Search Results (108)

Nanoparticle powders of a Ce_1−xRu_xO₂ mixed oxide (3.0% w/w), were synthesized to be used as catalytic supports, on which Pt and Ir nanoparticles were deposited as the active phase. The catalytic supports were prepared through a route involving microwave heating, while the Pt or Ir nanoparticles were incorporated via the wet incipient method. The {Pt, Ir/Ce_1−xRu_xO₂} catalytic systems were successfully tested as catalysts for low-temperature CO oxidation. To provide adequate support to our results, the compounds were characterized by SEM, EDS, XRD, DRS-UV-vis, and XPS techniques. In addition, BET isotherms were carried out to determine specific surface area features. The CO oxidation evolution was tested in the range of 25–350 °C. Both Pt and Ir supported Ce_1−xRu_xO₂ catalysts that remarkably improved the CO oxidation, reaching and sustaining 100% conversion from 125 °C onwards. Remarkably, the mixed oxide support, by itself, showed outstanding performance, achieving 100% conversion to CO₂, at a temperature of 225 °C. Full article

The reaction mechanism of the gold-catalyzed hydrothiolation of alkenes (1) with thiols (2) has been investigated in detail. The tetranuclear gold complex, (PPh₃)₄Au₄(SPh)₂(NTf)₂ (A), is a key intermediate in the catalytic hydrothiolation of alkenes. It forms instantaneously when PPh₃AuNTf₂ and PhSH are mixed in THF. Monitoring the reaction over time using ³¹P NMR spectroscopy revealed that gold complex A remained stable in the reaction system throughout the hydrothiolation process. In addition, we successfully observed a rapid ligand-exchange reaction between the thiolate group of gold complex A and thiols in solution. The gold-catalyzed alkene hydrothiolation reaction has been applied to the catalytic hydrothiolation of allenes, which have degenerate double bonds. Hydrothiolation of allenes proceeded regioselectively at the terminal double bond. However, the yield was lower than that observed for alkenes, and catalyst deactivation occurred. The hydrothiolation products of allenes were difficult to detach from the gold catalyst, necessitating an increase in the reaction temperature. Since high periodic transition metals such as gold and platinum are effective for hydrothiolation of alkenes and allenes, it is interesting to clarify whether iridium complexes, which belong to the same period as gold and platinum, could also catalyze alkene hydrothiolation. Through a detailed investigation of iridium ligands and reaction conditions, it was found that, in iridium systems, disulfide formation via oxidative coupling of thiols occurs preferentially over hydrothiolation reactions. This is likely due to steric hindrance around the iridium center, which inhibits alkene coordination to the iridium. Additionally, the hydrothiolation proceeding at low yields is believed to be a radical reaction involving electron transfer through the iridium complex. Full article

Catalytic materials are central to the advancement of hydrogen generation technologies, playing a pivotal role in enabling sustainable, carbon-neutral energy systems. Hydrogen can be produced via electrochemical water splitting, thermochemical reforming, or photocatalysis—each imposing unique performance requirements on catalysts in terms of activity, selectivity, stability, and efficiency. While traditional noble metals (e.g., platinum, ruthenium, iridium) provide benchmark catalytic activity, their widespread use is hindered by scarcity, high cost, and limited long-term durability. Consequently, researchers have increasingly focused on earth-abundant alternatives such as transition metals (Ni, Co, Fe, Mo), alloys, metal oxides, carbides, sulfides, nitrides, and carbon-based systems. Among these, two-dimensional materials, particularly the MXene family, have attracted significant attention due to their metallic conductivity, layered structure, and tunable surface chemistry. These features enable rapid charge transfer and abundant active sites, making MXenes and related nanostructured catalysts promising for both the Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER) across a wide range of electrochemical conditions. Parallel efforts have integrated novel semiconductors, plasmonic nanomaterials, and hybrid heterostructures to improve the efficiency of solar-to-hydrogen energy conversion. This paper reviews the main types of catalytic materials used in hydrogen production, explains their design strategies and structure–performance relationships, and discusses key engineering challenges such as integrating renewable energy sources, scaling up manufacturing, and ensuring long-term durability in real-world systems. Future research goals are also highlighted, including the development of affordable non-noble catalysts, enhancing catalyst stability through surface and defect engineering, and coupling hydrogen production with circular economy principles, all of which are essential to making hydrogen generation more efficient, scalable, and cost-effective as the world transitions to clean and sustainable energy. Full article

