Two derivatives of phenyl pyrimidine as acceptor unit and triphenylamino or 4,4'-dimethoxytriphenylamino donor groups were designed and synthesized as emitters for organic light-emitting diodes (OLEDs) aiming to utilize triplet excitons in the electroluminescence. Thermogravimetric analysis revealed high thermal stability of the compounds with 5% weight loss temperatures of 397 and 438 °C. The theoretical estimations and photophysical data show the contributions of local excited and charge transfer states into emission. The addition of the methoxy groups led to the significant improvement of hole-transporting properties and the bathochromic shift of the emission from blue to green-blue spectral diapason. It is shown that mixing of the compounds with the organic host results in facilitation of the delayed emission. The singlet-triplet energy splitting was found to be too big for the thermally activated delayed fluorescence. No thermal activation of the long-lived emission was detected. No experimental evidence for triplet-triplet annihilation and room temperature phosphorescence were detected making the hot exciton mechanism the most probable one. The OLEDs based on the compounds reached the maximum external quantum efficiency of up to 10.6%.
We investigated the effects of sterically nonrestricted electron-accepting substituents of three isomeric indolocarbazole derivatives on their aggregation-induced emission enhancement, mechanochromic luminescence and thermally activated delayed fluorescence. The compounds are potentially efficient emitters for host-free organic light-emitting diodes. The films of indolocarbazole derivatives exhibit emissions with wavelengths of fluorescence intensity maxima from 483 to 500 nm and photoluminescence quantum yields from 31 to 58%. The ionization potentials of the solid samples, measured by photoelectron emission spectrometry, are in the narrow range of 5.78-5.99 eV. The electron affinities of the solid samples are in the range of 2.99-3.19 eV. The layers of the derivatives show diverse charge-transporting properties with maximum hole mobility reaching 10-4 cm2/Vs at high electric fields. An organic light-emitting diode with a light-emitting layer of neat compound shows a turn-on voltage of 4.1 V, a maximum brightness of 24,800 cd/m2, a maximum current efficiency of 12.5 cd/A and an external quantum efficiency of ca. 4.8%. When the compounds are used as hosts, green electroluminescent devices with an external quantum efficiency of ca. 11% are obtained. The linking topology of the isomeric derivatives of indolo[2,3-a]carbazole and indolo[3,2-b]carbazole and the electron-accepting anchors influences their properties differently, such as aggregation-induced emission enhancement, mechanochromic luminescence, thermally activated delayed fluorescence, charge-transporting, and electroluminescent properties. The derivative indolo[3,2-b]carbazole displays good light-emitting properties, while the derivatives of indolo[2,3-a]carbazole show good hosting properties, which make them useful for application in electroluminescent devices.
The synthesis and optoelectronic properties of four simple-structure thioxanthone derivatives employing thioxanthone as an acceptor unit, coupled with moieties having very different electron-donating abilities such as phenoxazine, 3,6-di-tert-butylcarbazole, 3,7-di-tert-butylphenothiazine, or 2,7-di-tert-butyl-9,9-dimethylacridane, are reported. The compounds form molecular glasses with glass transition temperatures reaching 116 °C. Ionization potentials of the compounds estimated by photoelectron emission method range from 5.42 to 5.74 eV. Thioxanthone derivatives containing 3,6-tert-butylcarbazole or 2,7-di-tert-butyl-9,9-dimethylacridane moieties with weak electron-donating strengths were characterized by bipolar charge transport with relatively close hole and electron mobility values of 6.8 × 10-5/2.4 × 10-5 and 3.1 × 10-5/4.6 × 10-6 cm2/(V s) recorded at 3.6 × 105 V/cm. The other compounds demonstrated hole-transporting properties. The films of thioxanthones containing phenoxazine or 2,7-di-tert-butyl-9,9-dimethylacridane moieties showed efficient thermally activated delayed fluorescence with a photoluminescence quantum yield of up to 50% due to the solid-state luminescence enhancement. Organic-light-emitting diodes containing the synthesized compounds as emitters showed very different external quantum efficiencies (0.9-10.3%) and blue, sky blue, green, or yellow electroluminescence colors, thus reflecting the effects of donor substituents.
