From Smoothies to Dialysis: The Impact of Oxalate Nephropathy.

Oxalate nephropathy is a rare cause of acute kidney injury that can lead to end-stage renal disease. This case report describes a 54-year-old male with type 2 diabetes mellitus and chronic kidney disease who presented for a routine clinic follow-up. Laboratory tests revealed significant deterioration in renal function with an unrevealing history and symptoms suggestive of the process. Initial investigations for worsening renal function were inconclusive, prompting a renal biopsy that confirmed acute tubular injury with abundant calcium oxalate deposits. Further investigation into dietary history revealed that the patient regularly consumed high-oxalate foods, such as spinach and kale smoothies, under the impression they were beneficial for his diabetes. Despite the initiation of hemodialysis, the patient did not recover renal function and remains dialysis-dependent. This case underscores the need for a high index of suspicion for oxalate nephropathy in chronic kidney disease patients presenting with unexplained acute kidney injury. Diagnosis is confirmed through renal biopsy and should be considered in patients with relevant dietary histories.

Ion-Pairing Chromonic Liquid Crystals via Alternately Stacked Assembly of Amphiphilic Charged π-Electronic Systems.

In this study, a new assembly strategy for lyotropic chromonic liquid crystals (LCLCs) is proposed using iπ-iπ interactions, mainly comprising electrostatic and dispersion forces, between charged π-electronic systems to form stacking structures supported by the hydration of triethylene glycol (TEG) units.  Meso-TEG-aryl-substituted porphyrin AuIII complex, an amphiphilic π-electronic cation, showed diverse states and assembly modes in ion pairs depending on the coexisting counteranions.  The PCCp- ion pair formed a hexagonal columnar (Colh) LC phase based on a charge-by-charge assembly, suggesting the formation of an ordered arrangement of charged p-electronic systems through iπ-iπ interactions, with reduced interactions between the TEG chains.  Furthermore, in the presence of water, LCLC behaviors in the Colh and nematic columnar phases according to the amount of water were observed for the PCCp- ion pair via iπ-iπ interactions.  Magnetic-field-induced orientation of the charge-by-charge columnar structures upon dehydration was observed.  Furthermore, single-stranded charge-by-charge columnar structures, as components of the LCLCs, were observed using transmission electron microscopy (TEM).

Oriented Titanium-MOF Membrane for Hydrogen Purification.

Precise hydrogen sorting from purge gas (H2/N2) and coke gas (H2/CH4), commonly carried out by cryogenic distillation, still suffers from low separation efficiency, high energy consumption, and considerable capital cost. Though still in its infancy, membrane technology offers a potential to achieve more efficient hydrogen purification. In this study, an optimum separation of hydrogen towards both methane and nitrogen via a kinetically-driven mechanism is realized through preferred orientation control of a MOF membrane. Relying on the 0.3 nm-sized window aligned vertical to the substrate, b-oriented Ti-MOF membrane exhibits ultra-high hydrogen selectivity, surpassing the upper bound limit of separating H2/N2 and H2/CH4 gas pairs attained so far by inorganic membranes. This spectacular selectivity is combined with a high H2 permeability owing to the synergistic effect of the 1 nm-sized MOF channel.

Ionic Liquid Crystals as Chromogenic Materials.

Ionic liquid crystals (ILCs), a class of soft matter materials whose properties can be tuned by the wise pairing of the cation and anion, have recently emerged as promising candidates for different applications, combining the characteristics of ionic liquids and liquid crystals. Among those potential uses, this review aims to cover chromogenic ILCs. In this context, examples of photo-, electro- and thermochromism based on ILCs are provided. Furthermore, thermotropic and lyotropic ionic liquid crystals are also summarised, including the most common chemical and phase structures, as well as the advantages of confining these materials. This manuscript also comprises the following main experimental techniques used to characterise ILCs: Differential Scanning Calorimetry (DSC), Polarised Optical Microscopy (POM) and X-Ray Powder Diffraction (XRD). Chromogenic ILCs can be interesting smart materials for energy and health purposes.

