Crystal Morphology Research Articles

Investigation on thermoelectric properties of SnSe thin films as prepared by RF magnetron sputtering

In this work, we investigated the thermoelectric properties of SnSe (Tin Selenide) thin films onto SiO2/Si-wafer substrates as prepared by RF (radio frequency) magnetron sputtering technique. The sputtering conditions used base pressure below 5.5 10-4 Pa and working pressure at 0.93 Pa within the Ar atmosphere as a flow rate fixed 40 sccm. The RF sputtering power was applied at 80 W and sputtering time for 30 min. After thin film deposition, as-deposited thin films were annealed by the vacuum annealing method at 300-450 oC. The crystal structure, morphology and film thickness, and atomic composition of SnSe thin film were carried out by X-ray diffraction (XRD), the field emission scanning electron microscope (FE-SEM), and energy-dispersive X-ray spectroscopy (EDS) techniques, respectively. The thermoelectric properties (electrical resistivity; ρ) and Seebeck coefficient; S) were measured by the ZEM-3 method to calculate the power factor (PF) value. The results showed that the as-deposited thin films had improved the crystallography of SnSe from amorphous to crystalline phases after thin films were annealed at a temperature range of 300-400 oC. At room temperature, the maximum power factor of 0.35 mW m˗1 K˗2 (ρ = 202 mΩ m and S = 165 μV K˗1) could be found to estimate the dimensionless Figure of Merit (ZT) values around 0.44 for annealing thin film sample at 400 oC.

Prediction of morphology of CL-20/TFAZ cocrystal crystals in binary solvents based on modified attachment energy model

Crystal morphology of CL-20/TFAZ cocrystal in vacuum was predicted using the attachment energy (AE) model. Additionally, the modified attachment energy (MAE) model and molecular dynamics (MD) method were utilized to predict the crystal morphology of CL-20/TFAZ cocrystal in four different binary solvents, namely, isopropyl alcohol (IPA)/acetone (AC), IPA/dimethyl sulfoxide (DMSO), IPA/ethyl acetate (EA), and IPA/water (H2O). The radial distribution function (RDF) between the solvent and crystal surface and the mean square displacement (MSD) of the solvent were calculated. The findings showed that the morphology of CL-20/TFAZ cocrystal in vacuum was an irregular polyhedron with eleven important growth surfaces: (001), (1−10), (110), (100), (011), (0−11), (10−1), (020), (0−20), (11−1), and (1−1−1), with the (001) surface having the highest area ratio of 31.693 %. The crystalline morphology in IPA/AC, IPA/DMSO, and IPA/EA solvents was block-shaped, while it was rod-shaped in IPA/H2O. Comparing the RDF values of the four solvents, IPA/H2O exhibited the largest g(r) value and could more easily adsorb onto the crystal surface of CL-20/TFAZ cocrystal. Interestingly, IPA/H2O solvent had the smallest MSD value, suggesting the slowest diffusion rate, while IPA/AC solvent exhibited the fastest diffusion rate. Overall, IPA/EA solvents were more suitable for the formation of CL-20/TFAZ cocrystal.

Cuticle properties, wax composition, and crystal morphology of Hami melon cultivars (Cucumis melo L.) with differential resistance to fruit softening

Cuticle wax chemicals are cultivar-dependent and contribute to storage quality. Few research reported on wax analysis between melting flesh-type (MF; ‘Jinhuami 25’) and nonmelting flesh-type (NMF; ‘Xizhoumi 17’ and ‘Chougua’) Hami melons. Chemicals and crystal structures of Hami melon cuticular wax, cell wall metabolism related to fruit melting, and fruit physiology were analyzed to observe wax functions. Results showed that Hami melon cuticle wax predominantly consists of esters, alkanes, alcohols, aldehydes, and terpenoids. MF-type has a lower alkane/terpenoid ratio, concomitant to its higher weight loss and cuticle permeability. Micromorphology of wax crystals appears as numerous platelets with irregular crystals, and the transformation of wax structure in NMF Hami melon is delayed. Waxy components affect cell wall metabolism and physiological quality, which results in the pulp texture difference between MF-type and NMF-type during storage. Results provide a reference for the regulation of wax synthesis in both types of melons.

