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We performed spatially resolved near-ambient-pressure photoemission spectromicroscopy on graphene-coated copper in operando under oxidation conditions in an oxygen atmosphere (0.1 mbar). We investigated regions with bare copper and areas covered with mono- and bi-layer graphene flakes, in isobaric and isothermal experiments. The key method in this work is the combination of spatial and chemical resolution of the scanning photoemission microscope operating in a near-ambient-pressure environment, thus allowing us to overcome both the material and pressure gap typical of standard ultrahigh-vacuum X-ray photoelectron spectroscopy (XPS) and to observe in operando the protection mechanism of graphene toward copper oxidation. The ability to perform spatially resolved XPS and imaging at high pressure allows for the first time a unique characterization of the oxidation phenomenon by means of photoelectron spectromicroscopy, pushing the limits of this technique from fundamental studies to real materials under working conditions. Although bare Cu oxidizes naturally at room temperature, our results demonstrate that such a graphene coating acts as an effective barrier to prevent copper oxidation at high temperatures (over 300 °C), until oxygen intercalation beneath graphene starts from boundaries and defects. We also show that bilayer flakes can protect at even higher temperatures. The protected metallic substrate, therefore, does not suffer corrosion, preserving its metallic characteristic, making this coating appealing for any application in an aggressive atmospheric environment at high temperatures.
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http://dx.doi.org/10.1021/acsami.9b08918 | DOI Listing |
Chem Sci
August 2025
School of Chemical Engineering, The University of Adelaide Adelaide SA 5005 Australia
During the electrochemical conversion of CO to acetate on copper-based catalysts, the electrolyte concentration plays a crucial role in acetate selectivity. However, the correlation between the electrolyte concentration and the local microenvironment as well as the reaction kinetics remains unclear. In this work, we report for the first time the impact of KOH concentration on the solvent structure and reaction kinetics for CO reduction to acetate using advanced computational methods.
View Article and Find Full Text PDFAdv Mater
August 2025
Department of Chemistry, Northwestern University, Evanston, IL, 60208, USA.
Copper catalyst morphology, faceting, and oxidation state are each known to impact selectivity in the electroreduction of CO. Copper oxide precatalysts are synthesized using flash Joule heating and rapid cooling, and it is observed that temperature ramp rates can be used to control morphology, enabling us to implement ≈10 nm-sized intragrain features within ≈35 nm grains. It is found that the structural features of the precatalysts are substantially transferred to Cu catalysts that are formed when they are employed in CO electroreduction in a membrane electrode assembly electrolyzer.
View Article and Find Full Text PDFACS Nano
September 2025
Department of Chemical, Biological, and Materials Engineering, University of South Florida, Tampa, Florida 33620, United States.
The conversion and storage of solar energy as a chemical fuel are crucial technologies for the future of clean energy. Photocatalysis by the reverse water-gas shift (RWGS) reaction is a promising method to achieve this objective. This article investigates the photocatalytic effect of visible light on copper-based nanocatalysts for the RWGS reaction.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Center for Renewable Energy and Storage Technologies (CREST), Physical Science and Engineering (PSE), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
Ligand-modified metal nanoclusters (NCs) have emerged as candidate materials for catalysis owing to their well-defined yet tunable structure and their metal centers' high nuclearity. We posited that NC-based catalytic behavior will depend on ligand properties, the accessibility of active sites, and their atomic configuration. We synthesized a series of Cu NC-based catalysts, tuned local hydrophobicity through ligand adjustment, balanced the ligand coverage and active site exposure, and found that we were, in this way, able to engender efficient electrosynthesis of acetate via CO electroreduction.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Institute of Sustainability for Chemicals, Energy and Environment (ISCE2), Agency of Science, Technology, and Research (A*STAR), Singapore, 627833, Singapore.
Controlling product selectivity in electrochemical CO reduction (eCOR) is critical for efficient CO conversion. However, the dynamic structural changes of Cu-based catalysts during operation complicate mechanistic understanding. Here, we investigate fluorine-modified copper pre-catalysts with varying doping levels and reveal how their structural evolution governs eCOR activity and selectivity.
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