoride Nanocrystals Dispersed in Sol-Gel Materials

Nanocrystalline transparent BaF2:Eu3+ glass-ceramic materials emitting reddish-orange light were fabricated using a low-temperature sol-gel method. Several experimental techniques were used to verify structural transformation from precursor xerogels to sol-gel glass-ceramic materials containing fluoride nanocrystals. Thermal degradation of xerogels was analyzed by thermogravimetric analysis (TG) and di erential scanning calorimetry method (DSC). The presence of BaF2 nanocrystals dispersed in sol-gel materials was confirmed by the X-ray di raction (XRD) analysis and transmission electron microscopy (TEM). In order to detect structural changes in silica network during annealing process, the infrared spectroscopy (IR-ATR) was carried out. In particular, luminescence spectra of Eu3+ and their decays were examined in detail. Some spectroscopic parameters of Eu3+ ions in glass-ceramics containing BaF2 nanocrystals were determined and compared to the values obtained for precursor xerogels. It was observed, that the intensities of two main red and orange emission bands corresponding to the 5D0!7F2 electric-dipole transition (ED) and the 5D0!7F1 magnetic-dipole (MD) transition are changed significantly during transformation from xerogels to nanocrystalline BaF2:Eu3+ glass-ceramic materials. The luminescence decay analysis clearly indicates that the measured lifetime 5D0 (Eu3+) considerably enhanced in nanocrystalline BaF2:Eu3+ glass-ceramic materials compared to precursor xerogels. The evident changes in luminescence spectra and their decays suggest the successful migration of Eu3+ ions from amorphous silica network to low-phonon BaF2 nanocrystals

Long-lived emission from Eu3+:PbF2 nanocrystals distributed into sol-gel silica glass

This paper reports an optical investigation of Eu3+:PbF2 nanocrystals distributed into silica glasses fabricated by sol–gel methods. The sample microstructure was investigated using scanning transmission electron microscopy. The β-cubic PbF2 crystalline phase was identified using X-ray diffraction analysis. The observed emission bands correspond to 5D0 → 7FJ (J = 0–4) transitions of Eu3+. The spectroscopic parameters for Eu3+ ions were determined based on excitation and emission measurements as well as luminescence decay analysis. Emission originating from 5D0 state of Eu3+ ions in sample containing PbF2 nanocrystals is long-lived in comparison to precursor sol–gel silica glasses

Fabrication of fluoride nanocrystals and their spectroscopic properties

In this work, the fabrication of glass-ceramic materials containing MF3:Eu3+ (M = La, Gd) nanocrystals dispersed in silica sol-gel hosts has been presented. The transformation from liquid sols towards bulk samples was also examined based on IR measurements. The crystallization temperatures and formation of MF3 phases were verified based on TG/DSC analysis and XRD measurements. The optical properties of prepared Eu3+-doped samples were evaluated based on PLE and PL as well as luminescence decay analysis of the 5D0 excited state. Obtained samples exhibit a series of the 5D0 → 7FJ (J = 1–4) emission bands, which were recorded within the reddish-orange spectral area under near-UV illumination (λexc = 393 nm). Recorded luminescence spectra and double-exponential character of decay curves for prepared glass-ceramic samples indicated the successful migration of Eu3+ dopant ions from amorphous silica framework to low-phonon energy MF3 nanocrystal phases

Sol-Gel Glass-Ceramic Materials Containing CaF2:Eu3+ Fluoride Nanocrystals for Reddish-Orange Photoluminescence Applications

CaF2:Eu3+ glass-ceramic sol-gel materials have been examined for reddish-orange photoluminescence applications. The transformation from precursor xerogels to glass-ceramic materials with dispersed fluoride nanocrystals was verified using several experimental methods: di erential scanning calorimetry (DSC), thermogravimetric analysis (TG), X-ray di raction (XRD), transmission electron microscopy (TEM), infrared spectroscopy (IR-ATR), energy dispersive X-ray spectroscopy (EDS) and photoluminescence measurements. Based on luminescence spectra and their decays, the optical behavior of Eu3+ ions in fabricated glass-ceramics were characterized and compared to those of precursor xerogels. In particular, the determined luminescence lifetime of the 5D0 excited state of Eu3+ ions in nanocrystalline CaF2:Eu3+ glass-ceramic materials is significantly prolonged in comparison with prepared xerogels. The integrated intensities of emission bands associated to the 5D0 ! 7F2 electric-dipole transition (ED) and the 5D0 !7F1 magnetic-dipole transition (MD) are changed drastically during controlled ceramization process of xerogels. This implies the e cient migration of Eu3+ ions from amorphous silicate sol-gel network into low-phonon energy CaF2 nanocrystals

Studies of sol-gel evolution and distribution of Eu3+ ions in glassceramics containing LaF3 nanocrystals depending on initial sols composition

