This work reports an experimental study on an antiferromagnetic honeycomb lattice of MnPS that couples the valley degree of freedom to a macroscopic antiferromagnetic order. The crystal structure of MnPS is identified by high-resolution scanning transmission electron microscopy. Layer-dependent angle-resolved polarized Raman fingerprints of the MnPS crystal are obtained, and the Raman peak at 383 cm exhibits 100% polarity. Temperature dependences of anisotropic magnetic susceptibility of the MnPS crystal are measured in a superconducting quantum interference device. Anisotropic behaviors of the magnetic moment are explored on the basis of the mean field approximation model. Ambipolar electronic conducting channels in MnPS are realized by the liquid gating technique. The conducting channel of MnPS offers a platform for exploring the spin/valleytronics and magnetic orders in 2D limitation.
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http://dx.doi.org/10.1021/acsnano.7b05856 | DOI Listing |
Front Chem
December 2024
Research Center for Macromolecules and Biomaterials, National Institute for Materials Science (NIMS), Tsukuba, Japan.
Although the Diels-Alder reaction (DA) has garnered significant attention due to its numerous advantages, its long reaction time is a drawback. Herein, we investigated the effects of polarity difference on DA using Layer-by-Layer (LbL) films comprising polycationic polyallylamine hydrochloride and polyanionic poly (styrenesulfonic acid-co-furfuryl methacrylate) [poly (SS--FMA)] as the reaction environment. First, furan composition in poly (SS--FMA) was adjusted to be 19 mol% to achieve good water solubility and layer deposition.
View Article and Find Full Text PDFIn this work, 11-indeno[1,2-]quinoxalin-11-one (IQ), 7-nitro-11-indeno[1,2-]quinoxalin-11-one (NIQ), and 7-chloro-11-indeno[1,2-]quinoxalin-11-one (CIQ) as indenoquinoxalines (IQPs) and 7-nitro-2'-(4-nitrophenyl)-5',6',7',7a'-tetrahydrospiro[indeno[1,2-]quinoxaline-11,3'-pyrrolizine]-1',1'(2')-dicarbonitrile (SIQPNO) spiroheterocyclics were synthesized. These molecules photocatalytically reduced methylene blue (MB), methyl orange (MO), brilliant blue R (BBR), and Rhodamine B (RhB) in aqueous acetonitrile (aq-ACN) under sunlight (SL) for the first time. The IQPs and SIQPNO with a lanthanide graphene oxide template (LGT) of lanthanide sulfide nanorods (LnS, CeS, TbS, and HoS) photocatalytically reduced the dyes.
View Article and Find Full Text PDFSmall
December 2024
Institute of Physical and Theoretical Chemistry, Graz University of Technology, Stremayrgasse 9, Graz, 8010, Austria.
The one-pot synthesis of multicomponent hydrogen-bonded organic framework (HOF) biocomposites is reported. The co-immoblization of enzymes and magnetic nanoparticles (MNPs) into the HOF crystals yielded biocatalysts (MNPs-enzyme@BioHOF-1) with dynamic localization properties. Using a permanent magnet, it is possible to separate the MNPs-enzyme@BioHOF-1 particles from a solution.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
November 2024
Department of Inorganic Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech Republic.
ACS Appl Mater Interfaces
December 2024
Jiujiang Innovation Center of Biosensor Technology and Application, School of Medical Sciences, Jiujiang University, Jiujiang, Jiangxi 332005, P. R. China.
While noble metal nanoparticles (MNPs) exhibit remarkable performance in heterogeneous catalysis and their incorporation into crystalline materials can fully exploit the combined advantages of both, achieving introduction of nanoclusters during material crystallization, precisely controlling their interactions, and facilitating catalyst recovery remain significant challenges. In this study, Au NPs, Pt NPs, and Pd NPs are supported on magnetic FeO, enabling the modulation of the electronic states of MNPs by adjusting the introduction method. Notably, the catalysts (Pt/FeO, Au/FeO, and Pd/FeO) demonstrate excellent activity in chemoselective reactions: cinnamaldehyde (CAL) hydrogenation (turnover number: 20,135 h), nitrobenzene hydrogenation (with 99.
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