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Photoinduced charge‐trapping is a promising strategy for boosting the photosensitivity of organic photodetectors at the expense of their response time. In addition, they have a low carrier extraction yield due to the formation of low‐energy triplet excitons through the recombination of a photogenerated hole–electron pair. Materials with thermally activated delayed fluorescence (TADF) exhibit a long‐lived (≈µs) excited spin‐triplet nearly iso‐energetically aligned with that of an excited spin‐singlet, which results in suppressed exciton losses and is widely used in organic light‐emitting diodes. The extraction and population of triplet state excitons in TADFs is a sought‐after but underexplored aspect of photoinduced gating in photodetectors. A 1,2,3,5‐tetrakis(carbazol‐9‐yl)4,6‐Dicyanobenzene (4CzIPN) TADF blend with a high‐mobility Poly[2,5‐bis(3‐tetradecylthiophen‐2‐yl)thieno[3,2‐b]thiophene] (PBTTT‐C14) polymer via bulk type‐II offset can increase free carrier extraction yield (fast response) and retain trapped electrons in TADF triplet states (high gain). The PBTTT‐C14/4CzIPN ultraviolet photodetector device maintains a trade‐off between high photogain (≈103) and fast response time (79 ms) at 300 nm while operating at a shallow dark current (≈pA). Furthermore, the device shows high external quantum efficiency (≈104 %) and detectivity (≈1011 Jones) for low light power (

Multiple resonance (MR)‐type thermally activated delayed fluorescence (TADF) emitters have promising prospects for high‐color‐purity organic light‐emitting diodes (OLEDs), but they are seldom attempted in the fabrication of solution‐processed devices. In addition, another issue with MR‐TADF emitters is that their heteroatom patterns are very limited, hampering their diversity. Herein, a novel double boron (B)‐containing MR‐TADF paradigm that merges an unembedded organoboron unit and a B‐embedded π‐fused MR framework into one system, furnishing a unique para‐B‐π‐B′/meta‐N (nitrogen)‐π‐N molecular pattern is proposed. Based on this, a proof‐of‐concept molecule, BNB′‐1, is developed, simultaneously achieving a bright sharp emission peaking at 540 nm with a full width at half maximum (FWHM) of only 24.5 nm/98 meV, a nearly unity photoluminescence quantum yield and excellent organic solubility. A solution‐processed OLED using BNB′‐1 emitter delivers an impressive external quantum efficiency (EQE) as high as 36.2% with an emissive FWHM of only 30.0 nm/0.13 eV at ≈540 nm; both parameters set new records among the ever‐reported solution‐processed MR‐OLEDs. Moreover, BNB′‐1 also obtains a superhigh EQE of 40.3% in vacuum‐processed OLEDs, surpassing all MR‐OLEDs in the similar emission region. This work provides an interesting solution to develop high‐performance solution‐processable MR‐TADF emitters with diverse heteroatom patterns. [ABSTRACT FROM AUTHOR]

Deep‐red/near‐infrared (DR/NIR) organic light‐emitting diodes (OLEDs) are promising for applications such as night‐vision readable marking, bioimaging, and photodynamic therapy. To tune emission spectra into the DR/NIR region, red emitters generally require assistance from intermolecular interactions. But such interactions generally lead to sharp efficiency declines resulting from unwanted quenching events. To overcome this challenge, herein, an advanced method via strategically managing the intermolecular interactions of thermally activated delayed fluorescence (TADF) emitters is proposed. The proof‐of‐concept molecule called DCN‐SPTPA exhibits impressive resistance to quenching while delivering controllable aggregation behavior for redshifting the emission by installing an end‐spiro group. Consequently, two emitters demonstrate similar photophysical properties and device performance at very low doping levels; while DCN‐SPTPA‐based OLEDs demonstrate a 1.3–1.4‐fold enhancement of the external quantum efficiencies (EQEs) with respect to the control molecule at 5–20 wt.% doping ratios, affording DR/NIR emission at 656, 688, 696, and 716 nm with record‐breaking EQEs of 36.1%, 29.3%, 28.2%, and 24.0%, respectively. Moreover, DCN‐SPTPA‐based nondoped NIR device also retains a state‐of‐the‐art EQE of 2.61% peaked at 800 nm. This work first demonstrates instructive guidance for accurately manipulating the intermolecular interactions of red TADF emitters, which will spur future developments in high‐performance DR/NIR OLEDs. [ABSTRACT FROM AUTHOR]

