2019
DOI: 10.1016/j.dyepig.2019.107650
|View full text |Cite
|
Sign up to set email alerts
|

Solution-processed white organic light-emitting diodes with blue fluorescent and orange-red thermally activated delayed fluorescent dendritic luminogens

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
5
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 11 publications
(5 citation statements)
references
References 46 publications
0
5
0
Order By: Relevance
“…As shown in Figure 5b,Device Dshows ablue emission band at % 470 nm coming from BD-Cy,and ayellow emission band at % 550 nm from YD-TF,leading to white electroluminescence with CIE coordinates of (0.32, 0.45) at 5V .Asthe voltage increases,the relative intensity of blue emission to yellow emission is increased, accompanied by CIE coordinates moving to (0.31, 0.42) at 8V .R emarkably,D evice Dr eveals al ow turn-on voltage (V on )o f2 .8 Vt ogether with high device efficiency with the maximum LE (LE max )of57.6 cd A À1 ,maximum EQE (EQE max )of20.6 %and maximum PE (PE max )of58.9 lm W À1 , representing the state-of-the-art efficiency for solution-processed all-TADF white OLEDs (Table S6). [33][34][35][36][37][38][39][40][41] ForDevice E with 20 wt %BD-Cy and 1wt% YD-TF as emitter, the CIE coordinates move to (0.32, 0.44) at the voltage of 8V . Meanwhile,t he device efficiencies decline to 55.2 cd A À1 , 19.2 %and 55.6 lm W À1 for LE max ,EQE max and PE max, respectively due to exciton quenching at high dopant concentration.…”
Section: Devicementioning
confidence: 99%
See 1 more Smart Citation
“…As shown in Figure 5b,Device Dshows ablue emission band at % 470 nm coming from BD-Cy,and ayellow emission band at % 550 nm from YD-TF,leading to white electroluminescence with CIE coordinates of (0.32, 0.45) at 5V .Asthe voltage increases,the relative intensity of blue emission to yellow emission is increased, accompanied by CIE coordinates moving to (0.31, 0.42) at 8V .R emarkably,D evice Dr eveals al ow turn-on voltage (V on )o f2 .8 Vt ogether with high device efficiency with the maximum LE (LE max )of57.6 cd A À1 ,maximum EQE (EQE max )of20.6 %and maximum PE (PE max )of58.9 lm W À1 , representing the state-of-the-art efficiency for solution-processed all-TADF white OLEDs (Table S6). [33][34][35][36][37][38][39][40][41] ForDevice E with 20 wt %BD-Cy and 1wt% YD-TF as emitter, the CIE coordinates move to (0.32, 0.44) at the voltage of 8V . Meanwhile,t he device efficiencies decline to 55.2 cd A À1 , 19.2 %and 55.6 lm W À1 for LE max ,EQE max and PE max, respectively due to exciton quenching at high dopant concentration.…”
Section: Devicementioning
confidence: 99%
“…Solution-processed two-color white OLEDs based on blue and yellow p-stacked donor-acceptor dendrimers exhibit the maximum external quantum efficiencyof20.6 %and maximum power efficiency of 58.9 lm W À1 ,w hich are the state-of-the-art efficiencies for all-TADF white OLEDs by solution process (Table S6). [33][34][35][36][37][38][39][40][41]…”
Section: Introductionmentioning
confidence: 99%
“…32 However, meeting all the above requirements always needs to integrate multiple functional groups together into one molecule, which is generally associated with multi-step metal-catalyzed coupling reactions. 25–28,35–37 This will inevitably increase the difficulty of purification and the synthetic cost of TADF molecules. Therefore, it is of vital importance to develop efficient and solution-processable red TADF emitters via a simple and green synthetic route.…”
Section: Introductionmentioning
confidence: 99%
“…Huang and his coworkers [22] reported single-emissive-layer WOLEDs by solution process and obtained a high efficiency of 18.9 cd A −1 at 280 cd m −2 using Firpic, Ir(ppy) 2 (acac), Ir(bt) 2 (acac), and Ir(piq) 2 (acac) as dopants. Dong and his coworkers [23], using 3ICz-Tr as a blue emitter and Tri-tNID as an orange-red emitter, obtained a maximum external quantum efficiency (EQE max ) of 8.32% without the need for a host material. Lee and colleagues [24] produced hybrid WOLEDs with a single EML, which consisted of 5-(4-(4,6-diphenyl-1,3,5triazin-2-yl)phenyl)-10,10-diphenyl-5,10-dihydrodibenzo[b,e] [1,4]azasiline (DTPDDA) as a blue thermally activated delayed fluorescence (TADF) emitter and Ir(MDQ) 2 (acac) as a phosphorescent red emitter, and obtained an EQE max of 6.16%.…”
Section: Introductionmentioning
confidence: 99%