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Resonance interaction between a molecular transition and a confined electromagnetic field can lead to weak or strong light-matter coupling. Considering the substantial exciton–phonon coupling in thermally activated delayed fluorescence (TADF) materials, it is thus interesting to explore whether weak light-matter coupling can be used to redistribute optical density of states and to change the rate of radiative decay. Here, we demonstrate that the emission distribution of TADF emitters can be reshaped and narrowed in a top-emitting organic light-emitting device (OLED) with a weakly coupled microcavity. The Purcell effect of weak microcavity is found to be different for TADF emitters with different molecular orientations. We demonstrate that radiative rates of the TADF emitters with vertical orientation can be substantial increased in weakly coupled organic microcavity. These observations can enhance external quantum efficiencies, reduce efficiency roll-off, and improve color-purities of TADF OLEDs, especially for emitters without highly horizontal orientation., This work not only presents photophysical processes of thermally activated delayed fluorescent emitters in a weak Fabry-Pérot cavity, but also establishes a connection between emitter orientation and Purcell effect.

Encasing an OLED between two planar metallic electrodes creates a Fabry–Pérot microcavity, resulting in significant narrowing of the emission bandwidth. The emission from such microcavity OLEDs depends on the overlap of the resonant cavity modes and the comparatively broadband electroluminescence spectrum of the organic molecular emitter. Varying the thickness of the microcavity changes the mode structure, resulting in a controlled change in the peak emission wavelength. Employing a silicon wafer substrate with high thermal conductivity to dissipate excess heat in thicker cavities allows cavity thicknesses from 100 to 350 nm to be driven at high current densities. Three resonant modes, the fundamental and first two higher harmonics, are characterized, resulting in tunable emission peaks throughout the visible range with increasingly narrow bandwidth in the higher modes. Angle resolved electroluminescence spectroscopy reveals the outcoupling of the TE and TM waveguide modes which blue-shift with respect to the normal emission at higher angles. Simultaneous stimulation of two resonant modes can produce dual peaks in the violet and red, resulting in purple emission. These microcavity-based OLEDs employ a single green molecular emitter and can be tuned to span the entire color gamut, including both the monochromatic visible range and the purple line.

Despite widespread interest, ultrathin and highly flexible light-emitting devices that can be seamlessly integrated and used for flexible displays, wearables, and as bioimplants remain elusive. Organic light-emitting diodes (OLEDs) with µm-scale thickness and exceptional flexibility have been demonstrated but show insufficient stability in air and moist environments due to a lack of suitable encapsulation barriers. Here, we demonstrate an efficient and stable OLED with a total thickness of ≈ 12 µm that can be fully immersed in water or cell nutrient media for weeks without suffering substantial degradation. The active layers of the device are embedded between conformal barriers formed by alternating layers of parylene-C and metal oxides that are deposited through a low temperature chemical vapour process. These barriers also confer stability of the OLED to repeated bending and to extensive postprocessing, e.g. via reactive gas plasmas, organic solvents, and photolithography. This unprecedented robustness opens up a wide range of novel possibilities for ultrathin OLEDs., Though organic light-emitting diodes (OLEDs) with impressive flexibility have been reported, achieving stable operation in air and moist environments remains difficult. Here, the authors report ultrathin OLEDs with hybrid thin-film encapsulation barriers for stable operation in harsh environments.

Perovskite light-emitting diodes (PeLEDs) have showed significant progress in recent years; the external quantum efficiency (EQE) of electroluminescence in green and red regions has exceeded 20%, but the efficiency in blue lags far behind. Here, a large cation CH3CH2NH2+ is added in PEA2(CsPbBr3)2PbBr4 perovskite to decrease the Pb–Br orbit coupling and increase the bandgap for blue emission. X-ray diffraction and nuclear magnetic resonance results confirmed that the EA has successfully replaced Cs+ cations to form PEA2(Cs1-xEAxPbBr3)2PbBr4. This method modulates the photoluminescence from the green region (508 nm) into blue (466 nm), and over 70% photoluminescence quantum yield in blue is obtained. In addition, the emission spectra is stable under light and thermal stress. With configuration of PeLEDs with 60% EABr, as high as 12.1% EQE of sky-blue electroluminescence located at 488 nm has been demonstrated, which will pave the way for the full color display for the PeLEDs., Blue light-emitting diodes (LEDs) are critical for displays. Employing a large organic cation into a quasi-two dimensional perovskite with green emission, Chu et al. achieve LEDs exhibiting a high external quantum efficiency of 12.1% and stable spectra in the sky-blue region.