With the surging demand for ultra‐high‐resolution displays, the International Telecommunication Union (ITU) announce the next‐generation color gamut standard, named ITU‐R Recommendation BT.2020, which not only sets a seductive but challenging milestone for display technologies but also urges researchers to recognize the importance of color coordinates. Organic light‐emitting diodes (OLEDs) are an important display technology in current daily life, but they face challenges in approaching the BT.2020 standard. Thermally activated delayed fluorescence (TADF) emitters have bright prospects in OLEDs because they possess 100% theoretical exciton utilization. Thus, the development of TADF emitters emitting primary red (R), green (R), and blue (B) emission is of great significance. Here, a comprehensive overview of the latest advancements in TADF emitters that exhibit Commission Internationale de l'Éclairage (CIE) coordinates surpassing the National Television System Committee (NTSC) and approaching BT.2020 standards is presented. Rational strategies for molecular designs, as well as the resulting photophysical properties and OLED performances, are discussed to elucidate the underlying mechanisms for shifting the CIE coordinates of both donor‐acceptor and multiple resonance (MR) typed TADF emitters toward the BT.2020 standard. Finally, the challenges in realization of the wide‐color‐gamut BT.2020 standard and the prospects for this research area are provided. [ABSTRACT FROM AUTHOR]

Employing metal‐free thermally activated delayed fluorescence (TADF) materials as novel photosensitizers (PSs) for triplet–triplet annihilation upconversion (TTA‐UC) systems has received great attention. Nevertheless, how to choose suitable TADF materials is still a gap that deserves further in‐depth research. Herein, by systematically investigating the three TADF‐based TTA‐UC systems, it is found that TADF materials with multiple resonance (MR) effect are more suitable PSs for high‐performance TTA‐UC systems than those with intramolecular charge transfer (ICT) properties. Therefore, unlike a negligible maximum UC quantum efficiency (ΦUC', with a theoretical maximum of 100%) of 0.05% for ICT‐1 with a highly twisted molecular structure, MR‐TADF materials MR‐1 and MR‐2 offer superior UC performance with ΦUC' values above 12.7%. All these results suggest that employing MR‐TADF materials as the PS is the key to achieving efficient TTA‐UC performance. [ABSTRACT FROM AUTHOR]

Constructing donor‐π‐acceptor (D‐π‐A)‐type molecular structures by employing a phenyl as the π‐bridge to link donor (D) and acceptor (A) units has been recognized as an effective way to develop highly efficient red thermally activated delayed fluorescence (TADF) organic light‐emitting diodes (OLEDs). However, flexible and relatively planar structures would open potential energy loss channels, such as nonradiative inactivation and aggregation‐induced triplet quenching processes. Here, a bulky spiro‐9,9′‐bifluorene unit is first implemented to serve as a bridging group to construct a D‐π‐A molecule, enabling it to have higher overall rigidity, more sufficient steric hindrance, prolonged molecule length, and obvious aggregation‐induced emission characteristics compared with a common phenyl bridge. As a result, energy dissipation routes are effectively relieved at the unimolecular level, together with mitigated interchromophore quenching, rendering a 100% photoluminescence quantum yield and a larger horizontal dipole ratio of 89%. The OLED based on 3‐(2‐(diphenylamino)‐9,9′‐spirobi[fluoren]‐7‐yl)dibenzo[a,c]phenazine‐11,12‐dicarbonitrile exhibits an excellent external quantum efficiency of nearly 37% at 612 nm, which is over 1.38‐fold enhancement compared with the phenyl bridge‐based control molecule. This work provides an instructive solution to design highly efficient red TADF emitters exploiting D‐π‐A‐type molecular structures. [ABSTRACT FROM AUTHOR]

Hindered by spectral broadening issues with redshifted emission, long‐wavelength (e.g. maxima beyond 570 nm) multiple resonance (MR) emitters with full width at half maxima (FWHMs) below 20 nm remain absent. Herein, by strategically embedding diverse boron (B)/nitrogen (N) atomic pairs into a polycyclic aromatic hydrocarbon (PAH) skeleton, we propose a hybrid pattern for the construction of a long‐wavelength narrowband MR emitter. The proof‐of‐concept emitter B4N6‐Me realized orange‐red emission with an extremely small FWHM of 19 nm (energy unit: 70 meV), representing the narrowest FWHM among all reported long‐wavelength MR emitters. Theoretical calculations revealed that the cooperation of the applied para B‐π‐N and para B‐π‐B/N‐π‐N patterns is complementary, which gives rise to both narrowband and redshift characteristics. The corresponding organic light‐emitting diode (OLED) employing B4N6‐Me achieved state‐of‐the‐art performance, e.g. a narrowband orange‐red emission with an FWHM of 27 nm (energy unit: 99 meV), an excellent maximum external quantum efficiency (EQE) of 35.8 %, and ultralow efficiency roll‐off (EQE of 28.4 % at 1000 cd m−2). This work provides new insights into the further molecular design and synthesis of long‐wavelength MR emitters. [ABSTRACT FROM AUTHOR]

