Magneto-ionics allows for tunable control of magnetism by voltage-driven transport of ions, traditionally oxygen or lithium and, more recently, hydrogen, fluorine, or nitrogen. Here, magneto-ionic effects in single-layer iron nitride films are demonstrated, and their performance is evaluated at room temperature and compared with previously studied cobalt nitrides. Iron nitrides require increased activation energy and, under high bias, exhibit more modest rates of magneto-ionic motion than cobalt nitrides. Ab initio calculations reveal that, based on the atomic bonding strength, the critical field required to induce nitrogen-ion motion is higher in iron nitrides (≈6.6 V nm) than in cobalt nitrides (≈5.3 V nm). Nonetheless, under large bias (i.e., well above the magneto-ionic onset and, thus, when magneto-ionics is fully activated), iron nitride films exhibit enhanced coercivity and larger generated saturation magnetization, surpassing many of the features of cobalt nitrides. The microstructural effects responsible for these enhanced magneto-ionic effects are discussed. These results open up the potential integration of magneto-ionics in existing nitride semiconductor materials in view of advanced memory system architectures.
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http://dx.doi.org/10.1021/acsami.1c06138 | DOI Listing |
J Colloid Interface Sci
December 2024
School of Materials Science & Engineering, School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013, PR China; Zotye Automobile Co., Ltd, Jinhua 321399, PR China. Electronic address:
Biosensors (Basel)
December 2024
Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, No. 174, Shapingba Main Street, Chongqing 400030, China.
In this study, we have proposed an electrochemiluminescence (ECL) signal amplification system which is based on two-dimensional (2D) flower-like CdS@Co/Mo-MOF composites as a co-reaction accelerator of the g-CN/SO system for ultrasensitive detection of chlorpromazine hydrochloride (CPH). Specifically, the 2D flower-like Co/Mo-MOF with mesoporous alleviated the aggregation of CdS NPs while simultaneously fostering reactant-active site contact and improving the reactant-product transport rate. This allowed the material to act as a novel co-reaction accelerator, speeding up the transformation of the SO into SO and enhancing the cathodic ECL emission of g-CN.
View Article and Find Full Text PDFChemistry
December 2024
Lanzhou University, College of Chemistry and Chemical Engineering, Lanzhou Tianshui south street 222, 730000, Lanzhou, CHINA.
Dual single-atom catalysts have attracted considerable research interest due to their higher metal atom loading and more flexible active sites compared to single-atom catalysts (SACs). We pioneered the one-step synthesis of sheets copper-cobalt graphitic carbon nitride dual single-atom (S-Cu/Co-g-C3N4) using folding fan-shaped aluminum foil as a template, and used them as catalysts in the epoxidation of styrene respectively. Through XAFS(X-ray Absorption Fine Structure) and other characterizations, it is found that Cu and Co single atoms are stabilized separately on g-C3N4 via coordination with nitrogen (N), hindered the ordered growth of sheets, and formed more pore structures, which not only increased more catalytically active sites, but also effectively prevented the flakes re-aggregate during the catalytic process.
View Article and Find Full Text PDFJ Synchrotron Radiat
January 2025
Physikalisch-Technische Bundesanstalt, Abbestraße 2-12, Berlin, Germany.
This paper introduces a novel slit-less wavelength-dispersive spectrometer design that incorporates a single-bounce monocapillary with the goal of positioning the sample directly on the Rowland circle, thereby eliminating the need for a traditional entrance slit. This configuration enhances photon throughput while preserving energy resolution, demonstrated in comparative measurements on boron nitride and different lithium nickel manganese cobalt oxide cathodes. A common alternative to an entrance slit for limiting the source size on the Rowland circle is a customized design of the beamline involving a focusing optics unit consisting of two Kirkpatrick-Baez mirrors close to the end station.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Research Institute of Photocatalysis, State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou, 350116, China.
H and O evolutions occur simultaneously for conventional particulate photocatalytic overall water splitting (PPOWS), leading to a significant backward reaction and the formation of an explosive H/O gas mixture. This is an issue that must be addressed prior to industrialization of PPOWS. Here, a convenient, cost-effective, and scalable concept is introduced to uncouple hydrogen and oxygen production for PPOWS.
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