Reverse intersystem crossing (RISC), the uphill spin-flip process from a triplet to a singlet excited state, plays a key role in a wide range of photochemical applications. Understanding and predicting the kinetics of such processes in vastly different molecular structures would facilitate the rational material design. Here, we demonstrate a theoretical expression that successfully reproduces experimental RISC rate constants ranging over five orders of magnitude in twenty different molecules. We show that the spin flip occurs across the singlet–triplet crossing seam involving a higher-lying triplet excited state where the semi-classical Marcus parabola is no longer valid. The present model explains the counterintuitive substitution effects of bromine on the RISC rate constants of previously unknown molecules, providing a predictive tool for material design., Understanding and predicting the kinetics of reverse intersystem crossing (RISC) facilitates the design of materials. Here, the authors demonstrate a theoretical expression that reproduces experimental RISC rate constants ranging over five orders of magnitude in selected molecules.

Thin-film transistor (TFT)-driven full-color organic light-emitting diodes (OLEDs) with vertically stacked structures are developed herein using photolithography processes, which allow for high-resolution displays of over 2,000 pixels per inch. Vertical stacking of OLEDs by the photolithography process is technically challenging, as OLEDs are vulnerable to moisture, oxygen, solutions for photolithography processes, and temperatures over 100 °C. In this study, we develop a low-temperature processed Al2O3/SiNx bilayered protection layer, which stably protects the OLEDs from photolithography process solutions, as well as from moisture and oxygen. As a result, transparent intermediate electrodes are patterned on top of the OLED elements without degrading the OLED, thereby enabling to fabricate the vertically stacked OLED. The aperture ratio of the full-color-driven OLED pixel is approximately twice as large as conventional sub-pixel structures, due to geometric advantage, despite the TFT integration. To the best of our knowledge, we first demonstrate the TFT-driven vertically stacked full-color OLED., To realize organic light-emitting diodes (OLEDs) with improved resolution for display applications, a method for achieving high yield device fabrication is needed. Here, the authors report vertically-stacked transistor-driven full-color OLEDs with photolithography-processed intermediate electrodes.

Realizing of full-color quantum-dot LED display remains a challenge because of the poor stability of the blue quantum-dot and the immature inkjet-printing color patterning technology. Here, we develop a multifunctional tandem LED by stacking a yellow quantum-dot LED with a blue organic LED using an indium–zinc oxide intermediate connecting electrode. Under parallel connection and alternate-current driving, the tandem LED is full-color-tunable, which can emit red, green and blue primary colors as well as arbitrary colors that cover a 63% National Television System Committee color triangle. Under series connection and direct current driving, the tandem LED can emit efficient white light with a high brightness of 107000 cd m−2 and a maximum external quantum efficiency up to 26.02%. The demonstrated hybrid tandem LED, with multi-functionality of full-color-tunability and white light-emission, could find potential applications in both full-color-display and solid-state-lighting., Designing efficient light-emitting diodes with full-color-tunability and white-light-emission remains a challenge. Here, the authors demonstrate a multifunctional hybrid tandem LED by stacking a yellow quantum-dot LED with a blue organic LED using an indium–zinc oxide intermediate connecting electrode.