Noble metal-catalyzed C–H activation has transformed synthetic methodology by enabling direct modification of inert C–H bonds with high levels of efficiency, selectivity, and functional group tolerance. This mini-review provides a focused overview of the mechanistic foundations and emerging advances in C–H functionalization mediated by ruthenium, iridium, rhodium and palladium catalysts. Key activation modes including oxidative addition, concerted metalation deprotonation (CMD), and electrophilic pathways are discussed alongside the roles of high-valent intermediates and ligand control in determining reactivity and regioselectivity. Special emphasis is placed on recent electrochemical strategies, where anodic oxidation replaces traditional chemical oxidants, granting access to unique redox manifolds and expanding the scope of C–C, C–N, C–O, and C–X bond-forming reactions. Representative transformations highlight the versatility of noble metals in constructing heterocycles, enabling enantioselective processes, and facilitating late-stage functionalization of complex molecules. Current challenges and future perspectives are outlined, including the need for improved nondirected activation, deeper mechanistic insight, and enhanced scalability. Collectively, this review underscores the central role of noble metals in advancing sustainable and innovative C–H functionalization chemistry. Full article

Platinum group metals (PGMs)—comprising platinum (Pt), palladium (Pd), rhodium (Rh), iridium (Ir), ruthenium (Ru), and osmium (Os)—are indispensable strategic materials for key industries, including automotive manufacturing, petrochemical engineering, and the new energy sector. Given the uneven global distribution of primary PGM reserves and the widening supply–demand gap, recovering PGMs from secondary sources—primarily metallurgical by-products and spent catalysts—has become a strategic priority. synergistic smelting, leveraging “multi-feedstock complementarity” and “multi-technology coupling,” offers an efficient approach to overcoming challenges associated with secondary resources, such as low grades, complex matrices, and refractory separation. This paper systematically reviews the technological evolution of synergistic smelting for PGMs recovery, focusing on three aspects: the characteristics and processing bottlenecks of PGMs-bearing secondary resources, the development trajectory of traditional metallurgical technologies, and innovative breakthroughs in microwave-assisted synergistic smelting. A comparative analysis between traditional and microwave-based technologies is conducted across four dimensions: resource adaptability, technical performance, environmental sustainability, and industrial maturity. Finally, the core challenges currently confronting microwave-assisted synergistic smelting and future directions for industrial demonstration are elaborated on. This study serves as a comprehensive reference for the efficient and sustainable recovery of PGMs, with significant implications for the circular economy and strategic resource security. Full article