Modulating the Conductivity of Light-Responsive Ionic Liquid Crystals.

In this work, we describe the phase behaviour and the dielectric and conductivity response of new light-responsive ionic liquid crystals, ILCs, which can be applied as controllable electrolytes. The materials include two different dicationic viologens, the asymmetric 6BP18 and the symmetric EV2ON(Tf)2, containing bistriflimide as the counterions, mixed with 5% and 50% molar, respectively, of one new photoresponsive mesogen called CNAzO14. These mixtures exhibit liquid crystal behaviour, light responsiveness through the E-Z photoisomerisation of the azobenzene groups in CNAzO14, and strong dielectric responses. The 5%-CNAzO14/Ev2ON(Tf)2 mixture displays direct current conductivities in the 10-7 S·cm-1 range, which can be increased by a two-fold factor upon the irradiation of UV light at 365 nm. Our findings set the grounds for designing new smart ionic soft materials with nanostructures that can be tuned and used for energy conversion and storage applications.

Bioinspired Wearable Hydrogel Composite with Sustained Drug-Release for Wound Healing and Naked-Eye Visual Early Warning of Wound Dehiscence.

Wound healing is critical to the structural and functional restoration of damaged tissue. However, effective wound closure and healing are always great challenges in regenerative engineering. This study provided bioinspired wearable hydrogel composites with drug-releasing hydrogel and nonclose-packed photonic crystals (NPCs) for wound therapy and naked-eye visual early warning of wound dehiscence. Molecular dynamics models and drug-releasing results illustrated the sustained drug release of ibuprofen, and the mechanical properties of the drug-releasing hydrogel were optimized with 1410% tensile strain by introducing fish collagen; their biocompatibility and adhesion were also improved. The structural color of the NPCs blue-shifted from 630 to 500 nm with 15.0% strain, and the original color was customized with poly(methyl methacrylate) (PMMA) concentration and acrylamide content. Compared with the gauze and the traditional hydrogels, the composite provided a moist environment and an effectively closed wound; the debridement and released drug avoided inflammation, and the rat wound was healed 40.5% on the third day and essentially 100% on the 14th day. The work provided a novel strategy for wound healing and naked-eye visual early warning when a wound deforms, which is expected to promote the synergistic development of clinical treatment and visualized early warning.

Highly Tunable Light Absorber Based on Topological Interface Mode Excitation of Optical Tamm State.

Optical absorbers based on Tamm plasmon states are known for their simple structure and high operational efficiency. However, these absorbers often have limited absorption channels, and it is challenging to continuously adjust their light absorption rates. Here, we propose a Tamm plasmon state optical absorber composed of a layered stack structure consisting of one-dimensional topological photonic crystals and graphene nano-composite materials. Using the four-by-four transfer matrix method, we investigate the structural relationship of the absorber. Our results reveal that topological interface states (TISs) effectively excite the optical Tamm state (OTS), leading to multiple absorption peaks. This expands the number of absorption channels, with the coupling number of the TIS determining the transmission quality of these channels-a value further adjustable by the period number of the photonic crystals. Tuning the filling factor, refractive index, and thickness of the graphene nano-composite material allows for a wide range of control over the device's absorption rate, from 0 to 1. Additionally, adjusting the defect layer thickness, incident angle, and Fermi energy enables us to control the absorber's operational bandwidth and the switching of its absorption effect. This work presents a new approach to expanding the tunability of optoelectronic devices.

Magnetotransport and angle-resolved photoemission spectroscopy of MnSb12Te19: a new member of MnSb2nTe3n+1family.