Aromatic organic deep-blue emitters that exhibit thermally activated delayed fluorescence (TADF) can harvest all excitons in electrically generated singlets and triplets as light emission. However, blue TADF emitters generally have long exciton lifetimes, leading to severe efficiency decrease, i.e., rolloff, at high current density and luminance by exciton annihilations in organic light-emitting diodes (OLEDs). Here, we report a deep-blue TADF emitter employing simple molecular design, in which an activation energy as well as spin–orbit coupling between excited states with different spin multiplicities, were simultaneously controlled. An extremely fast exciton lifetime of 750 ns was realized in a donor–acceptor-type molecular structure without heavy metal elements. An OLED utilizing this TADF emitter displayed deep-blue electroluminescence (EL) with CIE chromaticity coordinates of (0.14, 0.18) and a high maximum EL quantum efficiency of 20.7%. Further, the high maximum efficiency were retained to be 20.2% and 17.4% even at high luminance., Deep-blue emitting organic materials with low exciton lifetime are required to realize efficient organic light-emitting diodes (OLEDs) at high brightness. Here, the authors report deep-blue OLEDs featuring thermally activated delayed fluorescence molecules with subnano-second exciton lifetime.

Organic optoelectronic devices combine high-performance, simple fabrication and distinctive form factors. They are widely integrated in smart devices and wearables as flexible, high pixel density organic light emitting diode (OLED) displays, and may be scaled to large area by roll-to-roll printing for lightweight solar power systems. Exceptionally thin and flexible organic devices may enable future integrated bioelectronics and security features. However, as a result of their low charge mobility, these are generally thought to be slow devices with microsecond response times, thereby limiting their full scope of potential applications. By investigating the factors limiting their bandwidth and overcoming them, we demonstrate here exceptionally fast OLEDs with bandwidths in the hundreds of MHz range. This opens up a wide range of potential applications in spectroscopy, communications, sensing and optical ranging. As an illustration of this, we have demonstrated visible light communication using OLEDs with data rates exceeding 1 gigabit per second., Organic LEDs (OLEDs) have generally been considered to be slow devices. Through engineering the structure and materials of OLEDs, the authors achieve a breakthrough in the high-speed operation of OLEDs and demonstrate a 1 Gbps optical wireless link using the OLEDs.

We herein present the results of a study on the novel fabrication process of uniform and homogeneous semiconducting polymer layers, in this case hole-injecting and fluorescent light-emitting layers that were produced by a simple solution-coating process for 3D conformal organic light-emitting diodes (3D OLEDs) on curvilinear surfaces. The solution-coating process used was a newly developed method of vortex-flow-assisted solution-coating with the support of spinning of the coating solution. It is shown that the vortex-flow-assisted spin-coating process can produce high-quality thin films at nanoscale thicknesses by controlling the liquid surface of the coating solutions, which can easily be adjusted by changing the spinning speed, even on complex curvilinear surfaces, i.e., a quasi-omnidirectional coating. This excellent film-forming ability without any serious film defects is mainly due to the reduction of line tension among the solution, air, and the substrate at the contact line due to vortex flows of the coating solution on the substrate during the vortex-spin-coating process. As a proof of concept, we present vortex-spin-coated 3D OLEDs fabricated on bi-convex lens substrates which exhibit excellent device performance with high brightness and current efficiency levels comparable to those of a conventional spin-coated 2D planar OLED on a flat substrate. It is also shown that the EL emission from the 3D OLED on the bi-convex lens substrate exhibits a diffusive Lambertian radiation pattern. The results here demonstrate that the vortex-flow-assisted spin-coating process is a promising approach for producing efficient and reliable next-generation OLEDs for 3D conformal opto-electronics.

Enhancing the injection of electron is an effective strategy to improve the performance of polymer light-emitting diodes (PLEDs). In this work, we reported a 286% improvement in current efficiency (CE) of PLEDs by using double-layered alkali halide electron injection layer (EIL) NaCl/LiF instead of LiF. A significant enhancement of electron injection was observed after inserting the NaCl layer. To understand the mechanism of such improvement, the devices with KBr/LiF and CsF/LiF as EILs were also investigated. Experimental results show that metal cation migrated under the effect of built-in electric field (Vbi), which plays the main role on the improvement of electron injection in PLEDs.

