PECULIAR PROPERTIES OF ELECTROMAGNETIC RADIATION PROPAGATION IN PHOTONIC CRYSTALLINE METAL-DIELECTRIC SYSTEMS BASED ON OPALS

The article studies the propagation of electromagnetic waves in metal-dielectric systems based on opals. We revealed anomalous transmission and absorption of light by hybrid plasmon- photonic layered heterostructures associated with the excitation of surface plasmon polaritons propagating along the metal-dielectric interface. The position of maxima in the reflection spectra of nanocomposites, obtained by filling the opal matrix with metal by the electrothermodiffusion method, is explained by the Bragg diffraction, and the asymmetric form of the spectral curves is attributed to the Fano resonance.

The Role of Endogenous Metal Nanoparticles in Biological Systems

The blood and tissues of vertebrate animals and mammals contain small endogenous metal nanoparticles. These nanoparticles were observed to be composed of individual atoms of iron, copper, zinc, silver, gold, platinum, and other metals. Metal nanoparticles can bind proteins and produce proteinaceous particles called proteons. A small fraction of the entire pool of nanoparticles is usually linked with proteins to form proteons. These endogenous metal nanoparticles, along with engineered zinc and copper nanoparticles at subnanomolar levels, were shown to be lethal to cultured cancer cells. These nanoparticles appear to be elemental crystalline metal nanoparticles. It was discovered that zinc nanoparticles produce no odor response but increase the odor reaction if mixed with an odorant. Some other metal nanoparticles, including copper, silver, gold, and platinum nanoparticles, do not affect the responses to odorants. The sources of metal nanoparticles in animal blood and tissues may include dietary plants and gut microorganisms. The solid physiological and biochemical properties of metal nanoparticles reflect their importance in cell homeostasis and disease.

Prediction of Europium Retention in Perovskite: Potential Candidates for an Engineering Barrier in the Disposal of Radioactive Waste

Perovskites, such as tausonite, are crystalline metal oxides with excellent optical and photocatalytic properties and have also been used successfully in the retention of metals, simulating the isotopes of uranium and plutonium. In this work, different pseudo-order and thermodynamic models were studied to achieve the prediction of the sorption of Eu3+ (chemical analogous for actinides) in tausonite. The effects of gamma irradiation and temperature on the structural characteristics of the material were determined, as an additional step in the evaluation of material as an engineering barrier in the disposal of radioactive waste. The results obtained show that the tausonite is resistant to the gamma irradiation and thermal energy. Likewise, it was possible to determine that europium sorption occurs through an exothermic and spontaneous reaction, as well as through the formation of surface complexes, where Eu3+ ions bind to sites on the tausonite by dipole-dipole interaction. Furthermore, it was shown that the sorption mechanism is influenced by diffusive phenomena, which participate in the formation of surface complexes. Additionally, a new sorption model with respect to pH was proposed, which allowed determining the physical parameter π. The evidence obtained suggests that π is a physical parameter that relates pH to an optimal value and could explain the equilibrium between the surface complexes that tausonite forms with europium. Likewise, the evidence suggests that 50 kg of tausonite would have the capacity to retain at least 26.59 g of alpha-emitting radionuclides, equivalent to a waste package (900 kg) with a maximum activity of 4000 Bq/g.

Electrocatalytic upcycling of polyethylene terephthalate to commodity chemicals and H2 fuel

Plastic wastes represent a largely untapped resource for manufacturing chemicals and fuels, particularly considering their environmental and biological threats. Here we report electrocatalytic upcycling of polyethylene terephthalate (PET) plastic to valuable commodity chemicals (potassium diformate and terephthalic acid) and H2 fuel. Preliminary techno-economic analysis suggests the profitability of this process when the ethylene glycol (EG) component of PET is selectively electrooxidized to formate (>80% selectivity) at high current density (>100 mA cm−2). A nickel-modified cobalt phosphide (CoNi0.25P) electrocatalyst is developed to achieve a current density of 500 mA cm−2 at 1.8 V in a membrane-electrode assembly reactor with >80% of Faradaic efficiency and selectivity to formate. Detailed characterizations reveal the in-situ evolution of CoNi0.25P catalyst into a low-crystalline metal oxy(hydroxide) as an active state during EG oxidation, which might be responsible for its advantageous performances. This work demonstrates a sustainable way to implement waste PET upcycling to value-added products.

