Phase-Dependent Magnetic Proximity Modulations on Valley Polarization and Splitting
Source abstract
Abstract
Proximate-induced magnetic interactions present a promising strategy for precise manipulation of valley degrees of freedom. Taking advantage of the splendid valleytronic platform of transition metal dichalcogenides, magnetic two-dimensional VSe 2 with different phases are introduced to intervene in the spin of electrons and modulate their valleytronic properties. When constructing the heterostructures, 1T-VSe 2 /WX 2 (X = S and Se) showcases significant improvement in the valley polarizations at room temperature, while 2H-VSe 2 /WX 2 exhibits superior performance at low temperatures and demonstrates heightened sensitivity to the external magnetic field. Simultaneously, considerable valley splitting with a large g eff factor up to −29.0 is observed in 2H-VSe 2 /WS 2, while it is negligible in 1T-VSe 2 /WX 2 . First-principles calculations reveal a phase-dependent magnetic proximity mechanism on the valleytronic modulations, which is dominated by interfacial charge transfer in 1T-VSe 2 /WX 2 and the proximity exchange field in 2H-VSe 2 /WX 2 heterostructures. The effective control over valley degrees of freedom will bridge the valleytronic physics and devices, rendering enormous potential in the field of valley quantum applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · Perovskite Materials and Applications · ZnO doping and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physics, Engineering Research Center for Micro-Nano Optoelectronic Materials and Devices of Ministry of Education, OSED, Fujian Provincial Key Laboratory of Semiconductor Materials and Applications, Xiamen University, Xiamen 361005, People’s Republic of China
Funding
Central University Basic Research Fund of China · Natural Science Foundation of Xiamen Municipality · National Natural Science Foundation of China
References (36)
Show source-provided references
1. 10.1038/s41565-019-0438-610.1038/s41565-019-0438-6 ↗
2. 10.1126/science.aav445010.1126/science.aav4450 ↗
3. 10.1002/adfm.20190141410.1002/adfm.201901414 ↗
4. 10.1021/acs.chemmater.9b0224310.1021/acs.chemmater.9b02243 ↗
5. 10.1007/s40843-022-2298-010.1007/s40843-022-2298-0 ↗
6. 10.1038/natrevmats.2017.3310.1038/natrevmats.2017.33 ↗
7. 10.1016/j.mattod.2016.10.00210.1016/j.mattod.2016.10.002 ↗
8. 10.1038/natrevmats.2016.5510.1038/natrevmats.2016.55 ↗
9. 10.1038/s41467-019-11966-410.1038/s41467-019-11966-4 ↗
10. 10.1039/C9TC04511B10.1039/C9TC04511B ↗
11. 10.1088/0022-3727/49/16/16510410.1088/0022-3727/49/16/165104 ↗
12. 10.1038/nnano.2017.6810.1038/nnano.2017.68 ↗
13. 10.1021/acsnano.7b0574310.1021/acsnano.7b05743 ↗
14. 10.1038/s41565-022-01115-210.1038/s41565-022-01115-2 ↗
15. 10.1126/sciadv.160311310.1126/sciadv.1603113 ↗
16. 10.1021/acsnano.1c0523210.1021/acsnano.1c05232 ↗
17. 10.1038/s41565-018-0063-910.1038/s41565-018-0063-9 ↗
18. 10.1021/acsami.0c0444910.1021/acsami.0c04449 ↗
19. 10.1038/s42005-022-01044-510.1038/s42005-022-01044-5 ↗
20. 10.1016/j.apsusc.2023.15711110.1016/j.apsusc.2023.157111 ↗
21. 10.1038/s41524-022-00932-210.1038/s41524-022-00932-2 ↗
22. 10.1016/j.apsusc.2022.15475410.1016/j.apsusc.2022.154754 ↗
23. 10.1002/smll.20120291910.1002/smll.201202919 ↗
24. 10.1039/c3nr03052k10.1039/c3nr03052k ↗
25. 10.1063/1.513503810.1063/1.5135038 ↗
26. 10.1007/s12274-022-4400-910.1007/s12274-022-4400-9 ↗
27. 10.1021/acs.nanolett.2c0413310.1021/acs.nanolett.2c04133 ↗
28. 10.1103/PhysRevB.90.16130210.1103/PhysRevB.90.161302 ↗
29. 10.1364/OE.39205210.1364/OE.392052 ↗
30. 10.1002/pssr.20151022410.1002/pssr.201510224 ↗
31. 10.1038/s42005-020-0377-410.1038/s42005-020-0377-4 ↗
32. 10.1038/nphys320110.1038/nphys3201 ↗
33. 10.1103/PhysRevB.92.12140310.1103/PhysRevB.92.121403 ↗
34. 10.1021/acsnano.0c0830510.1021/acsnano.0c08305 ↗
35. 10.1038/nnano.2014.15010.1038/nnano.2014.150 ↗
36. 10.1002/lpor.20220041610.1002/lpor.202200416 ↗