Engineering a low singlet-triplet energy gap (ΔEST) is necessary for efficient reverse intersystem crossing (rISC) in delayed fluorescence (DF) organic semiconductors but results in a small radiative rate that limits performance in LEDs. Here, we study a model DF material, BF2, that exhibits a strong optical absorption (absorption coefficient = 3.8 × 105 cm−1) and a relatively large ΔEST of 0.2 eV. In isolated BF2 molecules, intramolecular rISC is slow (delayed lifetime = 260 μs), but in aggregated films, BF2 generates intermolecular charge transfer (inter-CT) states on picosecond timescales. In contrast to the microsecond intramolecular rISC that is promoted by spin-orbit interactions in most isolated DF molecules, photoluminescence-detected magnetic resonance shows that these inter-CT states undergo rISC mediated by hyperfine interactions on a ~24 ns timescale and have an average electron-hole separation of ≥1.5 nm. Transfer back to the emissive singlet exciton then enables efficient DF and LED operation. Thus, access to these inter-CT states, which is possible even at low BF2 doping concentrations of 4 wt%, resolves the conflicting requirements of fast radiative emission and low ΔEST in organic DF emitters., A low singlet-triplet energy gap, necessary for delayed fluorescence organic semiconductors, results in a small radiative rate that limits performance in OLEDs. Here, the authors show that it is possible to reconcile these conflicting requirements in materials that can access both high oscillator strength intramolecular excitations and intermolecular charge transfer states.

Development of white organic light-emitting diodes based on purely thermally activated delayed fluorescence with a single-emissive-layer configuration has been a formidable challenge. Here, we report the rational design of a donor-acceptor energy-relaying exciplex and its utility in fabricating single-emissive-layer, thermally activated delayed fluorescence-based white organic light-emitting diodes that exhibit 100% internal quantum efficiency, 108.2 lm W−1 power efficiency, and 32.7% external quantum efficiency. This strategy enables thin-film fabrication of an 8 cm × 8 cm thermally activated delayed fluorescence white organic light-emitting diodes (10 inch2) prototype with 82.7 lm W−1 power efficiency and 25.0% external quantum efficiency. Introduction of a phosphine oxide-based acceptor with a steric group to the exciplex limits donor-acceptor triplet coupling, providing dual levels of high-lying and low-lying triplet energy. Transient spectroscopic characterizations confirm that a ladder-like energy relaying occurs from the high-lying triplet level of the exciplex to a blue emitter, then to the low-lying triplet level of the phosphine oxide acceptor, and ultimately to the yellow emitter. Our results demonstrate the broad applicability of energy relaying in multicomponent systems for exciton harvesting, providing opportunities for the development of third-generation white organic light-emitting diode light sources., Realizing efficient white organic light-emitting diodes (WOLEDs) with a single thermally-activated delayed fluorescence (TADF) emissive layer remains a challenge. Here, the authors design energy-relaying exciplex hosts with multi-triplet excited states for efficient single-emissive-layer TADF WOLEDs.

In this study, we report highly efficient green phosphorescent organic light-emitting diodes (OLEDs) with ultra-thin emission layers (EMLs). We use tris[2-phenylpyridinato-C2,N]iridium(III) (Ir(ppy)3), a green phosphorescent dopant, for creating the OLEDs. Under systematic analysis, the peak external quantum efficiency (EQE) of an optimized device based on the ultra-thin EML structure is found to be approximately 24%. This result is highest EQE among ultra-thin EML OLEDs and comparable to the highest efficiency achieved by OLEDs using Ir(ppy)3 that are fabricated via conventional doping methods. Moreover, this result shows that OLEDs with ultra-thin EML structures can achieve ultra-high efficiency.