Growth of Spontaneous Nucleation AlN Crystals by Al-Base Alloy Evaporation in Nitrogen Atmosphere

Aluminum nitride (AlN) crystals with areas ranging from 1 mm2 to 2 mm2 were successfully grown through spontaneous nucleation at 1700 °C using a modified vapor transport method. In this approach, Cu–Al alloy served as the source of aluminum (Al), and nitrogen (N2) was employed as the nitrogen source. The morphology and crystalline quality of the AlN crystals were characterized by a stereo microscope, Raman spectrometer, photoluminescence (PL) and secondary-ion mass spectrometry (SIMS). Deposited on the graphite lid, the as-grown AlN crystals exhibited both rectangular and hexagonal shapes, identified as m-plane and c-plane AlN, respectively, based on Raman spectroscopy. The full width half maximum (FWHM) values of E2 (high) for the rectangular and hexagonal grains were measured to be 6.00 cm−1 and 6.06 cm−1, respectively, indicating high crystalline quality. However, PL and SIMS analysis indicated the presence of impurities associated with oxygen in the crystals. This paper elucidates the growth mechanism of the modified vapor transport method and highlights the role of the Cu–Al alloy in sustaining reactions at lower temperatures. The addition of copper (Cu) not only facilitates sustainable reactions, but also provides a novel perspective for the growth of AlN single crystals.

Effects of the ZrO2 Crystalline Phase and Morphology on the Thermocatalytic Decomposition of Dimethyl Methylphosphonate.

Thermocatalytic decomposition is an efficient purification technology that is potentially applicable to degrading chemical warfare agents and industrial toxic gases. In particular, ZrO2 has attracted attention as a catalyst for the thermocatalytic decomposition of dimethyl methylphosphonate (DMMP), which is a simulant of the nerve gas sarin. However, the influence of the crystal phase and morphology on the catalytic performance of ZrO2 requires further exploration. In this study, monoclinic- and tetragonal-phase ZrO2 (m- and t-ZrO2, respectively) with nanoparticle, flower-like shape and hollow microsphere morphologies were prepared via hydrothermal and solvothermal methods, and their thermocatalytic decomposition of DMMP was systematically investigated. For a given morphology, m-ZrO2 performed better than t-ZrO2. For a given crystalline phase, the morphology of hollow microspheres resulted in the longest protection time. The exhaust gases generated by the thermocatalytic decomposition of DMMP mainly comprised H2, CO2, H2O and CH3OH, and the by-products were phosphorus oxide species. Thus, the deactivation of ZrO2 was attributed to the deposition of these phosphorous oxide species on the catalyst surface. These results are expected to help guide the development of catalysts for the safe disposal of chemical warfare agents.

Improving Photocatalytic Performance through Incorporation of Various Cations in A-site of Double Perovskite Material (Cs0.50MA0.50)2SnI6 for Degradation of Methylene Blue Dye Pollutant under Visible Light Irradiation

In this article, undoped double perovskite materials like caesium tin iodide (Cs2SnI6), methyl ammonium tin iodide [MA2SnI6: MA denotes CH3NH3+] and mixed double perovskite material [(Cs0.50MA0.50)2SnI6] were synthesized using a wet chemical methodology. The crystal structure confirmation, optical properties, thermal properties, surface morphology and presence of elemental composition of the prepared samples using XRD, UV, TGA and FESEM-EDAX analyses were thoroughly investigated. The synthesized materials were employed as photocatalysts to degrade methylene blue dye within 120 min under visible light. An increase in the optical properties of the synthesized double perovskite materials was confirmed by ultraviolet (UV) analysis, which showed that the introduction of various cations into the perovskite material at the A-site shifted the photoluminescence (PL) emission peak to the red. TGA results demonstrated that (Cs0.50MA0.50)2SnI6 has greater thermal stability, which was confirmed by the presence of 43% of sample despite the temperature reaching almost 870 ºC. Doped double perovskite material (Cs0.50MA0.50)2SnI6 exhibited increased photocatalytic activity, with methylene blue dye degradation efficiency attaining 89% after 120 min of visible light irradiation, which is greater than pure double perovskite materials. The photocatalytic degradation of methylene blue dye is mostly facilitated by hydroxyl radicals and holes, according to a radical trapping experiment that we conducted by employing different scavengers. The results of the current work showed that doped double perovskite materials [(Cs0.50MA0.50)2SnI6] exhibit high thermal stability as well as higher photocatalytic activity than pure double perovskite materials. A possible photocatalytic reaction process is also diagrammatically using the band positions of double perovskite materials found using Mott-Schottky plots , which confirms that the synthesized double perovskite material has an N-type semiconductor nature.

