journal article·2021-10-22

Size-Controlled Indium Phosphide Quantum Dots for Bright and Tunable Light Emission by Simple Hindered Diamine Addition

Rodolphe Valleix, Federico Cisnetti, Hanako Okuno, Philippe Boutinaud, Geneviève Chadeyron, Damien Boyer

ACS Applied Nano Materials· Volume 4· Issue 10
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Abstract

The use of sterically hindered N,N′-diisopropylbenzene-1,2-diamine (DIBA) for aminophosphine-based InP QDs synthesis in an oleylamine (OLAm) medium is evidenced as a powerful tool to finely control their size in a reproducible way. This diamine forms in situ a P(DIBA)(OLAm) species accounting for the observed size-tuning effect because the QDs crystallize as tetrahedra with an edge length (3.5 to 6.6 nm) depending on the DIBA concentration (0 to 7 eq./indium). This kinetically controlled size-tuning mechanism is proposed by combining 31P NMR and UV–vis spectroscopy. A proof-of-concept is established by coating the InP cores with ZnS shells. The luminescence of the as-synthesized InP/ZnS QDs is tunable over the 480–620 nm range, with photoluminescence internal quantum efficiencies of 45 to 60% suitable for applications as phosphors in LED lighting systems and LED displays.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Nanocluster Synthesis and Applications · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Université Clermont Auvergne, Clermont Auvergne INP, CNRS, ICCF, F-63000 Clermont−Ferrand, France

Université Grenoble Alpes, CEA, IRIG-MEM, 38000 Grenoble, France

References (45)

Show source-provided references
1. 10.1021/acsenergylett.9b0285110.1021/acsenergylett.9b02851 ↗
2. 10.3402/nano.v1i0.520210.3402/nano.v1i0.5202 ↗
3. 10.1155/2011/83413910.1155/2011/834139 ↗
4. 10.1126/science.281.5385.201310.1126/science.281.5385.2013 ↗
5. 10.1021/acsanm.1c0005410.1021/acsanm.1c00054 ↗
6. 10.1021/acsami.1c0239010.1021/acsami.1c02390 ↗
7. 10.1038/s41427-019-0141-y10.1038/s41427-019-0141-y ↗
8. 10.1021/acs.chemrev.0c0083110.1021/acs.chemrev.0c00831 ↗
9. 10.1021/ja00072a02510.1021/ja00072a025 ↗
10. 10.1021/j100019a06310.1021/j100019a063 ↗
11. 10.1016/j.impact.2019.10016810.1016/j.impact.2019.100168 ↗
12. 10.3389/fchem.2019.0046610.3389/fchem.2019.00466 ↗
13. 10.1021/acs.chemmater.5b0504410.1021/acs.chemmater.5b05044 ↗
14. 10.1039/C9SC04290C10.1039/C9SC04290C ↗
15. 10.1021/acs.chemrev.6b0011610.1021/acs.chemrev.6b00116 ↗
16. 10.1021/acs.chemmater.7b0025410.1021/acs.chemmater.7b00254 ↗
17. 10.1002/anie.20150597210.1002/anie.201505972 ↗
18. 10.1007/s11051-013-1750-y10.1007/s11051-013-1750-y ↗
19. 10.1021/acs.chemmater.5b0213810.1021/acs.chemmater.5b02138 ↗
20. 10.1039/D0CE00078G10.1039/D0CE00078G ↗
21. 10.1021/jacs.8b0697110.1021/jacs.8b06971 ↗
22. 10.1021/acs.chemmater.0c0055110.1021/acs.chemmater.0c00551 ↗
23. 10.1002/adfm.20200845310.1002/adfm.202008453 ↗
24. 10.1016/j.apsusc.2019.06.05910.1016/j.apsusc.2019.06.059 ↗
25. 10.1021/acs.langmuir.0c0178810.1021/acs.langmuir.0c01788 ↗
26. 10.1021/acs.chemmater.0c0156110.1021/acs.chemmater.0c01561 ↗
27. 10.1021/ja01167a00110.1021/ja01167a001 ↗
28. 10.1021/acs.nanolett.0c0481310.1021/acs.nanolett.0c04813 ↗
29. 10.1021/acs.organomet.7b0056410.1021/acs.organomet.7b00564 ↗
30. Nifant’ev E. E. · Z. Obs. Khimii · 1989 · 59 · 816
31. Nifant’ev E. E. · Z. Obs. Khimii · 1979 · 49 · 64
32. 10.1002/anie.20160028910.1002/anie.201600289 ↗
33. Several attempts have been made to change the nature of the substituent on the amines’ group. N,N′-Di(methyl)benzene-1,2-amine (DMBA) has been synthesized but appeared to be highly sensitive to light, and no reaction was observed when tested for InP QDs Syn.
34. 10.1038/s41586-019-1771-510.1038/s41586-019-1771-5 ↗
35. 10.1039/C8NR01286E10.1039/C8NR01286E ↗
36. 10.1021/acs.chemmater.6b0245610.1021/acs.chemmater.6b02456 ↗
37. 10.1002/anie.20170565010.1002/anie.201705650 ↗
38. 10.1063/1.200490110.1063/1.2004901 ↗
39. 10.1021/acsnano.9b0702710.1021/acsnano.9b07027 ↗
40. 10.1021/acsanm.8b0206310.1021/acsanm.8b02063 ↗
41. 10.1063/1.11580710.1063/1.115807 ↗
42. 10.1021/ja803687e10.1021/ja803687e ↗
43. 10.1109/IPCon.2012.635884410.1109/IPCon.2012.6358844 ↗
44. 10.1039/c2jm30760j10.1039/c2jm30760j ↗
45. 10.1021/jp100198910.1021/jp1001989 ↗