The quest for intrinsically ferromagnetic topological materials is a focal point in the study of topological phases of matter, as intrinsic ferromagnetism plays a vital role in realizing exotic properties such as the anomalous Hall effect (AHE) in quasi-two-dimensional materials, and this stands out as one of the most pressing concerns within the field. Here, we investigate a novel higher order member of the MnSb2nTe3n+1family, MnSb12Te19, for the first time combining magnetotransport and angle-resolved photoemission spectroscopy (ARPES) measurements. Our magnetic susceptibility experiments identify ferromagnetic transitions at temperatureTc= 18.7 K, consistent with our heat capacity measurements (T= 18.8 K). The AHE is observed for the field along thec-axis belowTc. Our study of Shubinikov-de-Haas oscillations provides evidence for Dirac fermions withπBerry phase. Our comprehensive investigation reveals that MnSb12Te19exhibits a FM ground state along with AHE, and hole-dominated transport properties consistent with ARPES measurements.

Electro-Optic Response of Polymer-Stabilized Cholesteric Liquid Crystals with Different Polymer Concentrations.

Polymer-stabilized cholesteric liquid crystals (PSCLCs) have emerged as promising candidates for one-dimensional photonic lattices that enable precise tuning of the photonic band gap (PBG). This work systematically investigates the effect of polymer concentrations on the AC electric field-induced tuning of the PBG in PSCLCs, in so doing it explores a range of concentrations and provides new insights into how polymer concentration affects both the stabilization of cholesteric textures and the electro-optic response. We demonstrate that low polymer concentrations (≈3 wt. %) cause a blue shift in the short wavelength band edge, while high concentrations (≈10 wt. %) lead to a contraction and deterioration of the reflection band. Polarization optical microscopy was conducted to confirm the phase transition induced by the application of an electric field. The observations confirm that increased polymer concentration stabilizes the cholesteric texture. Particularly, the highly desired fingerprint texture was stabilized in a sample with 10 wt. % of the polymer, whereas it was unstable for lower polymer concentrations. Additionally, higher polymer concentrations also improved the dissymmetry factor and stability of the lasing emission, with the dissymmetry factor reaching the value of around 2 for samples with 10 wt. % of polymer additive. Our results provide valuable comprehension into the design of advanced PSCLC structures with tunable optical properties, enhancing device performance and paving the way for innovative photonic applications.

Miscibility Studies of Bismesogen CBnCB Forming Nematic Twist-Bend Phase with Cyanobiphenyls nCB.

This work aims to determine how the nematic twist-bend phase (NTB) of bismesogens containing two rigid parts of cyanobiphenyls connected with a linking chain containing n = 7, 9, and 11 methylene groups behaves in mixtures with structurally similar cyanobiphenyls nCB, n = 4-12, 14. The whole phase diagrams are presented for the CB7CB-nCB system. For the other systems, CB9CB-nCB and CB11CB-nCB, only curves corresponding to NTB-N phase transition are presented. Based on the temperature-concentration range of the existence of NTB phase, it was established that an increase in the alkyl chain length of CBnCB causes an increase in the stability of the NTB phase. But surprisingly, an increase in the alkyl chain length of nCB compounds does not change the slope of the NTB-N equilibrium line on phase diagrams. It is slightly bigger when the nCB compound has the same length of alkyl chain as the length of the linking group of a bismesogen. XRD studies were carried out for two mixtures.

A Template Method Leads to Precisely Synthesize SiO2@Fe3O4 Nanoparticles at the Hundred-Nanometer Scale.

Constructing photonic crystals with core-shell structured nanoparticles is an important means for applications such as secure communication, anti-counterfeiting marking, and structural color camouflage. Nonetheless, the precise synthesis technology for core-shell structured nanoparticles at the hundred-nanometer scale faces significant challenges. This paper proposes a controlled synthesis method for core-shell structured nanoparticles using a template method. By using 100 nm diameter silica nanospheres as templates and coating them with a ferroferric oxide shell layer, SiO2@Fe3O4 core-shell structured nanoparticles with regular morphology and good uniformity can be obtained. The study experimentally investigated the effects of feed amount, modifiers, temperature, and feed order on the coating effect, systematically optimizing the preparation process. Centrifugal driving technology was used to achieve structural colors in the visible wavelength range. Additionally, the method successfully created well-defined and uniform core-shell structured nanoparticles using 200 nm diameter silica nanospheres as templates, demonstrating that this controllable synthesis method can effectively produce core-shell structured nanoparticles over a wide range of particle sizes. The template method proposed in this paper can significantly improve morphological regularity and size uniformity while effectively reducing the preparation cost of core-shell structured nanoparticles.