Two-stage repeat sintering: A modified method for fabricating hydroxyapatite scaffolds with enhanced mechano-therapeutic properties

A modified two-stage repeat sintering (TSRS) technique has been used to produce hydroxyapatite (HAp) from non-separated animal bones, and the energy consumption per cycle of the proposed TSRS was calculated. The TSRS technique was compared to the conventional one-step sintering method. The energy consumption per cycle of the proposed TSRS was calculated considering economies of scale and typical energy consumption billing in Nigeria. The synthesized powders from both techniques underwent comprehensive characterization through X-ray diffraction (XRD), Fourier transform infrared (FT-IR), and scanning electron microscopy (SEM). The XRD analysis revealed the main reflections of HAp in the (112), (300), and (202) planes. The FT-IR spectra exhibited characteristic bands representative of HAp at all measurement points. Notably, the TSRS-derived sample during the second sintering step showed carbonate bands, suggesting relevance in the bone structure makeup. SEM images unveiled varying crystal morphologies, ranging from irregular shapes in the raw bone (RB) sample to rounded shapes with nucleation in aggregates and agglomerates at micro and macro levels in the TSRS-derived samples. The samples obtained from the TSRS technique demonstrated a high Ca/P ratio that is potentially beneficial for osteoblast adhesion in vivo. The cost analysis of electricity consumption per TSRS cycle, factoring in economies of scale and typical energy consumption billing in Nigeria, amounted to approximately $8 with consideration of the exchange rates at the time of the study. The microhardness measured using the TSRS technique was 0.5 GPa with a 1 MPa compaction pressure, while the samples prepared using the conventional sintering method were too fragile to handle and measure. The obtained microhardness using the modified technique surpassed values reported in various studies. In conclusion, the samples produced using the TSRS technique exhibited promising results regarding energy efficiency, material characteristics, and microhardness compared to the samples produced through conventional sintering. The distinct crystal morphologies observed suggest potential advantages for biomedical applications, particularly in enhancing osteoblast adhesion.

Double-sided semitransparent titania photoelectrode with enhanced light harvesting

In this work, unique semitransparent electrodes were prepared by the anodization of titanium layers (540 nm thick) initially deposited on the both sides of glass substrates employing indium-tin oxide interface layers serving as a current collector for the induced photocurrent. The anodization strategy used in this study enables fabrication of semitransparent titanium dioxide nanotube arrays with either aligned or spaced architecture on the two sides of the planar substrate. This study aims to perform a detailed investigation of this novel photoelectrode system (crystal structure, morphology and optical properties) to reveal their photoelectrochemical features. It was found that the photoelectrode exhibits enhanced photocurrent density about 1.9 times higher (4.6 μAcm−2 at +0.5 V) for aligned nanotubes compared to a substrate overgrown symmetrically by separated nanotubes (2.4 μAcm−2 at +0.5 V). This can be effectively explained by the higher tube density in the case of aligned nanostructures, which provide more channels for charge percolation. In addition, both the high donor concentration (6.4 × 1020 cm−3) together with the low charge transfer resistance of the semitransparent electrode of the aligned nanotubes make the material promising for application in photoelectrochemical systems and smart light management.

Effects of high voltage electrostatic field assisted freezing enhanced with ultrahigh permittivity ceramic on quality attributes of grass carp (Ctenopharyngodon idella) fillets during frozen storage

Small sample capacity is a critical limitation for the industrialization of the high voltage electrostatic field assisted freezing (HVEFF) technique. In this study, using grass carp as a sample, the effects of ultrahigh permittivity ceramic enhanced HVEFF system on the quality attributes of grass carp (Ctenopharyngodon idella) fillets during freezing and frozen storage were investigated. The appropriate electrostatic field strength for freezing grass carp fillets was determined first with the HVEFF Peltier cooling platform and then used for the freezing and frozen storage of grass carp fillets in an HVEFF refrigerator at −18 °C. The biochemical qualities, and ice crystal morphology of the samples were measured every 2, 4, 6, and 8 weeks during frozen storage. Compared to the frozen control, this novel HVEFF system could effectively delay the deterioration of texture and water migration, and reduce TVB-N, TBARS and the equivalent ice crystal diameters. This study not only showed the positive effect of this novel HVEEF system on the frozen preservation of grass carp fillets but more importantly provided a solution to the bottleneck of HVEFF industrialization.

