One of the greatest challenges in the enhancement of the electrical properties of conductive mayenite [CaAlO](4e) (hereinafter C12A7:e) is the design of a more suitable/simple synthesis strategy that can be employed to obtain the required properties such as excellent stable electrical conductivity, a high electron concentration, outstanding mobility, and an exceptionally large surface area. Therefore, to synthesize C12A7:e in the metallic state, we proposed a facile, direct synthesis strategy based on an optimized sol-gel combustion method under a nitrogen gas environment using the low-cost precursors Ca(NO)·4HO and Al(NO)·9HO. Using this developed strategy, we successfully synthesized moderately conductive nanoscale C12A7:e powder, but with unexpected carbon components (reduced graphene oxide (rGO) and/or graphene oxide (GO)). The synthesized C12A7:e composite at room temperature has an electrical conductivity of about 21 S cm, a high electron concentration of approximately 1.5 × 10 cm, and a maximum specific surface area of 265 m g. Probably, the synthesized rGO was coated on nanocage C12A7:e particles. In general, the C12A7:e electride is sensitive to the environment (especially to oxygen and moisture) and protected by an rGO coating on C12A7:e particles, which also enhances the mobility and keeps the conductivity of C12A7:e electride stable over a long period. Doped mayenite electride exhibits a conductivity that is strongly dependent on the substitution level. The conductivity of gallium-doped mayenite electride increases with the doping level and has a maximum value of 270 S cm, which for the first time has been reported for the stable C12A7:e electride. In the case of Si-substituted calcium aluminate, the conductivity has a maximum value of 222 S cm at room temperature.
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http://dx.doi.org/10.1039/c7dt04543c | DOI Listing |
Adv Mater
January 2025
Department of Materials Science and Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
Interstitial quasi-atomic electrons (IQEs) in the quantized energy levels of positively charged cavities possess a substantial own magnetic moment and control the magnetism of crystalline electrides depending on the interaction with surrounding cations. However, weak spin-orbit coupling and gentle exchange interaction restricted by the IQEs preclude a large magnetic anisotropic, remaining a challenge for a hard magnetism. It is reported that 2D [ReC]·2e electrides (Re = Er, Ho, Dy, and Tb) show the permanent magnetism in a ferrimagnetic ground state, mimicking the ferrites composed of magnetic sublattices with different spin polarizations.
View Article and Find Full Text PDFAdv Mater
December 2024
National Research Center "Kurchatov Institute", Kurchatov Sq. 1, Moscow, 123182, Russia.
2D magnets have emerged as a class of materials highly promising for studies of quantum phenomena and applications in ultra-compact spintronics. Current research aims at design of 2D magnets with particular functional properties. A formidable challenge is to produce metallic monolayers: the material landscape of layered magnetic systems is strongly dominated by insulators; rare metallic magnets, such as FeGeTe, become insulating as they approach the monolayer limit.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
State Key Laboratory of Solidification Processing, School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an 710072, China.
Two-dimensional (2D) nanomaterials have garnered extensive attention owing to their unique properties and versatile application. Here, a family of 2D rare-earth metal phosphides (MP, M = Sc, Y, La) and their derivatives MPOT (T = F, OH) is developed to find their topological and electronic properties on the basis of density functional theory simulations. We show that the 2D MP compounds are most possibly obtained from thermodynamically stable MInP by chemical exfoliation.
View Article and Find Full Text PDFInorg Chem
December 2024
Department of Chemistry and Biochemistry, Institute for Inorganic and Materials Chemistry, University of Cologne, Cologne 50939, Germany.
Crystalline Ba(CH) was obtained by the reaction of elemental barium dissolved in liquid ammonia, forming a blue electride, and acetylene (CH) injected into the reaction vial with the electride solution. From the colorless precipitate that was obtained after evaporation of the ammonia, the crystal structure of Ba(CH) was solved and refined using synchrotron powder diffraction data. It crystallizes in the trigonal space group 3̅1 (no.
View Article and Find Full Text PDFJ Am Chem Soc
October 2024
Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.
We explore the eclipsed stacking of a metal-organic Kagome lattice containing heavy-metal nodes. Our model is Pt(HIB), a hypothetical but viable member of a well-known family of hexaaminobenzene based metal-organic frameworks (MOFs). Applying space group theory, it is shown how molecular diradicals, brought into play by a noninnocent ligand, become topologically nontrivial bands when moving in a periodic potential.
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