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Metal-bearing solid and liquid wastes are increasingly considered as secondary sources of critical and scarce metals. Undoubtedly, microorganisms are a cost-effective resource for extracting and concentrating diffuse elements from secondary sources. Microbial biotechnology for extracting base metals from ores and treatment of metal-laden wastewaters has already been applied at full scale. By contrast, microbe–metal interactions in the recovery of scarce metals and a few critical metals have received attention, whereas the recovery of many others has been barely explored. Therefore, this article explores and details the potential application of microbial biotechnologies in the recovery of critical and scarce metals. In the past decade bioelectrochemical systems have emerged as a new technology platform for metal recovery coupled to the removal of organic matter.

Single-atom catalysts make exceptionally efficient use of expensive noble metals and can bring out unique properties. However, applications are usually compromised by limited catalyst stability, which is due to sintering. Although sintering can be suppressed by anchoring the metal atoms to oxide supports, strong metal–oxygen interactions often leave too few metal sites available for reactant binding and catalysis, and when exposed to reducing conditions at sufficiently high temperatures, even oxide-anchored single-atom catalysts eventually sinter. Here we show that the beneficial effects of anchoring can be enhanced by confining the atomically dispersed metal atoms on oxide nanoclusters or ‘nanoglues’, which themselves are dispersed and immobilized on a robust, high-surface-area support. We demonstrate the strategy by grafting isolated and defective CeOx nanoglue islands onto high-surface-area SiO2; the nanoglue islands then each host on average one Pt atom. Further, we find that the Pt atoms remain dispersed under both oxidizing and reducing environments at high temperatures, and that the activated catalyst exhibits markedly increased activity for CO oxidation. We attribute the improved stability under reducing conditions to the support structure and the much stronger affinity of Pt atoms for CeOx than for SiO2, which ensures the Pt atoms can move but remain confined to their respective nanoglue islands. The strategy of using functional nanoglues to confine atomically dispersed metals and simultaneously enhance their reactivity is general, and we anticipate that it will take single-atom catalysts a step closer to practical applications.

Platinum group metals (PGMs) are a group of six metals with high market value and key importance to many industrial sectors. Due to their low prevalence in the Earth's crust and high demand, these metals have been recognized as critical materials for many years. Along with economic development, the natural resources of the platinum group metals are gradually depleting, which is accompanied by the need to recover PGMs from secondary sources. The solutions resulting from the processing of such materials are characterized by high content of impurities and low content of precious metals. For this reason, in order to obtain pure metals, it is extremely important to choose an effective, selective method for the recovery and separation of the platinum group metals. This review focuses on the most important aspects of the characteristics of the PGMs, including their properties and occurrence, the processing of natural and secondary raw materials and the role of liquid-liquid extraction in the selective separation of metals from this group, not only on a laboratory scale but, above all, on an industrial scale. In addition, this study collects information on the most commonly used, commercially available extractants, based on current reports, taken from the scientific literature.

This article presents studies on the precipitation of Pt, Pd, Rh, and Ru nanoparticles (NPs) from model and real multicomponent solutions using sodium borohydride, ascorbic acid, sodium formate, and formic acid as reducing agents and polyvinylpyrrolidone as a stabilizing agent. As was expected, apart from PGMs, non-precious metals were coprecipitated. The influence of the addition of non-precious metal ions into the feed solution on the precipitation yield and catalytic properties of the obtained precipitates was studied. A strong reducing agent, NaBH precipitates Pt, Pd, Rh, Fe and Cu NPs in most cases with an efficiency greater than 80% from three- and four-component model solutions. The morphology of the PGMs nanoparticles was analyzed via SEM-EDS and TEM. The size of a single nanoparticle of each precipitated metal was not larger than 5 nm. The catalytic properties of the obtained nanomaterials were confirmed via the reaction of the reduction of 4-nitrophenol (NPh) to 4-aminophenol (NAf). Nanocatalysts containing Pt/Pd/Fe NPs obtained from a real solution (produced as a result of the leaching of spent automotive catalysts) showed high catalytic activity (86% NPh conversion after 30 min of reaction at pH 11 with 3 mg of the nanocatalyst).

There is an increasing concern about the presence of various types of pharmaceuticals in drinking water, as long-term exposure of people to even low concentrations of drugs can lead to many problems, such as endocrine disorders or drug resistance. As the removal in sewage treatment plants is not effective enough, as indicated, among others, by the EC and OECD reports, it is justified to search for new materials that will allow for an effective and rapid reduction of these pollutants in water. Therefore, in our work, catalytically active nanomaterials containing platinum group metals (PGMs) were synthesized from model and real multicomponent solutions and examined in reactions of organic compounds. The nanoparticles (NPs) were obtained from real solutions from the hydrometallurgical processing of spent automotive converters (SACs), and to the best of our knowledge, the novelty of the proposed paper is the application of solutions from SAC processing as precursors for PGM-NPs. The synthesized PGM-NPs were deposited on a support (TiO ), characterized and, finally, examined as nanocatalysts in a degradation reaction of ibuprofen (IB) from model aqueous solutions. The degree of IB degradation reached more than 90%. The main products of IB degradation were p-isobutylphenol and CO .

