Establishing relationships between the surface atomic structure and activity of Cu-based electrocatalysts for CO and CO reduction is hindered by probable surface restructuring under working conditions. Insights into these structural evolutions are scarce as techniques for monitoring the surface facets in conventional experimental designs are lacking. To directly correlate surface reconstructions to changes in selectivity or activity, the development of surface-sensitive, electrochemical probes is highly desirable. Here, we report the underpotential deposition of lead over three low index Cu single crystals in alkaline media, the preferred electrolyte for CO reduction studies. We find that underpotential deposition of Pb onto these facets occurs at distinct potentials, and we use these benchmarks to probe the predominant facet of polycrystalline Cu electrodes . Finally, we demonstrate that Cu and Pb form an irreversible surface alloy during underpotential deposition, which limits this method to investigating the surface atomic structure after reaction.
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http://dx.doi.org/10.1021/acs.langmuir.1c02830 | DOI Listing |
Molecules
November 2024
Hunan Key Laboratory of Biomedical Nanomaterials and Devices, College of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou 412007, China.
A Pb-containing PtAu nanoflower electrocatalyst was deposited on the cathode via galvanic replacement reaction in a double-cabin galvanic cell (DCGC) with a Cu plate as the anode, a multiwalled carbon nanotube (MWCNT) modified glassy carbon electrode (GCE) as the cathode, 0.1 M HClO aqueous solution as the anolyte, and Pb-containing Pt salt and Au salt mixed aqueous solution as the catholyte, respectively, and the electrocatalytic performance of the modified electrode toward methanol oxidation in the alkaline medium was investigated. Electrochemical studies reveal that the stripping of bulk Cu can induce underpotential deposition (UPD) of Pb on Pt during the galvanic replacement reaction, which affects the morphology and composition of Pb-containing PtAu nanoparticles.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853-1301, United States.
Anion exchange membrane fuel cells (AEMFCs) have successfully eliminated anode carbonate precipitation through cation immobilization with the incorporation of alkaline polymer electrolytes (APEs). However, carbonation by CO in ambient air continues to induce significant AEMFC performance losses via mechanisms that remain unclear/elusive. In this multimodal investigation of AEMFC carbonation, we find that the increase in ionic resistance after carbonation accounts for only a small fraction of the cell voltage drop, especially at high current densities.
View Article and Find Full Text PDFSmall Methods
November 2024
Department of Materials Science & Engineering, University of Toronto, 184 College Street, Suite 140, Toronto, ON, M5S 3E4, Canada.
The complex compositional space of high entropy alloys (HEAs) has shown a great potential to reduce the cost and further increase the catalytic activity for hydrogen evolution reaction (HER) by compositional optimization. Without uncovering the specifics of the HER mechanism on a given HEA surface, it is unfeasible to apply compositional modifications to enhance the performance and save costs. In this work, a combination of density functional theory and Bayesian machine learning is used to demonstrate the unique catalytic mechanism of IrPdPtRhRu HEA catalysts for HER.
View Article and Find Full Text PDFSci Adv
November 2024
Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208-3113, USA.
Research drives development of sustainable electrocatalytic technologies, but efforts are hindered by inconsistent reporting of advances in catalytic performance. Iridium-based oxide catalysts are widely studied for electrocatalytic technologies, particularly for the oxygen evolution reaction (OER) for proton exchange membrane water electrolysis, but insufficient techniques for quantifying electrochemically accessible iridium active sites impede accurate assessment of intrinsic activity improvements. We develop mercury underpotential deposition and stripping as a reversible electrochemical adsorption process to robustly quantify iridium sites and consistently normalize OER performance of benchmark IrO electrodes to a single intrinsic activity curve, where other commonly used normalization methods cannot.
View Article and Find Full Text PDFMaterials (Basel)
October 2024
State Key Laboratory of Metal Matrix Composites, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Single-atom catalysts (SACs) have the advantages of good active site uniformity, high atom utilization, and high catalytic activity. However, the study of its controllable synthesis still needs to be thoroughly investigated. In this paper, we deposited Cu SAs on nanoporous N-doped graphene by underpotential deposition and further obtained a Pt SAC by a galvanic process.
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