Evaporative Thinning: A Facile Synthesis Method for High Quality Ultrathin Layers of 2D Crystals
Source abstract
Abstract
The palette of two-dimensional materials has expanded beyond graphene in recent years to include the chalcogenides among other systems. However, there is a considerable paucity of methods for controlled synthesis of mono- and/or few-layer two-dimensional materials with desirable quality, reproducibility, and generality. Here we show a facile top-down synthesis approach for ultrathin layers of 2D materials down to monolayer. Our method is based on controlled evaporative thinning of initially large sheets, as deposited by vapor mass-transport. Rather than optimizing conditions for monolayer deposition, our approach makes use of selective evaporation of thick sheets to control the eventual thickness, down to a monolayer, a process which appears to be self-stopping. As a result, 2D sheets with high yield, high reproducibility, and excellent quality can be generated with large (>10 μm) and thin (∼ 1-2 nm) dimensions. Evaporative thinning promises to greatly reduce the difficulty involved in isolating large, mono- and few-layers of 2D materials for subsequent studies.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · Metamaterials and Metasurfaces Applications · Graphene research and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, ‡Department of Electrical Engineering and Computer Science, §Department of Applied Physics, and ∥Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States
Funding
National Science Foundation · U.S. Department of Defense
References (30)
Show source-provided references
1. Schedin F. · Nat. Mater. · 2007 · 6 · 65210.1038/nmat1967 ↗
2. Geim A. K. · Nat. Mater. · 2007 · 6 · 18310.1038/nmat1849 ↗
3. Shanmugam M. · Appl. Phys. Lett. · 2012 · 100 · 15390110.1063/1.3703602 ↗
4. Han T. H. · J. Am. Chem. Soc. · 2011 · 133 · 1526410.1021/ja205693t ↗
5. Late D. J. · ACS Nano · 2013 · 7 · 487910.1021/nn400026u ↗
6. Rao C. N. R. · Angew. Chem., Int. Ed. · 2013 · 52 · 1316210.1002/anie.201301548 ↗
7. Nag A. · ACS Nano · 2010 · 4 · 153910.1021/nn9018762 ↗
8. Gorbachev R. V. · Small · 2011 · 7 · 46510.1002/smll.201001628 ↗
9. Splendiani A. · Nano Lett. · 2010 · 10 · 127110.1021/nl903868w ↗
10. Zhang W. · Sci. Rep. · 2014 · 4 · 382610.1038/srep03826 ↗
11. Late D. J. · Adv. Mater. · 2012 · 24 · 354910.1002/adma.201201361 ↗
12. Fang H. · Nano Lett. · 2012 · 12 · 378810.1021/nl301702r ↗
13. Kong D. S. · Nano Lett. · 2010 · 10 · 224510.1021/nl101260j ↗
14. Jana M. K. · Chem.—Eur. J. · 2013 · 19 · 911010.1002/chem.201300983 ↗
15. Novoselov K. S. · Science · 2004 · 306 · 66610.1126/science.1102896 ↗
16. Dang W. · Nano Lett. · 2010 · 10 · 287010.1021/nl100938e ↗
17. Lu X. · Nanoscale · 2013 · 5 · 890410.1039/C3NR03101B ↗
18. Wu J. · Small · 2013 · 9 · 331410.1002/smll.201301542 ↗
19. Zhang Y. · Nat. Phys. · 2010 · 6 · 58410.1038/nphys1689 ↗
20. Steinberg H. · Nano Lett. · 2010 · 10 · 503210.1021/nl1032183 ↗
21. Peng H. L. · Nat. Chem. · 2012 · 4 · 28110.1038/nchem.1277 ↗
22. Zakharchenko K. V. · J. Phys.: Condens. Matter · 2011 · 23 · 202202
23. Huang J. Y. · Proc. Natl. Acad. Sci. U.S.A. · 2009 · 106 · 1010310.1073/pnas.0905193106 ↗
24. March N. H. · 200210.1142/4717 ↗
25. Ziman J. M. · 197210.1017/CBO9781139644075 ↗
26. Landau L. D. · 1980
27. Zahn K. · Phys. Rev. Lett. · 2000 · 85 · 365610.1103/PhysRevLett.85.3656 ↗
28. Kresse G. · Comput. Mater. Sci. · 1996 · 6 · 1510.1016/0927-0256(96)00008-0 ↗
29. Kong D. S. · ACS Nano · 2011 · 5 · 469810.1021/nn200556h ↗
30. Hong S. S. · Nano Lett. · 2010 · 10 · 311810.1021/nl101884h ↗