Development and Characterization of Poly(butylene succinate‐co‐adipate)/Poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) with Cowpea Lignocellulosic Fibers as a Filler via Injection Molding and Extrusion Film‐Casting

AbstractBiodegradable poly(butylene succinate‐co‐adipate)/Poly(3‐hydroxybutyrate‐co‐3‐hydoxyvalerate) (PBSA/PHBV) filled with lignocellulosic sidestream/fibers from cowpea, a neglected and underutilized African crop are produced by injection molding and extrusion film casting. Differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) suggests that the fibers have more affinity and interfacial interaction with PBSA than PHBV. This is shown by a decrease in dampening of PBSA and an increase in dampening of PHBV with fiber addition. In addition, fiber addition results in more homogeneous crystal morphology of PBSA, while resulting in more heterogeneous crystal morphology of PHBV. The tensile strength of injection molded bio‐composites increases with fiber addition due to good interfacial adhesion between the matrix and fibers revealed by scanning electron microscope. In contrast, the tensile strength of bio‐composite films decreases with fiber addition due to the high‐volume fraction of pores in bio‐composite films that act as stress raisers. The stiffness of both injection molded, and bio‐composite films increase with fiber addition, as revealed by an increase in Young's modulus and storage modulus, while the tensile strain decreases. In conclusion, low‐value cowpea sidestream can be used as a filler to produce injection molded bio‐composites and bio‐composite films for potential application as rigid and flexible packaging.

Synthesis and Exploration of Barium Stannate-Zirconate BaSn1-xZrxO3 (0 ≤ X ≤ 1) Solid Solutions as Photocatalysts.

Employing ionic liquid-assisted microwave synthesis and moderate heat treatment allows for the preparation of otherwise difficult-to-obtain perovskite-type BaSn1-xZrxO3 solid solutions (0 ≤ x ≤ 1). The impact of substituting Sn for the crystal structure, crystallinity, morphology, and photocatalytic performance was investigated. The obtained materials are characterized by X-ray diffraction, scanning electron microscopy, Brunauer-Emmett-Teller (BET) surface area analysis, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectroscopy, photoluminescence spectroscopy, and Raman and IR spectroscopy. SEM images show that the morphology of the samples varies from rods for x = 0, 0.2 to spherical for x = 0.5, 0.8, 1. Upon Zr for Sn substitution, the band gap changes from 3.1 to 5.0 eV as the valence and conduction bands move to lower and higher energies. The photocatalytic activities of the BaSn1-xZrxO3 samples in the hydroxylation of terephthalic acid (TA) follow the order BaSn0.5Zr0.5O3> BaSn0.8Zr0.2O3> BaSnO3> BaSn0.2Zr0.8O3> BaZrO3. The superior photocatalytic activity of BaSn0.5Zr0.5O3 can be attributed to the synergistically favorable combination of a suitable band structure, band gap size, and increased surface area-to-volume ratio, resulting in a diminished crystalline particle size unattainable from samples prepared via traditional synthetic routes or without ionic liquid.

Investigation of Structural, Dielectric, Magnetic and Impedance Spectroscopy of MgO/CuFe2O4 Nanocomposites

