Strain-Induced Growth of Twisted Bilayers during the Coalescence of Monolayer MoS2 Crystals
Source abstract
Abstract
Tailoring the grain boundaries (GBs) and twist angles between two-dimensional (2D) crystals are two crucial synthetic challenges to deterministically enable envisioned applications such as moiré excitons, emerging magnetism, or single-photon emission. Here, we reveal how twisted 2D bilayers can be synthesized from the collision and coalescence of two growing monolayer MoS 2 crystals during chemical vapor deposition. The twisted bilayer (TB) moiré angles are found to preserve the misorientation angle (θ) of the colliding crystals. The shapes of the TB regions are rationalized by a kink propagation model that predicts the GB formed by the coalescing crystals. Optical spectroscopy measurements reveal a θ-dependent long-range strain in crystals with stitched grain boundaries and a sharp (θ > 20°) threshold for the appearance of TBs, which relieves this strain. Reactive molecular dynamics simulations explain this strain from the continued growth of the crystals during coalescence due to the insertion of atoms at unsaturated defects along the GB, a process that self-terminates when the defects become saturated. The simulations also reproduce atomic-resolution electron microscopy observations of faceting along the GB, which is shown to arise from the growth-induced long-range strain. These facets align with the axes of the colliding crystals to provide favorable nucleation sites for second-layer growth of a TB with twist angles that preserve the misorientation angle θ. This interplay between strain generation and aligned nucleation provides a synthetic pathway for the growth of TBs with deterministic angles.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Neural Networks and Applications · Distributed Control Multi-Agent Systems
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States
Computational Sciences and Engineering Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States
Department of Materials Science and Engineering, University of Tennessee, Knoxville, Tennessee 37996, United States
Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States
Funding
Basic Energy Sciences · Laboratory Directed Research and Development
References (53)
Show source-provided references
1. 10.1038/nature2616010.1038/nature26160 ↗
2. 10.1126/science.aaw378010.1126/science.aaw3780 ↗
3. 10.1038/s41586-020-2049-710.1038/s41586-020-2049-7 ↗
4. 10.1038/s41586-019-0975-z10.1038/s41586-019-0975-z ↗
5. 10.1038/s41586-019-0957-110.1038/s41586-019-0957-1 ↗
6. 10.1126/sciadv.aba852610.1126/sciadv.aba8526 ↗
7. 10.1126/sciadv.170169610.1126/sciadv.1701696 ↗
8. 10.1038/s41586-019-0976-y10.1038/s41586-019-0976-y ↗
9. 10.1021/acsnano.5b0780710.1021/acsnano.5b07807 ↗
10. 10.1021/acs.nanolett.5b0501510.1021/acs.nanolett.5b05015 ↗
11. 10.1002/aelm.20160029810.1002/aelm.201600298 ↗
12. 10.1038/s41586-019-1308-y10.1038/s41586-019-1308-y ↗
13. 10.1126/science.aar841210.1126/science.aar8412 ↗
14. 10.1038/s41467-019-13488-510.1038/s41467-019-13488-5 ↗
15. 10.1038/s41586-019-1147-x10.1038/s41586-019-1147-x ↗
16. 10.1021/acs.chemmater.9b0377910.1021/acs.chemmater.9b03779 ↗
17. 10.1021/nl502961e10.1021/nl502961e ↗
18. 10.1021/jacs.6b1255910.1021/jacs.6b12559 ↗
19. 10.1039/C6SC04535A10.1039/C6SC04535A ↗
20. 10.1021/acsnano.6b0831510.1021/acsnano.6b08315 ↗
21. 10.1103/PhysRevMaterials.3.01400410.1103/PhysRevMaterials.3.014004 ↗
22. 10.1038/nmat363310.1038/nmat3633 ↗
23. 10.1038/nmat367310.1038/nmat3673 ↗
24. 10.1039/C8NR02280A10.1039/C8NR02280A ↗
25. 10.1021/nl304004210.1021/nl3040042 ↗
26. 10.1021/nn302099q10.1021/nn302099q ↗
27. 10.1021/acsami.9b1565410.1021/acsami.9b15654 ↗
28. 10.1038/ncomms1042610.1038/ncomms10426 ↗
29. 10.1021/nl400747910.1021/nl4007479 ↗
30. 10.1126/sciadv.aav402810.1126/sciadv.aav4028 ↗
31. 10.1021/nn500228r10.1021/nn500228r ↗
32. 10.1063/1.505196510.1063/1.5051965 ↗
33. 10.1038/s41467-018-02830-y10.1038/s41467-018-02830-y ↗
34. 10.1002/smll.20120287610.1002/smll.201202876 ↗
35. 10.1109/JMEMS.2018.287798310.1109/JMEMS.2018.2877983 ↗
36. 10.1103/PhysRevB.87.08130710.1103/PhysRevB.87.081307 ↗
37. 10.1021/nl401474810.1021/nl4014748 ↗
38. 10.1038/s41467-017-00516-510.1038/s41467-017-00516-5 ↗
39. 10.1021/acsami.8b2139110.1021/acsami.8b21391 ↗
40. 10.1063/1.173603610.1063/1.1736036 ↗
41. 10.1007/BF0281326210.1007/BF02813262 ↗
42. 10.1103/PhysRev.78.27510.1103/PhysRev.78.275 ↗
43. 10.1063/1.135256310.1063/1.1352563 ↗
44. 10.1557/mrs2002.1510.1557/mrs2002.15 ↗
45. 10.1103/PhysRevLett.88.15610310.1103/PhysRevLett.88.156103 ↗
46. 10.1021/acsnano.7b0368110.1021/acsnano.7b03681 ↗
47. 10.1006/jcph.1995.103910.1006/jcph.1995.1039 ↗
48. 10.1103/PhysRevB.79.24511010.1103/PhysRevB.79.245110 ↗
49. 10.1088/0965-0393/21/4/04500310.1088/0965-0393/21/4/045003 ↗
50. 10.1021/acsnano.8b0071210.1021/acsnano.8b00712 ↗
51. 10.1038/nmat503810.1038/nmat5038 ↗
52. 10.1021/acs.nanolett.9b0182910.1021/acs.nanolett.9b01829 ↗
53. 10.1038/s41567-020-0958-x10.1038/s41567-020-0958-x ↗