Tunable synthesis of atomic one-dimensional V<sub>x</sub>Te<sub>y</sub> magnets within single-walled carbon nanotubes.
basic_science · Level V
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- Record sourced from PubMed, PMID 40628742.
- Also identified by DOI 10.1038/s41467-025-61591-7 and PMC identifier 12238426.
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Abstract
The unstable configurations and uncontrollable stoichiometric ratios of atomically-thick one-dimensional (1D) magnets pose challenges for practical applications. Here, we employ a spatially confined domain strategy to obtain 1D vanadium tellurides (V<sub>x</sub>Te<sub>y</sub>) with distinctive stoichiometry within single-walled carbon nanotubes (SWCNTs). Confined by SWCNTs with different inner diameters, three unconventional air-stable V<sub>x</sub>Te<sub>y</sub> can be generated: 1D 1H-VTe<sub>2</sub>, V<sub>6</sub>Te<sub>6</sub>, and VTe<sub>3</sub>. Atomically resolved electron microscopy systematically unveils the conformational distributions of these three phases inside SWCNTs. Density functional theory (DFT) calculations indicate that these diverse V<sub>x</sub>Te<sub>y</sub> phases exhibit different intrinsic electronic structures, which correspond to ferromagnetic, antiferromagnetic, and non-magnetic properties. Furthermore, the magnetic response and magnetic anisotropy of the 1D V<sub>x</sub>Te<sub>y</sub>@SWCNTs assembly are experimentally confirmed. This work highlights the preparation of air-stable atomic 1D magnets, offering promising solutions for the design of next-generation spintronic devices.