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Spin-phonon coupling and magnetic transition in an organic molecule intercalated Cr2Ge2Te6
Published
Author(s)
Angela R. Hight Walker, Thuc Mai, Adam Biacchi
Abstract
The manipulation of spin-phonon coupling in both formations and explorations of magnetism in two-dimensional van der Waals ferromagnetic semiconductors facilitates unprecedented prospects for spintronic devices. The interlayer engineering with spin-phonon coupling promises for controllable magnetism via organic cation intercalation. Here, spectroscopic evidences reveal the intercalation effect on the intrinsic magnetic and electronic transitions in quasi-two-dimensional Cr2Ge2Te6 using tetrabutyl ammonium (TBA+) as the intercalant. The temperature-evolution of Raman modes E_g^3 and A_g^1, along with the magnetization measurements, unambiguously captures the enhancement of the ferromagnetic Curie temperature in the intercalated heterostructure. Moreover, the E_g^4 mode highlights the increased effect of spin-phonon interaction in magnetic order-induced lattice distortion. Combined with the first-principle calculations, we observed a substantial number of electrons transferred from TBA+ to Cr through the interface. The interplay between spin-phonon coupling and magnetic ordering in van der Waals magnets appeals for further understanding of the manipulation of magnetism in layered heterostructures.
Hight Walker, A.
, Mai, T.
and Biacchi, A.
(2024),
Spin-phonon coupling and magnetic transition in an organic molecule intercalated Cr2Ge2Te6, Nano Letters, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=958059
(Accessed October 13, 2025)