journal article·2022-04

Peri‐Acenoacene for Solution Processed Distributed Feedback Laser: The Effect of 1,2‐Oxaborine Doping

Yanwei Gu, Rafael Muñoz‐Mármol, Wei Fan, Yi Han, Shaofei Wu, Zhengtao Li, Víctor Bonal, José M. Villalvilla, José A. Quintana, Pedro G. Boj, María A. Díaz‐García, Jishan Wu

Advanced Optical Materials· Volume 10· Issue 7
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Abstract

Abstract Zigzag edged nanographenes such as peri‐acenoacenes are promising materials for organic lasers, but the effects of heteroatom doping on the electronic properties and gain medium performance remain unclear. Herein, the facile synthesis of a new 1,2‐oxaborine (BO) doped peri‐tetracenotetracene derivative, the bis(1,2‐oxaborine)peri‐tetracenotetracene (BOTT‐Mes), is reported. X‐ray crystallographic analysis confirms the BO‐doped planar structure and the nonexistence of intermolecular π–π stacking in solid state. Compared with the all‐carbon peri‐tetracenotetracene derivative (TT‐Ar), the BO‐doped BOTT‐Mes exhibits more disrupted π‐conjugation at the BO sites, a lower‐lying highest occupied molecular orbital, and a larger energy gap. Due to its rigid skeleton and nonaggregative feature, it displays well‐resolved absorption and emission spectra with a small Stokes shift (8 nm) and high photoluminescence quantum yield (80%) when it is dispersed in a polystyrene (PS) thin film. Notably, 1,2‐oxaborine doping improves the film amplified spontaneous emission (ASE) performance, with a lower ASE threshold (Eth‐ASE = 66 µJ cm–2) as compared to the TT‐Ar doped PS film (Eth‐ASE = 100 µJ cm–2). Furthermore, a low threshold (22 µJ cm–2) solution‐processed distributed feedback laser is fabricated, indicating the feasibility of using BOTT‐Mes as gain medium for practical laser applications.
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Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Synthesis and Properties of Aromatic Compounds · Organic Electronics and Photovoltaics

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

Affiliations

Department of Chemistry National University of Singapore 3 Science Drive 3 Singapore 117543 Singapore

Departamento de Física Aplicada and Instituto Universitario de Materiales de Alicante Universidad de Alicante Alicante 03080 Spain

Departamento de Óptica Farmacología y Anatomía and Instituto Universitario de Materiales de Alicante Universidad de Alicante Alicante 03080 Spain

References (59)

Show source-provided references
1. 10.1126/science.110289610.1126/science.1102896 ↗
2. 10.1038/nmat184910.1038/nmat1849 ↗
3. 10.1021/cr068010r10.1021/cr068010r ↗
4. 10.1021/ar500240e10.1021/ar500240e ↗
5. 10.1038/nphoton.2010.18610.1038/nphoton.2010.186 ↗
6. 10.1038/nnano.2014.21410.1038/nnano.2014.214 ↗
7. 10.1143/JPSJ.65.192010.1143/JPSJ.65.1920 ↗
8. 10.1002/anie.20180427610.1002/anie.201804276 ↗
9. 10.1002/ange.20180427610.1002/ange.201804276 ↗
10. 10.1002/anie.20180281810.1002/anie.201802818 ↗
11. 10.1002/ange.20180281810.1002/ange.201802818 ↗
12. 10.1126/sciadv.aav771710.1126/sciadv.aav7717 ↗
13. 10.1002/anie.20200032610.1002/anie.202000326 ↗
14. 10.1002/ange.20200032610.1002/ange.202000326 ↗
15. 10.1038/s41467-019-11336-010.1038/s41467-019-11336-0 ↗
16. 10.1002/adfm.20210507310.1002/adfm.202105073 ↗
17. 10.1039/C5CS00183H10.1039/C5CS00183H ↗
18. 10.1021/acs.chemrev.6b0007610.1021/acs.chemrev.6b00076 ↗
19. 10.1016/j.tet.2016.01.05410.1016/j.tet.2016.01.054 ↗
20. 10.1002/anie.20190582310.1002/anie.201905823 ↗
21. 10.1002/anie.20190582310.1002/anie.201905823 ↗
22. 10.1021/jacs.6b0167410.1021/jacs.6b01674 ↗
23. 10.1021/jacs.6b0409210.1021/jacs.6b04092 ↗
24. 10.1039/C9CC01986C10.1039/C9CC01986C ↗
25. 10.1039/jr960000134410.1039/jr9600001344 ↗
26. 10.1021/jo049343w10.1021/jo049343w ↗
27. Crystallographic data with CCDC number 1985806 are deposited in the Cambridge Crystallographic Data Centre.
28. 10.1016/S0022-328X(00)81488-610.1016/S0022-328X(00)81488-6 ↗
29. 10.1107/S056774086800184610.1107/S0567740868001846 ↗
30. 10.1021/cr03008810.1021/cr030088 ↗
31. 10.1021/cr030090110.1021/cr0300901 ↗
32. 10.1021/cr050966z10.1021/cr050966z ↗
33. 10.1002/anie.20090253210.1002/anie.200902532 ↗
34. 10.1016/j.optlastec.2019.10581410.1016/j.optlastec.2019.105814 ↗
35. 10.1002/anie.20170073010.1002/anie.201700730 ↗
36. 10.1039/D1MH00846C10.1039/D1MH00846C ↗
37. 10.1021/acs.jpcc.8b0692510.1021/acs.jpcc.8b06925 ↗
38. 10.1038/ncomms945810.1038/ncomms9458 ↗
39. 10.7567/1882-0786/ab1b9010.7567/1882-0786/ab1b90 ↗
40. 10.1021/acs.chemrev.6b0017210.1021/acs.chemrev.6b00172 ↗
41. 10.1201/b2232710.1201/b22327 ↗
42. 10.1063/1.166149910.1063/1.1661499 ↗
43. 10.1002/adom.20200115310.1002/adom.202001153 ↗
44. 10.1002/adom.20130030110.1002/adom.201300301 ↗
45. 10.1038/s41598-019-47589-410.1038/s41598-019-47589-4 ↗
46. 10.1039/D0CS00037J10.1039/D0CS00037J ↗
47. 10.1021/cm900568k10.1021/cm900568k ↗
48. 10.1063/1.46491310.1063/1.464913 ↗
49. 10.1103/PhysRevB.37.78510.1103/PhysRevB.37.785 ↗
50. 10.1016/j.cplett.2004.06.01110.1016/j.cplett.2004.06.011 ↗
51. 10.1063/1.167490210.1063/1.1674902 ↗
52. 10.1063/1.167752710.1063/1.1677527 ↗
53. 10.1007/BF0053348510.1007/BF00533485 ↗
54. 10.1002/jcc.2288510.1002/jcc.22885 ↗
55. 10.1016/j.tsf.2019.13758010.1016/j.tsf.2019.137580 ↗
56. 10.3390/polym1315254510.3390/polym13152545 ↗
57. 10.1364/AO.49.00046310.1364/AO.49.000463 ↗
58. 10.1002/adom.20170023810.1002/adom.201700238 ↗
59. 10.1016/j.optlastec.2020.10676610.1016/j.optlastec.2020.106766 ↗