Motivated to minimize the effects of solid-state solvation and conformation disorder on emission properties of donor-acceptor-type emitters, we developed five new asymmetric multiple donor-acceptor type derivatives of tert-butyl carbazole and trifluoromethyl benzene exploiting different electron-accepting anchoring groups. Using this design strategy, for a compound containing four di-tert-butyl carbazole units as donors as well as 5-methyl pyrimidine and trifluoromethyl acceptor moieties, small singlet-triplet splitting of ca. 0.03 eV, reverse intersystem crossing rate of 1 × 106 s-1, and high photoluminescence quantum yield of neat film of ca. 75% were achieved. This compound was also characterized by the high value of hole and electron mobilities of 8.9 × 10-4 and 5.8 × 10-4 cm2 V-1 s-1 at an electric field of 4.7 × 105 V/cm, showing relatively good hole/electron balance, respectively. Due to the lowest conformational disorder and solid-state solvation effects, this compound demonstrated very similar emission properties (emission colors) in non-doped and differently doped organic light-emitting diodes (OLEDs). The lowest conformational disorder was observed for the compound with the additional accepting moiety inducing steric hindrance, limiting donor-acceptor dihedral rotational freedom. It can be exploited in the multi-donor-acceptor approach, increasing the efficiency. Using an emitter exhibiting the minimized solid-state solvation and conformation disorder effects, the sky blue OLED with the emitting layer of this compound dispersed in host 1,3-bis(N-carbazolyl)benzene displayed an emission peak at 477 nm, high brightness over 39 000 cd/m2, and external quantum efficiency up to 15.9% along with a maximum current efficiency of 42.6 cd/A and a maximum power efficiency of 24.1 lm/W.
Aiming to design bipolar organic semiconductors with high electron mobility and efficient red thermally activated delayed fluorescence (TADF), three donor-acceptor compounds were designed and synthesized selecting 1,8-naphthalimide as an acceptor and phenoxazine, 3,7-di-tert-butylphenothiazine or 2,7-di-tert-butyldimethyl-9,10-dihydroacridine as donor moieties. Aggregation induced emission enhancement was detected for the compounds causing efficient TADF in the solid-state. Photoluminescence quantum yields up to 77% were observed for the films of the compounds doped in a host. The compounds exhibited small singlet-triplet splitting (0.03-0.05 eV), and high reverse intersystem crossing rates of 2.08 × 105-1.13 × 106 s-1. The compounds were characterized by satisfactory hole and electron-injecting properties with ionization potentials of 5.72-5.83 eV and electron affinities of 2.79-2.91 eV. Bipolar charge transport was revealed by time of flight measurements. Electron transport with low dispersity and mobilities exceeding 2 × 10-3 cm2 V-1 s-1 was observed at an electric field of 4.6 × 105 V cm-1. The compounds were used as emitters in red electroluminescent devices, which showed maximum external quantum efficiencies up to 8.2%. Utilization of host-guest systems as light-emitting materials with hosts preferably transporting holes and TADF guests which preferably transport electrons allowed maximum efficiencies to be achieved at a practical brightness of 700-2200 cd m-2. DFT calculations of the geometry, electronic structure, absorption and photoluminescence spectra of all compounds were carried out to prove the conclusions drawn from the experiment. The results of the calculations clearly show that the first excited state for all compounds is the intramolecular charge transfer state. Quantitative analysis of the separation degree of electronic density during excitation allows the observed dependence of the blue shift value in the absorption and emission spectra on the increasing polarity of the solvent to be explained.
INTRODUCTION: Evolution of organic light-emitting diodes (OLEDs) reached the point, which allows to obtain maximum internal quantum efficiency of 100% partly using heavy-metal-free emitters exhibiting thermally activated delayed fluorescence (TADF). Such emitters are also predictively perfect candidates for new generation of optical sensors since triplet harvesting can be sensitive to different analytes (at least to oxygen). Although many organic TADF emitters have been reported so far as OLED emitters, the investigation of materials suitable for both OLEDs and optical sensors remains extremely rare. OBJECTIVES: Aiming to achieve high photoluminescence quantum yields in solid-state and triplet harvesting abilities of organic semiconductors with efficient bipolar charge transport required for application in both blue OLEDs and optical sensors, symmetrical donor-acceptor-donor organic emitters containing pyrimidine-5-carbonitrile electron-withdrawing scaffold and carbazole, tert-butylcarbazole and methoxy carbazole donor moieties were designed, synthesized and investigated as the main objectives of this study. METHODS: New compounds were tested by many experimental methods including optical and photoelectron spectroscopy, time of flight technique, electrochemistry and thermal analyses. RESULTS: Demonstrating advantages of the molecular design, the synthesized emitters exhibited sky-blue efficient TADF with reverse intersystem crossing rates exceeding 106 s-1, aggregation-induced emission enhancement with photoluminescence quantum yields in solid state exceeding 50%, hole and electron transporting properties with charge mobilities exceeding 10-4 cm2/V·s, glass-forming properties with glass transition temperatures reaching 177 °C. Sky-blue OLEDs with non-doped light-emitting layers of the synthesized emitter showed maximum external efficiency of 12.8% while the doped device with the same emitter exhibited maximum external efficiency of 14%. The synthesized emitters were also used as oxygen probes for optical sensors with oxygen sensitivity estimated by the Stern-Volmer constant of 3.24·10-5 ppm-1. CONCLUSION: The developed bipolar TADF emitters with pyrimidine-5-carbonitrile and carbazole moieties showed effective applicability in both blue OLEDs and optical sensors.