Building blocks and heteroatom alignments are two determining factors in designing multiple resonance (MR)‐type thermally activated delayed fluorescence (TADF) emitters. Carbazole‐fused MR emitters, represented by CzBN derivatives, and the heteroatom alignments of ν‐DABNA are two star series of MR‐TADF emitters that show impressive performances from the aspects of building blocks and heteroatom alignments, respectively. Herein, a novel CzBN analog, Π‐CzBN, featuring ν‐DABNA heteroatom alignment is developed via facile one‐shot lithium‐free borylation. Π‐CzBN exhibits superior photophysical properties with a photoluminescence quantum yield close to 100 % and narrowband sky blue emission with a full width at half maximum (FWHM) of 16 nm/85 meV. It also gives efficient TADF properties with a small singlet‐triplet energy offset of 40 meV and a fast reverse intersystem crossing rate of 2.9×105 s−1. The optimized OLED using Π‐CzBN as the emitter achieves an exceptional external quantum efficiency of 39.3 % with a low efficiency roll‐off of 20 % at 1000 cd m−2 and a narrowband emission at 495 nm with FWHM of 21 nm/106 meV, making it one of the best reported devices based on MR emitters with comprehensive performance. [ABSTRACT FROM AUTHOR]

Multiple resonance (MR) type thermally activated delayed fluorescence (TADF) emitters are very promising in the high‐resolution and high‐efficiency displays, due to their narrow and highly efficient optical emissions. Early MR‐TADF cores that show only short‐range charge‐transfer (CT) electronic excitations hardly afford ideal performances (e.g., show low efficiencies) in organic light‐emitting diodes (OLEDs). This work thus designs and synthesizes two MR‐TADF emitters (TCzBN‐BP and TCzBN‐FP), where the same MR core TCzBN is chemically modified by the acceptor fragments benzophenone/9‐fluorenone (BP/FP) to incorporate long‐range CT excitations in the two molecules. OLEDs exploiting TCzBN‐BP as emitter, in which short‐range CT excitation is dominant in the first singlet (S1) excited state, achieve a maximum external quantum efficiency (EQE) of 35.6% and a narrow emission bandwidth of 35 nm. In contrast, OLEDs exploiting TCzBN‐FP with an overloaded long‐range CT excitation in the S1 state exhibit a maximum EQE of 27.2% and a broadened emission bandwidth of 56 nm. This work not only shows the importance of careful management of long‐ and short‐range CT excitations, but also provides a new insight into the structure–property relationship in the MR‐TADF emitters, which thus promotes the design of more novel MR‐TADF emitters with high efficiencies and high color purity. [ABSTRACT FROM AUTHOR]

High‐performance nondoped organic light‐emitting diodes (OLEDs) are promising technologies for future commercial applications. Herein, we synthesized two new thermally activated delayed fluorescence (TADF) emitters that enable us, for the first time, to combine three effective approaches for enhancing the efficiency of nondoped OLEDs. First, the two emitters are designed to have high steric hindrances such that their emitting cores will be suitably isolated from those of their neighbors to minimize concentration quenching. On the other hand, each of the two emitters has two stable conformations in solid films. In their neat films, molecules with the minority conformation behave effectively as dopants in the matrix composing of the majority conformation. One hundred percent exciton harvesting is thus theoretically feasible in this unique architecture of "self‐doped" neat films. Furthermore, both emitters have relatively high aspect ratios in terms of their molecular shapes. This leads to films with preferred molecular orientations enabling high populations of horizontal dipoles beneficial for optical out‐coupling. With these three factors, OLEDs with nondoped emitting layers of the respective emitters both achieve nearly 100% exciton utilization and deliver over 30% external quantum efficiencies and ultralow efficiency roll‐off at high brightness, which have not been observed in reported nondoped OLEDs. [ABSTRACT FROM AUTHOR]