The barrier layer in Cu technology is essential to prevent Cu from diffusing into the dielectric layer at high temperatures; therefore, it must have a high stability and good adhesion to both Cu and the dielectric layer. In the past three decades, tantalum/tantalum nitride (Ta/TaN) has been widely used as an inter-layer to separate the dielectric layer and the Cu. However, to fulfill the demand for continuous down-scaling of the Cu technology node, traditional materials and technical processes are being challenged. Direct electrochemical deposition of Cu on top of Ta/TaN is not realistic, due to its high resistivity. Therefore, pre-deposition of a Cu seed layer by physical vapor deposition (PVD) or chemical vapor deposition (CVD) is necessary, but the non-uniformity of the Cu seed layer has a devastating effect on the defect-free fill of modern sub-20 or even sub-10 nm Cu technology nodes. New Cu diffusion barrier materials having ultra-thin size, high resistivity and stability are needed for the successful super-fill of trenches at the nanometer scale. In this review, we briefly summarize recent advances in the development of Cu diffusion-proof materials, including metals, metal alloys, self-assembled molecular layers (SAMs), two-dimensional (2D) materials and high-entropy alloys (HEAs). Also, challenges are highlighted and future research directions are suggested.

Platinum alloy gauzes are employed for the high-temperature oxidation of NH3 to NO used in the industrial production of HNO3 for application in agricultural fertilizers. To enhance the efficiency of NH3 oxidation, various Pt–Pd–Rh alloys are employed for the production of such catalytic gauzes. To understand the role of these metals in NH3 oxidation, scanning electron microscopy, energy-dispersive spectroscopy and X-ray diffraction were applied to investigate the morphology, composition and structure of Pt, Pd and Rh foils after annealing in O2 and oxidation of NH3 with air at 1133 K. After annealing in O2 and NH3 oxidation, the metallic microgranular structure was detected on Pt(poly), whereas oxide layers of Rh2O3 and PdO were observed on Rh(poly) and Pd(poly). At the onset of NH3 oxidation (t = 1 h), fibrous metal-oxide agglomerates of nanofibers formed on these oxide layers. The long-term (5–10 h) oxidation of NH3 led to the formation of a continuous layer of pyramidal crystals on Rh(poly) and palladium “cauliflowers” on Pd(poly). The highly exothermic reaction of NH3 with oxygen on metals and PdO or Rh2O3 initiates strong catalytic etching forming grains and facets on Pt, fibrous metal-oxide agglomerates, pyramidal crystals and metallic “cauliflowers” on Rh and Pd.

Developing highly efficient and durable catalysts for future electrochemical and energy applications is one of the main subjects of current studies in renewable energy generation. In the past several years, researchers have developed Pt-based alloy electrocatalyst nanomaterials that exhibit promising electrocatalytic properties for various electrochemical applications. The efficient structural and morphological control of Pt-based alloy materials plays a decisive role in achieving these enhanced electrocatalytic properties. The present review article emphasizes the recent progress and important developments in the synthesis and electrocatalytic applications of Pt-group-based nanodendrite materials. The following review will help the exploration and development of better catalysts for practical applications and aims to elucidate the nanodendrite structure of Pt-group metals.

This manuscript reviews the current trends in the recovery of Platinum Group Metals (PGMs) from end-of-life autocatalysts and the aims of the recently funded Marie Sklodowska-Curie Project “Chemistry of Platinum Group Metals-CHemPGM” towards the greening of PGMs recovery processes and the reusing of recovered PGMs for preparation of new catalysts. Together with the analysis of the state of the art recovery of PGMs from spent autocatalysts through pyrometallurgical and hydrometallurgical routes and the recent trends in reducing their environmental impact, also emerging sustainable and green technologies are analyzed. Particular focus is given on the mechanochemical processing as a promising sustainable route not only for the pretreatment of waste materials but also for direct PGMs leaching. The present review identifies also the trends in catalysts for carbon neutrality and the few recent efforts in developing PGM-based catalysts starting directly from the liquor of the leach solutions of spent catalysts envisaging therefore a possible key to close PGMs loop in a more efficient and sustainable way.

Chemistry of Schiff base (SB) ligands began in 1864 due to the discovery made by Hugo Schiff (Schiff, H., 1864, (1), 118-119). However, there is still a vivid interest in coordination compounds based on imine ligands. The aim of this paper is to review the most recent concepts on construction of homo- and hetero-oligonuclear Schiff base coordination compounds narrowed down to the less frequently considered complexes of platinum group metals (PGM). The combination of SB and PGM in oligonuclear entities has several advantages over mononuclear or polynuclear species. Such complexes usually exhibit better electroluminescent, magnetic and/or catalytic properties than mononuclear ones due to intermetallic interactions and frequently have better solubility than polymers. Various construction strategies of oligodentate imine ligands for coordination of PGM are surveyed including simple imine ligands, non-innocent 1,2-diimines, chelating imine systems with additional N/O/S atoms, classic N O -compartmental Schiff bases and their modifications resulting in acyclic fused ligands, macrocycles such as calixsalens, metallohelical structures, nano-sized molecular wheels and hybrid materials incorporating mesoionic species. Co-crystallization and formation of metallophilic interactions to extend the mononuclear entities up to oligonuclear coordination species are also discussed.