Here, we report on three new triphenylamine-based enamines synthesized by condensation of an appropriate primary amine with 2,2-diphenylacetaldehyde and characterized by experimental techniques and density functional theory (DFT) computations. Experimental results allow highlighting attractive properties including solid-state ionization potential in the range of 5.33-5.69 eV in solid-state and hole mobilities exceeding 10-3 cm2/V·s, which are higher than those in spiro-OMeTAD at the same electric fields. DFT-based analysis points to the presence of several conformers close in energy at room temperature. The newly synthesized hole-transporting materials (HTMs) were used in perovskite solar cells and exhibited performances comparable to that of spiro-OMeTAD. The device containing one newly synthesized hole-transporting enamine was characterized by a power conversion efficiency of 18.4%. Our analysis indicates that the perovskite-HTM interface dominates the properties of perovskite solar cells. PL measurements indicate smaller efficiency for perovskite-to-new HTM hole transfer as compared to spiro-OMeTAD. Nevertheless, the comparable power conversion efficiencies and simple synthesis of the new compounds make them attractive candidates for utilization in perovskite solar cells.
Capability of exciplex energy transfer through a spacer was investigated using three exciplex-forming solid mixtures which contained the well-known electron accepting 2,4,6-tris[3-(diphenylphosphinyl)phenyl]-1,3,5-triazine and appropriately designed bipolar cyanocarbazolyl-based derivatives functionalized by attachment of carbazolyl, acridanyl or phenyl units. These novel cyanocarbazolyl-based derivatives were used as both the spacer and exciplex-forming donor. Efficient organic light-emitting diodes with electroluminescence in cyan-yellow region and maximum external quantum efficiency of up to 7.7% were fabricated owing to efficient thermally activated fluorescence (TADF) of the newly discovered exciplexes. An approach of exciton separation by the spacer between the studied exciplexes and selected orange TADF emitter was proposed for the fabrication of white electroluminescent devices with prolonged lifetime comparing to that of single-color exciplex-based devices. Exciplex-forming systems were tested for exciton separation between inter- and intramolecular TADF. Exciplex energy transfer through a spacer was observed on relatively long distance for one system due to the energy resonance between triplet levels of the exciplex and spacer. First time observed here exciplex energy transfer through a spacer can be useful for both improvement of device stability and obtaining of white electroluminescence.
Aiming to design blue fluorescent emitters with high photoluminescence quantum yields in solid-state, nitrogen-containing heteroaromatic 9,9-dimethylacridine was refined by tetraphenylethene and triphenylethene. Six tetra-/triphenylethene-substituted 9,9-dimethylacridines were synthesized by the Buchwald-Hartwig method with relatively high yields. Showing effects of substitution patterns, all emitters demonstrated high fluorescence quantum yields of 26-53% in non-doped films and 52-88% in doped films due to the aggregation induced/enhanced emission (AIE/AIEE) phenomena. In solid-state, the emitters emitted blue (451-481 nm) without doping and deep-blue (438-445 nm) with doping while greenish-yellow emission was detected for two compounds with additionally attached cyano-groups. The ionization potentials of the derivatives were found to be in the relatively wide range of 5.43-5.81 eV since cyano-groups were used in their design. Possible applications of the emitters were demonstrated in non-doped and doped organic light-emitting diodes with up to 2.3 % external quantum efficiencies for simple fluorescent devices. In the best case, deep-blue electroluminescence with chromaticity coordinates of (0.16, 0.10) was close to blue color standard (0.14, 0.08) of the National Television System Committee.
