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Tetrahedron‐based nitrides offer a wide range of properties and applications. Highly condensed nitridophosphates are examples of nitrides that exhibit fascinating luminescence properties when doped with Eu2+, making them appealing for industrial applications. Here, we present the first nitridomagnesophosphate solid solution series Ba3−xSrx[Mg2P10N20] : Eu2+ (x=0–3), synthesized by a high‐pressure high‐temperature approach using the multianvil technique (3 GPa, 1400 °C). Starting from the binary nitrides P3N5 and Mg3N2 and the respective alkaline earth azides, we incorporate Mg into the P/N framework to increase the degree of condensation κ to 0.6, the highest observed value for alkaline earth nitridophosphates. The crystal structure was elucidated by single‐crystal X‐ray diffraction, powder X‐ray diffraction, energy‐dispersive X‐ray spectroscopy (EDX), and solid‐state NMR. DFT calculations were performed on the title compounds and other related highly condensed nitridophosphates to investigate the influence of Mg in the P/N network. Eu2+‐doped samples of the solid solution series show a tunable narrow‐band emission from cyan to green (492–515 nm), which is attributed to the preferred doping of a single crystallographic site. Experimental confirmation of this assumption was provided by overdoping experiments and STEM‐HAADF studies on the series as well on the stoichiometric compound Ba2Eu[Mg2P10N20] with additional atomic resolution energy‐dispersive X‐ray spectroscopy (EDX) mapping. [ABSTRACT FROM AUTHOR]

In the field of nitride phosphors, which are crucial for phosphor‐converted light‐emitting diodes, mixed tetrahedral networks hold a significant position. With respect to the wide range of compositions, the largely unexplored (Si, P)–N networks are investigated as potential host structures. In this work, two highly condensed structures, namely Sr2SiP2N6 and Sr5Si2P6N16 are reported to address the challenges that arise from the similarities of the network‐forming cations Si4+ and P5+ in terms of charge, ionic radius, and atomic scattering factor, a multistep workflow is employed to elucidate their structure. Using single‐crystal X‐ray diffraction, energy‐dispersive X‐ray spectroscopy (EDX), atomic‐resolution scanning transmission electron microscopy (STEM)‐EDX maps, and straightforward crystallographic calculations, it is found that Sr2SiP2N6 is the first ordered, and Sr5Si2P6N16 the first disordered, anionic tetrahedral (Si, P)–N network. After doping with Eu2+, Sr2SiP2N6:Eu2+ shows narrow cyan emission (λmax = 506 nm, fwhm = 60 nm/2311 cm−1), while for Sr5Si2P6N16:Eu2+ a broad emission with three maxima at 534, 662, and 745 nm upon irradiation with ultraviolet light is observed. An assignment of Sr sites as probable positions for Eu2+ and their relation to the emission bands of Sr5Si2P6N16:Eu2+ is discussed. [ABSTRACT FROM AUTHOR]

This study presents the synthesis and characterization of oxonitridosilicate phosphates Sr3SiP3O2N7, Sr5Si2P4ON12, and Sr16Si9P9O7N33 as the first of their kind. These compounds were synthesized under high‐temperature (1400 °C) and high‐pressure (3 GPa) conditions. A unique structural feature is their common fundamental building unit, a vierer single chain of (Si, P)(O, N)4 tetrahedra. All tetrahedra comprise substitutional disorder which is why we refer to it as the fundamental disorder unit (FDU). We classified four different FDU motifs, revealing systematic bonding patterns. Including literature known Sr5Si2P6N16, three of the four patterns were found in the presented compounds. Common techniques like single‐crystal X‐ray diffraction (SCXRD), elemental analyses, and 31P nuclear magnetic resonance (NMR) spectroscopy were utilized for structural analysis. Additionally, low‐cost crystallographic calculations (LCC) provided insights into the structure of Sr16Si9P9O7N33 where NMR data were unavailable due to the lack of bulk samples. The optical properties of these compounds, when doped with Eu2+, were investigated using photoluminescence excitation (PLE), photoluminescence (PL) measurements, and density functional theory (DFT) calculations. Factors influencing the emission properties, including thermal quenching mechanisms, were discussed. This research reveals the new class of oxonitridosilicate phosphates with unique systematic structural features that offer potential for theoretical studies of luminescence and band gap tuning in insulators. [ABSTRACT FROM AUTHOR]