The field of electrochemical devices, encompassing energy storage, fuel cells, electrolysis, and sensing, is fundamentally reliant on the electrode materials that govern their performance, efficiency, and sustainability. Traditional materials, while foundational, often face limitations such as restricted reaction kinetics, structural deterioration, and dependence on costly or scarce elements, driving the need for continuous innovation. Emerging electrode materials are designed to overcome these challenges by delivering enhanced reaction activity, superior mechanical robustness, accelerated ion diffusion kinetics, and improved economic feasibility. In energy storage, for example, the shift from conventional graphite in lithium-ion batteries has led to the exploration of silicon-based anodes, offering a theoretical capacity more than tenfold higher despite the challenge of massive volume expansion, which is being mitigated through nanostructuring and carbon composites. Simultaneously, the rise of sodium-ion batteries, appealing due to sodium’s abundance, necessitates materials like hard carbon for the anode, as sodium’s larger ionic radius prevents efficient intercalation into graphite. In electrocatalysis, the high cost of platinum in fuel cells is being addressed by developing Platinum-Group-Metal-free (PGM-free) catalysts like metal–nitrogen–carbon (M-N-C) materials for the oxygen reduction reaction (ORR). Similarly, for the oxygen evolution reaction (OER) in water electrolysis, cost-effective alternatives such as nickel–iron hydroxides are replacing iridium and ruthenium oxides in alkaline environments. Furthermore, advancements in materials architecture, such as MXenes—two-dimensional transition metal carbides with metallic conductivity and high volumetric capacitance—and Single-Atom Catalysts (SACs)—which maximize metal utilization—are paving the way for significantly improved supercapacitor and catalytic performance. While significant progress has been made, challenges related to fundamental understanding, long-term stability, and the scalability of lab-based synthesis methods remain paramount for widespread commercial deployment. The future trajectory involves rational design leveraging advanced characterization, computational modeling, and machine learning to achieve holistic, system-level optimization for sustainable, next-generation electrochemical devices. Full article

This study investigates amorphous anodized porous TiO₂ (a-TiO₂) as a substrate for iridium-based oxygen evolution catalysts. The substrates were prepared via anodization of Ti foil in a glycerol-based solution for 15 min @ 60 V. Nickel was subsequently electrodeposited to act both as a conductive and sacrificial layer for the galvanic deposition of iridium from an Ir(IV) chloro-complex solution. Electrochemical anodization resulted in a uniform IrO_x layer on the a-TiO₂ substrate, featuring Ir aggregates ~250 nm in size and an Ir:Ni atomic ratio of ca. 7, as determined by EDS analysis. The quantity of Ni determined by ICP-MS bulk analysis indicated that Ni resided also within the porous matrix. Varying the Ni deposition charge density (q_Ni) revealed that an intermediate loading (1463 mC cm⁻²) provided the best balance between Ir accessibility during the galvanic replacement step and electronic continuity. The optimized IrO_x/Ir-Ni/a-TiO₂ electrode achieved excellent OER performance (η = 344 mV @ 10 mA cm⁻²; 1.68 mA μg_Ir⁻¹ @ η = 300 mV) at an ultra-low Ir loading of 2.15 μg_Ir cm⁻² and demonstrated good short-term stability, with only a 20 mV potential increase over 4 h of continuous operation at 5.5 mA cm⁻². Overall, this strategy offers a scalable pathway for producing efficient OER electrodes with minimal noble metal loading. Full article

Parahydrogen-induced hyperpolarization (PHIP), introduced nearly four decades ago, provides an elegant solution to one of the fundamental limitations of nuclear magnetic resonance (NMR)—its notoriously low sensitivity. By converting the spin order of parahydrogen into nuclear spin polarization, NMR signals can be boosted by several orders of magnitude. Here we present a portable, compact, and cost-effective setup that brings PHIP and Signal Amplification by Reversible Exchange (SABRE) experiments within easy reach, operating seamlessly across ultra-low-field (0–10 μT) and high-field (>1 T) conditions at 50% parahydrogen enrichment. The system provides precise control over bubbling pressure, temperature, and gas flow, enabling systematic studies of how these parameters shape hyperpolarization performance. Using the benchmark Chloro(1,5-cyclooctadiene)[1,3-bis(2,4,6-trimethylphenyl)imidazole-2-ylidene]iridium(I) (Ir–IMes) catalyst, we explore the catalyst activation time and response to parahydrogen flow and pressure. Polarization transfer experiments from hydrides to [1-¹³C]pyruvate leading to the estimation of heteronuclear J-couplings are also presented. We further demonstrate the use of Chloro(1,5-cyclooctadiene)[1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene]iridium(I) (Ir–SIPr), a recently introduced catalyst that can also be used for pyruvate hyperpolarization. The proposed design is robust, reproducible, and easy to implement in any laboratory, widening the route to explore and expand the capabilities of parahydrogen-based hyperpolarization. Full article