Realizing blue‐hazard‐free emission is an important goal for white organic light‐emitting diodes (OLEDs) toward healthy lighting applications. However, conventional blue organic emitters with broad emission spectra would generally cover the high‐energy emission region and thus cannot meet the demand. Here a blue multiple resonance type thermally activated delayed fluorescence (TADF) emitter DPMX‐CzDABNA is newly designed. The DPMX‐CzDABNA‐based OLEDs can realize blue narrowband emission peaked at 484 nm with a full width at half maximum of 29 nm, and external quantum efficiencies (EQEs) around 26%, which allows DPMX‐CzDABNA to precisely avoid the high‐energy photon contribution and thus be a promising blue component to construct high‐performance white OLEDs with human‐eye‐friendly emission spectra. Using DPMX‐CzDABNA and a reported TADF emitter BPPZ‐DPXZ, respectively, as blue and orange components in white OLEDs, the single‐emitting‐layer devices approach white emission with outstanding EQE up to 35.8%; the double‐emitting‐layer OLEDs achieve blue‐hazard‐free white emissions with a maximum EQE of 26.5% and very stable Commission Internationale de l'Eclairage coordinates of ≈(0.38,0.43) over a wide luminance range from 100 to 10 000 cd m−2. It is expected that this strategy can pave a new way for developing highly efficient all‐TADF white OLEDs without blue‐hazard emission. [ABSTRACT FROM AUTHOR]

Multiple resonance (MR) type thermally activated delayed fluorescence (TADF) material is currently a research hotspot in organic light‐emitting diodes (OLEDs) due to their high color purity and high exciton utilization. However, there are only a handful of MR‐TADF emitters with emissions beyond the blue‐to‐green region. The very limited emission colors for MR‐TADF emitters are mainly caused by the fact that so far molecular modifications of MR‐TADF do not offer much change in the emission colors. Here, we report a new approach to modifying a prototypical MR core of DABNA by fusing carbazoles to the MR framework. The carbazole‐fused molecule (TCZ‐F‐DABNA) basically maintains the MR‐dominated features of DABNA while red‐shifting the emission. Its OLED achieves an external quantum efficiency of 39.2 % with a peak at 588 nm, which is a record‐high efficiency for OLEDs with peaks beyond 560 nm. This work provides a new approach for significantly tunning emission colors of MR‐TADF emitters. [ABSTRACT FROM AUTHOR]

Thermally activated delayed fluorescence (TADF) emitters induced by the multiple resonance (MR) effect have garnered considerable attention. However, it is difficult to develop MR‐TADF emitters that maintain high color purities in the red region. In this work, the importance of excited state alignments of MR‐based donor‐acceptor (D‐A) molecules in determining their preferring characteristics is clarified. By using the newly designed molecule mBDPA‐TOAT whose apparent excited states show hybridization of MR and intersegmental charge‐transfer features as an emitter in an organic light‐emitting diode (OLED), a high external quantum efficiency of 17.3% is achieved with a full width at half‐maximum of 45 nm (154 meV) and Commission Internationale de L'Éclairage coordinate of (0.61, 0.39). This work demonstrates when introducing D‐A typed structures, features, and alignments of molecular excited states determine ultimate material properties. This could help to develop high efficiency and high color purity TADF emitters toward long wavelength range. [ABSTRACT FROM AUTHOR]

The conformational distribution and mutual interconversion of thermally activated delayed fluorescence (TADF) emitters significantly affect the exciton utilization. However, their influence on the photophysics in amorphous film states is still not known due to the lack of a suitable quantitative analysis method. Herein, we used temperature‐dependent time‐resolved photoluminescence spectroscopy to quantitatively measure the relative populations of the conformations of a TADF emitter for the first time. We further propose a new concept of "self‐doping" for realizing high‐efficiency nondoped OLEDs. Interestingly, this "compositionally" pure film actually behaves as a film with a dopant (quasi‐equatorial form) in a matrix (quasi‐axial form). The concentration‐induced quenching that may occur at high concentrations is thus expected to be effectively relieved. The "self‐doping" OLED prepared with the newly developed TADF emitter TP2P‐PXZ as a neat emitting layer realizes a high maximum external quantum efficiency of 25.4 % and neglectable efficiency roll‐off. [ABSTRACT FROM AUTHOR]