Light‐emitting diodes (LEDs) producing pure, highly saturated colors are the industry standard for efficient backlighting of high‐color gamut displays. Vivid color reproduction, matching the eye's perception of nature, is the central paradigm in the design of narrow‐band emitting phosphors. To cover a wide range of naturally occurring color tones, expansion of the color gamut in the green spectral region, and therefore an advanced applicable green phosphor, is highly desired. Herein, the oxonitridoberyllosilicate Ba[BeSiON2]:Eu2+ showing outstanding narrow‐band green emission (λmax ≈526 nm with FWHM ≈1600 cm−1 (≈45 nm), x = 0.212, y = 0.715) when excited with InGaN‐based blue LEDs is presented. High quantum efficiency and low thermal quenching (>90% rel. quantum efficiency at 100 °C) as well as excellent scalability make the material suitable for industrial application in high color‐gamut LED displays. A prototype phosphor‐converted‐LED (pc‐LED), with green‐emitting Ba[BeSiON2]:Eu2+ and K2SiF6:Mn4+ as red phosphor shows an extraordinary coverage in the CIE 1931 color space of 109% compared to the DCI‐P3 standard, topping the widely applied β‐SiAlON:Eu2+ phosphor (104%), making it suitable for use in phone displays, monitors, and television screens. [ABSTRACT FROM AUTHOR]

We have previously presented a computational protocol that is based on an embedded cluster model and operates in the framework of TD-DFT in conjunction with the excited state dynamics (ESD) approach. The protocol is able to predict the experimental absorption and emission spectral shapes of Eu2+-doped phosphors. In this work, the applicability domain of the above protocol is expanded to Eu2+-doped phosphors bearing multiple candidate Eu doping centers. It will be demonstrated that this protocol provides full control of the parameter space that describes the emission process. The stability of Eu doping at various centers is explored through local energy decomposition (LED) analysis of DLPNO-CCSD(T) energies. This enables further development of the understanding of the electronic structure of the targeted phosphors, the diverse interactions between Eu and the local environment, and their impact on Eu doping probability, and control of the emission properties. Hence, it can be employed to systematically improve deficiencies of existing phosphor materials, defined by the presence of various intensity emission bands at undesired frequencies, towards classes of candidate Eu2+-doped phosphors with desired narrow band red emission. For this purpose, the chosen study set consists of three UCr4C4-based narrow-band phosphors, namely the known alkali lithosilicates RbNa[Li3SiO4]2:Eu2+ (RNLSO2), RbNa3[Li3SiO4]4:Eu2+ (RNLSO) and their isotypic nitridolithoaluminate phosphors consisting of CaBa[LiAl3N4]2:Eu2+ (CBLA2) and the proposed Ca3Ba[LiAl3N4]4:Eu2+ (CBLA), respectively. The theoretical analysis presented in this work led us to propose a modification of the CBLA2 phosphor that should have improved and unprecedented narrow band red emission properties. Finally, we believe that the analysis presented here is important for the future rational design of novel Eu2+-doped phosphor materials, with a wide range of applications in science and technology. [ABSTRACT FROM AUTHOR]