The viewing angle characteristics and light extraction efficiency of organic light-emitting diodes (OLEDs) with a micro-cavity structure were enhanced. This was accomplished by inserting a diffusion layer composed of nano-sized structures of a transparent polymer poly(methyl methacrylate) (PMMA) combined with a zinc oxide (ZnO) semi-planarization layer with a high refractive index (n = 2.1) into the devices. The PMMA nanostructures were fabricated by employing a reactive ion etching (RIE) process. The height and density of the PMMA nanostructures were controlled by varying the speed at which the PMMA was spin-coated onto the substrate. The insertion of the diffusion layer into the micro-cavity OLEDs (MC-OLEDs) improved the external quantum efficiency (EQE) by as much as 17% when compared to that of a MC-OLED without a diffusion layer. Furthermore, adjustment of the viewing angle from 0° to 60° halved the peak shift distance of the electroluminescence (EL) spectra from 42 to 20 nm. Additionally, changing the viewing angle from 0° to 60° changed the color coordinate movement distance of the MC-OLED with the diffusion layer to 0.078, less than half of the distance of the MC-OLED without the diffusion layer (0.165).

Perovskite light emitting diodes suffer from poor operational stability, exhibiting a rapid decay of external quantum efficiency within minutes to hours after turn-on. To address this issue, we explore surface treatment of perovskite films with phenylalkylammonium iodide molecules of varying alkyl chain lengths. Combining experimental characterization and theoretical modelling, we show that these molecules stabilize the perovskite through suppression of iodide ion migration. The stabilization effect is enhanced with increasing chain length due to the stronger binding of the molecules with the perovskite surface, as well as the increased steric hindrance to reconfiguration for accommodating ion migration. The passivation also reduces the surface defects, resulting in a high radiance and delayed roll-off of external quantum efficiency. Using the optimized passivation molecule, phenylpropylammonium iodide, we achieve devices with an efficiency of 17.5%, a radiance of 1282.8 W sr−1 m−2 and a record T50 half-lifetime of 130 h under 100 mA cm−2., Perovskite light emitting diodes suffer from operational stability, showing rapid decay of performance within minutes to hours after turn-on. Here, the authors investigate how the steric and Coulomb interaction of ammonium passivation molecules with varying alkyl chain length can improve device stability by suppressing iodide ion migration.

Molecular organic fluorophores are currently used in organic light-emitting diodes, though non-emissive triplet excitons generated in devices incorporating conventional fluorophores limit the efficiency. This limit can be overcome in materials that have intramolecular charge-transfer excitonic states and associated small singlet-triplet energy separations; triplets can then be converted to emissive singlet excitons resulting in efficient delayed fluorescence. However, the mechanistic details of the spin interconversion have not yet been fully resolved. We report transient electron spin resonance studies that allow direct probing of the spin conversion in a series of delayed fluorescence fluorophores with varying energy gaps between local excitation and charge-transfer triplet states. The observation of distinct triplet signals, unusual in transient electron spin resonance, suggests that multiple triplet states mediate the photophysics for efficient light emission in delayed fluorescence emitters. We reveal that as the energy separation between local excitation and charge-transfer triplet states decreases, spin interconversion changes from a direct, singlet-triplet mechanism to an indirect mechanism involving intermediate states., Despite advances in the design of thermally activated delayed fluorescence (TADF) emitters for devices, the effect of spin interactions is not well understood. Here, the authors report the role of spin-vibronic coupling in TADF organic emitters using transient electron spin resonance spectroscopy.

Stretchable organic light-emitting diodes are ubiquitous in the rapidly developing wearable display technology. However, low efficiency and poor mechanical stability inhibit their commercial applications owing to the restrictions generated by strain. Here, we demonstrate the exceptional performance of a transparent (molybdenum-trioxide/gold/molybdenum-trioxide) electrode for buckled, twistable, and geometrically stretchable organic light-emitting diodes under 2-dimensional random area strain with invariant color coordinates. The devices are fabricated on a thin optical-adhesive/elastomer with a small mechanical bending strain and water-proofed by optical-adhesive encapsulation in a sandwiched structure. The heat dissipation mechanism of the thin optical-adhesive substrate, thin elastomer-based devices or silicon dioxide nanoparticles reduces triplet-triplet annihilation, providing consistent performance at high exciton density, compared with thick elastomer and a glass substrate. The performance is enhanced by the nanoparticles in the optical-adhesive for light out-coupling and improved heat dissipation. A high current efficiency of ~82.4 cd/A and an external quantum efficiency of ~22.3% are achieved with minimum efficiency roll-off., A transparent twistable and stretchable MoO3/Au/MoO3 electrode is demonstrated by Choi et al. for organic light-emitting diodes. The device fabricated on thin elastomer shows enhanced EQE with minimum efficiency roll-off owing to the improved charge injection and heat dissipation from the substrate.

