A 2D heavy fermion CePb kagome material on silicon: emergence of unique spin polarized states for spintronics
We report on the successful synthesis of a 2D atomically thin heavy-fermion CePb 3 kagome compound on a Si(111) surface. Growth and morphology were controlled and characterized through scanning tunneling microscopy observations revealing the high crystalline quality of the sample. Angle-resolved pho...
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Veröffentlicht in: | Nanoscale 2022-10, Vol.14 (39), p.14732-1474 |
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Zusammenfassung: | We report on the successful synthesis of a 2D atomically thin heavy-fermion CePb
3
kagome compound on a Si(111) surface. Growth and morphology were controlled and characterized through scanning tunneling microscopy observations revealing the high crystalline quality of the sample. Angle-resolved photoelectron spectroscopy measurements revealed the giant highly-anisotropic Rashba-like spin splitting of the surface states and semi-metallic character of the spectrum. According to the DFT calculations, the occupied hole and unoccupied electron states with huge spin-orbit splitting and out-of-plane spin polarization reside at the M&cmb.macr; points near the Fermi level
E
F
, which is 100 meV above the experimental one. The out-of-plane FM magnetization was found to be preferred with Ce spin and orbital magnetic momenta values of 0.895
μ
B
and −0.840
μ
B
, respectively. The spin-split states near
E
F
are primarily formed by Pb p
xy
orbitals with the admixing of Ce d and f electrons due to the Ce f-d hybridization acquired asymmetry with respect to the sign of
k
. The observed electronic structure of the CePb
3
/Si(111)√3 × √3 system is rather unique and in the hole-doped state, like in our experiment, can be enabled in the tunable spin current regime, which makes it a prospective 2D material for spintronic applications.
We report on the successful synthesis of a 2D atomically thin heavy-fermion CePb
3
kagome compound on a Si(111) surface, which holds intriguing spin-polarized states relevant for spintronic applications. |
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ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d2nr04280k |