This study investigates the properties of (MgO)x/(CuFe2O4)1-x x= 10–50 wt.% nanocomposites (NCPs) prepared by physical mixing of both materials. The crystal structure, phase identification and morphology were analyzed by x-ray Diffraction (XRD) and Scanning Electron Microscope (SEM). The investigation revealed the formation of required phases which are in nanometer dimension (22–54 nm) computed by Debye-Sherrer’s formula. Both the real and imaginary parts of dielectric constant (ε/ & ε//), a.c. conductivity (σac), and impedance were measured in the frequency range of 1kHz to 2MHz by LCR meter. The ε/ and ε// revealed a decreasing trend with frequency, while MgO weight fractions in NCPs enhance the permittivity values. The real and imaginary parts of impedance (Z/ & Z//) demonstrate a decreasing trend with frequency which is ascribed to increase in σac. The complex impedance spectroscopy (CIS) analysis shows semicircular arcs at higher frequency, which are due to electrical transport properties of conducting grains. The effect of MgO contents on magnetic properties were analyzed by measuring M-H loops at room temperature through vibrating sample magnetometer (VSM). Both the saturation magnetization (Ms) and coercivity (Hc) values show a decreasing profile with MgO fractions, which are due to increase in nonmagnetic contents and decrease in surface anisotropy respectively. 

Soft-templating synthesis of hierarchical mordenite as high-performance catalyst for cyclic acetals production via acetylation of glycerol and benzaldehyde

Highly active hierarchical mordenite zeolite with micro/mesoporosity (TM-n) for selective synthesis of cyclic acetals via acetylation reaction is reported. The hierarchical zeolite is synthesized using soft-templating approach with variations in octadecyltrimethoxysilane (OTMS/Al2O3 ratio, n = 0.2, 0.3 and 0.4) in precursor hydrogels. The results reveal that OTMS not only creates secondary mesoporosity in zeolite framework (larger mesopore volume, external surface area, average pore diameter), but also influences the crystallization process, altering the crystal morphology, crystallinity and Si/Al ratios. Among TM-n zeolites prepared, TM-0.3 hierarchical mordenite has the optimum OTMS amount incorporated while further increasing the OTMS amount leads to the formation of ANA/GIS intergrowth. Thanks to the accessible hierarchical porosity, reduced acidity and morphological effects, the TM-0.3 hierarchical mordenite exhibits excellent catalytic performance (84.1% conversion, TOF = 0.087 s−1, 61.5% dioxolane selectivity) in acetylation of glycerol and benzaldehyde (160 °C, 20 min) better than pristine mordenite. The catalyst is reusable for five runs with minimal loss of activity (TOF = 0.087 → 0.084 s−1), making it a promising catalyst for chemical productions involving bulky molecules. In addition, comparative catalytic tests with classical homogeneous and heterogeneous catalysts, including H2SO4, HCl, CH3COOH, H–Y, H-LTL, Na-X, Na-A, were performed.

Long-Lived Charge Separation in Single Crystals of an Electron Donor Covalently Linked to Four Acceptor Molecules.

Crystalline donor-acceptor (D-A) systems serve as an excellent platform for studying CT exciton creation, migration, and dissociation into free charge carriers for solar energy conversion. Donor-acceptor cocrystals have been utilized to develop an understanding of CT exciton formation in ordered organic solids; however, the strong electronic coupling of the D and A units can sometimes limit charge separation lifetimes due to their close proximity. Covalent D-A systems that preorganize specific donor-acceptor structures can assist in engineering crystal morphologies that promote long-lived charge separation to overcome this limitation. Here we investigate photogenerated CT exciton formation in a single crystal of a 2,5,8,11-tetraphenylperylene (PerPh4) donor to which four identical naphthalene-(1,4:5,8)-bis(dicarboximide) (NDI) electron acceptors are covalently attached at the para positions of the PerPh4 phenyl groups to yield PerPh4-NDI4. X-ray crystallography shows that the four NDIs pack pairwise into two distinct motifs. Two NDI acceptors of one PerPh4-NDI4 are positioned over the PerPh4 donors of adjacent PerPh4-NDI4 molecules with the donor and acceptor π-systems having a large dihedral angle between them, while the other two NDIs of PerPh4-NDI4 form xylene-NDI van der Waals π-stacks with the corresponding NDIs in adjacent PerPh4-NDI4 molecules. Upon selective photoexcitation of PerPh4 in the single crystal, CT exciton formation occurs in <300 fs yielding electron-hole pairs that live for more than ∼16 μs. This demonstrates the effectiveness of covalently linked D-A systems for engineering single crystal structures that promote efficient and long-lived charge separation for solar energy conversion.

