Optimizing Solid-State Ligand Exchange for Colloidal Quantum Dot Optoelectronics: How Much Is Enough?
Source abstract
Abstract
Progress in chalcogenide and perovskite CQD optoelectronics has relied to a significant extent on solid-state ligand exchanges (SSEs): the replacement of initial insulating ligands with shorter conducting linkers on CQD surfaces. Herein we develop a mechanistic model of SSE employing 3-mercaptopropionic acid (MPA) and 1,2-ethanedithiol (EDT) as the linkers. The model suggests that optimal linker concentrations lead to efficient exchange, resulting in ca. 200–300 exchanged ligands per CQD, a 50% thickness reduction of the initial film, decreased interdot spacing, a 15 nm red-shift in the excitonic absorption peak, and a 10× reduction in carrier lifetime. It is the combined effect of these physicochemical changes that has traditionally made 1% MPA and 10–2% EDT (v:v) the concentrations of choice for efficient CQD optoelectronics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Perovskite Materials and Applications · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Physical Sciences and Engineering Division, KAUST Solar Center (KSC), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia
Department of Electrical and Computer Engineering, University of Toronto, Toronto, Ontario M5S 3G4, Canada
Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695, United States
Funding
King Abdullah University of Science and Technology
References (50)
Show source-provided references
1. 10.1038/nnano.2015.17810.1038/nnano.2015.178 ↗
2. 10.1126/sciadv.aao420410.1126/sciadv.aao4204 ↗
3. 10.1038/nmat500010.1038/nmat5000 ↗
4. 10.1038/nnano.2017.18910.1038/nnano.2017.189 ↗
5. 10.1126/science.aac552310.1126/science.aac5523 ↗
6. 10.1038/nature2142410.1038/nature21424 ↗
7. 10.1002/adma.20180166110.1002/adma.201801661 ↗
8. 10.1038/s41565-018-0117-z10.1038/s41565-018-0117-z ↗
9. 10.1557/mrc.2013.1710.1557/mrc.2013.17 ↗
10. 10.1002/adma.20140328110.1002/adma.201403281 ↗
11. 10.1002/adma.20140057710.1002/adma.201400577 ↗
12. 10.1021/acsenergylett.6b0042910.1021/acsenergylett.6b00429 ↗
13. 10.1021/nn700334810.1021/nn7003348 ↗
14. 10.1002/adma20130280210.1002/adma201302802 ↗
15. 10.1002/adma.20140441110.1002/adma.201404411 ↗
16. 10.1002/adma.20140449510.1002/adma.201404495 ↗
17. 10.1063/1.486921610.1063/1.4869216 ↗
18. 10.1002/adma.20120504110.1002/adma.201205041 ↗
19. 10.1016/j.nanoen.2015.08.01010.1016/j.nanoen.2015.08.010 ↗
20. 10.1021/nn401918d10.1021/nn401918d ↗
21. 10.1021/acs.chemrev.5b0006310.1021/acs.chemrev.5b00063 ↗
22. 10.1002/adma.20150365710.1002/adma.201503657 ↗
23. 10.1002/adma.20120282510.1002/adma.201202825 ↗
24. 10.1002/pssa.20153247010.1002/pssa.201532470 ↗
25. 10.1021/acsnano.5b0454710.1021/acsnano.5b04547 ↗
26. 10.1021/acsenergylett.7b0054010.1021/acsenergylett.7b00540 ↗
27. 10.1002/adma.20170757210.1002/adma.201707572 ↗
28. 10.1038/s41467-019-10856-z10.1038/s41467-019-10856-z ↗
29. 10.1002/adma.20030539510.1002/adma.200305395 ↗
30. 10.1038/nnano.2012.12710.1038/nnano.2012.127 ↗
31. 10.1021/jz300048y10.1021/jz300048y ↗
32. 10.1021/cr900137k10.1021/cr900137k ↗
33. 10.1021/nn503569p10.1021/nn503569p ↗
34. 10.1021/acs.nanolett.5b0327110.1021/acs.nanolett.5b03271 ↗
35. 10.1021/cm501739h10.1021/cm501739h ↗
36. 10.1063/1.514325210.1063/1.5143252 ↗
37. 10.1021/acsphotonics.9b0105010.1021/acsphotonics.9b01050 ↗
38. 10.1021/acs.jpclett.0c0058710.1021/acs.jpclett.0c00587 ↗
39. 10.1038/s41563-019-0582-210.1038/s41563-019-0582-2 ↗
40. 10.1038/s41566-019-0362-110.1038/s41566-019-0362-1 ↗
41. 10.1021/ja308861d10.1021/ja308861d ↗
42. 10.1021/acs.nanolett.8b0302010.1021/acs.nanolett.8b03020 ↗
43. 10.1016/0021-9797(71)90338-910.1016/0021-9797(71)90338-9 ↗
44. 10.1021/nn303364d10.1021/nn303364d ↗
45. 10.1103/PhysRevLett.110.19680210.1103/PhysRevLett.110.196802 ↗
46. 10.1021/jacs.5b1307710.1021/jacs.5b13077 ↗
47. 10.1021/acsnano.9b0019110.1021/acsnano.9b00191 ↗
48. 10.1039/C6CC08114B10.1039/C6CC08114B ↗
49. 10.1002/adma.20170492810.1002/adma.201704928 ↗
50. 10.1002/adma.20190619910.1002/adma.201906199 ↗