In this work, we performed a systematic analysis of the impact of selected chemical reagents used in sol-gel synthesis (i.e., N,N-dimethylformamide) and different catalyst agents (i.e., CH3COOH, HNO3) on the formation and luminescence of Eu3+-doped SiO2–LaF3 nano-glass–ceramics. Due to the characteristic nature of intra-configurational electronic transitions of Eu3+ ions within the 4f6 manifold (5D0 → 7FJ, J = 0–4), they are frequently used as a spectral probe. Thus, the changes in the photoluminescence profile of Eu3+ ions could identify the general tendency of rare earth materials to segregate inside low-phonon energy fluoride nanocrystals, which allows us to assess their application potential in optoelectronics. Fabricated sol-gel materials, from sols to gels and xerogels to nano-glass–ceramics, were examined using several experimental techniques: X-ray diffraction (XRD), transmission electron microscopy (TEM), infrared spectroscopy (IR), and luminescence measurements. It was found that the distribution of Eu3+ ions between the amorphous silicate solgel host and LaF3 nanocrystals is strictly dependent on the initial composition of the obtained sols, and the lack of N,N-dimethylformamide significantly promotes the segregation of Eu3+ ions inside LaF3 nanocrystals. As a result, we detected long-lived luminescence from the 5D0 excited state equal to 6.21 ms, which predisposes the obtained glass–ceramic material for use as an optical element in reddish-orange emitting devices

Structural and photoluminescence investigations of Tb3+/Eu3+ codoped silicate sol-gel glass-ceramics containing CaF2 nanocrystals

In this work, the series of Tb3+/Eu3+ co-doped xerogels and derivative glass-ceramics containing CaF2 nanocrystals were prepared and characterized. The in situ formation of fluoride crystals was verified by an X-ray diffraction technique (XRD) and transmission electron microscopy (TEM). The studies of the Tb3+/Eu3+ energy transfer (ET) process were performed based on excitation and emission spectra along with luminescence decay analysis. According to emission spectra recorded under near-ultraviolet (NUV) excitation (351 nm, 7F6 ! 5L9 transition of Tb3+), the mutual coexistence of the 5D4 ! 7FJ (J = 6–3) (Tb3+) and the 5D0 ! 7FJ (J = 0–4) (Eu3+) luminescence bands was clearly observed. The co-doping also resulted in gradual shortening of a lifetime from the 5D4 state of Tb3+ ions, and the ET efficiencies were varied from ET = 11.9% (Tb3+:Eu3+ = 1:0.5) to ET = 22.9% (Tb3+:Eu3+ = 1:2) for xerogels, and from ET = 25.7% (Tb3+:Eu3+ = 1:0.5) up to ET = 67.4% (Tb3+:Eu3+ = 1:2) for glass-ceramics. Performed decay analysis from the 5D0 (Eu3+) and the 5D4 (Tb3+) state revealed a correlation with the change in Tb3+–Eu3+ and Eu3+–Eu3+ interionic distances resulting from both the variable Tb3+:Eu3+ molar ratio and their partial segregation in CaF2 nanophase

Luminescence of SiO2-BaF2:Tb3+, Eu3+ nano-glass-ceramics made from sol-gel method at low temperature

The synthesis and characterization of multicolor light-emitting nanomaterials based on rare earths (RE3+) are of great importance due to their possible use in optoelectronic devices, such as LEDs or displays. In the present work, oxyfluoride glass-ceramics containing BaF2 nanocrystals co-doped with Tb3+, Eu3+ ions were fabricated from amorphous xerogels at 350 C. The analysis of the thermal behavior of fabricated xerogels was performed using TG/DSC measurements (thermogravimetry (TG), differential scanning calorimetry (DSC)). The crystallization of BaF2 phase at the nanoscale was confirmed by X-ray diffraction (XRD) measurements and transmission electron microscopy (TEM), and the changes in silicate sol–gel host were determined by attenuated total reflectance infrared (ATR-IR) spectroscopy. The luminescent characterization of prepared sol–gel materials was carried out by excitation and emission spectra along with decay analysis from the 5D4 level of Tb3+. As a result, the visible light according to the electronic transitions of Tb3+ (5D4 ! 7FJ (J = 6–3)) and Eu3+ (5D0 ! 7FJ (J = 0–4)) was recorded. It was also observed that co-doping with Eu3+ caused the shortening in decay times of the 5D4 state from 1.11 ms to 0.88 ms (for xerogels) and from 6.56 ms to 4.06 ms (for glass-ceramics). Thus, based on lifetime values, the Tb3+/Eu3+ energy transfer (ET) efficiencies were estimated to be almost 21% for xerogels and 38% for nano-glass-ceramics. Therefore, such materials could be successfully predisposed for laser technologies, spectral converters, and three-dimensional displays