Novel D-A-D conjugated polymers based on tetraphenylethylene monomer for electrochromism
Source abstract
Abstract
Abstract A monomer (E)-4′,4‴-(1,2-diphenylethene-1,2-diyl)bis([1,1′-biphenyl]-4-carbaldehyde) (DDBC) with AIE properties and two novel DDBC-basing polyazomethines (coded as P1 and P2) were prepared. They were gained in short time, low cost and mild reaction conditions by a straightforward synthetic path. Fluorescent testing shows that DDBC owns an intense aggregation-induced emission (AIE) characteristics. But unfortunately, the polymers based on DDBC do not have AIE effect. It may be attributed that the molecules in the excited state consume light energy in the form of electron transfer, reducing the proportion of energy outputted from light, thus causing the disappearance of macroscopic fluorescence. Another guess is that the tetraphenylethylene (TPE) unit takes part of the conjugated backbone of the polymer. However, P1 have high coloration efficiency (346.94 cm2 C−1) and P2 have short response time (the color switching time is 3.43 s and the bleaching time is 1.41 s at 470 nm). Moreover, P1 has electrochromic properties in the near-infrared field. Thus, these features demonstrate that these two novel polymers have great potential as electrochromic materials in optoelectronics applications.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Conducting polymers and applications · Luminescence and Fluorescent Materials · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (38)
Show source-provided references
1. High-performance asymmetric electrochromic-supercapacitor device based on poly (indole-6-carboxylicacid)/TiO2 nanocomposites10.1021/acsami.8b19505 ↗
2. Redox-active and electrochromic polymers from triarylamine end-capped, 2,7-bis (diphenylamino) naphthalene-cored dicarboxamides10.1016/j.eurpolymj.2017.03.016 ↗
3. Four shades of brown: tuning of electrochromic polymer blends toward high-contrast eyewear10.1021/am507063d ↗
4. Soluble high coloration efficiency electrochromic polymers based on (N-phenyl) carbazole, triphenylamine and 9,9-dioctyl-9H-fluorene10.1016/j.synthmet.2018.11.015 ↗
5. Synthesis and tunability of highly electron-accepting, N-benzylated “phosphaviologens”10.1021/ja513258j ↗
6. Colorless to neutral color electrochromic devices based on asymmetric viologens10.1021/acsami.6b11321 ↗
7. Synthesis, photoluminescence, and electrochromism of polyamides containing (3,6-di-tert-butylcarbazol-9-yl) triphenylamine units10.1002/pola.24269 ↗
8. Conjugated polymers for flexible energy harvesting and storage10.1002/adma.201704261 ↗
9. Conjugated polymer-based photoelectrochemical cytosensor with turn-on enable signal for sensitive cell detection10.1021/acsami.7b18275 ↗
10. Unusual doping of donor-acceptor-type conjugated polymers using lewis acids10.1021/ja501024n ↗
11. A rational design and synthesis of cross-conjugated small molecule acceptors approaching high-performance fullerene-free polymer solar cells10.1021/acs.chemmater.8b01491 ↗
12. Vapor-Phase processable novel nonplanar donor-acceptor quateraryls for blue OLEDs10.1021/ol8008182 ↗
13. Molecular engineering of organic sensitizers for dye-sensitized solar cell applications10.1021/ja800066y ↗
14. Effect of Substituents of thienylene-vinylene-thienylene-based conjugated polymer donors on the performance of fullerene and nonfullerene solar cells10.1021/acs.jpcc.8b05184 ↗
15. Trifunctional CdSe quantum dots-polymer composite film with electrochromic, electrofluorescent and light-induced coloration effects10.1016/j.solmat.2017.04.024 ↗
16. Multifunctional AIE-active polymers containing TPA-TPE moiety for electrochromic, electrofluorochromic and photodetector10.1021/acsami.8b02560 ↗
17. High-performance electrofluorochromic devices based on aromatic polyamides with AIE-active tetraphenylethene and electro-active triphenylamine moieties10.1039/C8PY00809D ↗
18. Realizing highly efficient solution-processed homojunction-like sky-blue OLEDs by using thermally activated delayed fluorescent emitters featuring an aggregation-induced emission property10.1021/acs.jpclett.8b00344 ↗
19. A light-up probe with aggregation-induced emission for real-time bio-orthogonal tumor labeling and image-guided photodynamic therapy10.1002/ange.201805446 ↗
20. Probing cancer cells through intracellular aggregation-induced emission kinetic rate of copper nanoclusters10.1021/acsami.8b05160 ↗
21. DNA quadruplexes as molecular scaffolds for controlled assembly of fluorogens with aggregation-induced emission10.1039/C8SC00001H ↗
22. Multifunctional AIE-active polymers containing TPA-TPE moiety for electrochromic, electrofluorochromic and photodetector10.1016/j.dyepig.2019.03.040 ↗
23. Aggregation-induced emission10.1039/c1cs15113d ↗
24. Colorless to all-black full-NIR high-contrast switching in solid electrochromic films prepared with organic mixed valence systems based on dibenzofulvene derivatives10.1021/acs.chemmater.8b01665 ↗
25. Novel blue and red electrochromic poly (azomethine ether)s based on electroactive triphenylamine moieties10.1016/j.orgel.2009.11.009 ↗
26. Simple approach to regulate the spectra of novel kinds of polyazomethines containing bulky triphenylamine: electrochemistry, electrochromism and photophysical responsive to environment10.1016/j.dyepig.2012.08.003 ↗
27. Novel poly-Schiff bases containing 4, 4’-diamino-triphenylamine as hole transport material for organic electronic device10.1016/j.matlet.2004.05.007 ↗
28. Hyperbranched polytriazoles with high molecular compressibility: aggregation-induced emission and superamplified explosive detection10.1039/c0jm04100a ↗
29. Benzo[c][1,2,5]thiadiazole donor-acceptor dyes: a synthetic, spectroscopic, and computational study10.1021/acs.jpca.6b00447 ↗
30. Polymers with aggregation-induced emission characteristics
31. Synthesis and photovoltaic properties of silafluorene copolymers substituted by carbazole and triphenylamine pendants10.1016/j.dyepig.2017.07.011 ↗
32. Colorless to all-black full-NIR high-contrast switching in solid electrochromic films prepared with organic mixed valence systems based on dibenzofulvene derivatives10.1021/acs.chemmater.8b01665 ↗
33. Synthesis, fluorescence, electrochromic properties of aromatic polyamide with triarylamine unit serving as functional group10.1016/j.eurpolymj.2017.06.014 ↗
34. Synthesis and electrochromic properties of electrochromic polymers based on propylenedioxythiophene, diketopyrrolopyrrole and benzodithiophene units10.1016/j.orgel.2018.10.035 ↗
35. A new electrochromic material from an indole derivative and its application in high-quality electrochromic devices10.1016/j.elecom.2009.11.013 ↗
36. Color control in π-conjugated organic polymers for use in electrochromic devices10.1021/cr900129a ↗
37. Three novel donor-acceptor type electrochromic polymers containing 2,3-bis (5-methylfuran-2-yl) thieno [3,4-b] pyrazine acceptor and different thiophene donors: low-band-gap, neutral green-colored, fast-switching materials10.1016/j.jelechem.2018.10.020 ↗
38. Electrochemical polymerization of triphenylamine end-capped dendron: electrochromic and electrofluorochromic switching behaviors10.1016/j.jelechem.2018.06.015 ↗