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Recognizing the substantial effects of carbon dioxide on human health and the environment, monitoring CO levels has become increasingly vital. Owing to energy constraints and the widespread application of CO gas sensors, it is important to design cost-effective, more efficient, and faster response CO gas sensors that operate at room temperature and involve a low-cost technique. This study aims to develop a cost-effective and efficient CO gas detector that functions at room temperature and uses less power than traditional high-temperature CO sensors. In this study, we achieved this by employing innovative CoO thin films with optimized spinel-structured p-type semiconductors through spin-coating, facilitated by Li and Na doping as well as Li/Na codoping. Doping with 3% Li/Na reduced the crystallite size from 92.4 to 8.03 nm and increased the band gap from 3.31 to 3.69 eV. At room temperature (30 °C), the sensor response improved significantly, increasing from 50% to 345.01% for 3% Li-CoO upon the addition of 3% Na at a concentration of 9990 ppm. This performance surpasses that of most metal-oxide-based CO sensors reported in the literature. Additionally, this optimized sensor demonstrated a very short response time of 18.8 s and a recovery time of 16.4 s at a CO concentration of 9990 ppm diluted with air. It outperformed other films in terms of sensitivity, stability, response and recovery times, and performance across a wide range of relative humidity levels (43-90%). The sensor exhibited superior selectivity for CO than for N, H, and NH. Overall, the 3% Li, Na-CoO sensor is well-suited for climate change mitigation and industrial applications.
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http://dx.doi.org/10.1039/d4ra06847e | 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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