Acridones/chemistry , Luminescence , Acridones/chemical synthesis , Calorimetry, Differential Scanning , Electricity , Electrochemistry , Furans/chemistry , Spectrophotometry, Ultraviolet , Temperature , Toluene/chemistry
The synthesis of new iridium(III) complexes containing a 2-(benzo[b]selenophen-2-yl)pyridine ligand is reported along with their photophysical, thermal, electrochemical and electroluminescent properties. These complexes are characterized by deep red phosphorescence with photoluminescence quantum yields exceeding 31% in the solid state. Solid layers of the complexes were characterized by ionization potentials of 5.17-5.27 eV and electron affinities of 2.87-2.95 eV. Their thermal and electrochemical stabilities were proved by cyclic voltammetry and thermogravimetric analysis. Deep red selenium-based iridium phosphorescent emitters were used in red electroluminescent devices which were characterized by a deep red color with Commission Internationale de l'Eclairage (CIE 1931) chromaticity coordinates (x, y) of (0.69, 0.31). This color is deeper than that defined by the red color standard (0.67, 0.33) of the National Television System Committee (NTSC) or CIE 1931 of (0.68, 0.32) of the widely known red phosphorescent emitter bis(1-phenylisoquinoline)(acetylacetonate)iridium(III) (Ir(piq)2(acac)). Using newly developed deep red iridium complexes, white hybrid wet-processable light-emitting devices were fabricated, the electroluminescence of which was characterized by a white color with a color rendering index (CRI) reaching 85. White hybrid OLEDs were obtained by mixing blue fluorescence, green thermally activated delayed fluorescence, and red phosphorescence. They showed a maximum brightness exceeding 10000 cd/m2 and a high external quantum efficiency of 6.3% as for solution-processed white devices.
With the aim of developing all-organic bipolar semiconductors with high charge mobility and efficient E-type fluorescence (so-called TADF) as environmentally friendly light-emitting materials for optoelectronic applications, four noble metals-free dyes with linear and V-shapes were designed using accepting pyridine-3,5-dicarbonitrile and donating carbazole units. By exploiting a donor-acceptor design strategy and using moieties with different donating and accepting abilities, TADF emitters with a wide variety of molecular weights were synthesized to achieve the optimum combination of charge-transporting and fluorescent properties in one TADF molecule. Depending on molecule structures, different TADF emitters capable of emitting in the range from 453 to 550â nm with photoluminescence quantum yields up to 98 % for the solutions in oxygen-free toluene were obtained. All compounds showed bipolar charge-transport. Hole mobility of 2.8×10-3 â cm2 /Vs at 7×105 â V cm-1 was observed for the compound containing two di-tert-butyl-substituted carbazole moieties. The compounds were tested in both non-doped and doped organic light-emitting diodes using different hosts. It was shown that the developed TADF emitters are suitable for different color devices with electroluminescence ranging from blue to yellow and with brightness, maximum current and external quantum efficiencies exceeding 10 000â cd m-2 , 15â cd/A, and 7 %, respectively.
The synthesis and full characterization of new derivatives of indolo[3,2-b]carbazole with differently substituted phenyl groups at nitrogen atoms is reported. Comparative study on their thermal, optical electrochemical, and photoelectrical properties is presented. The synthesized compounds are electrochemically stable. Their highest occupied molecular orbital energy values range from -5.14 to -5.07 eV. The electron photoemission spectra of the films of synthesized materials revealed the ionization potentials of 5.31-5.47 eV. Hole drift mobility of the amorphous film of 5,11-bis(3-methoxyphenyl)-6-pentyl-5,11-dihydroindolo[3,2-b]carbazole exceed 10(-3) cm(2)/V·s at high electric fields, as it was established by xerographic time-of-flight technique. In contrast to diphenylamino substituted derivatives of carbazole, no effect of the position of methoxy groups on the photoelectrical properties was observed for the synthesized methoxyphenyl-substituted derivatives of indolo[3,2-b]carbazole. The indolo[3,2-b]carbazole core has a larger resonance structure that includes 3 phenyl rings, and thus the energy gap of the HOMO and LUMO π orbitals is lower as compared to that of carbazoles. With a larger energy difference between the phenyl substituents and the core moiety, the indolo[3,2-b]carbazole derivatives studied all have a weaker coupling between the phenyl group and a much weaker dependence of the molecular properties on the position of substituents on the phenyl groups as compared to those observed in substituted carbazoles.
