Reduced Fracture Anisotropy yet Enhanced Deformability of Multilayer MoS2 Straps
Source abstract
Abstract
The mechanical properties of two-dimensional transition metal dichalcogenides (2D TMDs), molybdenum disulfide (MoS 2 ) in particular, are crucial for their reliable applications in advanced flexible electronics and phototransistors. This study systematically investigated the influence of geometrical factors on MoS 2 ’s mechanical property and fracture behavior by performing in situ tensile tests on submicroscale strap specimens with different thicknesses ranging from 7 to 95 nm inside SEM and TEM. Results demonstrated a strong correlation between the apparent fracture strength and Young’s modulus of MoS 2 and the specimen thickness, where thinner samples exhibited a significantly elevated fracture strength and Young’s modulus. Moreover, a distinct mechanism transition in the fracture modes was revealed: in thin samples, cracks tend to propagate along the low surface energy ( 10 1 ¯ 0 ) plane, whereas in thick samples, crack paths comply with the plane stress distribution rule and reside on the ( 11 2 ¯ 0 ) principal stress plane, exhibiting reduced fracture anisotropy. Additionally, an interlayer sliding behavior was discovered as a mechanical energy dissipating mechanism to enhance the deformability of MoS 2 and retard rupture. These discoveries provide fundamental insights into the mechanical stability of MoS 2, boosting the development of high-performance 2D materials for flexible electronics and nanomechanical systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Graphene research and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physical Science and Technology
ShanghaiTech University
Shanghai Key Laboratory of High-resolution Electron Microscopy
Funding
Science and Technology Commission of Shanghai Municipality · School of Physical Science and Technology, ShanghaiTech University · National Natural Science Foundation of China
References (61)
Show source-provided references
1. 10.1126/science.110289610.1126/science.1102896 ↗
2. 10.1021/nl903963610.1021/nl9039636 ↗
3. 10.1038/nnano.2010.27910.1038/nnano.2010.279 ↗
4. 10.1038/nnano.2014.30910.1038/nnano.2014.309 ↗
5. 10.1039/C5CS00275C10.1039/C5CS00275C ↗
6. 10.1142/S021797921850148510.1142/S0217979218501485 ↗
7. 10.1021/acs.chemrev.0c0050510.1021/acs.chemrev.0c00505 ↗
8. 10.1016/j.mtchem.2022.10133310.1016/j.mtchem.2022.101333 ↗
9. 10.1109/IEDM.2012.647898010.1109/IEDM.2012.6478980 ↗
10. 10.1021/nl302015v10.1021/nl302015v ↗
11. 10.1126/science.aah469810.1126/science.aah4698 ↗
12. 10.1021/acs.nanolett.6b0273910.1021/acs.nanolett.6b02739 ↗
13. 10.1038/s41928-021-00566-010.1038/s41928-021-00566-0 ↗
14. 10.1002/adma.20220247210.1002/adma.202202472 ↗
15. 10.1007/s40820-023-01273-510.1007/s40820-023-01273-5 ↗
16. 10.1016/j.mattod.2016.10.00210.1016/j.mattod.2016.10.002 ↗
17. 10.1016/j.pmatsci.2018.03.00710.1016/j.pmatsci.2018.03.007 ↗
18. 10.1007/s42247-021-00241-210.1007/s42247-021-00241-2 ↗
19. 10.1021/jp111514610.1021/jp1115146 ↗
20. 10.1016/j.jmat.2015.03.00310.1016/j.jmat.2015.03.003 ↗
21. 10.3390/photonics201028810.3390/photonics2010288 ↗
22. 10.1016/j.jphotochemrev.2017.12.00210.1016/j.jphotochemrev.2017.12.002 ↗
23. 10.1016/j.psep.2018.06.02510.1016/j.psep.2018.06.025 ↗
24. 10.1002/chem.20180101810.1002/chem.201801018 ↗
25. 10.1063/1.503432010.1063/1.5034320 ↗
26. 10.1016/j.mtsust.2021.10007310.1016/j.mtsust.2021.100073 ↗
27. 10.1016/j.colsurfa.2020.12583610.1016/j.colsurfa.2020.125836 ↗
28. 10.1149/2162-8777/ac5a6f10.1149/2162-8777/ac5a6f ↗
29. 10.1021/accountsmr.0c0006310.1021/accountsmr.0c00063 ↗
30. 10.1103/PhysRevLett.78.214810.1103/PhysRevLett.78.2148 ↗
31. 10.1103/PhysRevB.76.06412010.1103/PhysRevB.76.064120 ↗
32. 10.1016/j.jmps.2024.10557910.1016/j.jmps.2024.105579 ↗
33. 10.1016/j.apmt.2018.12.01910.1016/j.apmt.2018.12.019 ↗
34. 10.1016/j.nanoso.2019.01.00610.1016/j.nanoso.2019.01.006 ↗
35. 10.1002/advs.20220070010.1002/advs.202200700 ↗
36. 10.1126/science.115799610.1126/science.1157996 ↗
37. 10.1021/nn203879f10.1021/nn203879f ↗
38. 10.1002/adma.20110396510.1002/adma.201103965 ↗
39. 10.1038/ncomms478210.1038/ncomms4782 ↗
40. 10.1002/adma.20160420110.1002/adma.201604201 ↗
41. 10.1038/s41467-019-14130-010.1038/s41467-019-14130-0 ↗
42. 10.1016/j.xcrp.2020.10017210.1016/j.xcrp.2020.100172 ↗
43. 10.1126/sciadv.abc228210.1126/sciadv.abc2282 ↗
44. 10.1016/j.matt.2021.01.00110.1016/j.matt.2021.01.001 ↗
45. 10.1038/s41586-021-03488-110.1038/s41586-021-03488-1 ↗
46. 10.1021/acs.nanolett.4c0120210.1021/acs.nanolett.4c01202 ↗
47. 10.1038/s41467-024-45657-610.1038/s41467-024-45657-6 ↗
48. 10.1021/nn506052d10.1021/nn506052d ↗
49. 10.1039/C7NR02171B10.1039/C7NR02171B ↗
50. 10.1021/acsnano.6b0506310.1021/acsnano.6b05063 ↗
51. 10.1126/science.109899310.1126/science.1098993 ↗
52. 10.1021/jacs.1c1113610.1021/jacs.1c11136 ↗
53. 10.1088/2053-1591/3/9/09400210.1088/2053-1591/3/9/094002 ↗
54. 10.1103/PhysRevLett.102.23680510.1103/PhysRevLett.102.236805 ↗
55. 10.1016/j.jmst.2014.11.01910.1016/j.jmst.2014.11.019 ↗
56. 10.1088/2053-1583/3/2/02200210.1088/2053-1583/3/2/022002 ↗
57. 10.1021/acs.nanolett.6b0156510.1021/acs.nanolett.6b01565 ↗
58. 10.1103/PhysRevB.96.18410810.1103/PhysRevB.96.184108 ↗
59. 10.1021/acsnano.0c0966610.1021/acsnano.0c09666 ↗
60. 10.1063/5.006155610.1063/5.0061556 ↗
61. 10.1103/PhysRevLett.110.14430110.1103/PhysRevLett.110.144301 ↗