Nondoped organic light‐emitting diodes (OLEDs) have drawn enormous attention for their merits of process simplicity, reduced fabrication cost, and phase stability. Herein, a novel approach of utilizing intermolecular hydrogen bonding for enhancing performance of nondoped OLEDs with a new thermally activated delayed fluorescence (TADF) emitter 10‐(4‐(2,6‐di(pyrimidin‐5‐yl)pyridin‐4‐yl)phenyl)‐10H‐phenoxazine (DPmP‐PXZ) is investigated. Endowing with suitable intermolecular hydrogen bonds linking the ends of neighboring DPmP‐PXZ molecules, the molecules tend to form extended 1D molecular chain in solid. This 1D structure effectively keeps the electron‐rich PXZ cores in neighboring molecules apart from each other such that triplet‐related exciton quenching can be well suppressed. In addition, it also improves the balance of carrier mobilities and the optical out‐coupling from the emitting layer. With these merits, OLEDs using DPmP‐PXZ as a dopant emitter, from 10 to 100 wt%, can maintain high external quantum efficiencies (EQEs) of over 20%. More importantly, its nondoped OLED shows a yellow emission and an excellent maximum EQE of 21.8% with little efficiency roll‐off which is even comparable with state‐of‐the‐art yellow OLEDs. These results provide new insight on the role of hydrogen bonding in molecular packing and its subsequent influences on the performance of OLEDs. [ABSTRACT FROM AUTHOR]

While monochrome organic light‐emitting diodes (OLEDs) based on thermally activated delayed fluorescence (TADF) emitters have achieved over 30% external quantum efficiencies (EQEs), all‐TADF white OLEDs (WOLEDs) are still lagging behind. Herein, a simple system based on two color‐complementary TADF emitters is exploited to realize high‐performance WOLEDs. By doping a high‐performance orange–red TADF fluorophor (BPPZ‐DPXZ) into a blue TADF host (DBFCz‐Trz), energy transfer, and triplet‐to‐singlet conversion in the host‐dopant system can be optimized to simultaneously achieve full exciton utilization and color balance. With this design, all‐TADF single‐emitting‐layer WOLEDs with a maximum EQE up to 32.8% are demonstrated. This high efficiency surpasses EQEs of reported WOLEDs based on both TADF as well as phosphorescence. It is expected that this finding can provide new insight for designing highly efficient all‐TADF WOLEDs. [ABSTRACT FROM AUTHOR]

Developing red thermally activated delayed fluorescence (TADF) emitters for high‐performance OLEDs is still facing great challenge. Herein, three red TADF emitters, pDBBPZ‐DPXZ, pDTBPZ‐DPXZ, and oDTBPZ‐DPXZ, are designed and synthesized with same donor–acceptor (D‐A) backbone with different peripheral groups attaching on the A moieties. Their lowest triplet states change from locally excited to charge transfer character leading to significantly enhance reverse intersystem crossing process. In particular, oDTBPZ‐DPXZ exhibits efficient TADF feature and exciton utilization. It not only achieves an external quantum efficiency (EQE) of 20.1 % in red vacuum‐processed OLED, but also realize a high EQE of 18.5 % in a solution‐processed OLED, which is among the best results in solution‐processed red TADF OLEDs. This work provides an effective strategy for designing red TADF molecules by managing energy level alignments to facilitate the up‐conversion process and thus enhance exciton harvesting. [ABSTRACT FROM AUTHOR]

Developing red thermally activated delayed fluorescence (TADF) emitters, attainable for both high‐efficient red organic light‐emitting diodes (OLEDs) and non‐doped deep red/near‐infrared (NIR) OLEDs, is challenging. Now, two red emitters, BPPZ‐PXZ and mDPBPZ‐PXZ, with twisted donor–acceptor structures were designed and synthesized to study molecular design strategies of high‐efficiency red TADF emitters. BPPZ‐PXZ employs the strictest molecular restrictions to suppress energy loss and realizes red emission with a photoluminescence quantum yield (ΦPL) of 100±0.8 % and external quantum efficiency (EQE) of 25.2 % in a doped OLED. Its non‐doped OLED has an EQE of 2.5 % owing to unavoidable intermolecular π–π interactions. mDPBPZ‐PXZ releases two pyridine substituents from its fused acceptor moiety. Although mDPBPZ‐PXZ realizes a lower EQE of 21.7 % in the doped OLED, its non‐doped device shows a superior EQE of 5.2 % with a deep red/NIR emission at peak of 680 nm. [ABSTRACT FROM AUTHOR]

Sind gründlich studiert worden, allerdings verlief die Entwicklung von roten/nahinfraroten TADF-Emittern viel langsamer als die von grünen und blauen Emittern (TADF: thermisch aktivierte verzögerte Fluoreszenz). Sind gründlich studiert worden, allerdings verlief die Entwicklung von roten/nahinfraroten TADF-Emittern viel langsamer als die von grünen und blauen Emittern (TADF: thermisch aktivierte verzögerte Fluoreszenz). Zhang et al. präsentieren in ihrem Forschungsartikel auf S. 14808 zwei neuartige rote TADF-Emitter. [Extracted from the article]