Oxonitridophosphates exhibit the potential for broad structural diversity, making them promising host‐compounds in phosphor‐converted light‐emitting diode applications. The novel monophyllo‐oxonitridophosphate β‐MgSrP3N5O2 was obtained by using the high‐pressure multianvil technique. The crystal structure was solved and refined based on single‐crystal X‐ray diffraction data and confirmed by powder X‐ray diffraction. β‐MgSrP3N5O2 crystallizes in the orthorhombic space group Cmme (no. 67, a=8.8109(6), b=12.8096(6), c=4.9065(3) Å, Z=4) and has a structure related to that of Ba2CuSi2O7. DFT calculations were performed to investigate the phase transition from α‐ to β‐MgSrP3N5O2 and to confirm the latter as the corresponding high‐pressure polymorph. Furthermore, the luminescence properties of Eu2+ doped samples of both polymorphs were investigated and discussed, showing blue and cyan emission, respectively (α‐MgSrP3N5O2; λmax=438 nm, fwhm=46 nm/2396 cm−1; β‐MgSrP3N5O2; λmax=502 nm, fwhm=42 nm/1670 cm−1). [ABSTRACT FROM AUTHOR]

Brexanolone, a formulation of the neurosteroid allopregnanolone (ALLO), is approved for treating postpartum depression (PPD) and is being investigated for therapeutic efficacy across numerous neuropsychiatric disorders. Given ALLO's beneficial effects on mood in women with PPD compared to healthy control women, we sought to characterize and compare the cellular response to ALLO in women with (n = 9) or without (n = 10, i.e., Controls) past PPD, utilizing our previously established patient-derived lymphoblastoid cell lines (LCLs). To mimic in vivo PPD ALLO-treatment, LCLs were exposed to ALLO or DMSO vehicle for 60 h and RNA-sequenced to detect differentially expressed genes (DEGs, pnominal < 0.05). Between ALLO-treated Control and PPD LCLs, 269 DEGs were identified, including Glutamate Decarboxylase 1 (GAD1), which was decreased 2-fold in PPD. Network analysis of PPD:ALLO DEGs revealed enriched terms related to synaptic activity and cholesterol biosynthesis. Within-diagnosis analyses (i.e., DMSO vs. ALLO) detected 265 ALLO-induced DEGs in Control LCLs compared to only 98 within PPD LCLs, with just 11 DEGs overlapping. Likewise, the gene ontologies underlying ALLO-induced DEGs in PPD and Control LCLs were divergent. These data suggest that ALLO may activate unique and opposing molecular pathways in women with PPD, which may be tied to its antidepressant mechanism. [ABSTRACT FROM AUTHOR]

Background: The development of adipose tissue during adolescence may provide valuable insights into obesity-associated diseases. We propose an automated convolutional neural network (CNN) approach using Dixon-based magnetic resonance imaging (MRI) to quantity abdominal subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) in children and adolescents. Methods: 474 abdominal Dixon MRI scans of 136 young healthy volunteers (aged 8–18) were included in this study. For each scan, an axial fat-only Dixon image located at the L2–L3 disc space and another image at the L4–L5 disc space were selected for quantification. For each image, an outer and an inner region around the abdomen wall, as well as SAT and VAT pixel masks, were generated by expert readers as reference standards. A standard U-Net CNN architecture was then used to train two models: one for region segmentation and one for fat pixel classification. The performance was evaluated using the dice similarity coefficient (DSC) with fivefold cross-validation, and by Pearson correlation and the Student's t-test against the reference standards. Results: For the DSC results, means and standard deviations of the outer region, inner region, SAT, and VAT comparisons were 0.974 ± 0.026, 0.997 ± 0.003, 0.981 ± 0.025, and 0.932 ± 0.047, respectively. Pearson coefficients were 1.000 for both outer and inner regions, and 1.000 and 0.982 for SAT and VAT comparisons, respectively (all p = NS). Conclusion: These results show that our method not only provides excellent agreement with the reference SAT and VAT measurements, but also accurate abdominal wall region segmentation. The proposed combined region- and pixel-based CNN approach provides automated abdominal wall segmentation as well as SAT and VAT quantification with Dixon MRI and enables objective longitudinal assessment of adipose tissues in children during adolescence. [ABSTRACT FROM AUTHOR]

