范德瓦尔斯力
凝聚态物理
异质结
材料科学
物理
纳米技术
量子力学
分子
作者
Junho Choi,Christopher Lane,Jian–Xin Zhu,S. A. Crooker
出处
期刊:Nature Materials
[Springer Nature]
日期:2022-12-19
卷期号:22 (3): 305-310
被引量:17
标识
DOI:10.1038/s41563-022-01424-w
摘要
Magnetic proximity interactions between atomically thin semiconductors and two-dimensional magnets provide a means to manipulate spin and valley degrees of freedom in non-magnetic monolayers, without using applied magnetic fields1–3. In such van der Waals heterostructures, magnetic proximity interactions originate in the nanometre-scale coupling between spin-dependent electronic wavefunctions in the two materials, and typically their overall effect is regarded as an effective magnetic field acting on the semiconductor monolayer4–8. Here we demonstrate that magnetic proximity interactions in van der Waals heterostructures can in fact be markedly asymmetric. Valley-resolved reflection spectroscopy of MoSe2/CrBr3 van der Waals structures reveals strikingly different energy shifts in the K and K′ valleys of the MoSe2 due to ferromagnetism in the CrBr3 layer. Density functional calculations indicate that valley-asymmetric magnetic proximity interactions depend sensitively on the spin-dependent hybridization of overlapping bands and as such are likely a general feature of hybrid van der Waals structures. These studies suggest routes to control specific spin and valley states in monolayer semiconductors9,10. The authors demonstrate that magnetic proximity interactions in a hexagonal boron nitride-encapsulated MoSe2/CrBr3 van der Waals heterostructure have a striking difference in the two (K, K′) valleys of a monolayer MoSe2.
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