Multi-resonance (MR) thermally activated delayed fluorescence (TADF) materials with planar rigidity show great potential as emitters in organic light-emitting diodes (OLEDs) due to their high photoluminescence quantum yields and narrowband emission. However, their strong intermolecular interaction trends usually result in redshifted and broadened emission spectra as well as low device efficiencies due to the aggregation-caused quenching (ACQ) effect. In this paper, a bulky spirobifluorene unit was appended onto an asymmetric carbazole/diphenylamine-embedded MR skeleton to relieve such trends, thus affording a new MR-TADF blue emitter, BNSF-1. Introducing spirobifluorene significantly relieves the intermolecular interaction trends of MR backbones without affecting their original photophysical properties. The corresponding sensitizer-free OLED devices based on BNSF-1 exhibit narrowband sky-blue electroluminescence peaking at 475 nm with a full width at half-maximum of 25 nm, as well as a maximum external quantum efficiency of 25.9 %. More importantly, BNSF-1 exhibited negligible spectral broadening and ACQ trends as the doping ratio increased. Our work provides a feasible method for constructing doping concentration-insensitive MR-TADF emitters. [Display omitted] • A novel multi-resonance TADF emitter with spirobifluorene unit is developed. • The emitter exhibits blue emission at 475 nm with a small FWHM of 25 nm. • Maximum external quantum efficiency of 25.9 % and PLQY of 92.6 % are realized. [ABSTRACT FROM AUTHOR]

In this work, by combining conformational isomeric moiety to MR-emitting core, we propose a new pathway to reduce the concentration sensitivity without compromising color purity of MR-TADF emitters. [Display omitted] • Two novel MR-TADF emitters with conformational isomerism were designed. • Conformational isomerism is introduced to deal with poor concentration dependence. • Concentration quenching can be suppressed with barely harming color purity. • BNCz-aDMAC-based OLEDs achieve superior performance with low concentration dependence. Electroluminescent performance of multiple resonance (MR) type thermally activated delayed fluorescence (TADF) emitters is highly dependent to the doping concentration due to the flat molecular structures, which is a major issue toward practical applications. Herein, an effective approach reducing the concentration dependence is proposed by introducing conformational isomerism for MR-TADF emitters. Two novel MR-TADF emitters were designed by decorating 10H-spiro[acridine-9,2′-adamantane] (a-DMAc) as a dual-conformational moiety onto the MR-core BNCz with different connection methods, which could induce different conformational distributions. In particular, the conformational isomerism of BNCz-aDMAC leads to a lower fraction of QE forms compared to the QE-dominant BNCz-PDMAC in amorphous doped film states with identical doping weights, thus enabling effective suppression of concentration quenching with barely harming color purity. Therefore, BNCz-aDMAC-based organic light-emitting diodes (OLEDs) demonstrate consistent and high efficiency over a wide doping range, maintaining a maximum external quantum efficiency of 23.8 % and a full width at half maximum of 31 nm even at a high doping ratio of 30 wt%. [ABSTRACT FROM AUTHOR]

[Display omitted] • Two multiple resonance derivatives with heavy atom-containing chains are developed. • A new heavy atom effect involvement method for enhancing RISC of MR emitters. • TCzBN-S based evaporated OLEDs afford a low roll-off of 44% at 1000 cd m−2. • Both emitters are feasible for solution-process OLEDs with high performance. Multiple resonance (MR)-based thermally activated delayed fluorescence (TADF) emitters are promising candidates for ultra-high definition (UHD) organic light-emitting diodes (OLEDs). However, the device performances of MR-TADF emitters are usually encumbered with their slow reverse intersystem crossing (RISC) rates (k RISC s). Recently, applying heavy atom effect to MR emitters has been proved to be a plausible solution for enhancing their k RISC and improving TADF properties. Nevertheless, to date, heavy atoms have all been directly fused in MR frameworks, leading to limitations in molecular design and additional structure relaxation from heavy atoms. Herein, we incorporate heavy atom effect via facilely hanging heavy atom-containing chains onto a MR framework and thus synthesize two MR emitters (sulfur ether group for TCzBN-S and sulfone group for TCzBN-SO). An enhanced k RISC of 1.40 × 105 s−1 is reached for TCzBN-S due to sufficient natural transition orbital (NTO) contributions from the heavy atom, which is absent for TCzBN-SO, with a relatively slow k RISC of 5.6 × 104 s−1. Consequently, OLEDs employing TCzBN-S as emitter achieve a maximum external quantum efficiency (EQE) of 30.0% and an alleviated efficiency roll-off of 44% at 1000 cd m−2. In contrast, OLEDs based on TCzBN-SO achieve a maximum EQE of 33.0% but a more severe efficiency roll-off 1000 of 65%. Moreover, solution-process OLEDs based on TCzBN-S and TCzBN-SO are also fabricated and achieved high EQEs of 23.3% and 25.5%, respectively, demonstrating that peripheral flexible and hanging heavy atom chains are also beneficial to solution processing. Our work not only extends heavy atom involving modes in MR emitters, which are important for further developing MR derivatives by using the heavy atom effect, but also confirms that such MR derivatives with hanging chains are applicable to both vacuum-evaporation and solution-process OLEDs. [ABSTRACT FROM AUTHOR]