Construction of Patterned Cu2O Photonic Crystals on Textile Substrates for Environmental Dyeing with Excellent Antibacterial Properties.

Structural dyeing has attracted much attention due to its advantages such as environmental friendliness, vivid color, and resistance to fading. Herein, we propose an alternative strategy for fabric coloring based on Cu2O microspheres. The strong Mie scattering effect of Cu2O microspheres enables the creation of vibrant structural colors on fabric surfaces. These colors are visually striking and can potentially be adjusted by tuning the diameter of the microspheres. Importantly, the Cu2O spheres were firmly bonded to the fabrics by using the industrial adhesive PDMS, and the Cu2O structural color fabrics exhibited excellent color fastness to washing, rubbing, and bending. Cu2O structural color fabrics also demonstrated excellent antimicrobial properties against bacteria such as Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). The bactericidal rates of Cu2O structural color textiles after washing for E. coli and S. aureus reached 92.40% and 94.53%, respectively. This innovative approach not only addresses environmental concerns associated with traditional dyeing processes but also enhances fabric properties by introducing vibrant structural colors and antimicrobial functionality.

Crystal structure of new quaternary intermetallic compounds R2MoSi2C (R = Y, Gd).

The discovery of novel quaternary intermetallic compounds R2MoSi2C (R = Y, Gd) in the R-Mo-Si-C system is reported. Their crystal structure was investigated using single-crystal X-ray diffraction. It is shown that the Y2MoSi2C and Gd2MoSi2C compounds crystallize in the tetragonal space group P4/mbm (Pearson symbol tP12) with unit-cell parameters a = 6.9525 (18) Å, c = 4.1962 (16) Å, and a = 6.9945 (16) Å, c = 4.2020 (14) Å, respectively.

Repurposing weather modification for cloud research showcased by ice crystal growth.

The representation of cloud processes in models is one of the largest sources of uncertainty in weather forecast and climate projections. While laboratory settings offer controlled conditions for studying cloud processes, they cannot reproduce the full range of conditions and interactions present in natural cloud systems. To bridge this gap, here we leverage weather modification, specifically glaciogenic cloud seeding, to investigate ice growth rates within natural clouds. Seeding experiments were conducted in supercooled stratus clouds (at - 8 to - 5 ∘ C) using an uncrewed aerial vehicle, and the created ice crystals were measured 4-10 min downwind by in situ and ground-based remote sensing instrumentation. We observed substantial variability in ice crystal growth rates within natural clouds, attributed to variations in ice crystal number concentrations and in the supersaturation, which is difficult to reproduce in the laboratory and which implies faster precipitation initiation than previously thought. We found that for the experiments conducted at - 5.2 ∘ C, the ice crystal populations grew nearly linearly during the time interval from 6 to 10 min. Our results demonstrate that the targeted use of weather modification techniques can be employed for fundamental cloud research (e.g. ice growth processes, aerosol-cloud interactions), helping to advance cloud microphysics parameterizations and to improve weather forecasts and climate projections.

Dynamic Luminescence Vapochromism of Pyridinium-Based Organic Salts.