Large external quantum efficiency rolloff at high current densities in organic light-emitting diodes (OLEDs) is frequently caused by the quenching of radiative singlet excitons by long-lived triplet excitons [singlet–triplet annihilation (STA)]. In this study, we adopted a triplet scavenging strategy to overcome the aforementioned STA issue. To construct a model system for the triplet scavenging, we selected 2,6-dicyano-1,1-diphenyl-λ5σ4-phosphinine (DCNP) as the emitter and 4,4′-bis[(N-carbazole)styryl]biphenyl (BSBCz) as the host material by considering their singlet and triplet energy levels. In this system, the DCNP’s triplets are effectively scavenged by BSBCz while the DCNP’s singlets are intact, resulting in the suppressed STA under electrical excitation. Therefore, OLEDs with a 1 wt.%-DCNP-doped BSBCz emitting layer demonstrated the greatly suppressed efficiency rolloff even at higher current densities. This finding favourably provides the advanced light-emitting performance for OLEDs and organic semiconductor laser diodes from the aspect of the suppressed efficiency rolloff., Though organic light-emitting diodes are highly desirable for display and lighting applications, efficiency roll-off at high current densities limits its applicability. Here, the authors report a triplet scavenging strategy for improved triplet exciton management and reduced efficiency roll-off.

Compared to red and green organic light-emitting diodes (OLEDs), blue OLEDs are still the bottleneck due to the lack of efficient emitters with simultaneous high exciton utilization efficiency (EUE) and short excited-state lifetime. Different from the fluorescence, phosphorescence, thermally activated delayed fluorescence (TADF), and organic radical materials traditionally used in OLEDs, we demonstrate herein a new type of emitter, cerium(III) complex Ce-1 with spin-allowed and parity-allowed d–f transition of the centre Ce3+ ion. The compound exhibits a high EUE up to 100% in OLEDs and a short excited-state lifetime of 42 ns, which is considerably faster than that achieved in efficient phosphorescence and TADF emitters. The optimized OLEDs show an average maximum external quantum efficiency (EQE) of 12.4% and Commission Internationale de L’Eclairage (CIE) coordinates of (0.146, 0.078)., OLEDs: deep blue emission from cerium(III) complex A luminescent cerium(III) complex could be promising for realizing efficient and stable deep-blue organic-LEDs required for display and lighting applications, arising from its theoretical high exciton utilization efficiency and short excited-state lifetime. Liding Wang, Zifeng Zhao, and coworkers from China have shown that a new cerium (III) complex called Ce-1, which supports a d-f energy level transition, can efficiently emit blue light with a high photoluminescence quantum yield up to 93% and a short excited-state lifetime of 42 ns. OLEDs fabricated from the complex offered a maximum external quantum efficiency of 12.4% and a luminance of about 1000 cd m−2, and their emission is characterized as being deep blue with CIE colour coordinates of (0.146, 0.078).

The realisation of a cathode with various work functions (WFs) is required to maximise the potential of organic semiconductors that have various electron affinities. However, the barrier-free contact for electrons could only be achieved by using reactive materials, which significantly reduce the environmental stability of organic devices. We show that a stable electrode with various WFs can be produced by utilising the coordination reaction between several phenanthroline derivatives and the electrode. Although the low WF of the electrode realised by using reactive materials is specific to the material, the WF of the phenanthroline-modified electrode is tunable depending on the amount of electron transfer associated with the coordination reaction. A phenanthroline-modified electrode that has a higher electron injection efficiency than lithium fluoride has been demonstrated. The observation of various WFs induced by the coordination reaction affords strategic perspectives on the development of stable cathodes unique to organic electronics., Despite recent studies aimed at realizing efficient charge injection and collection in organic electronics, developing stable organic injection materials remains a challenge. Here, the authors report phenanthroline derivative-based materials for improved charge injection in organic devices.