The Signal Amplification By Reversible Exchange (SABRE) technique provides enhancement of Nuclear Magnetic Resonance (NMR) signals up to several orders of magnitude using chemical exchange of a substrate and parahydrogen on an iridium complex. Therefore, the availability of such a catalytic complex to a broader community is an absolutely vital step for dissemination of the groundbreaking SABRE methodology. The most common SABRE catalyst, which is activated in situ, is based on Ir-IMes system (IMes = 1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene). Earlier approaches for the synthesis of this catalyst often relied on specialized equipment and were limited to a comparatively small scale. This, in turn, increased the barrier of entry for new scientists to the area of SABRE hyperpolarization. Here, we present a robust, inexpensive, and easy to reproduce synthetic procedure for the preparation of this SABRE catalyst, which does not require specialized inert atmosphere equipment like a glove box or Schlenk line. The synthesis was validated on the scale of several grams vs. tens of milligrams scale in the reported approaches. The resulting SABRE catalyst, [Ir(IMes)(COD)Cl], was activated in situ and further evaluated in hyperpolarization experiments resulting in signal enhancements comparable to (or higher than) those for the catalyst prepared using Schlenk line equipment. Full article

As part of the GreenRAIM activity of the European Space Agency (ESA), an extensive test campaign involving various monopropellants was undertaken. In this work, design and test results of an additively manufactured 1-Newton monopropellant thruster are shown. The detailed design of the thruster and the experimental setup are presented. The first part of the test campaign was conducted with 98 wt.% hydrogen peroxide as the propellant and a commercially available Pt/Al₂O₃ catalyst. The second part was carried out with the same thruster but using nitrous oxide as the propellant and an iridium-based catalyst. The test data acquired was used to validate a comprehensive, generic model for monopropellant thrusters within the simulation software EcosimPro/ESPSS v3.7, which was developed within the activity. Full article

In the water splitting process for sustainable hydrogen production, the oxygen evolution reaction (OER) stands as one of the pivotal half-reactions. Nevertheless, the sluggish four-electron transfer process inherent to OER has emerged as a kinetic bottleneck that impedes water electrolysis. To address this challenge, researchers have been devoting substantial efforts to developing high-performance OER electrocatalysts. Currently, iridium (Ir)-based or ruthenium (Ru)-based oxides are widely acknowledged as benchmark catalysts for OER. However, their scarcity and exorbitant cost render large-scale applications impractical. In recent years, transition metal carbides have garnered extensive attention in the realm of OER electrocatalysts, exhibiting tremendous application prospects owing to their advantages of low cost, high catalytic activity, and excellent stability. This review briefly introduces the fundamental characteristics and synthesis methodologies of transition metal carbides, summarizes the recent research advances in their application as OER catalysts, elaborates on the modification strategies and catalytic mechanisms of transition metal carbide nanomaterials, and finally discusses the challenges confronted by these metal carbides as well as the future research directions. Full article

Industrial catalysts are accelerating the global transition toward renewable energy, serving as enablers for innovative technologies that enhance efficiency, lower costs, and improve environmental sustainability. This review explores the pivotal roles of industrial catalysts in hydrogen production, biofuel generation, and biomass conversion, highlighting their transformative impact on renewable energy systems. Precious-metal-based electrocatalysts such as ruthenium (Ru), iridium (Ir), and platinum (Pt) demonstrate high efficiency but face challenges due to their cost and stability. Alternatives like nickel-cobalt oxide (NiCo₂O₄) and Ti₃C₂ MXene materials show promise in addressing these limitations, enabling cost-effective and scalable hydrogen production. Additionally, nickel-based catalysts supported on alumina optimize SMR, reducing coke formation and improving efficiency. In biofuel production, heterogeneous catalysts play a crucial role in converting biomass into valuable fuels. Co-based bimetallic catalysts enhance hydrodeoxygenation (HDO) processes, improving the yield of biofuels like dimethylfuran (DMF) and γ-valerolactone (GVL). Innovative materials such as biochar, red mud, and metal–organic frameworks (MOFs) facilitate sustainable waste-to-fuel conversion and biodiesel production, offering environmental and economic benefits. Power-to-X technologies, which convert renewable electricity into chemical energy carriers like hydrogen and synthetic fuels, rely on advanced catalysts to improve reaction rates, selectivity, and energy efficiency. Innovations in non-precious metal catalysts, nanostructured materials, and defect-engineered catalysts provide solutions for sustainable energy systems. These advancements promise to enhance efficiency, reduce environmental footprints, and ensure the viability of renewable energy technologies. Full article

