Pith. sign in

REVIEW

Quantum-Confined Tunable Ferromagnetism on the Surface of a van der Waals Antiferromagnet NaCrTe2

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2410.14196 v1 pith:US5X7AAN submitted 2024-10-18 cond-mat.mtrl-sci cond-mat.str-el

Quantum-Confined Tunable Ferromagnetism on the Surface of a van der Waals Antiferromagnet NaCrTe2

classification cond-mat.mtrl-sci cond-mat.str-el
keywords surfacenacrte2quantum-confinedcrte2ferromagneticferromagnetismantiferromagnetband
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
0 comments
read the original abstract

The surface of three-dimensional materials provides an ideal and versatile platform to explore quantum-confined physics. Here, we systematically investigate the electronic structure of Na-intercalated CrTe2, a van der Waals antiferromagnet, using angle-resolved photoemission spectroscopy and ab-initio calculations. The measured band structure deviates from the calculation of bulk NaCrTe2 but agrees with that of ferromagnetic monolayer CrTe2. Consistently, we observe an unexpected exchange splitting of the band dispersions, persisting well above the N\'eel temperature of bulk NaCrTe2. We argue that NaCrTe2 features a quantum-confined 2D ferromagnetic state in the topmost surface layer due to strong ferromagnetic correlation in the CrTe2 layer. Moreover, the exchange splitting and the critical temperature can be controlled by surface doping of alkali-metal atoms, suggesting a feasible tunability of the surface ferromagnetism. Our work not only presents a simple platform to explore tunable 2D ferromagnetism but also provides important insights into the quantum-confined low-dimensional magnetic states.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.