The low efficiency and fast degradation of devices from ink-jet printing process hinders the application of quantum dot light emitting diodes on next generation displays. Passivating the trap states caused by both anion and cation under-coordinated sites on the quantum dot surface with proper ligands for ink-jet printing processing reminds a problem. Here we show, by adapting the idea of dual ionic passivation of quantum dots, ink-jet printed quantum dot light emitting diodes with an external quantum efficiency over 16% and half lifetime of more than 1,721,000 hours were reported for the first time. The liquid phase exchange of ligands fulfills the requirements of ink-jet printing processing for possible mass production. And the performance from ink-jet printed quantum dot light emitting diodes truly opens the gate of quantum dot light emitting diode application for industry., Designing efficient and scalable quantum dot LEDs meeting industrial requirements remains a challenge. Here, the authors, by leveraging the liquid phase exchange of d-MX2 ligands, present printed quantum dot LEDs with external quantum efficiency over 16% and half lifetime of more than 1,721,000 hours.

To extract the confined waveguided light in organic light-emitting diodes (OLEDs), inserting a low refractive index (RI) periodic structure between the anode and organic layer has been widely investigated as a promising technology. However, the periodic-structure-based light extraction applied inside devices has been shown to severely distort spectrum and affect EL characteristics. In this study, a simple light extraction technology using periodic low-RI nanodot array (NDA) as internal light extraction layer has been demonstrated. The NDA was fabricated simply via laser interference lithography (LIL). The structural parameters of periodic pattern, distance, and height were easily controlled by the LIL process. From computational analysis using finite-difference time-domain (FDTD) method, the NDA with 300 nm pitch and 0.3 coverage ratio per unit cell with 60 nm height showed the highest enhancement with spectral-distortion-minimized characteristics. Through both computational and experimental systematic analysis on the structural parameters of low-RI NDA-embedded OLEDs, highly efficient OLEDs have been fabricated. Finally, as representative indicators, hexagonal and rectangular positioned NDA-embedded OLEDs showed highly improved external quantum efficiencies of 2.44 (+29.55%) and 2.77 (+57.38%), respectively. Furthermore, the disadvantage originating from the nanoscale surface roughness on the transparent conductive oxide was minimized.

Bio-hybrid light-emitting diodes (Bio-HLEDs) based on color down-converting filters with fluorescent proteins (FPs) have achieved moderate efficiencies (50 lm/W) and stabilities (300 h) due to both thermal- and photo-degradation. Here, we present a significant enhancement in efficiency (~130 lm/W) and stability (>150 days) using a zero-thermal-quenching bio-phosphor design. This is achieved shielding the FP surface with a hydrophilic polymer allowing their homogenous integration into the network of a light-guiding and hydrophobic host polymer. We rationalize how the control of the mechanical and optical features of this bio-phosphor is paramount towards highly stable and efficient Bio-HLEDs, regardless of the operation conditions. This is validated by the relationships between the stiffness of the FP-polymer phosphor and the maximum temperature reached under device operation as well as the transmittance of the filters and device efficiency., Bio-hybrid LEDs (HLED) are an environmental friendly alternative to LEDs based on inorganic phosphors but achieving long term is challenging. Here, the authors present a long-living Bio-HLED based on a zero-thermal-quenching biophosphor design and investigate the photo-induced heat generation and dissipation processes.