cis-Bis(L-DOPA-κ2 N,O)copper(II) monohydrate: synthesis, crystal structure, and approaches to the analysis of pseudosymmetry

The crystal structure of the cis isomer of cis-bis(L-DOPA-κ2 N,O)copper(II) monohydrate (L-DOPA is 3,4-dihydroxy-L-phenylalanine) (CuLD), [Cu(C9H10NO4)2]·H2O, is a singular example of a structurally characterized, homoleptic, crystalline metal L-DOPA complex. CuLD crystallizes in the space group P21, with Z′ = 2. The two independent molecules are square planar, and are interconnected by a linear hydrogen-bonded chain containing 12 independent hydrogen bonds. The copper ions in both molecules have weak apical intermolecular Cu...O interactions [2.739 (2) and 2.973 (2) Å] with catechol –OH groups. A survey of the Cambridge Structural Database suggested that cis and trans isomers of Cu(NH2–C–CO2)2 amino acid complexes are equally likely to occur. 12 strong O—H...O and N—H...O hydrogen bonds stabilize an unusual linear arrangement of the Cu complexes. The Cu...Cu′ distances along the chain are nearly equal [5.0739 (3) and 5.1107 (3) Å] and the Cu...Cu′...Cu angles are nearly linear [176.75 (1)°]. The MATCH procedure available in the Oxford University Crystals for Windows package was used to carry out a detailed analysis of the relationship between the two independent molecules. MATCH has some particular advantages in studying the details of pseudosymmetry, which include: (i) no atomic-order requirements; (ii) the pseudosymmetry matrix is readily available, which allows quick insight into the symmetry elements involved and their location; and (iii) the differences between molecular centroids, as well as between all atomic positions and torsion angles, are listed. A tutorial presentation is designed to attract new users to the technique. In the present case, a search for a pseudosymmetric relationship between the two independent molecules showed that they are related by a pseudo-42 axis along the crystallographic c direction. A detailed analysis shows that the pseudo-42 symmetry is disrupted by torsions about the CH2—C(ipso) bonds, and that there is no supergroup that can be used to describe the crystal structure.

A strain rate dependent thermo-elasto-plastic constitutive model for crystalline metallic materials

The strain rate and temperature effects on the deformation behavior of crystalline metal materials have always been a research hotspot. In this paper, a strain rate dependent thermo-elasto-plastic constitutive model was established to investigate the deformation behavior of crystalline metal materials. Firstly, the deformation gradient was re-decomposed into three parts: thermal part, elastic part and plastic part. Then, the thermal strain was introduced into the total strain and the thermo-elastic constitutive equation was established. For the plastic behavior, a new relation between stress and plastic strain was proposed to describe the strain rate and temperature effects on the flow stress and work-hardening. The stress–strain curves were calculated over wide ranges of strain rates (10–6–6000 s−1) and temperatures (233–730 K) for three kinds of crystalline metal materials with different crystal structure: oxygen free high conductivity copper for face centered cubic metals, Tantalum for body centered cubic metals and Ti–6Al–4V alloy for two phase crystal metals. The comparisons between the calculation and experimental results reveal that the present model describes the deformation behavior of crystalline metal materials well. Also, it is concise and efficient for the practical application.

Physical properties of porphyrin-based crystalline metal‒organic frameworks

Metal‒organic frameworks (MOFs) are widely studied molecular assemblies that have demonstrated promise for a range of potential applications. Given the unique and well-established photophysical and electrochemical properties of porphyrins, porphyrin-based MOFs are emerging as promising candidates for energy harvesting and conversion applications. Here we discuss the physical properties of porphyrin-based MOFs, highlighting the evolution of various optical and electronic features as a function of their modular framework structures and compositional variations.