General Strategy for Two-Dimensional Transition Metal Dichalcogenides by Ion Exchange
Source abstract
Abstract
The ability to control and vary the atomic compositions of two-dimensional (2D) layered semiconductors is of considerable importance for tailoring their electronic and optoelectronic properties. The current methods to tailor chemical composition of 2D layered semiconductors is largely limited to vapor phase chemistry, and solution phase chemistry is insufficiently explored to date. Here, we report a general approach to prepare 2D layered transition metal dichalcogenides (TMDs) by ion exchange reactions in solution phase. By choosing four typical layered metal dichalcogenides including MoS 2, MoSe 2, WS 2 and SnS 2 as representative cases, the feasibility and versatility of both cation and anion exchange reactions in layered metal dichalcogenides are confirmed. Transient absorption results indicate that exciton lifetime of these samples as excitation energy is increased. The optoelectronic properties of these TMD nanosheets after the ion exchange exhibit potential for future devices. Our strategy can be employed not only to modulate the atomic composition and electronic structures of layered TMDs, but also open up a new pathway for the fabrication of various hybrid heterostructures.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States
Funding
National Natural Science Foundation of China
References (53)
Show source-provided references
1. 10.1038/nnano.2012.19310.1038/nnano.2012.193 ↗
2. 10.1073/pnas.050284810210.1073/pnas.0502848102 ↗
3. 10.1038/nnano.2013.21910.1038/nnano.2013.219 ↗
4. 10.1038/nphys54710.1038/nphys547 ↗
5. 10.1126/science.aac782010.1126/science.aac7820 ↗
6. 10.1126/science.124650110.1126/science.1246501 ↗
7. 10.1002/anie.20150993310.1002/anie.201509933 ↗
8. 10.1038/nmat368710.1038/nmat3687 ↗
9. 10.1126/science.122641910.1126/science.1226419 ↗
10. 10.1038/ncomms309610.1038/ncomms3096 ↗
11. 10.1002/adma.20110479810.1002/adma.201104798 ↗
12. 10.1021/nl204361210.1021/nl2043612 ↗
13. 10.1039/C2CS35386E10.1039/C2CS35386E ↗
14. 10.1021/jacs.5b0277210.1021/jacs.5b02772 ↗
15. 10.1002/anie.20151002910.1002/anie.201510029 ↗
16. 10.1021/ja507994310.1021/ja5079943 ↗
17. 10.1021/acs.chemmater.7b0160510.1021/acs.chemmater.7b01605 ↗
18. 10.1021/ja405203e10.1021/ja405203e ↗
19. 10.1021/nn203009v10.1021/nn203009v ↗
20. 10.1002/adma.20160239110.1002/adma.201602391 ↗
21. 10.1039/C5CS00507H10.1039/C5CS00507H ↗
22. 10.1021/ja200400n10.1021/ja200400n ↗
23. 10.1021/ja308984510.1021/ja3089845 ↗
24. 10.1126/science.110375510.1126/science.1103755 ↗
25. 10.1126/science.118476910.1126/science.1184769 ↗
26. 10.1039/C2CS35241A10.1039/C2CS35241A ↗
27. 10.1002/adma.20130240010.1002/adma.201302400 ↗
28. 10.1021/ja309416c10.1021/ja309416c ↗
29. 10.1021/ja404523s10.1021/ja404523s ↗
30. 10.1021/jp405989z10.1021/jp405989z ↗
31. 10.1149/1.295572610.1149/1.2955726 ↗
32. 10.1021/ja401348510.1021/ja4013485 ↗
33. 10.1038/ncomms956910.1038/ncomms9569 ↗
34. 10.1039/qr956100028310.1039/qr9561000283 ↗
35. Lide D. R. · 2009
36. 10.1021/nl501441w10.1021/nl501441w ↗
37. 10.1038/ncomms874910.1038/ncomms8749 ↗
38. 10.1021/nn500432710.1021/nn5004327 ↗
39. 10.1021/acsnano.6b0758010.1021/acsnano.6b07580 ↗
40. 10.1002/smll.20130289310.1002/smll.201302893 ↗
41. 10.1364/OE.21.00490810.1364/OE.21.004908 ↗
42. 10.1002/adfm.20110211110.1002/adfm.201102111 ↗
43. 10.1103/PhysRevB.85.20530210.1103/PhysRevB.85.205302 ↗
44. 10.1021/acs.nanolett.6b0053610.1021/acs.nanolett.6b00536 ↗
45. 10.1021/nl201874w10.1021/nl201874w ↗
46. 10.1021/nn504760x10.1021/nn504760x ↗
47. 10.1021/acs.jpclett.6b0241310.1021/acs.jpclett.6b02413 ↗
48. 10.1021/nn303973r10.1021/nn303973r ↗
49. 10.1002/adfm.20150070910.1002/adfm.201500709 ↗
50. 10.1103/PhysRevLett.94.09740110.1103/PhysRevLett.94.097401 ↗
51. 10.1103/PhysRevB.89.12542710.1103/PhysRevB.89.125427 ↗
52. 10.1021/nl502197510.1021/nl5021975 ↗
53. 10.1021/acs.nanolett.6b0351310.1021/acs.nanolett.6b03513 ↗