Low‐Threshold, Highly Stable Colloidal Quantum Dot Short‐Wave Infrared Laser enabled by Suppression of Trap‐Assisted Auger Recombination
Source abstract
Abstract
Abstract Pb‐chalcogenide colloidal quantum dots (CQDs) are attractive materials to be used as tuneable laser media across the infrared spectrum. However, excessive nonradiative Auger recombination due to the presence of trap states outcompetes light amplification by rapidly annihilating the exciton population, leading to high gain thresholds. Here, a binary blend is employed of CQDs and ZnO nanocrystals in order to passivate the in‐gap trap states of PbS‐CQD gain medium. Using transient absorption, a fivefold increase is measured in Auger lifetime demonstrating the suppression of trap‐assisted Auger recombination. By doing so, a twofold reduction is achieved in amplified spontaneous emission (ASE) threshold. Finally, by integrating the proposed binary blend to a distributed feedback (DFB) resonator, single‐mode lasing emission is demonstrated at 1650 nm with a linewidth of 1.23 nm (0.62 meV), operating at a low lasing threshold of ≈385 μJ cm–2. The Auger suppression in this system has allowed to achieve unprecedented lasing emission stability for a CQD laser with recorded continuous operation of 5 h at room temperature and ambient conditions.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Semiconductor Quantum Structures and Devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
ICFO Institut de Ciències Fotòniques The Barcelona Institute of Science and Technology Castelldefels 08860 Spain
Laboratory of Ultrafast Science Department of Physics University of Cyprus Nicosia 1678 Cyprus
ICREA—Institució Catalana de Recerca i Estudis Avançats Barcelona 08010 Spain
Funding
European Research Council
References (29)
Show source-provided references
1. 10.1126/science.290.5490.31410.1126/science.290.5490.314 ↗
2. 10.1038/nnano.2012.6110.1038/nnano.2012.61 ↗
3. 10.1038/nature2142410.1038/nature21424 ↗
4. 10.1126/science.aax348910.1126/science.aax3489 ↗
5. 10.1038/s41578-020-00274-910.1038/s41578-020-00274-9 ↗
6. 10.1021/acs.nanolett.0c0185910.1021/acs.nanolett.0c01859 ↗
7. 10.1038/s41566-021-00878-910.1038/s41566-021-00878-9 ↗
8. 10.1126/science.287.5455.101110.1126/science.287.5455.1011 ↗
9. 10.1038/nnano.2017.18910.1038/nnano.2017.189 ↗
10. 10.1038/s41467-020-17032-810.1038/s41467-020-17032-8 ↗
11. 10.1021/nl403289w10.1021/nl403289w ↗
12. 10.1002/adma.20090148210.1002/adma.200901482 ↗
13. 10.1038/nature0583910.1038/nature05839 ↗
14. 10.1021/nl500775p10.1021/nl500775p ↗
15. 10.1021/acs.nanolett.5b0259510.1021/acs.nanolett.5b02595 ↗
16. 10.1002/adma.20140029710.1002/adma.201400297 ↗
17. 10.1038/ncomms718010.1038/ncomms7180 ↗
18. 10.1002/smll.20170059810.1002/smll.201700598 ↗
19. Cao Y. · Nat. Energy · 2016 · 16035 · 1
20. 10.1038/s41565-018-0312-y10.1038/s41565-018-0312-y ↗
21. 10.1002/adma.20140463610.1002/adma.201404636 ↗
22. 10.1103/PhysRevB.86.16520210.1103/PhysRevB.86.165202 ↗
23. 10.1021/acs.jpca.0c0177510.1021/acs.jpca.0c01775 ↗
24. 10.1021/acsomega.8b0096210.1021/acsomega.8b00962 ↗
25. 10.1017/CBO978051147076910.1017/CBO9780511470769 ↗
26. 10.1038/ncomms1394110.1038/ncomms13941 ↗
27. 10.1021/nl402803h10.1021/nl402803h ↗
28. 10.1021/cr900137k10.1021/cr900137k ↗
29. 10.1021/acsaem.0c0038910.1021/acsaem.0c00389 ↗