The surface atomic coordination and arrangement largely determine photocatalytic properties. Whereas, the intrinsic impact of surface microstructures on the reaction mechanism and pathway is still unclear. Herein, via constructing N-doped BiOCO photocatalysts with diverse exposed facets, (1 1 0) and (0 0 1) facet, we testify that the pivotal roles of crystal facet and doping effect on the intermediate production and reactivity for photocatalytic nitric oxide (NO) abatement. The photoreactivity of N-doped BiOCO is documented to be higher than that of the pure samples because of the enhanced light absorption and charge transfer. Further in situ probing experiments and theoretical calculations verify that the unique adsorption patterns and activated intermediates on the (1 1 0) facet facilitate the formation of final products and inhibit the generation of toxic NO by-product in terms of thermodynamics. More importantly, we found that the selective and nonselective oxidation processes are emerged over (1 1 0) and (0 0 1) facets of BiOCO, respectively.
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http://dx.doi.org/10.1016/j.jcis.2021.07.018 | DOI Listing |
Sci Adv
January 2025
Department of Structural Biochemistry, Max Planck Institute of Molecular Physiology, Otto-Hahn-Str. 11, 44227 Dortmund, Germany.
Tc toxins are pore-forming virulence factors of many pathogenic bacteria. Following pH-induced conformational changes, they perforate the target membrane like a syringe to translocate toxic enzymes into a cell. Although this complex transformation has been structurally well studied, the reaction pathway and the resulting temporal evolution have remained elusive.
View Article and Find Full Text PDFPLoS One
January 2025
Department of Sport Studies, Faculty of Education Studies, Universiti Putra Malaysia, Selangor, Malaysia.
Introduction: Mental fatigue, a psychobiological state induced by prolonged and sustained cognitive tasks, impairs both cognitive and physical performance. Several studies have investigated strategies to counteract mental fatigue. However, potential health risks and contextual restrictions often limit these strategies, which hinder their practical application.
View Article and Find Full Text PDFJ Phys Chem A
January 2025
Liaoning Key Laboratory of Manufacturing System and Logistics Optimization, Shenyang 110819, China.
Artificial intelligence technology has introduced a new research paradigm into the fields of quantum chemistry and materials science, leading to numerous studies that utilize machine learning methods to predict molecular properties. We contend that an exemplary deep learning model should not only achieve high-precision predictions of molecular properties but also incorporate guidance from physical mechanisms. Here, we propose a framework for predicting molecular properties based on data-driven electron density images, referred to as D3-ImgNet.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
January 2025
Department Chemical and Food Engineering, UFSC, Florianópolis, 88040-900, SC, Brazil.
Produced water management is a significant challenge for the oil and gas industry. Due to the large volumes and complex composition of this water, treatment requires special attention, resulting in high costs for companies in the sector. Naphthenic acids, known for their recalcitrance, add a layer of complexity to the treatment process.
View Article and Find Full Text PDFJ Mol Model
January 2025
Laboratorio de Química Teórica Computacional (QTC), Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, Avenida Vicuña Mackenna 4860, 7820436, Santiago de Chile, Chile.
Context: Dopamine -monooxygenase (D M) is an essential enzyme in the organism that regioselectively converts dopamine into R-norepinephrine, the key step of the reaction, studied in this paper, is a hydrogen atom transfer (HAT) from dopamine to a superoxo complex on D M, forming a hydroperoxo intermediate and dopamine radical. It was found that the formation of a hydrogen bond between dopamine and the D M catalyst strengthens the substrate-enzyme interaction and facilitates the HAT which takes place selectively to give the desired enantiomeric form of the product. Six reactions leading to the hydroperoxo intermediate were analyzed in detail using theoretical and computational tools in order to identify the most probable reaction mechanism.
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