1.42-Fold Enhancement of Blue OLED Device Performance by Simply Changing Alkyl Groups on the Acridine Ring
Source abstract
Abstract
Developing high-efficiency blue thermally activated delayed fluorescence (TADF) emitters is still a formidable challenge. Here, we report five blue TADF emitters designed by simply changing the frequently used methyl group (C1) to a longer one gradually to subtly adjust the energy levels. DAc-C1–DAc-C5 are developed by using diphenylsulfone (DPS) as the acceptor and acridine with different-length alkyl chains on C(9) as the donor groups. These five compounds have high photoluminescence quantum yields (PLQYs) (75%–84%) with blue emission. The DAc-C2-based OLED device exhibits the maximum external quantum efficiency (EQE) of up to 24.1% with CIE (0.15, 0.19), which is 1.42 times higher than that of state-of-the-art TADF OLEDs based on DAc-C1 (EQE: 17.0%) under the same conditions, confirming the power of the molecular design strategy. Furthermore, the crystal analyses partially explain the influence of the alkyl chain on the device property, demonstrating a new approach for achieving TADF luminogens with high performance.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (73)
Show source-provided references
1. Highly efficient organic light-emitting diodes from delayed fluorescence10.1038/nature11687 ↗
2. Efficient blue organic light-emitting diodes employing thermally activated delayed fluorescence10.1038/nphoton.2014.12 ↗
3. Highly efficient blue electroluminescence based on thermally activated delayed fluorescence10.1038/nmat4154 ↗
4. Nearly 100% internal quantum efficiency in undoped electroluminescent devices employing pure organic emitters10.1002/adma.201405474 ↗
5. Electroluminescence in conjugated polymers10.1038/16393 ↗
6. Improved energy transfer in electrophosphorescent devices10.1063/1.123055 ↗
7. Highly phosphorescent bis-cyclometalated iridium complexes: synthesis, photophysical characterization, and use in organic light emitting diodes10.1021/ja003693s ↗
8. Highly efficient phosphorescent emission from organic electroluminescent devices10.1038/25954 ↗
9. Nearly 100% internal phosphorescence efficiency in an organic light-emitting device10.1063/1.1409582 ↗
10. Evidence of the Reverse Intersystem Crossing in Intra-Molecular Charge-Transfer Fluorescence-Based Organic Light-Emitting Devices Through Magneto-Electroluminescence Measurements10.1002/adom.201300028 ↗
11. Controlling Synergistic Oxidation Processes for Efficient and Stable Blue Thermally Activated Delayed Fluorescence Devices10.1002/adma.201602127 ↗
12. Luminous butterflies: efficient exciton harvesting by benzophenone derivatives for full-color delayed fluorescence OLEDs10.1002/anie.201402992 ↗
13. Triplet harvesting with 100% efficiency by way of thermally activated delayed fluorescence in charge transfer OLED emitters10.1002/adma.201300753 ↗
14. Stable blue thermally activated delayed fluorescent organic light-emitting diodes with three times longer lifetime than phosphorescent organic light-emitting diodes10.1002/adma.201500267 ↗
15. Molecular Design Strategies for Color Tuning of Blue TADF Emitters10.1021/acsami.9b06364 ↗
16. Efficient and Stable Organic Light-Emitting Diodes Employing Indolo[2,3-b]indole-Based Thermally Activated Delayed Fluorescence Emitters10.1021/acsami.9b19474 ↗
17. Dibenzo[a,j]phenazine-Cored Donor-Acceptor-Donor Compounds as Green-to-Red/NIR Thermally Activated Delayed Fluorescence Organic Light Emitters10.1002/anie.201600113 ↗
18. Improving the Efficiency of Red Thermally Activated Delayed Fluorescence Organic Light-Emitting Diode by Rational Isomer Engineering10.1002/adfm.202002681 ↗
19. Highly Efficient Nondoped OLEDs with Negligible Efficiency Roll-Off Fabricated from Aggregation-Induced Delayed Fluorescence Luminogens10.1002/anie.201706752 ↗
20. Highly Efficient Thermally Activated Delayed Fluorescence via J-Aggregates with Strong Intermolecular Charge Transfer10.1002/adma.201808242 ↗
21. A Multifunctional Bipolar Luminogen with Delayed Fluorescence for High-Performance Monochromatic and Color-Stable Warm-White OLEDs10.1002/adfm.202000019 ↗
