TADF and HLCT emission switching by changing the intramolecular charge transfer properties through modification of substituent orientation
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OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Photochemistry and Electron Transfer Studies
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References (62)
Show source-provided references
1. High-efficiency single emissive layer white organic light-emitting diodes based on solution-processed dendritic host and new orange-emitting iridium complex10.1002/adma.201104758 ↗
2. Spiro‐based thermally activated delayed fluorescence emitters for organic light‐emitting diodes10.1002/adom.202402464 ↗
3. A brief history of OLEDs—Emitter development and industry milestones
4. Boron‐dipyrromethene emitters with strengthened rigidity and restricted scissoring vibration for high‐performance OLEDs with deep‐red narrowband emission10.1002/adom.202402333 ↗
5. Management of charges and excitons for high-performance white organic light-emitting diodes10.1039/b909057f ↗
6. Two birds with one stone: polymerized thermally activated delayed fluorescence small molecules10.1002/chem.202304095 ↗
7. Nearly 100% internal phosphorescence efficiency in an organic light-emitting device10.1063/1.1409582 ↗
8. Highly phosphorescent bis-cyclometalated iridium complexes: synthesis, photophysical characterization, and use in organic light emitting diodes10.1021/ja003693s ↗
9. Excitonic singlet-triplet ratio in a semiconducting organic thin film10.1103/PhysRevB.60.14422 ↗
10. Hot exciton versus hot exciplex TADF mechanism–effect of the donor‐acceptor functionalization pattern on anthracene‐based emitters10.1002/cptc.202400141 ↗
11. Organic electroluminescent materials and devices
12. Electroluminescence from triplet metal—ligand charge-transfer excited state of transition metal complexes10.1016/S0379-6779(97)04166-0 ↗
13. Thermally activated delayed fluorescence (TADF) materials based on earth‐abundant transition metal complexes: synthesis, design and applications
14. Recent progress in metal-organic complexes for optoelectronic applications10.1039/C3CS60449G ↗
15. Narrowband emissive solution‐processed polymer organic light‐emitting diodes with external quantum efficiency above 30%
16. Recent progress of green thermally activated delayed fluorescent emitters10.1080/15980316.2017.1333046 ↗
17. High-efficiency, long-lifetime deep-blue organic light-emitting diodes10.1038/s41566-021-00763-5 ↗
18. Universal blue emitters for high efficiency thermally activated delayed fluorescence and fluorescent organic light-emitting diodes10.1016/j.dyepig.2019.108070 ↗
19. Efficient OLEDs with alleviated efficiency Roll‐off based on MR‐TADF materials containing indolo [3, 2, 1‐jk] carbazole10.1002/adom.202400200 ↗
20. Deep‐blue OLEDs with BT. 2020 blue gamut, external quantum efficiency approaching 40
21. Simple‐structure and anti‐quenching deep‐blue multi‐resonance TADF emitters enable high‐efficiency OLEDs with BT. 2020 blue gamut10.1002/adfm.202414635 ↗
22. Advancing photocatalytic overall water splitting with Z-Scheme heterojunctions by interfacial manipulation
23. Rigid heterocyclic modification promoted nitrogen/carbonyl multi-resonance thermally activated delayed fluorescence emitters for high-efficiency electroluminescence
24. Integration of through-space conjugation of an adjacent arene with a nitrogen/carbonyl framework for narrowband emission
25. Rational molecular design via cyanobenzene integration for constructing efficient yellow‐orange thermally activated delayed fluorescence emitters10.1002/adom.202303299 ↗
26. Regulating the spatially folded arrangement of donor and acceptor units to achieve efficient orange‐red thermally activated delayed fluorescence
27. High‐performance solution processable red TADF‐OLED with external quantum efficiency exceeding 28% using a multi‐resonance emitter host
28. Molecular engineering of Donor/π‐Bridge enables high‐efficiency and long‐lifetime near‐infrared TADF‐OLEDs10.1002/adfm.202412780 ↗
29. Highly and deep red‐luminescent Bisphenylamine‐Appended benzocarcogendiazole fluorophores10.1002/cphc.202400426 ↗