[Display omitted] • Developing red TADF emitters by simultaneously employing polycyclic large-conjugation donor and acceptor units. • The first example of delicate management of 3LE D and 3LE A for constructing a high-performance red TADF emitter. • DBBPZ-IDPZ delivers fast k RISC and high PLQY of 98.1% thanks to the joint contribution of 3LE D and 3LE A. • DBBPZ-IDPZ based OLED affords an improved EQE of 26.0 %, peaking at 628 nm. Accelerating reverse intersystem crossing (RISC) rates of red thermally activated delayed fluorescence (TADF) emitters is crucial yet remains ongoing challenges. Herein, we disclose an ingenious molecular design to dramatically boost such an up-conversion process by leveraging effective participation of localized excited triplet states from both donor and acceptor segments (3LE D and 3LE A). Inspiringly, energy level alignment with 3LE A -3LE D close to the charge-transfer singlet and triplet (1CT and 3CT) states are obtained in the case of DBBPZ-IDPZ, by simultaneously employing polycyclic large-conjugation donor and acceptor units. Due to the joint contribution of 3LE D and 3LE A , DBBPZ-IDPZ shows 15.7 folds accelerated RISC rate and delivers a higher photoluminescence quantum yield of 98.1 % relative to the control molecule (36.7 %). Eventually, the red OLED based on DBBPZ-IDPZ presents a significantly improved external quantum efficiency of 26.0 % with an emission maximum at 628 nm, which is approximately triple that of the control device (8.9 %). This is the first example of a delicate management of 3LE D and 3LE A to simultaneously participate in RISC process for developing highly efficient red TADF emitters. Our work provides new insights into the molecular design tactic of high-performance red TADF OLEDs. [ABSTRACT FROM AUTHOR]

In this text, by linking a phenoxazine donor (D) into different positions of the 11,12-diphenyldipyrido[3,2-a:2′,3′-c]phenazine acceptor (A), Two novel red thermally activated delayed fluorescence (TADF) isomers, PPZBP and BPZPP, were designed and synthesized. The different connection modes bring different steric hindrance between D and A segments, which lead to tunable conjugation of the whole molecule, resulting in the change of locally excited triplet (3LE) state. Beneficial from the suitable conjugation, PPZBP shows better energy level alignments than BPZPP for superior triplet up conversion. PPZBP-based red organic light-emitting diode realizes a higher EQE of 22.0% than that (14.8%) of the BPZPP-based one. This work not only demonstrates the importance of controlling D-A conjugations on the 3LE states and the resultant influences on RISC rates, it also gives a deep insight into preferred design strategies for high-efficiency red TADF emitters. [Display omitted] • Structure-property investigation of two D-A type red TADF isomers. • Different linking modes greatly affecting conjugations and 3LE. • Small Δ E ST , well-located 3LE, high RISC process can be realized simultaneously. • PPZBP -based OLED realizes higher EQE of 22.0% compared to its counterparts. [ABSTRACT FROM AUTHOR]