22. Achieving Nearly 30% External Quantum Efficiency for Orange-Red Organic Light Emitting Diodes by Employing Thermally Activated Delayed Fluorescence Emitters Composed of 1,8-Naphthalimide-Acridine Hybrids10.1002/adma.201704961 ↗
23. A Significantly Twisted Spirocyclic Phosphine Oxide as a Universal Host for High-Efficiency Full-Color Thermally Activated Delayed Fluorescence Diodes10.1002/adma.201506286 ↗
24. Intermolecular Charge-Transfer Transition Emitter Showing Thermally Activated Delayed Fluorescence for Efficient Non-Doped OLEDs10.1002/anie.201804483 ↗
25. A Red Thermally Activated Delayed Fluorescence Emitter Simultaneously Having High Photoluminescence Quantum Efficiency and Preferentially Horizontal Emitting Dipole Orientation10.1002/adfm.201908839 ↗
26. Sky-Blue Organic Light Emitting Diode with 37% External Quantum Efficiency Using Thermally Activated Delayed Fluorescence from Spiroacridine-Triazine Hybrid10.1002/adma.201601675 ↗
27. A versatile thermally activated delayed fluorescence emitter for both highly efficient doped and non-doped organic light emitting devices10.1039/C5CC05022G ↗
28. Evaporation- and Solution-Process-Feasible Highly Efficient Thianthrene-9,9′,10,10′-Tetraoxide-Based Thermally Activated Delayed Fluorescence Emitters with Reduced Efficiency Roll-Off10.1002/adma.201503225 ↗
29. High-Efficiency Blue Organic Light-Emitting Diodes Based on Thermally Activated Delayed Fluorescence from Phenoxaphosphine and Phenoxathiin Derivatives10.1002/adma.201506391 ↗
30. Highly efficient blue thermally activated delayed fluorescence emitters based on symmetrical and rigid oxygen-bridged boron acceptors10.1038/s41566-019-0415-5 ↗
31. The odd-even effect of alkyl chain in organic room temperature phosphorescence luminogens and the corresponding in vivo imaging10.1039/C9QM00108E ↗
32. Effect of Carbon Chain Length in the Substituent of PCBM-like Molecules on Their Photovoltaic Properties10.1002/adfm.200902447 ↗
33. Significantly improved performance of dye-sensitized solar cells by optimizing organic dyes with pyrrole as the isolation spacer and utilizing alkyl chain engineering10.1039/C8TA06258G ↗
34. Unraveling the Main Chain and Side Chain Effects on Thin Film Morphology and Charge Transport in Quinoidal Conjugated Polymers10.1002/adfm.201801874 ↗
35. N-Alkyl substituted di(perylene bisimides) as air-stable electron transport materials for solution-processible thin-film transistors with enhanced performance10.1039/c3tc30156g ↗
36. The Strong Light-Emission Materials in the Aggregated State: What Happens from a Single Molecule to the Collective Group
37. Similar or different: the same Spiro-core but different alkyl chains with apparently improved device performance of perovskite solar cells10.1007/s11426-018-9432-x ↗
38. Oxadiazole-and triazole-based highly-efficient thermally activated delayed fluorescence emitters for organic light-emitting diodes10.1039/c3tc30699b ↗
39. An organic molecule with asymmetric structure exhibiting aggregation-induced emission, delayed fluorescence, and mechanoluminescence10.1002/anie.201409767 ↗
40. A Simple Organic Molecule Realizing Simultaneous TADF, RTP, AIE, and Mechanoluminescence: Understanding the Mechanism Behind the Multifunctional Emitter10.1002/anie.201910719 ↗
41. Achieving High-Performance Nondoped OLEDs with Extremely Small Efficiency Roll-Off by Combining Aggregation-Induced Emission and Thermally Activated Delayed Fluorescence10.1002/adfm.201606458 ↗
42. Avoiding Energy Loss on TADF Emitters: Controlling the Dual Conformations of D-A Structure Molecules Based on the Pseudoplanar Segments10.1002/adma.201701476 ↗
43. Manipulation of successive crystalline transformations to control electron transfer and switchable functions10.1093/nsr/nwy033 ↗
44. Hydrogen-Bonding-Assisted Intermolecular Charge Transfer: A New Strategy to Design Single-Component White-Light-Emitting Materials10.1002/adfm.201703918 ↗
45. Sterically Shielded Electron Transporting Material with Nearly 100% Internal Quantum Efficiency and Long Lifetime for Thermally Activated Delayed Fluorescent and Phosphorescent OLEDs10.1021/acsami.7b04391 ↗
