journal article·2021-12-31Open access

Shortwave infrared-absorbing squaraine dyes for all-organic optical upconversion devices

Karen Strassel, Wei-Hsu Hu, Sonja Osbild, Daniele Padula, Daniel Rentsch, Sergii Yakunin, Yevhen Shynkarenko, Maksym Kovalenko, Frank Nüesch, Roland Hany, Michael Bauer

Abstract

Shortwave infrared (SWIR) optical sensing and imaging are essential to an increasing number of next-generation applications in communications, process control or medical imaging. An all-organic SWIR upconversion device (OUC) consists of an organic SWIR sensitive photodetector (PD) and an organic light-emitting diode (OLED), connected in series. OUCs directly convert SWIR to visible photons, which potentially provides a low-cost alternative to the current inorganic compound-based SWIR imaging technology. For OUC applications, only few organic materials have been reported with peak absorption past 1000 nm and simultaneous small absorption in the visible. Here, we synthesized a series of thermally stable high-extinction coefficient donor-substituted benz[cd]indole-capped SWIR squaraine dyes. First, we coupled the phenyl-, carbazole-, and thienyl-substituted benz[cd]indoles with squaric acid (to obtain the SQ dye family). We then combined these donors with the dicyanomethylene-substituted squaraine acceptor unit, to obtain the dicyanomethylene-functionalized squaraine DCSQ family. In the solid state, the absorbance of all dyes extended considerably beyond 1100 nm. For the carbazole- and thienyl-substituted DCSQ dyes, even the peak absorptions in solution were in the SWIR, at 1008 nm and 1014 nm. We fabricated DCSQ PDs with an external photon-to-current efficiency over 30%. We then combined the PD with a fluorescent OLED and fabricated long-term stable OUCs with peak sensitivity at 1020 nm, extending to beyond 1200 nm. Our OUCs are characterized by a very low dark luminance (<10−2 cd m−2 at below 6 V) in the absence of SWIR light, and a low turn-on voltage of 2 V when SWIR light is present.
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Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Luminescence Properties of Advanced Materials

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

Affiliations

Laboratory for Functional Polymers, Empa, Swiss Federal Laboratories for Materials Science and Technology, Dübendorf, Switzerland

Ecole Polytechnique Fédérale de Lausanne, EPFL, Institute of Chemical Sciences and Engineering, Lausanne, Switzerland

Ecole Polytechnique Fédérale de Lausanne, EPFL, Institute of Materials Science and Engineering, Lausanne, Switzerland

Dipartimento di Biotecnologie, Chimica e Farmacia, Università di Siena, Siena, Italy

Department of Chemistry and Applied Biosciences, Laboratory of Inorganic Chemistry, Zürich, Switzerland

Laboratory for Thin Films and Photovoltaics, Empa, Swiss Federal Laboratories for Materials Science and Technology, Dübendorf, Switzerland

Funding

Italian Ministry of Education, University, and Research · Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

References (59)