Organic vapochromic materials which undergo a drastic change in their photophysical properties upon exposure to vapors or gases are attracting growing scientific attention because of their low price and wide range of possible applications. In this work, luminescence vapochromism of carbazole-pyridinium-based organic salts with a general structure of (CzPy)X (CzPy+ = 2,3-di(9H-carbazol-9-yl)pyridinium ion; X = Cl, Br or I) is reported. It was found that (CzPy)X compounds form J-aggregates, which rearranged back to monomeric form upon exposure to methanol, ethanol, acetone, and water vapors. In contrast, acetonitrile was found to promote the J-aggregation in (CzPy)X compounds by occupying the voids in their crystal lattice and pushing cations closer together. It was further demonstrated that the efficiency of J-aggregation in (CzPy)X compounds depends on the size of the anion, which was employed to realize dynamic luminescence vapochromism, with vapochromic response times ranging from a couple of minutes in (CzPy)Cl to more than an hour in (CzPy)I. In addition, (CzPy)X compounds exhibited high melting points of about 250 °C and excellent thermal stability. (CzPy)Cl and (CzPy)Br have also shown good photoluminescence quantum yields at room temperature in a solid state.

Stretchable Distributed Bragg Reflectors as Strain-Responsive Mechanochromic Sensors.

Mechanochromic materials exhibit color changes upon external mechanical stimuli, finding wide-ranging applications in colorimetric sensing, display technology, and anticounterfeiting measures. Many of these materials rely on fluorescence properties and therefore necessitate external optical or electrical excitation. However, for broader applicability, the detection of color changes by the naked eye only or without complicated detection instrumentation is highly desirable. Photonic crystals offer a promising avenue for attaining such performances. In this work, we present elastomeric distributed Bragg reflectors (DBRs) characterized by a series of photonic bandgaps exhibiting mechanochromic response from the near-infrared to the visible wavelengths. To achieve this, we engineered alternating thin films of a thermoplastic fluoropolymer and a styrene-butadiene copolymer using different elastomeric substrates to attain different behaviors. The reported system demonstrates a reversible and instantaneous shift of the photonic bandgaps in response to 100% strain in multiple deformation cycles. Comparing the DBR stress-strain response with the optical strain response confirms a mechanochromic sensitivity of ∼1.7-6.9 nm/% and ∼80 nm/MPa, with an optical Poisson's ratio in the range 0.3-0.7. All these properties are spectrally dependent, as demonstrated by exploiting the properties of different diffraction order photonic band gaps.

An alternative method to the Takagi-Taupin equations for studying dark-field X-ray microscopy of deformed crystals.

This study introduces an alternative method to the Takagi-Taupin equations for investigating the dark-field X-ray microscopy (DFXM) of deformed crystals. In scenarios where dynamical diffraction cannot be disregarded, it is essential to assess the potential inaccuracies of data interpretation based on the kinematic diffraction theory. Unlike the Takagi-Taupin equations, this new method utilizes an exact dispersion relation, and a previously developed finite difference scheme with minor modifications is used for the numerical implementation. The numerical implementation has been validated by calculating the diffraction of a diamond crystal with three components, wherein dynamical diffraction is applicable to the first component and kinematic diffraction pertains to the remaining two. The numerical convergence is tested using diffraction intensities. In addition, the DFXM image of a diamond crystal containing a stacking fault is calculated using the new method and compared with the experimental result. The new method is also applied to calculate the DFXM image of a twisted diamond crystal, which clearly shows a result different from those obtained using the Takagi-Taupin equations.

Facile Synthesis of Soft Core-Shell Nanospheres for Constructing Multiresponsive Photonic Crystal Security Patterns.

