Crown Ethers Enable Room-Temperature Synthesis of CsPbBr3 Quantum Dots for Light-Emitting Diodes
Source abstract
Abstract
The synthesis of all-inorganic cesium lead halide perovskite quantum dots (QDs) typically requires high temperatures, stringent conditions, large quantities of surface ligands, and judicious purification steps to overcome ligand-induced charge injection barriers in optoelectronic devices. Low-temperature syntheses generally require lower ligand concentrations but are severely limited by the low solubility of the Cs precursor. We describe an innovative and general approach employing crown ethers under ambient conditions to overcome these solubility limitations. The crown ethers facilitate complete dissolution of the CsBr precursor, rendering CsPbBr3 QD inks practical for device fabrication. The resultant light-emitting diodes (LEDs) displayed bright green emission, with a current efficiency and external quantum efficiency of 9.22 cd A–1 and 2.64%, respectively. This represents the first LED based on CsPbBr3 QDs prepared at room temperature. Lastly, the crown ethers form core–shell structures, opening new avenues to exploit their strong coordination strength.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Energy Research Institute at NTU (ERI@N), Research Techno Plaza, X-Frontier Block Level 5, 50 Nanyang Drive, Singapore 637553
Interdisciplinary Graduate School, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798
School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798
Funding
National Research Foundation Singapore
References (33)
Show source-provided references
1. 10.1002/adma.20160066910.1002/adma.201600669 ↗
2. 10.1126/science.aam709310.1126/science.aam7093 ↗
3. 10.1073/pnas.160747111310.1073/pnas.1607471113 ↗
4. 10.1126/science.aad181810.1126/science.aad1818 ↗
5. 10.1021/acs.nanolett.7b0097610.1021/acs.nanolett.7b00976 ↗
6. 10.1021/nl504877910.1021/nl5048779 ↗
7. 10.1021/acsnano.6b0386310.1021/acsnano.6b03863 ↗
8. 10.1002/adma.20160388510.1002/adma.201603885 ↗
9. 10.1021/acsami.6b0852810.1021/acsami.6b08528 ↗
10. 10.1021/acs.jpclett.6b0222410.1021/acs.jpclett.6b02224 ↗
11. 10.1002/adma.20160006410.1002/adma.201600064 ↗
12. 10.1002/adma.20160078410.1002/adma.201600784 ↗
13. 10.1002/adfm.20160095810.1002/adfm.201600958 ↗
14. 10.1002/adfm.20160010910.1002/adfm.201600109 ↗
15. 10.1038/nenergy.2016.19410.1038/nenergy.2016.194 ↗
16. 10.1021/acsnano.5b0819310.1021/acsnano.5b08193 ↗
17. 10.1038/srep3769310.1038/srep37693 ↗
18. 10.1039/C6CC01500J10.1039/C6CC01500J ↗
19. 10.1021/acsnano.5b0115410.1021/acsnano.5b01154 ↗
20. 10.1021/j100854a04910.1021/j100854a049 ↗
21. 10.1039/C7CS00128B10.1039/C7CS00128B ↗
22. 10.1039/C6CS00619A10.1039/C6CS00619A ↗
23. 10.1007/BF0051821810.1007/BF00518218 ↗
24. 10.1039/C6CC01088A10.1039/C6CC01088A ↗
25. 10.1039/C6CC01056C10.1039/C6CC01056C ↗
26. 10.1038/ncomms1519810.1038/ncomms15198 ↗
27. 10.1021/acsnano.5b0629510.1021/acsnano.5b06295 ↗
28. 10.1021/jacs.7b0400010.1021/jacs.7b04000 ↗
29. 10.1002/adma.20150256710.1002/adma.201502567 ↗
30. 10.1021/nn203728t10.1021/nn203728t ↗
31. 10.1016/j.nanoen.2017.05.00210.1016/j.nanoen.2017.05.002 ↗
32. 10.1021/acsnano.6b0761710.1021/acsnano.6b07617 ↗
33. 10.1021/acsnano.6b0154010.1021/acsnano.6b01540 ↗