journal article·2020-09-22Open access

Luminescent sp2-Carbon-Linked 2D Conjugated Polymers with High Photostability

Shunqi Xu, Yungui Li, Bishnu P. Biswal, Matthew A. Addicoat, Silvia Paasch, Paulius Imbrasas, SangWook Park, Huanhuan Shi, Eike Brunner, Marcus Richter, Simone Lenk, Sebastian Reineke, Xinliang Feng

Chemistry of Materials· Volume 32· Issue 18

Abstract

Luminescent organic materials with high photostability are essential in optoelectronics, sensor, and photocatalysis applications. However, small organic molecules are generally sensitive to UV irradiation, giving rise to chemical decompositions. In this work, we demonstrate two novel CN-substituted two-dimensional sp2-carbon-linked conjugated polymers (2D CCPs) containing a chromophore triphenylene unit. The Knoevenagel polymerization between 2,3,6,7,10,11-hexakis(4-formylphenyl)triphenylene (HFPTP) and 1,4-phenylenediacetonitrile (PDAN) or 2,2′-(biphenyl-4,4′-diyl)diacetonitrile (BDAN), provides the crystalline 2D CCP-HFPTP-PDAN (2D CCP-1) and 2D CCP-HFPTP-BDAN (2D CCP-2) with dual pore structures, respectively. 2D CCP-1 and 2D CCP-2 exhibit the photoluminescence quantum yield (PLQY) up to 24.9 and 32.3%, which are the highest values among the reported 2D conjugated polymers and π-conjugated 2D covalent organic frameworks. Furthermore, compared with the well-known emissive small molecule tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN), both 2D CCPs show superior photostability under UV irradiation for 2 h, profiting from the twisted and rigid structures of the CN-substituted vinylene linkages. The present work will trigger the further explorations of novel organic emitters embedded in 2D CCPs with high PLQY and photostability, which can be useful for optoelectronic devices.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Luminescence and Fluorescent Materials · Metal-Organic Frameworks: Synthesis and Applications

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

Affiliations

Center for Advancing Electronics Dresden (CFAED) and Faculty of Chemistry and Food Chemistry, Chair of Molecular Functional Materials, Technische Universität Dresden, Mommsenstraße 4, Dresden 01069, Germany

Dresden Integrated Center for Applied Physics and Photonic Materials (IAPP), Chair for Organic Semiconductors, Technische Universität Dresden, Nöthnitzer Straße 61, Dresden 01069, Germany

School of Science and Technology, Nottingham Trent University Clifton Lane, Nottingham NG118NS, United Kingdom

Department of Chemistry and Food Chemistry, Chair of Bioanalytical Chemistry, Technische Universität Dresden, Bergstraße 66, Dresden 01069, Germany

Funding

European Commission · Deutsche Forschungsgemeinschaft · H2020 Marie Sklodowska-Curie Actions · H2020 European Research Council · Center of Advancing Electronics Dresden · German Science Council · Coordination Networks: Building Blocks for Functional Systems

References (33)

Show source-provided references
1. 10.1103/RevModPhys.85.124510.1103/RevModPhys.85.1245 ↗
2. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
3. 10.1038/s41565-019-0370-910.1038/s41565-019-0370-9 ↗
4. 10.1021/acs.chemrev.6b0017210.1021/acs.chemrev.6b00172 ↗
5. 10.1021/acs.chemrev.8b0064410.1021/acs.chemrev.8b00644 ↗
6. 10.1038/nature0800310.1038/nature08003 ↗
7. 10.1038/s41467-019-11032-z10.1038/s41467-019-11032-z ↗
8. Shahid I. · Adv. Mater. Process. · 2004 · 162 · 51
9. 10.1021/jp412614k10.1021/jp412614k ↗
10. 10.1021/acs.jpcc.5b0708410.1021/acs.jpcc.5b07084 ↗
11. 10.1002/anie.20190429110.1002/anie.201904291 ↗
12. 10.1039/D0CS00236D10.1039/D0CS00236D ↗
13. 10.1038/ncomms748610.1038/ncomms7486 ↗
14. 10.1021/jacs.7b1066310.1021/jacs.7b10663 ↗
15. 10.1002/anie.20170027110.1002/anie.201700271 ↗
16. 10.1038/s41467-018-04769-610.1038/s41467-018-04769-6 ↗
17. 10.3390/molecules2308194710.3390/molecules23081947 ↗
18. 10.1038/s41467-018-06719-810.1038/s41467-018-06719-8 ↗
19. 10.1002/chem.20180638510.1002/chem.201806385 ↗
20. 10.1021/jacs.5b1075410.1021/jacs.5b10754 ↗
21. 10.1021/jacs.8b0831210.1021/jacs.8b08312 ↗
22. 10.1021/jacs.8b0745010.1021/jacs.8b07450 ↗
23. 10.1021/jacs.8b0838010.1021/jacs.8b08380 ↗
24. 10.1039/C6CC01476C10.1039/C6CC01476C ↗
25. 10.1038/nature1168710.1038/nature11687 ↗
26. 10.1038/s41598-019-51718-410.1038/s41598-019-51718-4 ↗
27. 10.3389/fchem.2019.0068810.3389/fchem.2019.00688 ↗
28. 10.1002/anie.20181268510.1002/anie.201812685 ↗
29. 10.1063/1.494864710.1063/1.4948647 ↗
30. 10.1021/acsmacrolett.5b0080410.1021/acsmacrolett.5b00804 ↗
31. 10.1038/s41598-019-51718-410.1038/s41598-019-51718-4 ↗
32. 10.1039/C8TC01998C10.1039/C8TC01998C ↗
33. 10.1021/jacs.0c0199010.1021/jacs.0c01990 ↗