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Wearable hydrogen (H) sensing is necessary to monitor the H leakage in its transportation and storage, of which ppm-concentration detection limit and fast response at room temperature are highly desired. Here, a wearable H sensing working at room temperature is developed with palladium and iron framework intermixed with reduced graphene oxide (rGO//Pd-Fe FW), which is synthesized by combined Pd-Fe cyanogel immobilized with graphene oxide as precursor and in situ reduction. As-prepared rGO//Pd-Fe FW is observed with porous FW structure composed of interconnected Pd-Fe nanoparticles, in which rGO is evenly intermixed. Beneficially, rGO//Pd-Fe FW exhibits 2 ppm low detection limit and 2 s fast response (1 v/v% H) at room temperature. Such excellent H sensing performance may be attributed to the synergistic effect of the optimized Pd-Fe FW's catalytic activity, boosted electron transfers between Pd hydride and rGO, and enriched adsorption sites over porous FW's surface. Practically, the perceptron learning algorithm combined with principal component analysis is conducted to identify the H leakage, and the wearable H sensing devices are built by integrating rGO//Pd-Fe FW over the paper and flexible printed circuit board with reliable sensing responses.
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http://dx.doi.org/10.1002/smll.202408117 | DOI Listing |
J Org Chem
September 2025
College of Chemistry and Pharmaceutical Engineering, Nanyang Normal University, Nanyang, Henan 473061, China.
A visible-light-induced cascade cyclization of isocyanobiaryls with hydrosilanes has been developed for the synthesis of 6-silylated phenanthridines. Readily available hydrosilanes were employed as silyl radical precursors under room-temperature conditions. The merits of the transformation include operational simplicity, mild conditions, high atom economy, and good functional group compatibility.
View Article and Find Full Text PDFLangmuir
September 2025
Product & Process Engineering, Department of Chemical Engineering, Faculty of Applied Sciences, Delft University of Technology, 2629 HZ Delft, The Netherlands.
Noble metal nanoparticles (NPs), particularly platinum (Pt), are widely used in heterogeneous catalysis due to their exceptional activity. However, controlling their size and preventing sintering during synthesis remains a major challenge, especially when aiming for high dispersion and stability on supports such as graphene. Atomic layer deposition (ALD) has emerged as a promising method to address these issues, yet conventional processes often lead to broad particle size distributions (PSDs).
View Article and Find Full Text PDFJ Am Soc Mass Spectrom
September 2025
Chemistry Department, Indiana University, 800 E Kirkwood Ave, Bloomington, Indiana 47405.
In charge detection mass spectrometry (CD-MS) ions are trapped in an electrostatic linear ion trap (ELIT) where they oscillate back and forth through a conducting cylinder. The oscillating ions induce a periodic charge separation that is detected by a charge sensitive amplifier (CSA) connected to the cylinder. The resulting time domain signal is analyzed using short-time Fourier transforms to give the mass-to-charge ratio and charge for each ion, which are then multiplied to give the mass.
View Article and Find Full Text PDFOrg Lett
September 2025
School of Molecular Sciences, The University of Western Australia, Crawley, WA 6009, Australia.
We report the synthesis of three nickel complexes based on Ni(NHC)[P(OR)](Ar)Cl and their application in C()-N cross-coupling reactions. Reactions involving secondary amines proceeded at room temperature, while anilines and primary alkyl amines coupled under mild heating. The reported complexes are air-stable as solids, operate at low catalytic loading, and do not require an exogenous ligand.
View Article and Find Full Text PDFLangmuir
September 2025
School of Light Industry Science and Engineering, Beijing Technology and Business University, Beijing 100048, People's Republic of China.
The study of the self-assembly of surfactants in aqueous solutions, though a traditional field, remains fascinating and full of novelty. In this article, the anionic perfluorodecanoic acid surfactant (PFA) is separately complexed with three hydroxyalkylamines (monoethanolamine (MEA), diethylamine (DEA), and triethanolamine (TEA)) in aqueous solutions. The transformation of aggregate morphologies from spherical unilamellar to nanotubes and then to spherical bilamellar is observed at room temperature, which is confirmed by cryo-transmission electron microscopy (cryo-TEM).
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