Show source-provided references
1. 10.1364/AO.58.00987610.1364/AO.58.009876 ↗
2. 10.1038/ncomms1542110.1038/ncomms15421 ↗
3. 10.1039/C5NH00073D10.1039/C5NH00073D ↗
4. 10.1002/anie.20170697410.1002/anie.201706974 ↗
5. 10.1038/nature2475510.1038/nature24755 ↗
6. 10.1039/C8CS00234G10.1039/C8CS00234G ↗
7. 10.1073/pnas.171891711510.1073/pnas.1718917115 ↗
8. 10.1080/14686996.2019.159073110.1080/14686996.2019.1590731 ↗
9. Hansen MP · Proc of SPIE · 2008 · 6939
10. 10.1117/1.JBO.20.3.03090110.1117/1.JBO.20.3.030901 ↗
11. 10.1038/s41928-020-0388-x10.1038/s41928-020-0388-x ↗
12. 10.1021/acsphotonics.9b0066910.1021/acsphotonics.9b00669 ↗
13. Li N · Adv Sci · 2020 · 200044410.1002/advs.202000444 ↗
14. 10.1002/adma.20090331210.1002/adma.200903312 ↗
15. 10.1080/14686996.2019.161005710.1080/14686996.2019.1610057 ↗
16. 10.1063/1.512473510.1063/1.5124735 ↗
17. 10.1109/ACCESS.2020.298704310.1109/ACCESS.2020.2987043 ↗
18. 10.1016/j.orgel.2019.07.00210.1016/j.orgel.2019.07.002 ↗
19. 10.1002/adom.20180003810.1002/adom.201800038 ↗
20. 10.1021/acs.macromol.5b0085910.1021/acs.macromol.5b00859 ↗
21. 10.1002/adfm.20180039110.1002/adfm.201800391 ↗
22. 10.1021/acs.accounts.8b0044610.1021/acs.accounts.8b00446 ↗
23. 10.1002/tcr.20160001310.1002/tcr.201600013 ↗
24. 10.1002/asia.20090059610.1002/asia.200900596 ↗
25. 10.1016/j.chemphys.2018.11.00210.1016/j.chemphys.2018.11.002 ↗
26. 10.1002/chem.20200112610.1002/chem.202001126 ↗
27. 10.1016/j.dyepig.2015.05.01610.1016/j.dyepig.2015.05.016 ↗
28. 10.1002/anie.20090253210.1002/anie.200902532 ↗
29. 10.1021/cm801911n10.1021/cm801911n ↗
30. 10.1039/c3ra23048a10.1039/c3ra23048a ↗
31. 10.1002/ejoc.20090129710.1002/ejoc.200901297 ↗
32. 10.1016/j.dyepig.2019.04.00710.1016/j.dyepig.2019.04.007 ↗
33. 10.1021/am300467w10.1021/am300467w ↗
34. 10.1021/cm403492910.1021/cm4034929 ↗
35. 10.1021/acs.bioconjchem.9b0048210.1021/acs.bioconjchem.9b00482 ↗
36. 10.1016/j.dyepig.2004.05.00310.1016/j.dyepig.2004.05.003 ↗
37. 10.1002/chem.20120278310.1002/chem.201202783 ↗
38. 10.1021/acsami.8b0004710.1021/acsami.8b00047 ↗
39. 10.1021/acsami.9b0673210.1021/acsami.9b06732 ↗
40. Véron AC. Near-infrared absorbing cyanine dyes and organic-inorganic perovskites for electronic applications [Doctoral thesis]. Switzerland: University Zurich; 2017.
41. 10.1139/v90-08110.1139/v90-081 ↗
42. 10.1016/j.dyepig.2015.02.01910.1016/j.dyepig.2015.02.019 ↗
43. 10.1016/j.dyepig.2018.12.00710.1016/j.dyepig.2018.12.007 ↗
44. 10.1021/acsami.9b2014710.1021/acsami.9b20147 ↗
45. 10.1021/jp000139w10.1021/jp000139w ↗
46. 10.1016/S0143-7208(96)00101-510.1016/S0143-7208(96)00101-5 ↗
47. 10.1016/j.saa.2018.11.06110.1016/j.saa.2018.11.061 ↗
48. 10.1021/acs.jmedchem.8b0069410.1021/acs.jmedchem.8b00694 ↗
49. 10.1021/acs.jpcc.9b0529710.1021/acs.jpcc.9b05297 ↗
50. 10.1080/0026897700010017110.1080/00268977000100171 ↗
51. 10.1021/jp971577e10.1021/jp971577e ↗
52. 10.1039/C2TA00883A10.1039/C2TA00883A ↗
53. 10.1002/pip.228910.1002/pip.2289 ↗
54. 10.1039/C9EE01508F10.1039/C9EE01508F ↗
55. 10.1039/C3MH00098B10.1039/C3MH00098B ↗
56. 10.1002/adfm.20110156510.1002/adfm.201101565 ↗
57. 10.1002/adma.20100455410.1002/adma.201004554 ↗
58. 10.1002/adom.20180127810.1002/adom.201801278 ↗
59. 10.1063/1.9879910.1063/1.98799 ↗