High-performance electrocatalysts for the hydrogen evolution reaction are of interest in the development of next-generation sustainable hydrogen production systems. Although expensive platinum-group metals have been recognized as the most effective HER catalysts, there is an ongoing requirement for the discovery of cost-effective electrode materials. This paper reveals the prospects of two-dimensional (2D) noble metals, possessing a large surface area and a high density of active sites available for hydrogen proton adsorption, as promising catalytic materials for water splitting. An overview of the synthesis techniques is given. The advantages of wet chemistry approaches for the growth of 2D metals over deposition techniques show the potential for kinetic control that is required as a precondition to prevent isotropic growth. An uncontrolled presence of surfactant-related chemicals on a 2D metal surface is however the main disadvantage of kinetically controlled growth methods, which stimulates the development of surfactant-free synthesis approaches, especially template-assisted 2D metal growth on non-metallic substrates. Recent advances in the growth of 2D metals using a graphenized SiC platform are discussed. The existing works in the field of practical application of 2D noble metals for hydrogen evolution reaction are analyzed. This paper shows the technological viability of the "2D noble metals" concept for designing electrochemical electrodes and their implementation into future hydrogen production systems, thereby providing an inspirational background for further experimental and theoretical studies.
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http://dx.doi.org/10.1039/d3cp00156c | DOI Listing |
J Am Chem Soc
January 2025
Institute for Chemical Research, Kyoto University, Gokasho, Uji 611-0011, Japan.
Nanoclusters are nanometer-sized molecular compounds characterized by significant metal-metal bonding and low average oxidation states, and they exhibit unique properties distinct from those of small metal complexes or nanoparticles. Unlike noble metals stable in metallic forms, the synthesis of nanometer-sized iron clusters has been precluded by the relatively weak iron-iron bonds and the high reactivity of low oxidation state iron, despite the extensive history of molecular iron compounds. Here, we report the synthesis and characterization of a cationic 55-atom iron cluster with a 1.
View Article and Find Full Text PDFNanoscale
January 2025
Research Center for Materials Nanoarchitectonics (MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Loading cocatalysts on semiconductor-based photocatalysts to create active reaction sites is a preferable method to enhance photocatalytic activity and a widely adopted strategy to achieve effective photocatalytic applications. Although theoretical calculations suggest that the broad density of states of noble metal cocatalysts, such as Pt, act as a recombination center, this has never been experimentally demonstrated. Herein, we employed pico-nano and nano-micro second transient absorption spectroscopy to investigate the often overlooked photogenerated holes, instead of the widely studied electrons on Pt- and Ni-loaded SrTiO to evaluate the effects of cocatalysts as a recombination center.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Central South University, chemistry, CHINA.
The two-dimensional lamellar materials disperse platinum sites and minimize noble-metal usage for fuel cells, while mass transport resistance at the stacked layers spurs device failure with a significant performance decline in membrane electrode assembly (MEA). Herein, we implant porous and rigid sulfonated covalent organic frameworks (COF) into the graphene-based catalytic layer for the construction of steric mass-charge channels, which highly facilitates the activity of oxygen reduction reactions in both the rotating disk electrode (RDE) measurements and MEA device tests. Specifically, the normalized mass activity is remarkably boosted by 3.
View Article and Find Full Text PDFPNAS Nexus
January 2025
Thrust of Earth, Ocean and Atmospheric Sciences Function Hub, The Hong Kong University of Science and Technology (Guangzhou), Guangzhou 511453, China.
Modulating the electronic structure of noble metals via electronic metal-support interaction (EMSI) has been proven effectively for facilitating molecular oxygen activation and catalytic oxidation reactions. Nevertheless, the investigation of the fundamental mechanisms underlying activity enhancement has primarily focused on metal oxides as supports, especially in the catalytic degradation of volatile organic compounds. In this study, a novel Pt catalyst supported on nitrogen-doped carbon encapsulating FeNi alloy, featuring ultrafine Pt nanoparticles, was synthesized.
View Article and Find Full Text PDFChemSusChem
January 2025
Brandenburgische Technische Universitat Cottbus-Senftenberg, Angewandte Physik und Halbleiterspektroskopie, Konrad-Zuse-Str. 1, 03046, Cottbus, GERMANY.
Ultrathin atomic layer deposited ceria films (< 20 nm) are capable of H2 heterolytic activation at room temperature, undergoing a significant reduction regardless of the absolute pressure, as measured under in-situ conditions by near ambient pressure X-ray photoelectron spectroscopy. ALD-ceria can gradually reduce as a function of H2 concentration under H2/O2 environments, especially for diluted mixtures below 10%. At room temperature, this reduction is limited to the surface region, where the hydroxylation of the ceria surface induces a charge transfer towards the ceria matrix, reducing Ce4+ cations to Ce3+.
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