Rational design of high-performance catalysts for CO electroreduction is crucial for achieving carbon neutrality, yet effective modification strategies remain scarce. In this study, we present the microwave heating approach to incorporate La ions into Sn-based perovskite oxides, significantly enhancing their electrocatalytic performance for the reduction of CO to formate. Through comprehensive characterization techniques, including X-ray photoelectron spectroscopy, synchrotron radiation X-ray absorption spectroscopy, electrochemical measurements (Tafel analysis and impedance spectroscopy), and density functional theory calculations, we demonstrate that La substitution effectively modulates the Sn-O bond distance in BaSnO. This structural modification induces local charge density enrichment, facilitates CO adsorption, and enhances electron transfer kinetics, resulting in a substantial improvement in the formate Faradaic efficiency. In situ Raman spectroscopic analysis and postreaction XPS characterization confirmed the structural integrity of the perovskite framework and the preservation of Sn valence states under negative potentials. This work provides fundamental insights into the CO reduction reaction mechanism on perovskite electrocatalysts and establishes a framework for the design of advanced tin-based electrocatalysts.
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http://dx.doi.org/10.1021/acsami.4c21829 | DOI Listing |
Chemistry
March 2025
Nagoya University School of Science Graduate School of Science: Nagoya Daigaku Rigakubu Daigakuin Rigaku Kenkyuka, Integrated Research Consortium on Chemical Sciences (IRCCS), Furo-cho, Chikusa-ku, 464-8602, Nagoya, JAPAN.
The efficient conversion of carbon dioxide (CO2) into valuable products remains a keystone of sustainable energy research. Achieving this goal requires catalytic methodologies that can adapt to diverse energy sources such as light, heat, or electricity. This concept highlights the remarkable versatility of tetradentate PNNP-ligated iridium complexes, (PNNP)Ir, as multifunctional catalysts, which demonstrate outstanding performance in CO2 reduction across photochemical, thermal, and electrochemical systems.
View Article and Find Full Text PDFChem Sci
March 2025
School of Chemistry and Molecular Biosciences, University of Queensland Brisbane 4072 Australia
Formate dehydrogenase (FdsDABG) from is a Mo-containing enzyme capable of catalysing both formate oxidation to CO and the reverse CO reduction to formate by utilising NAD or NADH, respectively. This enzyme is part of the NADH dehydrogenase superfamily. Its subcomplex, FdsBG, lacking the formate oxidizing/CO-reducing Mo-cofactor, but harbouring an FMN as well as [2Fe-2S] and [4Fe-4S] clusters, reversibly interconverts the NAD/NADH redox pair.
View Article and Find Full Text PDFPLoS One
March 2025
Aix-Marseille Université, Université du Sud Toulon-Var, CNRS/INSU, IRD, MIO, UM 110, Marseille, France.
A novel thermophilic (optimum growth temperature ~ 60 °C) anaerobic Gram-negative bacterium, designated strain V6Fe1T, was isolated from sediments heated by the hydrothermal circulation of the Aeolian Islands (Vulcano, Italy) on the seafloor. Strain V6Fe1T belongs to the recently described family Deferrivibrionaceae in the phylum Deferribacterota. It grows chemoorganotrophically by fermentation of proteinaceous substrates and organic acids or by respiration of organic compounds using fumarate, nitrate, Fe(III), S°, and Mn(IV) as electron acceptors.
View Article and Find Full Text PDFChemistry
March 2025
Georgia Institute of Technology, Biomedical Engineering, 901 Atlantic Drive, MoSE 3100J, 30332, Atlanta, UNITED STATES OF AMERICA.
Noble-metal open nanostructures have remarkable catalytic capabilities toward a wide range of reactions. In particular, Pd-based open nanostructures have been synthesized and validated for superior catalytic performance toward formic acid oxidation. However, most of the syntheses are based on dropwise addition, making it challenging to increase the production volume.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
Northwestern University, Department of Chemistry, 2145 Sheridan Rd, 60208, United States, 60208, Evanston, UNITED STATES OF AMERICA.
The reduction of carbon dioxide (CO2) into valuable products will contribute to sustainable carbon use. Here we report the photocatalytic reduction of CO2 to carbon monoxide, formate, and oxalate ions using a redox-active phenazine-based two-dimensional covalent organic framework (Phen-COF) and its phenazine monomer. Under similar irradiation conditions, Phen-COF produced 2.
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