Efficient Two‐Photon Excited Fluorescence from Charge‐Transfer Cocrystals Based on Centrosymmetric Molecules
Source abstract
Abstract
Abstract Two‐photon excited chromophores are widely applied for photon upconversion in organic optoelectronics. In this work, efficient two‐photon excited fluorescence is observed from charge‐transfer cocrystals where the molecular architectures of donor and acceptor molecules are both centrosymmetric. The superior structural symmetry of cocrystals eliminates the second harmonic generation of incident near‐infrared laser. The nonlinear optical properties of cocrystals are found to be strongly correlated with the intermolecular charge‐transfer interaction, bringing a wide window of excitation wavelength for the upconverted light emission. The work demonstrates that the cocrystallization of small molecules provides opportunities for the design and synthesis of novel organic optofunctional materials.
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Research context
OpenAlex topics: Nonlinear Optical Materials Studies · Luminescence and Fluorescent Materials · Photochromic and Fluorescence Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Microelectronics State Key Laboratory of Crystal Materials Shandong University Jinan 250100 P. R. China
School of Physics Shandong University Jinan 250100 P. R. China
Technical Institute of Physics and Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China
Institute of Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Shandong Province
References (45)
Show source-provided references
1. 10.1038/1798910.1038/17989 ↗
2. 10.1002/adfm.20060051810.1002/adfm.200600518 ↗
3. 10.1002/anie.20090542810.1002/anie.200905428 ↗
4. 10.1021/ja200549v10.1021/ja200549v ↗
5. 10.1002/adfm.20140440210.1002/adfm.201404402 ↗
6. 10.1039/c1jm12566d10.1039/c1jm12566d ↗
7. 10.1039/C1JM13556B10.1039/C1JM13556B ↗
8. 10.1039/C6TC04129A10.1039/C6TC04129A ↗
9. 10.1039/C8MH01130C10.1039/C8MH01130C ↗
10. 10.1126/science.281.5383.165310.1126/science.281.5383.1653 ↗
11. 10.1021/jp034986l10.1021/jp034986l ↗
12. 10.1021/jp063930z10.1021/jp063930z ↗
13. 10.1021/jp710682z10.1021/jp710682z ↗
14. 10.1002/adma.20120423710.1002/adma.201204237 ↗
15. 10.1002/adma.20160526010.1002/adma.201605260 ↗
16. 10.1002/anie.20080525710.1002/anie.200805257 ↗
17. 10.1021/acs.accounts.6b0020910.1021/acs.accounts.6b00209 ↗
18. 10.1039/b009769l10.1039/b009769l ↗
19. 10.1021/ja044584710.1021/ja0445847 ↗
20. 10.1039/C5SC04920B10.1039/C5SC04920B ↗
21. 10.1021/acs.chemmater.7b0241710.1021/acs.chemmater.7b02417 ↗
22. 10.1021/acs.nanolett.6b0349910.1021/acs.nanolett.6b03499 ↗
23. 10.1002/anie.20171252410.1002/anie.201712524 ↗
24. 10.1039/c3cp55205e10.1039/c3cp55205e ↗
25. 10.1002/anie.20170343910.1002/anie.201703439 ↗
26. 10.1021/acsami.8b1629410.1021/acsami.8b16294 ↗
27. 10.1002/adfm.20130207210.1002/adfm.201302072 ↗
28. 10.1002/anie.20160771210.1002/anie.201607712 ↗
29. 10.1002/adma.20150592710.1002/adma.201505927 ↗
30. 10.1039/P2973000052010.1039/P29730000520 ↗
31. 10.1107/S056774087500503110.1107/S0567740875005031 ↗
32. 10.1002/ange.20171294910.1002/ange.201712949 ↗
33. 10.1021/j100315a02810.1021/j100315a028 ↗
34. 10.1002/aelm.20160020310.1002/aelm.201600203 ↗
35. 10.1016/S0039-6028(01)00715-410.1016/S0039-6028(01)00715-4 ↗
36. 10.1002/adma.20140005610.1002/adma.201400056 ↗
37. 10.1246/bcsj.53.194910.1246/bcsj.53.1949 ↗
38. 10.1063/1.44976510.1063/1.449765 ↗
39. 10.1039/C8TC02748J10.1039/C8TC02748J ↗
40. 10.1039/C7NJ03127K10.1039/C7NJ03127K ↗
41. 10.1002/adma.20160028010.1002/adma.201600280 ↗
42. 10.1016/0009-2614(77)85381-510.1016/0009-2614(77)85381-5 ↗
43. 10.1002/adma.20170596310.1002/adma.201705963 ↗
44. 10.1039/b822395e10.1039/b822395e ↗
45. 10.1021/jacs.5b1152510.1021/jacs.5b11525 ↗