Electronic Hybridization of Large-Area Stacked Graphene Films
Source abstract
Abstract
Direct, tunable coupling between individually assembled graphene layers is a next step toward designer two-dimensional (2D) crystal systems, with relevance for fundamental studies and technological applications. Here we describe the fabrication and characterization of large-area (>cm(2)), coupled bilayer graphene on SiO(2)/Si substrates. Stacking two graphene films leads to direct electronic interactions between layers, where the resulting film properties are determined by the local twist angle. Polycrystalline bilayer films have a "stained-glass window" appearance explained by the emergence of a narrow absorption band in the visible spectrum that depends on twist angle. Direct measurement of layer orientation via electron diffraction, together with Raman and optical spectroscopy, confirms the persistence of clean interfaces over large areas. Finally, we demonstrate that interlayer coupling can be reversibly turned off through chemical modification, enabling optical-based chemical detection schemes. Together, these results suggest that 2D crystals can be individually assembled to form electronically coupled systems suitable for large-scale applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Graphene research and applications · 2D Materials and Applications · Topological Materials and Phenomena
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Naval Research Laboratory, Washington, D.C. 20007, United States
Sandia National Laboratories, Albuquerque, New Mexico 87185, United States
References (51)
Show source-provided references
1. Geim A. K. · Nat. Mater. · 2007 · 6 · 18310.1038/nmat1849 ↗
2. Geim A. K. · Science · 2009 · 324 · 153010.1126/science.1158877 ↗
3. Novoselov K. S. · Proc. Natl. Acad. Sci. U.S.A. · 2005 · 102 · 1045110.1073/pnas.0502848102 ↗
4. Ponomarenko L. A. · Nat. Phys. · 2011 · 7 · 95810.1038/nphys2114 ↗
5. Britnell L. · Science · 2012 · 335 · 94710.1126/science.1218461 ↗
6. Gao G. · Nano Lett. · 2012 · 12 · 351810.1021/nl301061b ↗
7. Zalalutdinov M. K. · Nano Lett. · 2012 · 12 · 421210.1021/nl3018059 ↗
8. Liu Z. · Nano Lett. · 2011 · 11 · 203210.1021/nl200464j ↗
9. Shi Y. · Nano Lett. · 2012 · 12 · 278410.1021/nl204562j ↗
10. Haigh S. J. · Nat. Mater. · 2012 · 11 · 76410.1038/nmat3386 ↗
11. Havener R. W. · Nano Lett. · 2012 · 12 · 316210.1021/nl301137k ↗
12. Li G. · Nat. Phys. · 2010 · 6 · 10910.1038/nphys1463 ↗
13. Kim K. · Phys. Rev. Lett. · 2012 · 108 · 24610310.1103/PhysRevLett.108.246103 ↗
14. Luican A. · Phys. Rev. Lett. · 2011 · 106 · 12680210.1103/PhysRevLett.106.126802 ↗
15. MacDonald A. H. · Nature · 2011 · 474 · 45310.1038/474453a ↗
16. Lopes dos Santos J. M. B. · Phys. Rev. Lett. · 2007 · 99 · 25680210.1103/PhysRevLett.99.256802 ↗
17. Trambly de Laissardière G. · Nano Lett. · 2010 · 10 · 80410.1021/nl902948m ↗
18. Mele E. J. · Phys. Rev. B · 2011 · 84 · 23543910.1103/PhysRevB.84.235439 ↗
19. Ni Z. · Phys. Rev. B · 2009 · 80 · 12540410.1103/PhysRevB.80.125404 ↗
20. Wang Y. · ACS Nano · 2010 · 4 · 407410.1021/nn1004974 ↗
21. Ohta T. · Phys. Rev. Lett. · 2012 · 109 · 18680710.1103/PhysRevLett.109.186807 ↗
22. Zhan D. · Adv. Mater. · 2012 · 24 · 405510.1002/adma.201200011 ↗
23. Righi A. · Phys. Rev. B · 2011 · 84 · 24140910.1103/PhysRevB.84.241409 ↗
24. Ferrari A. C. · Phys. Rev. Lett. · 2006 · 97 · 18740110.1103/PhysRevLett.97.187401 ↗
25. Yang L. · Phys. Rev. Lett. · 2009 · 103 · 18680210.1103/PhysRevLett.103.186802 ↗
26. Mak K. F. · Phys. Rev. Lett. · 2008 · 101 · 19640510.1103/PhysRevLett.101.196405 ↗
27. Novoselov K. S. · Science · 2004 · 306 · 66610.1126/science.1102896 ↗
28. Blake P. · Appl. Phys. Lett. · 2007 · 91 · 063124-310.1063/1.2768624 ↗
29. Li X. · J. Am. Chem. Soc. · 2011 · 133 · 281610.1021/ja109793s ↗
30. Kim K. S. · Nature · 2009 · 457 · 70610.1038/nature07719 ↗
31. Reina A. · Nano Lett. · 2009 · 9 · 3010.1021/nl801827v ↗
32. Bae S. · Nat. Nanotechnol. · 2010 · 5 · 57410.1038/nnano.2010.132 ↗
33. 450 PMMA A2 spun at 2000 rpm and baked at 85°C for 5 minutes.10.1046/j.1464-410X.2000.00089-2.x ↗
34. Kim K. · Phys. Rev. B · 2011 · 83 · 24543310.1103/PhysRevB.83.245433 ↗
35. Zhu W. · Nano Lett. · 2012 · 12 · 343110.1021/nl300563h ↗
36. Ishigami M. · Nano Lett. · 2007 · 7 · 164310.1021/nl070613a ↗
37. Ohta T. · Phys. Rev. B · 2012 · 85 · 07541510.1103/PhysRevB.85.075415 ↗
38. Ni Z. H. · Nano Lett. · 2007 · 7 · 275810.1021/nl071254m ↗
39. Palik E. D. · 1998
40. Sato K. · Phys. Rev. B · 2012 · 86 · 12541410.1103/PhysRevB.86.125414 ↗
41. Knox K. R. · Phys. Rev. B · 2008 · 78 · 20140810.1103/PhysRevB.78.201408 ↗
42. Locatelli A. · ACS Nano · 2010 · 4 · 487910.1021/nn101116n ↗
43. Wofford J., M. · New J. Phys. · 2012 · 14 · 05300810.1088/1367-2630/14/5/053008 ↗
44. Chan J. · ACS Nano · 2012 · 6 · 322410.1021/nn300107f ↗
45. Robinson J. T. · Nano Lett. · 2010 · 10 · 300110.1021/nl101437p ↗
46. Ferrari A. C. · Phys. Rev. B · 2000 · 61 · 1409510.1103/PhysRevB.61.14095 ↗
47. Ohta T. · Science · 2006 · 313 · 95110.1126/science.1130681 ↗
48. Zhang Y. · Nature · 2009 · 459 · 82010.1038/nature08105 ↗
49. Herzinger, C. M.; Johs, B. D.Dielectric Function Parametric Model, and Method of Use. U.S. Patent 5796983, 1998
50. Herzinger C. M. · J. Appl. Phys. · 1998 · 83 · 332310.1063/1.367101 ↗
51. Lafkioti M. · Nano Lett. · 2010 · 10 · 114910.1021/nl903162a ↗