To investigate the reactions of oxygen atoms with ethene and silane in a crossed-beam condition, we developed a stable, highly intense, and short-pulsed source of atomic oxygen with a transient high-voltage discharge. Mixtures of O(2) and He served as discharge media. Utilizing a crossed molecular-beam apparatus and direct vacuum-ultraviolet ionization, we measured the temporal profiles of oxygen atoms and the time-of-flight spectra of reaction products. With O(2) 3% seeded in He as a discharge medium, oxygen atoms might have a full width as small as 13.5 micros at half maximum at a location 193 mm downstream from the discharge region. Most population of oxygen atoms is in the ground state (3)P but some in the first excited state (1)D, depending on the concentration of precursor O(2). This discharge device analogously generates carbon, nitrogen, and fluorine atoms from precursors CO, N(2), and F(2), respectively.
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http://dx.doi.org/10.1063/1.2772090 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
East China University of Science and Technology, Key Laboratory for Advanced Materials and Institute of Fine Chemicals, 130 Meilong Road, 200237, Shanghai, CHINA.
Nanoconfinement at the interface of heterogeneous Fenton-like catalysts offers promising avenues for advancing oxidation processes in water purification. Herein, we introduce a template-free strategy for synthesizing nanoconfined catalysts from municipal sludge (S-NCCs), specifically engineered to optimize reactive oxygen species (ROS) generation and utilization for rapid pollutant degradation. Using selective hydrofluoric acid corrosion, we create an architecture that confines atomically dispersed Fe centers within a micro-mesoporous carbon matrix in situ.
View Article and Find Full Text PDFSmall
January 2025
Department of Energy and Materials Engineering, Dongguk University-Seoul, Seoul, 04620, South Korea.
The MXene, which is usually transition metal carbide, nitride, and carbonitride, is one of the emerging family of 2D materials, exhibiting considerable potential across various research areas. Despite theoretical versatility, practical application of MXene is prohibited due to its spontaneous oxidative degradation. This review meticulously discusses the factors influencing the oxidation of MXenes, considering both thermodynamic and kinetic point of view.
View Article and Find Full Text PDFAdv Mater
January 2025
Shenzhen Key Laboratory of Energy Electrocatalytic Materials, Guangdong Provincial Key Laboratory of New Energy Materials Service Safety, College of Materials Science and Engineering, Shenzhen University, Shenzhen, Guangdong, 518055, P. R. China.
Engineering nanomaterials at single-atomic sites can enable unprecedented catalytic properties for broad applications, yet it remains challenging to do so on RuO-based electrocatalysts for proton exchange membrane water electrolyzer (PEMWE). Herein, the rational design and construction of Bi-RuO single-atom alloy oxide (SAAO) are presented to boost acidic oxygen evolution reaction (OER), via phase engineering a novel hexagonal close packed (hcp) RuBi single-atom alloy. This Bi-RuO SAAO electrocatalyst exhibits a low overpotential of 192 mV and superb stability over 650 h at 10 mA cm, enabling a practical PEMWE that needs only 1.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Chang Chun Institute of Applied Chemistry Chinese Academy of Sciences, State Key Laboratory of Electroanalytical Chemistry, 5625 Renmin Street, 130022, Changchun, CHINA.
Single-atom catalysts (SACs) with high metal loadings are highly desirable but still challenging for large scale synthesis. Here we report a new technique named as dry-solid-electrochemical synthesis (DSES) for a general large-scale synthesis of SACs with high metal loadings in an energy-conservation and environment-friendly way. With it, a series of pure carbon-supported metal SACs (Platinum up to 35.
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January 2025
Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
Nitrogen doping emerges as a potent approach to enhance the oxidase-like activity of carbon nanozymes. However, the unclear knowledge of the active nitrogen species within nitrogen-doped carbon nanozymes hinders the advancement of high-performance carbon nanozymes. Herein, a group of nitrogen-doped carbon (N/C) nanozymes with controllable nitrogen dopants are successfully synthesized via a dicyandiamide-assisted pyrolysis method.
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