Developing high-performance oxygen evolution reaction (OER) electrocatalysts remains a critical challenge for sustainable hydrogen production via water electrolysis. Herein, we present a self-supported atomic iridium-decorated FeOOH nanostructure on iron foam (Ir-FeOOH/IF) by a facile impregnation reduction method. The self-supported Ir-FeOOH/IF electrode integrates the high electrical conductivity and outstanding mass transfer performance of IF. The FeOOH features abundant active sites, while the Ir modification regulated the electronic structure of FeOOH. As a result, the as-prepared Ir-FeOOH/IF catalyst (with the optimized synthesis time) achieves a low overpotential of 145 and 284 mV at current densities of 0.1 and 1 A cm⁻², respectively, and exhibits excellent long-term catalytic stability for 135 h at 0.1 A cm⁻² in a 1 M KOH solution. This work provides a new strategy for the design of low-cost and highly stable OER electrocatalysts. Full article

Producing hydrogen by water electrolysis has attracted significant attention as a potential renewable energy solution. In this work, a catalyst with reduced graphene oxide (rGO) loaded on IrO₂/TiO₂ (called rGO/IrO₂/TiO₂) was designed for the catalytic oxygen evolution reaction (OER). The catalyst was synthesized by coating graphene oxide onto a pretreated IrO₂/TiO₂ precursor, followed by thermal treatment at 450 °C to achieve reduction and the adhesion of graphene to the substrate. The graphene support retained its intact sp² carbon framework with minor oxygen-containing functional groups, which enhanced electrical conductivity and hydrophilicity. Benefiting from the synergistic effect of an rGO, IrO₂, and TiO₂ matrix, the rGO/IrO₂/TiO₂ catalyst only needed overpotentials of 240 mV and 320 mV to reach 10 mA cm⁻² and 100 mA cm⁻² in the OER, along with excellent stability over 50 h. Its morphology and crystalline structure were characterized by SEM and XRD spectroscopy, and its electrochemical performance was tested by LSV analysis, EIS impedance spectrum, and double-layer capacitance (C_dl) measurements. This work introduces an innovative and eco-friendly strategy for constructing a high-performance, functionalized Ir-based catalyst. Full article

This study develops iridium (Ir)-based catalysts for the hydrogenation of dodecanoic acid, a medium-chain fatty acid abundant in palm kernel and coconut oils, for producing fatty alcohols and alkanes. Among various supports such as AlOOH, SiO₂, TiO₂, Nb₂O₅, MoO₃, Ta₂O₅, ZrO₂, and WO₃ for 7.5 wt% Ir loading, an Ir-impregnated Nb₂O₅ (Ir/Nb₂O₅) catalyst demonstrated remarkable performance with 100% conversion and a high dodecanol yield (89.1%) under mild conditions (170 °C, 4.0 MPa H₂), while at higher temperatures and pressures (200 °C, 8.0 MPa H₂), Ir-impregnated MoO₃ (Ir/MoO₃) produced dodecane as the main product with a yield of 90.7%. These findings can tailor product selectivity toward desired bio-based chemicals and fuels, offering sustainable pathways for fatty acid hydrogenation by optimizing catalyst supports and reaction conditions in the Ir-based catalyst. Full article