Oct 2026· Advancement of science· 0 citations· 52 references
Medicine
Abstract
ABSTRACT Transition‐metal dichalcogenides provide a versatile platform for the intercalation of magnetic ions in their van der Waals gaps, enabling tuning of correlated electronic and magnetic states. Despite extensive studies on sulfide‐based systems, Cr x NbSe2 remains poorly understood due to scarcity of single‐crystals and uncertainties in structural analyses leading to contradictory reports on its magnetic behavior. Here, high‐quality single crystals of Cr1/4NbSe2 via chemical vapor transport were synthesized, along with comprehensive investigation of chemical, structural, electronic, optical, electrical, and magnetic properties, supported by density‐functional theory calculations, presented for the first time. Single crystal x‐ray diffraction, scanning transmission electron microscopy, and selected area electron diffraction reveal ordered Cr intercalation forming a centrosymmetric 2 × 2 superlattice with hexagonal symmetry P63/mmc. Optical reflectivity indicates an enhanced electron scattering rate. DFT calculations predict antiferromagnetic ground state induced by Cr intercalation. Consistently, SQUID magnetometry and specific heat measurements hint a correlated antiferromagnetic state at T N ≈ 107 K, while resistivity measurements show metallic transport, with no signatures of superconductivity. Electron spin resonance suggests weak internal field which possibly arise from subtle magnetic anisotropy, undetectable in angle‐resolved magnetometry. These findings resolve longstanding inconsistencies and establish Cr1/4NbSe2 as a benchmark vdW antiferromagnet for next‐generation spintronic and quantum materials.
Dual intercalation provides an effective crystal-chemical route to tune magnetic interactions and functional transport properties in layered dichalcogenides. Here, we grow dual-intercalated (Fe,Cr)1/3NbS2 single crystals by chemical vapor transport and establish the structure-property relationships through single-cryst...
Ming-Hui Gao, Dian-Wei Luo, Kai-Ying Yang et al.· Journal of Physical Chemistr...· 0 citations
Layered transition‐metal dichalcogenides (TMDs) have emerged as an incipient class of low‐dimensional quantum materials owing to their highly tunable electronic, optical, magnetic, and catalytic properties. In recent years, controlled electronic modulation through substitution, intercalation, surface doping, and inters...
Z. Urrehman· Physica Status Solidi (a)· 0 citations
Transition metal ditellurides exhibit structural and electronic properties distinct from their selenide and sulfide counterparts, including the stabilization of multiple charge density wave (CDW) phases. Within the niobium compound family, notable differences in structure are also observed: bulk NbTe2 crystallizes in t...
Noor Ul Ain, A. Amiri, F. Calleja et al.· ACS Nano· 0 citations
Two-dimensional van der Waals antiferromagnets have emerged as a promising platform for low-dimensional spintronics. NiPS3 is a representative system because of its negligible stray fields and ultrafast spin dynamics. However, the relationship between local structural evolution and the establishment of long-range ant...
Si-Yu Wang, Lin Ma, Dan-Min Liu et al.· Inorganic Chemistry· 0 citations
Cr1+δTe2, a family among two-dimensional (2D) van der Waals (vdW) transition-metal dichalcogenides, has garnered significant interest owing to its tunable structural, electrical, and magnetic properties controlled by the concentration of self-intercalated Cr atoms. Among various external stimuli, pressure provides an...
S. Rastogi, U. Dutta, Ajit K. Jena et al.· ACS Applied Electronic Mater...· 0 citations
Electronic structure, local bonding, and magnetic order are intimately coupled in correlated antiperovskites, making it challenging to distinguish the contributions of individual crystallographic sites to their collective properties. Here, we combine element-specific X-ray spectroscopy, temperature-dependent X-ray abso...
Aryan Keshri, Sourav Chowdhury, Naveen Goyal et al.· Journal of the American Chem...· 0 citations
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