Controllable synthesis of snowflake‐like α‐calcium sulfate hemihydrate microstructures using Na2EDTA as morphology modifier

AbstractIn this work, snowflake‐like α‐CaSO4·0.5H2O (α‐CSH) hierarchical architectures were successfully synthesized by a facile one‐pot method in an ethylene glycol‐water system using Na2EDTA as a crystal morphology modifier. Characterization techniques including X‐ray diffraction (XRD), thermogravimetric (TG) analysis, differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR) confirmed the progressive morphological evolution of α‐CSH from rods to snowflake‐like structures ultimately to hexagonal plates with increased Na2EDTA concentrations. The results revealed that Na2EDTA concentration played a critical role in directing the crystallization and self‐assembly of α‐CSH, and a mechanism is proposed where Na2EDTA modulated crystal orientation through preferential adsorption and regulated the driving forces between ion‐mediated crystallization and particle‐mediated assembly. This work puts forward a simple yet effective strategy for facilely regulating the morphology of α‐CSH microstructures, which could potentially expand their applications across diverse fields such as composites, construction, biomedicine, and drug delivery.

Potential of Y2Sn2O7:Eu3+, Dy3+ Inorganic Nanophosphors in Latent Fingermark Detection

In this work, we investigated the potential of Eu3+/Dy3+-codoped Y2Sn2O7 fluorescent nanophosphors to visualize latent fingermarks. We prepared these nanophosphors with various doping concentrations by the conventional coprecipitation reaction. The crystal structure, morphology, luminescence properties, and energy transfer mechanisms were studied. The crystalline phase was characterized by X-ray diffraction and crystal structure refinement using the Rietveld method. XRD measurements showed that the samples crystallized in the pure single pyrochlore phase with few more peaks originated from secondary phases and impurities generated during phosphor production, and that Eu3+ ions occupied D3d symmetry sites. The average crystallite size after mechanical grinding was less than 100 nm for all compositions. The optical characterization showed that, when excited under 532 nm, the Eu3+/Dy3+-codoped Y2Sn2O7 samples’ main intense emission peaks were located at 580–707 nm, corresponding to the 5D0→7Fj (j = l, 2, 3, and 4) transitions of europium. In fact, the 5D0→7F2 hypersensitive transition is strongly dependent on the local environment and was quite weak in Eu3+:Y2Sn2O7 at low Eu3+ doping levels. We found that the presence of Dy3+ as a codopant permitted enhancing the emission from this transition. The calculated PL CIE coordinates for the synthesized nanophosphors were very close to those of the reddish-orange region and only slightly dependent on the doping level. Various surfaces, including difficult ones (wood and ceramic), were successfully tested for latent fingerprint development with the prepared Eu3+/Dy3+-codoped Y2Sn2O7 fluorescent nanophosphor powder. Thanks to the high contrast obtained, fingerprint ridge patterns at all three levels were highlighted: core (level 1) islands, bifurcation, and enclosure (level 2), and even sweat pores (level 3).

Synthesis of millimetre-scale HZSM-5 single crystals by secondary hydrothermal treatment

Millimetre-scale HZSM-5 single crystals were successfully synthesized by a two-step hydrothermal method. In the first step, millimetre-sized silicalite-1 single crystals were prepared by hydrothermal synthesis using quartz tube as siliceous source. In the second step, framework Al atoms were inserted into the single crystals of silicalite-1 by another hydrothermal treatment involving NaAlO2 as aluminium source. Through the characterizations of power and single crystal X-ray diffraction, optical microscope, ICP, 27Al MAS NMR, 29Si MAS NMR, and n-propylamine temperature-programmed decomposition (NPA-TPD), it was confirmed framework Al atoms with uniform spatial distribution can be inserted into giant single crystals of silicalite-1 with no obvious effects on the crystal structure, size and morphology. Such giant HZSM-5 single crystals are a promise candidate for the probe adsorption investigations, which can be applied in the measurement of framework Al spatial distribution. The strategy of insertion of aluminium or other heteroatoms of pure siliceous zeolite through secondary hydrothermal method provides a possible route to prepare giant single crystals that is difficult to synthesize directly.