By controlling the conjugation extension of acceptor (A) frameworks, making 3LE A energy levels gradually reduced while their CT energy levels are well maintained with semblable photophysical and electrochemical properties. In the case of pDPBPZ-PXZ, the ideal molecular energy level alignments are obtained with near-degenerate 1CT, 3CT and 3LE A states. Consequently, resulting in enhancement of the rates of reverse intersystem crossing (RISC), and boosting the device efficiencies in red OLEDs. [Display omitted] • Two red TADF emitters were designed and synthesized. • Modulating conjugation extension can shift 3LE A states without affecting CT ones. • Ideal energy alignments achieved with improved k RISC. • Both emitters show similar CT properties and Δ E ST , but different exciton harvests. Increasing the reverse intersystem crossing (RISC) rates remains a challenge for red thermally activated delayed fluorescence (TADF) emitters, and energy level alignments play an important role. In this work, we demonstrate that locally excited triplet energy levels from acceptor segments (3LE A) can be well modulated by changing the conjugation extension inside acceptors. Our newly designed compounds pDPAPQ-PXZ and pDPBPZ-PXZ show nearly identical charge-transfer (CT) properties because of similar donor and acceptor strengths. On the other hand, the 3LE A state of pDPBPZ-PXZ was significantly lower than that of pDPAPQ-PXZ only because of its greater π-delocalization. In the case of pDPBPZ-PXZ, ideal molecular energy level alignments are obtained with near-degenerate CT featuring singlet and triplet states (1CT, 3CT) and 3LE A. As a result, pDPBPZ-PXZ simultaneously achieves an approximately 10-fold improved k RISC and a dramatically improved photoluminescence quantum yield of 85.6% compared with pDPAPQ-PXZ. The corresponding OLED successfully doubles the external quantum efficiency to 20.3%. This work demonstrates that the conjugation extensions of acceptors play a fatal role in determining 3LE A levels and that they can be isolated from controlling the acceptor strengths. This provides a promising approach toward enhancing RISC efficiency and developing highly efficient red TADF emitters. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fullerene fragments are used as acceptor to prepare TADF emitters for the first time. • OLED using one of the fullerenes fragment-based TADF emitter shows high EQE of 20.2%. • Acceptor without heteroatom can be used for designing efficient TADF emitter. • This strategy may open a new path for enhancing operation stability of TADF emitters. Fragments of fullerene are used as acceptor segments for the first time to construct two thermally activated delayed fluorescence (TADF) compounds DBCP and FAP. Both compounds exhibit similar highly twisted geometries and separated frontier molecular orbital distributions. While on the other hand, their locally exited triplet energy levels from acceptor moieties (3LE A) are fine-tunable owning to the different structural stress in the fragments, resulting in different lowest triplet excited state (T 1) features. In DBCP, the 3LE A is the high lying state and thus DBCP exhibits a small singlet–triplet energy difference of 0.10 eV and a high photoluminescence quantum yield (Φ PL) of 89% with excellent TADF characteristics; while T 1 of FAP is 3LE A , and thus, FAP displays poor triplet exciton utilization with Φ PL of only 54%. In organic light-emitting diodes (OLEDs) based on DBCP and FAP as dopants, maximum external quantum efficiencies of 20.2% and 12.8% are respectively achieved. This work not only demonstrates for the first time that fullerene fragments can be used as key building blocks for TADF emitters, it also proves in principle that pure hydrocarbon mobilities without any electronegative heteroatom can also be employed as acceptor segment in high performance TADF emitters. [ABSTRACT FROM AUTHOR]

By enhancing electron-withdrawing abilities of the secondary acceptor attachments into the main acceptor core, their charge transfer triplet (3CT) energy levels are gradually reduced, while the locally excited triplet (3LE A) levels are well maintained. The well-aligned excited states, consequently, results in the enhancement of the rates of reverse intersystem crossing (RISC), and boosting the device efficiencies in red OLEDs. [Display omitted] • A facile strategy to modulate CT states while maintaining LE state is proposed. • CT energy levels are gradually reduced, while the 3LE A ones are well maintained. • Fast k RISC , small ΔE ST and high PLQY can be realized simultaneously. • mDPBPZ-DPXZ-based red OLED exhibits much higher EQE compared to its counterparts. Realizing highly efficient reverse intersystem crossing (RISC) process for red thermally activated delayed fluorescence (TADF) emitters remains a formidable challenge. Herein we demonstrate that charge transfer (CT) energy levels are gradually reduced with enhancing electron-withdrawing abilities of the secondary acceptor (A) attachments. Meanwhile, their local excited triplet (3LE A) state levels are well maintained due to the conjugations between the main framework and the attachments are all similar for these A segments. The optimized molecular energy level alignments are obtained in the case of mDPBPZ-DPXZ, in which 3CT and the 3LE A states are almost degenerate, and gives rise to a small singlet–triplet energy difference (ΔE ST) of 0.02 eV, a fast RISC rate of 1.54 × 106 s−1 and a high photoluminescence quantum yield of 93%, simultaneously. And the corresponding device achieves an external quantum efficiency of 21.6%, significantly higher than the other counterparts. This work demonstrates that the energy alignment between the CT and 3LE A state can be easily managed by introducing secondary A attachments on original A framework, which shifts the 1CT and 3CT state to lower energies without affecting the 3LE A energy. It provides a facile design strategy to promote the RISC process, which is particular useful in designing highly efficient red TADF emitters. [ABSTRACT FROM AUTHOR]