An Efficient, Thermally Stable Cerium-Based Silicate Phosphor for Solid State White Lighting
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A novel air-stable sodium iron hexacyanoferrate (R-Na1.92Fe[Fe(CN)(6)]) with rhombohedral structure is demonstrated to be a scalable, low-cost cathode material for sodium-ion batteries exhibiting high capacity, long cycle life, and good rate capability. The cycling mechanism of the iron redox is clarified and understood through synchrotron-based soft X-ray absorption spectroscopy, which also reveals the correlation between the physical properties and the cell performance of this novel material. More importantly, successful preparation of a dehydrated iron hexacyanoferrate with high sodium-ion concentration enables the fabrication of a discharged sodium-ion battery with a non-sodium metal anode, and the manufacturing feasibility of low cost sodium-ion batteries with existing lithium-ion battery infrastructures has been tested.
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Mechanisms of hexagonal close-packed (HCP) to body-centered cubic (BCC) phase transformation in Mg single crystals are observed using a combination of polychromatic beam Laue diffraction and monochromatic beam powder diffraction techniques under quasi-hydrostatic pressures of up to 58 ± 2 GPa at ambient temperature. Although experiments were performed with both He and Ne pressure media, crystals inevitably undergo plastic deformation upon loading to 40–44 GPa. The plasticity is accommodated by dislocation glide causing local misorientations of up to 1°–2°. The selected crystals are tracked by mapping Laue diffraction spots up to the onset of the HCP to BCC transformation, which is determined to be at a pressure of 56.6 ± 2 GPa. Intensity of the Laue reflections from HCP crystals rapidly decrease but no reflections from crystalline BCC phase are observed with a further increase of pressure. Nevertheless, the powder diffraction shows the formation of 110 BCC peak at 56.6 GPa. The peak intensity increases at 59.7 GPa. Upon the full transformation, a powder-like BCC aggregate is formed revealing the destructive nature of the HCP to BCC transformation in single crystals of Mg.
An efficient and stable palladium based excimer emitter was developed capable of exhibiting maximum EQE over 27% and achieved nearly 3000 h at 1000 cd m −2 .
A facile and effective templated synthetic strategy to prepare extremely stable CsPbX 3 nanocomposites by anchoring CsPbX 3 NCs onto silica particles.
Small-angle X-ray scattering was utilized to investigate the morphological transition of glycerol monooleate under various compositions, temperatures, and additives such as water and fatty acids.
Porous silicon layers were embedded with ZnTe using the isothermal close space sublimation technique. The presence of ZnTe was demonstrated using cross-sectional energy dispersive spectroscopy maps. ZnTe embedded samples present intense room temperature photoluminescence along the whole visible range. We ascribe this PL to ZnTe nanocrystals of different sizes grown on the internal pore surface. Such crystals, with different orientations and sizes, were observed in transmission electron microscopy images, while transmission electron diffraction images of the same regions reveal ZnTe characteristic patterns.
Keeping in view of the recent increased interest towards phosphor materials and its applications, an attempt has been made in the present paper to analyze the new NaPbB{sub 5}O{sub 9}:Dy{sub 3+} phosphor with different Dy{sub 3+} concentrations. Special attention is paid to investigate their crystal structure, morphology and luminescence properties. X-ray diffraction (XRD) results confirm the formation of NaPbB{sub 5}O{sub 9}:Dy{sub 3+} phosphor powder. The scanning electron microscope (SEM) images show that the grains are in micrometer range. Photoluminescence spectra are recorded with different excitation wavelengths for the investigated phosphor and analyzed the variation of intensity of emission bands with Dy{sub 3+} ion concentration. Color co-ordinates are calculated and are used to characterize the color of the phosphor.
The study reported herein presents results on the room-temperature photoluminescence (PL) dynamics of chemically synthesized SiC{sub x}O{sub y≤1.6} (0.19 < x < 0.6) thin films and corresponding nanowire (NW) arrays. The PL decay transients of the SiC{sub x}O{sub y} films/NWs are characterized by fast luminescence decay lifetimes that span in the range of 350–950 ps, as determined from their deconvoluted PL decay spectra and their stretched-exponential recombination behavior. Complementary steady-state PL emission peak position studies for SiC{sub x}O{sub y} thin films with varying C content showed similar characteristics pertaining to the variation of their emission peak position with respect to the excitation photon energy. A nearly monotonic increase in the PL energy emission peak, before reaching an energy plateau, was observed with increasing excitation energy. This behavior suggests that band-tail states, related to C-Si/Si-O-C bonding, play a prominent role in the recombination of photo-generated carriers in SiC{sub x}O{sub y}. Furthermore, the PL lifetime behavior of the SiC{sub x}O{sub y} thin films and their NWs was analyzed with respect to their luminescence emission energy. An emission-energy-dependent lifetime was observed, as a result of the modulation of their band-tail states statistics with varying C content and with the reduced dimensionality of the NWs.
Silica optical fiber sensors offer a fast, distributed measurement solution in various cryogenic and radiation environments, such as magnets for fusion power. Under these conditions, light-absorbing point defects limit lifetime via radiation-induced attenuation (RIA). To support RIA kinetics prediction, we present an in situ, broadband absorption spectroscopy setup combining gamma irradiation with liquid nitrogen cooling. The apparatus enables continuous monitoring of narrowband RIA levels and the use of secondary optical annealing light sources, alongside broadband spectrum measurements to characterize RIA defects through spectrum decomposition. Initial results confirm the inevitable photobleaching effect of the probe light source, which must be accounted for. In addition, we report RIA kinetics during cycles of gamma irradiation at 77 K and isochronal thermal annealing steps from liquid nitrogen to room temperature, showcasing the setup’s ability to replicate real fiber operation scenarios. These instruments form an ideal platform to further study the kinetics of RIA coupled with thermal and optical annealing.
Significance We analyze the evolution of ligninolytic peroxidases from wood-rotting fungi using conifer and angiosperm lignin as representatives of 2 steps of lignin evolution. By enzyme resurrection, we show that during fungal evolution, these enzymes improved their activity and switched their degradative preferences with the rise of a surface tryptophan conferring on them the ability to oxidize nonphenolic lignin. We calibrated the peroxidase phylogeny and determined that this residue appeared coincident with angiosperm diversification, characterized by the synthesis of a more complex and less phenolic lignin due to the general incorporation of a new unit in its structure. This way, we show that fungal evolution followed that of lignin synthesis, pointing to a coevolution between fungal saprotrophs and their plant hosts.