30. Understanding and modulating the horizontal orientations and short‐range charge transfer excited states for high‐performance narrowband emitters10.1002/flm2.15 ↗
31. Purely organic room temperature phosphorescent materials toward organic light‐emitting diodes10.1002/flm2.23 ↗
32. High-efficiency red thermally activated delayed fluorescence emitters based on benzothiophene-fused spiro-acridine donor - ScienceDirect10.1016/j.cej.2020.126663 ↗
33. Exchange functionals with improved long-range behavior and adiabatic connection methods without adjustable parameters: the mPW and mPW1PW models10.1063/1.475428 ↗
34. Density‐functional thermochemistry. III. The role of exact exchange10.1063/1.464913 ↗
35. Density-functional exchange-energy approximation with correct asymptotic behavior10.1103/PhysRevA.38.3098 ↗
36. Inhomogeneous electron gas10.1103/PhysRev.136.B864 ↗
37. The performance of a family of density functional methods10.1063/1.464906 ↗
38. Self-ConsistentEquations including exchange and correlation effects10.1103/PhysRev.140.A1133 ↗
39. Development of the colle-salvetti correlation-energy into a function of the electron density10.1103/PhysRevB.37.785 ↗
40. Density-functional approximation for the correlation energy of the inhomogeneous electron gas10.1103/PhysRevB.33.8822 ↗
41. Generalized gradient approximation made simple10.1103/PhysRevLett.77.3865 ↗
42. The calculation of atomic fields10.1017/S0305004100011683 ↗
43. Approximate density functional theory as a practical tool in molecular energetics and dynamics10.1021/cr00005a001 ↗
44. Ab initio calculation of vibrational absorption and circular dichroism spectra using density functional force fields10.1021/j100096a001 ↗
45. Toward reliable density functional methods without adjustable parameters: the PBE0 model10.1063/1.478522 ↗
46. Development of novel density functionals for thermochemical kinetics10.1063/1.1774975 ↗
47. Zhao · Theor. Chem. Acc. · 2008 · 11910.1007/s00214-007-0401-8 ↗
48. Assessment of functionals for TD-DFT calculations of singlet-triplet transitions10.1021/ct100005d ↗
49. Structure and Dynamics of Liquid Water from ab Initio Molecular Dynamics-Comparison of BLYP, PBE, and revPBE Density Functionals with and without van der Waals Corrections10.1021/ct3001848 ↗
50. Time-dependent density functional theory calculations for core-excited states: assessment of standard exchange-correlation functionals and development of a novel hybrid functional10.1063/1.2173987 ↗
51. Performance of B3LYP density functional methods for a large set of organic molecules10.1021/ct700248k ↗
52. Frisch · 2009
53. Insights from QM/MM-ONIOM calculations: the TADF phenomenon of phenanthro [9, 10-d] imidazole-anthraquinone in the solid state10.1039/D1CP00578B ↗
54. Theoretical study on the origin of the dual phosphorescence emission from organic aggregates at room temperature
55. Efficient and long-lived room-temperature organic phosphorescence: theoretical descriptors for molecular designs10.1021/jacs.8b11224 ↗
56. MOlecular MAterials property prediction package (MOMAP) 1.0: a software package for predicting the luminescent properties and mobility of organic functional materials10.1080/00268976.2017.1402966 ↗
57. Theoretical study of conversion and decay processes of excited triplet and singlet states in a thermally activated delayed fluorescence molecule10.1021/acs.jpcc.7b00692 ↗
58. Thermal vibration correlation function formalism for molecular excited state decay rates10.1002/cjoc.202000226 ↗
59. GROMACS: high performance molecular simulations through multi-level parallelism from laptops to supercomputers10.1016/j.softx.2015.06.001 ↗
60. VMD: visual molecular dynamics10.1016/0263-7855(96)00018-5 ↗
61. A practical method for the use of curvilinear coordinates in calculations of normal-mode-projected displacements and Duschinsky rotation matrices for large molecules10.1063/1.1412875 ↗
62. K.A.C. Angeli, K. Bak, V. Bakken, R. Bast, L. Boman, O. Christiansen, R. Cimiraglia, S. Coriani, J. Cukras, P. Dahle, Dalton2018. 2–Dalton Program Manual.