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1,3-Butadiene (CH), the main raw material for producing important chemicals (nylon, synthetic resin, rubber), relies on petroleum cracking with intensive carbon emissions. The electrocatalytic dimeric hydrogenation of natural gas/coal-derived CH to CH provides a nonpetroleum pathway. However, CH, as a byproduct of CH hydrogenation, is usually neglected because of its very low Faradaic efficiency. Here, we theoretically and experimentally report a mechanism comprising acetylene dimerization and subsequent hydrogenation. The first dimerization process can be accelerated under appropriate coverage of acetylene and water. A ligand-modifying strategy is subsequently proposed to regulate the wettability of Cu nanoarrays to enable suitable coverages. The optimized 1-dodecanethiol-modified Cu nanoarrays deliver a 65.3% CH Faradaic efficiency at 100 mA cm. The CH formation kinetics become sluggish at the two ends of the surface CH/HO ratios, and moderate CH/HO coverage accelerates the C‒C coupling process to promote CH production. Moreover, life cycle assessment demonstrates its sustainability.
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http://dx.doi.org/10.1038/s41467-025-60881-4 | DOI Listing |
Angew Chem Int Ed Engl
August 2025
Institute of Molecular Plus, Department of Chemistry, School of Science, Tianjin University, Tianjin, 300072, China.
Electrocatalytic semihydrogenation of alkynes to alkenes with water at nearly industrial current densities is highly important. However, a low interfacial alkyne-water ratio leads to severe hydrogen evolution, making it extremely challenging to obtain alkenes with a high Faradaic efficiency (FE). Here, a strategy involving fluorine···π interaction-induced alkyne concentration and orderly arranged sulfonate-repelled interfacial water-cation is developed over commercial Nafion-modified palladium nanotips, enabling electrolysis of 2-methyl-3-buten-2-ol (MBE) with up to 83% FE under -100 mA cm.
View Article and Find Full Text PDFNat Commun
July 2025
Department of Chemistry, School of Science, Tianjin University, Tianjin, China.
1,3-Butadiene (CH), the main raw material for producing important chemicals (nylon, synthetic resin, rubber), relies on petroleum cracking with intensive carbon emissions. The electrocatalytic dimeric hydrogenation of natural gas/coal-derived CH to CH provides a nonpetroleum pathway. However, CH, as a byproduct of CH hydrogenation, is usually neglected because of its very low Faradaic efficiency.
View Article and Find Full Text PDFJ Phys Chem A
July 2025
Department of Materials Science and Engineering, Stanford University, 450 Jane Stanford Way, Stanford, California 94305, United States.
An open-source and modular Python package, Catalight, is developed and demonstrated to automate (photo)catalysis measurements. (Photo)catalysis experiments require studying several parameters to evaluate performance, including the temperature, gas flow rate and composition, illumination power, and spectral profile. Catalight orchestrates measurements over this complicated parameter space and systematically stores, analyzes, and visualizes the results.
View Article and Find Full Text PDFACS Chem Biol
July 2025
Biological Chemistry Department, David Geffen School of Medicine, UCLA, Los Angeles, California 90095, United States.
Cysteine residues play key roles in protein structure and function and can serve as targets for chemical probes and even drugs. Chemoproteomic studies have revealed that heightened cysteine reactivity toward electrophilic probes, such as iodoacetamide alkyne (IAA), is indicative of likely residue functionality. However, while the cysteine coverage of chemoproteomic studies has increased substantially, these methods still provide only a partial assessment of proteome-wide cysteine reactivity, with cysteines from low-abundance proteins and tough-to-detect peptides still largely refractory to chemoproteomic analysis.
View Article and Find Full Text PDFHydrosilylation of terminal alkenes and alkynes on the surfaces of hydrogen-terminated silicon nanoparticles (H-SiNPs) has provided a convenient approach toward tailoring surface chemistry. These reactions have traditionally required thermal, photochemical, or chemical activation and are not necessarily compatible with all substrates and particle sizes. Herein, we demonstrate that hydrosilylation on silicon nanoparticles (Si NPs) can be promoted at room temperature by exposing the reaction mixture to a standard ultrasonic bath.
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