Structural and Photoluminescence Characteristics of a Novel Single‐Phase White‐Emitting Phosphor SrBi2Nb2O9:Dy3+

A group of white light‐emitting phosphors SrBi2Nb2O9:xDy3+ (SBN:xDy3+) are prepared by high‐temperature solid reaction. The crystal phase, morphology, and photoluminescence (PL) characteristics of the prepared SBN:xDy3+ are analyzed. The X‐ray diffraction results prove that the synthesized samples are pure phase, in which the shift of the main peak depicted that crystal interplanar distance decreases after Dy3+ replacing Bi3+. The scanning electron microscope results show that the average crystal size of the sample is ≈1–10 μm. Energy dispersive X‐ray spectroscopy shows that the ratio of element composition of the SBN:xDy3+ is similar to the theoretical calculation. The PL excitation illustrates the excitation peaks mainly exist at 389, 399, 426, and 450 nm due to the transitions of Dy3+. For PL, the emission peaks of samples with different doping concentrations are centered at 479 and 573 nm. The ratio of yellow intensity to blue intensity indicates that Dy3+ is located at a high symmetry site, which has the possibility to produce suitable white light. The Commission Internationale de l’Eclairage coordinates of the SBN:xDy3+ are located near the standard white light coordinate. All these results prove that SrBi2Nb2O9:xDy3+ can be a potential material in the white light application.

Enhancing the Luminescence of La3Mg2NbO9:Mn4+ Phosphor through H3BO3 and Charge Compensator Co-Doping for Use in Plant Growth Lamps.

Mn4+-doped red-light-emitting phosphors have become a research hotspot that can effectively enhance photosynthesis and promote morphogenesis in plants. Herein, the red phosphor La3Mg2NbO9:Mn4+ was synthesized through the solid-state reaction method. The effects of adding H3BO3 and a charge compensator R+ (R = Li, Na, K) on the crystal structure, morphology, quantum efficiency, and luminous performance of the La3Mg2NbO9:Mn4+ phosphor were systematically analyzed, respectively. The results showed that adding H3BO3 flux and a charge compensator improved the quantum efficiency and luminescence intensity. The emission intensity of the phosphor was enhanced about 5.9 times when Li+ was used as the charge compensator, while it was enhanced about 240% with the addition of H3BO3 flux. Remarkably, it was also found that the addition of H3BO3 flux and a charge compensator simultaneously improved the thermal stability at 423 K from 47.3% to 68.9%. The prototype red LED fabricated using the La3Mg2NbO9:Mn4+,H3BO3,Li+ phosphor exhibited a perfect overlap with the phytochrome absorption band for plant growth. All of these results indicate that the La3Mg2NbO9:Mn4+,H3BO3,Li+ phosphor has great potential for use in agricultural plant lighting.

Crystallization of Ethylene Plant Hormone Receptor-Screening for Structure.

The plant hormone ethylene is a key regulator of plant growth, development, and stress adaptation. Many ethylene-related responses, such as abscission, seed germination, or ripening, are of great importance to global agriculture. Ethylene perception and response are mediated by a family of integral membrane receptors (ETRs), which form dimers and higher-order oligomers in their functional state as determined by the binding of Cu(I), a cofactor to their transmembrane helices in the ER-Golgi endomembrane system. The molecular structure and signaling mechanism of the membrane-integral sensor domain are still unknown. In this article, we report on the crystallization of transmembrane (TM) and membrane-adjacent domains of plant ethylene receptors by Lipidic Cubic Phase (LCP) technology using vapor diffusion in meso crystallization. The TM domain of ethylene receptors ETR1 and ETR2, which is expressed in E. coli in high quantities and purity, was successfully crystallized using the LCP approach with different lipids, lipid mixtures, and additives. From our extensive screening of 9216 conditions, crystals were obtained from identical crystallization conditions for ETR1 (aa 1-316) and ETR2 (aa 1-186), diffracting at a medium-high resolution of 2-4 Å. However, data quality was poor and not sufficient for data processing or further structure determination due to rotational blur and high mosaicity. Metal ion loading and inhibitory peptides were explored to improve crystallization. The addition of Zn(II) increased the number of well-formed crystals, while the addition of ripening inhibitory peptide NIP improved crystal morphology. However, despite these improvements, further optimization of crystallization conditions is needed to obtain well-diffracting, highly-ordered crystals for high-resolution structural determination. Overcoming these challenges will represent a major breakthrough in structurally determining plant ethylene receptors and promote an understanding of the molecular mechanisms of ethylene signaling.