Responsive photonic crystals (RPCs) presenting tunable structural colors under external stimuli are widely applied in the fields of dynamic displays, sensors, and anticounterfeiting. However, the development of multiresponsive photonic crystal (MRPC) films possessing versatile variable optical properties remains a significant challenge due to the tedious synthetic procedure of multifunctional building blocks and complex assembly processes, thereby constraining their extensive applications. In the present work, a series of soft nanospheres with a hydrophobic cores and responsive hydrophilic shells have been synthesized by a facile one-step surfactant-free emulsion polymerization method. The MRPC patterns were then prepared by depositing soft nanosphere emulsions onto the 3D-printed substrates with a topological structure followed by drying at room temperature. The shells of soft nanospheres deformed and fused with each other, resulting in the formation of transparent MRPC film patterns. The MRPC patterns exhibited brilliant structural color in a wet state but lost the color again after complete drying. Such a reversible structural color was ascribed to the change of the refractive index (RI) of the hydrophilic shell layers of nanospheres according to wetting/drying state shifting. Moreover, the on-demand designed MRPC patterns could rapidly respond to external stimuli of temperature, pH, and organic solvents in a reversible manner, and multichannel encrypted security labels were also demonstrated. We postulate that our facile and feasible approach can be applied to the systematic design and large-scale production of MRPC patterns for a variety of applications.

Cold and Liquid Crystal Properties of Square-Planar Copper(II) Versus Nickel(II)-iminophenolate/naphthalen-2-olate Schiff Base Complexes.

Reaction of  the phenolate or naphthalen-2-olate based Schiff base ligands, (E)-1-((2-ethylphenylimino)methyl)phenol (HL1) or (E)-1-((2-ethylphenylimino)methyl)naphthalen-2-ol (HL2) with nickel(II) and copper(II) acetate provides the complexes bis[(E)-1-((2-ethylphenylimino)methyl)phenolato-ĸ2N,O]Ni/Cu(II), [Ni(L1)2] (1) and [Cu(L1)2] (2), or bis[(E)-1-((2-ethylphenylimino)methyl)naphthalen-2-olato-ĸ2N,O]Ni/Cu(II), [Ni(L2)2] (3) and [Cu(L2)2] (4), respectively. Single crystal X-ray structure determinations for 1, 3 and 4 reveal N2,O2-metal coordination of two chelating Schiff base ligands in a square-planar geometry. Powder X-ray diffractograms confirm the phase purity of the bulk microcrystalline samples. Thermal analyses by differential scanning calorimetry (DSC) and polarized light microscopic (PLM) indicate the copper(II) complexes to exhibit cold crystal (2) and liquid crystal (4) property. Cyclic voltammograms suggest an irreversible electrochemical process with two one electron charge transfer processes in N,N-dimethylformamide. Variable temperature magnetic measurements at the solid-state prove the diamagnetic nature of the low-spin Ni2+ centres in 1 or 3, as expected from the square-planar coordination geometry with rather strong ligands. The complexes expose medium level of antioxidant activity in methanol. Optimized geometry and excited state property by DFT/TD-DFT correspond well to the experimental results of the electronic and molecular structure at the ground state.

Analysis of Ca1-xSrxCO3 phases generated by competitive Sr2+ replacement in pre-formed aragonite.

The ratio of Sr/Ca ions in marine biogenic minerals is considered advantageous for tracking geochemical and biomineralization processes that occur in the oceans. It is debatable, though, whether the ratio in biominerals such as coral skeleton is simply related to values in the seawater environment or controlled by the organism. Recent data show that coral larvae produce partially disordered immature aragonite in Mg-containing Sr-poor calcifying fluids, which transforms into well-ordered aragonite in Mg-depleted Sr-enriched environments, upon animal metamorphosis into the sessile polyp state. Inspired by the process in young coral, we explored in vitro substitution of Ca by Sr in aragonite by exposing aragonite crystals precipitated a priori to Sr solutions with variable concentrations. The resulting biphasic material, comprised of Sr-doped aragonite and Ca-doped strontianite, was carefully analyzed for foreign cation substitution in each polymorph. This allowed to establish a linear correlation between Sr levels in mineralizing solutions and Sr in aragonite as well as Ca in strontianite. It indicated that ca. 5-fold higher Sr solution concentration is needed for substitution in the crystal to reach the level found in corals. It also provided with Sr levels required for a putative strontianite phase to form.