Understanding electronic structure properties of narrow-band emitting phosphor materials is important for finding and tailoring novel materials for fabrication of phosphor converted (pc)-LEDs. Thereby, illumination quality can be improved while further reduction in worldwide energy consumption is achieved. In pc-LEDs, the energetic position of the Eu2+ 5d1 states with respect to conduction band and valence band of the host lattice determines the electronic structure and the optical properties, such as thermal quenching and quantum efficiency under application conditions. Here, we experimentally determine the energetic position of the Eu2+ 5d1 state for the narrow-band red-emitting phosphor SrLi2Al2O2N2:Eu2+ (SALON) employing resonant inelastic X-ray scattering (RIXS) measurements. The position of the 5d1 energy level of the dopant Eu2+ is determined directly from RIXS measurements at the N K- and O K-edges and is found to be 0.53 ± 0.04 eV (N K-edge) and 0.48 ± 0.10 eV (O K-edge) below the conduction band. We further use X-ray excited optical luminescence measurements to provide a deeper understanding of the energy levels and radiative processes involved in SALON, as the method allows determination of the 4f7 energy levels thus confirming the narrow-band luminescence in the red spectral region at 610 nm due to the 4f65d1 → 4f7 transition. [ABSTRACT FROM AUTHOR]

The oxonitridosilicate La7Sr[Si10N19O3] : Eu2+ and its substitutional variants RE8‐xAEx[Si10N20‐xO2+x] : Eu2+ with RE=La, Ce; AE=Ca, Sr, Ba and 0≤x≤2 were synthesized starting from REN, SrN/Ca3N2/Ba2N, SiO2, amorphous Si3N4 and Eu2O3 as doping agent at 1600 °C in a radiofrequency furnace. The crystal structure of La7Sr[Si10N19O3] was solved and refined based on single‐crystal X‐ray diffraction data. La7Sr[Si10N19O3] crystallizes in the orthorhombic space group Pmn21 (no. 31). The crystal structures of the isotypic compounds RE8‐xAEx[Si10N20‐xO2+x] were confirmed by Rietveld refinements based on powder X‐ray diffraction data using the single‐crystal data of La7Sr[Si10N19O3] as starting point. Crystal structure elucidation reveals a 3D network of vertex sharing SiN4 and SiN2(N1/2‐x/4O1/2+x/4)2 (0≤x≤2) tetrahedra. When excited with UV to blue light, La7Sr[Si10N19O3] : Eu2+ shows amber luminescence with λem=612 nm and fwhm=84 nm/2194 cm−1, which makes it interesting for application in amber phosphor‐converted light emitting diodes. [ABSTRACT FROM AUTHOR]

The nitridoberylloaluminate Ba2[BeAl3N5]:Eu2+ and solid solutions Sr2−xBax[BeAl3N5]:Eu2+ (x=0.5, 1.0, 1.5) were synthesized in a hot isostatic press (HIP) under 50 MPa N2 atmosphere at 1200 °C. Ba2[BeAl3N5]:Eu2+ crystallizes in triclinic space group P1‾ (no. 2) (Z=2, a=6.1869(10), b=7.1736(13), c=8.0391(14) Å, α=102.754(8), β=112.032(6), γ=104.765(7)°), which was determined from single‐crystal X‐ray diffraction data. The lattice parameters of the solid solution series have been obtained from Rietveld refinements and show a nearly linear dependence on the atomic ratio Sr : Ba. The electronic properties and the band gaps of M2[BeAl3N5] (M=Sr, Ba) have been investigated by a combination of soft X‐ray spectroscopy and density functional theory (DFT) calculations. Upon irradiation with blue light (440–450 nm), the nitridoberylloaluminates exhibit intense orange to red luminescence, which can be tuned between 610 and 656 nm (fwhm=1922–2025 cm−1 (72–87 nm)). In contrast to the usual trend, the substitution of the smaller Sr2+ by larger Ba2+ leads to an inverse‐tunable luminescence to higher wavelengths. Low‐temperature luminescence measurements have been performed to exclude anomalous emission. [ABSTRACT FROM AUTHOR]