46. Optical tuning by the self-assembly and disassembly of chain-like plasmonic superstructures10.1093/nsr/nwx067 ↗
47. A stable tetraphenylethene derivative: aggregation-induced emission, different crystalline polymorphs, and totally different mechanoluminescence properties10.1039/C6MH00025H ↗
48. AIEgen with Fluorescence-Phosphorescence Dual Mechanoluminescence at Room Temperature10.1002/anie.201610453 ↗
49. Miracles of Molecular Uniting10.1007/s40843-019-1172-2 ↗
50. Triboluminescence: recalling interest and new aspects10.1016/j.chempr.2018.01.001 ↗
51. Aggregation-induced emission: a coming-of-age ceremony at the age of eighteen10.1007/s11426-019-9512-x ↗
52. Recent Advances in Purely Organic Room Temperature Phosphorescence Polymer10.1007/s10118-019-2218-z ↗
53. Frisch · 2009
54. Localized orbital scaling correction for systematic elimination of delocalization error in density functional approximations10.1093/nsr/nwx111 ↗
55. Efficient up-conversion of triplet excitons into a singlet state and its application for organic light emitting diodes10.1063/1.3558906 ↗
56. Ultrahigh-Efficiency Green PHOLEDs with a Voltage under 3 V and a Power Efficiency of Nearly 110 lm W−1 at Luminance of 10 000 cd m−210.1002/adma.201702847 ↗
57. Polycyclic Aromatic Hydrocarbon Derivatives toward Ideal Electron-Transporting Materials for Organic Light-Emitting Diodes10.1021/acs.jpclett.9b00526 ↗
58. Multifunctional Organic Emitters for High-Performance and Low-Cost Organic Light-Emitting Didoes10.1002/tcr.201900005 ↗
59. Singlet-Triplet Splitting Energy Management via Acceptor Substitution: Complanation Molecular Design for Deep-Blue Thermally Activated Delayed Fluorescence Emitters and Organic Light-Emitting Diodes Application10.1002/adfm.201603520 ↗
60. Engineering the excited-state properties of purely organic intramolecular and intermolecular charge transfer emitters towards high-performance fluorescent OLEDs10.1039/C7TC04014H ↗
61. High-efficiency deep-blue organic light-emitting diodes based on a thermally activated delayed fluorescence emitter10.1039/C3TC31936A ↗
62. The role of fluorine-substitution on the π-bridge in constructing effective thermally activated delayed fluorescence molecules10.1039/C8TC01158C ↗
63. Narrowband deep-blue organic light-emitting diode featuring an organoboron-based emitter10.1038/s41566-019-0476-5 ↗
64. Molecular design of deep blue fluorescent emitters with 20% external quantum efficiency and narrow emission spectrum10.1016/j.orgel.2015.12.001 ↗
65. Full-Color Delayed Fluorescence Materials Based on Wedge-Shaped Phthalonitriles and Dicyanopyrazines: Systematic Design, Tunable Photophysical Properties, and OLED Performance10.1002/adfm.201505106 ↗
66. Simultaneous improvement of emission color, singlet-triplet energy gap, and quantum efficiency of blue thermally activated delayed fluorescent emitters using a 1-carbazolylcarbazole based donor10.1039/C6CC04516B ↗
67. Blue TADF Emitters Based on Indenocarbazole Derivatives with High Photoluminescence and Electroluminescence Efficiencies10.1021/acsami.8b20699 ↗
68. Isobenzofuranone- and Chromone-Based Blue Delayed Fluorescence Emitters with Low Efficiency Roll-Off in Organic Light-Emitting Diodes10.1021/acs.chemmater.7b03371 ↗
69. Management of singlet and triplet excitons for efficient white organic light-emitting devices10.1038/nature04645 ↗
70. Management of Singlet and Triplet Excitons: A Universal Approach to High-Efficiency All Fluorescent WOLEDs with Reduced Efficiency Roll-Off Using a Conventional Fluorescent Emitter10.1002/adom.201600117 ↗
71. Molecular Packing: Another Key Point for the Performance of Organic and Polymeric Optoelectronic Materials10.1021/acs.accounts.0c00060 ↗
72. Fluorescence of Non-aromatic Organic Systems and Room Temperature Phosphorescence of Organic Luminogens: The Intrinsic Principle and Recent Progress10.1002/smll.201801560 ↗
73. The influence of the molecular packing on the room temperature phosphorescence of purely organic luminogens10.1038/s41467-018-03236-6 ↗