journal article·2020-01-27

Heavy-Atom-Free Red-to-Yellow Photon Upconversion in a Thiosquaraine Composite

Sarah R. Pristash, Kathryn L. Corp, Emily J. Rabe, Cody W. Schlenker

ACS Applied Energy Materials· Volume 3· Issue 1
Publisher page

Abstract

We demonstrate a completely heavy-atom-free red-to-yellow triplet–triplet annihilation (TTA) photon upconversion system using a thionated squaraine sensitizer, both in fluid solution and in a solid-state composite architecture. Previous works have shown that thionation introduces sulfur nonbonding (n) orbitals that invert the native energy ordering of the ππ*(S1) and nπ*(S2) singlet transitions on the squaraine core, opening a channel for efficient intersystem crossing in the thiosquaraine without relying on the heavy-atom effect, as expected based on El-Sayed’s rule. Our thiosquaraine [2-(4-(dibutylamino)phenyl)-4-(4-(dibutyliminio)cyclohexa-2,5-dien-1-ylidene)-3-thioxocyclobut-1-enethiolate] exhibits an intense red absorption band, no measurable room-temperature fluorescence, and a native triplet lifetime on the order of 20 μs. This triplet is readily quenched (kQ = 1.4 × 109 M–1 s–1) upon sensitizing the triplet excited state of rubrene as a model upconversion emitter. We observe a 0.27 eV anti-Stokes shift, with selective 685 nm excitation of the thiosquaraine resulting in upconverted rubrene fluorescence centered at 570 nm. The system shows an upconversion quantum efficiency of ∼1.5% in deaerated toluene solution. This quantum efficiency is defined based on a maximum 50% quantum efficiency for TTA upconversion. This system exhibits upconversion under filtered (650 nm long-pass) simulated solar illumination and an intensity transition from quadratic to linear optical power dependence at ∼150 W/cm2 under 685 nm laser diode illumination. We also apply this thiosquaraine system to demonstrate red-to-yellow photon upconversion in a solid-state polymer composite, a prerequisite for light-harvesting device integration. In contrast with traditional TTA upconversion photosensitizers incorporating cost-prohibitive precious metals or photolabile arylhalide groups, we present an easily tunable squaraine dye that serves as a promising red-absorbing heavy-atom-free upconversion sensitizer for increased scalability and photostability.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Luminescence Properties of Advanced Materials · Nanoplatforms for cancer theranostics

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

Affiliations

Department of Chemistry, University of Washington, Seattle, Washington 98195, United States

Molecular Engineering & Sciences Institute, University of Washington, Seattle, Washington 98195, United States

Clean Energy Institute, University of Washington, Seattle, Washington 98195, United States

Funding

Division of Graduate Education · Clean Energy Institute

References (46)

Show source-provided references
1. 10.1063/1.173603410.1063/1.1736034 ↗
2. 10.1021/acsenergylett.7b0023710.1021/acsenergylett.7b00237 ↗
3. 10.1021/jp309636m10.1021/jp309636m ↗
4. 10.1039/C5SC03215F10.1039/C5SC03215F ↗
5. 10.1021/acsphotonics.8b0049810.1021/acsphotonics.8b00498 ↗
6. 10.1039/C1CC16015J10.1039/C1CC16015J ↗
7. 10.1002/anie.20060161510.1002/anie.200601615 ↗
8. 10.1039/C6TC05113H10.1039/C6TC05113H ↗
9. 10.1021/acsami.7b1792910.1021/acsami.7b17929 ↗
10. 10.1016/j.ccr.2010.01.00310.1016/j.ccr.2010.01.003 ↗
11. 10.1039/c3cc45843a10.1039/c3cc45843a ↗
12. 10.1021/jp711187810.1021/jp7111878 ↗
13. 10.1039/C4CC05718J10.1039/C4CC05718J ↗
14. 10.1002/anie.20100813410.1002/anie.201008134 ↗
15. 10.1016/0022-2852(61)90236-310.1016/0022-2852(61)90236-3 ↗
16. 10.1021/jp021263d10.1021/jp021263d ↗
17. 10.1021/jo200990y10.1021/jo200990y ↗
18. 10.1021/acs.accounts.7b0023510.1021/acs.accounts.7b00235 ↗
19. 10.1039/C7TC04096B10.1039/C7TC04096B ↗
20. 10.1021/jp902116310.1021/jp9021163 ↗
21. 10.1039/C8OB00421H10.1039/C8OB00421H ↗
22. 10.1039/C8CC01553H10.1039/C8CC01553H ↗
23. 10.1021/jp400276g10.1021/jp400276g ↗
24. 10.1021/jz100381v10.1021/jz100381v ↗
25. 10.1021/acs.jpcc.7b0837310.1021/acs.jpcc.7b08373 ↗
26. 10.1021/acs.joc.7b0164710.1021/acs.joc.7b01647 ↗
27. 10.1021/ja00769a02510.1021/ja00769a025 ↗
28. 10.1021/acs.accounts.7b0062910.1021/acs.accounts.7b00629 ↗
29. 10.1021/cr300471v10.1021/cr300471v ↗
30. 10.1021/cm301241410.1021/cm3012414 ↗
31. 10.1021/acsami.7b1778910.1021/acsami.7b17789 ↗
32. 10.1021/ja075014k10.1021/ja075014k ↗
33. 10.1021/ja904696n10.1021/ja904696n ↗
34. 10.1021/jacs.7b0286910.1021/jacs.7b02869 ↗
35. 10.18637/jss.v049.i0310.18637/jss.v049.i03 ↗
36. 10.1021/ja108493b10.1021/ja108493b ↗
37. 10.1039/C4CP00744A10.1039/C4CP00744A ↗
38. 10.1016/0022-2313(88)90331-610.1016/0022-2313(88)90331-6 ↗
39. 10.1098/rspa.1958.008010.1098/rspa.1958.0080 ↗
40. 10.1039/c3cc40778k10.1039/c3cc40778k ↗
41. 10.1021/acsphotonics.5b0069410.1021/acsphotonics.5b00694 ↗
42. 10.1021/acs.jpcc.6b0022310.1021/acs.jpcc.6b00223 ↗
43. 10.1021/acsami.8b0004710.1021/acsami.8b00047 ↗
44. 10.1021/jp503708d10.1021/jp503708d ↗
45. 10.1039/c000137f10.1039/c000137f ↗
46. 10.1021/j100304a01210.1021/j100304a012 ↗