Visible light communication (VLC) is a wireless technology that relies on optical intensity modulation and is potentially a game changer for internet-of-things (IoT) connectivity. However, VLC is hindered by the low penetration depth of visible light in non-transparent media. One solution is to extend operation into the “nearly (in)visible” near-infrared (NIR, 700–1000 nm) region, thus also enabling VLC in photonic bio-applications, considering the biological tissue NIR semitransparency, while conveniently retaining vestigial red emission to help check the link operativity by simple eye inspection. Here, we report new far-red/NIR organic light-emitting diodes (OLEDs) with a 650–800 nm emission range and external quantum efficiencies among the highest reported in this spectral range (>2.7%, with maximum radiance and luminance of 3.5 mW/cm2 and 260 cd/m2, respectively). With these OLEDs, we then demonstrate a “real-time” VLC setup achieving a data rate of 2.2 Mb/s, which satisfies the requirements for IoT and biosensing applications. These are the highest rates ever reported for an online unequalised VLC link based on solution-processed OLEDs., Long-wavelength OLEDs: visible light communication Highly efficient organic light-emitting diodes (OLEDs) that operate in the red and near-infrared region bring new opportunities for applications involving visible light communication (VLC). Alessandro Minotto and coworkers from the UK, Poland and Italy have designed and fabricated heavy-metal-free OLEDs featuring a polymeric light-generating active region composed of a fluorescent 𝜋-expanded diketopyrrolopyrrole dye called eDPP blended in a host charge-transport matrix called F8BT. The devices emit light at 650–800 nm with an external quantum efficiency of around 2.7% and a radiance of 3.5 mW/cm2. When employed in a data communications link, error-free data rates of ~2.2 Mb/s were achieved making them suitable for a variety of internet-of-things (IoT) applications such as data-enabled biosensing implants where shorter-wavelength visible light cannot be used due to the issue of strong absorption.

The harvesting of excitons as luminescence by organic fluorophores forms the basis of light-emitting applications. Although high photoluminescence quantum yield is essential for efficient light emission, concentration-dependent quenching of the emissive exciton is generally observed. Here we demonstrate generation and accumulation of concentration-dependent “long-lived” (i.e., over 1 h) photo-generated carriers and the successive release of their energy as electroluminescence in a solid-state film containing a polar fluorophore. While fluorophore excitons are generally believed to be stable because of their high exciton binding energies, our observations show that some of the excitons undergo spontaneous exciton dissociation in a solid-state film by spontaneous orientation polarization even without an external electric field. These results lead to the reconsideration of the meaning of “luminescence quantum yield” for the solid films containing polar organic molecules because it can differ for optical and electrical excitation., Though highly emissive charge-transfer type molecules in a host matrix is an attractive material for organic opto-electronics, concentration quenching limits photoluminescence quantum yield. Here, the authors report concentration quenching in fluorophores based on spontaneous exciton dissociation.

The light-emitting electrochemical cell promises cost-efficient, large-area emissive applications, as its characteristic in-situ doping enables use of air-stabile electrodes and a solution-processed single-layer active material. However, mutual exclusion of high efficiency and high brightness has proven a seemingly fundamental problem. Here we present a generic approach that overcomes this critical issue, and report on devices equipped with air-stabile electrodes and outcoupling structure that deliver a record-high efficiency of 99.2 cd A−1 at a bright luminance of 1910 cd m−2. This device significantly outperforms the corresponding optimized organic light-emitting diode despite the latter employing calcium as the cathode. The key to this achievement is the design of the host–guest active material, in which tailored traps suppress exciton diffusion and quenching in the central recombination zone, allowing efficient triplet emission. Simultaneously, the traps do not significantly hamper electron and hole transport, as essentially all traps in the transport regions are filled by doping., Cost-efficient light-emitting electrochemical cells can deliver unique functions, but suffer because strong brightness has only been obtained at modest efficiency. Tang et al. report on rationally designed devices that are both bright and efficient, thus representing a major step towards commercialization.

Advanced 1.5-µm emitting materials that can be used to fabricate electrically driven light-emitting devices have the potential for developing cost-effective light sources for integrated silicon photonics. Sensitized erbium (Er3+) in organic materials can give bright 1.5-µm luminescence and provide a route for realizing 1.5-µm organic light emitting diodes (OLEDs). However, the Er3+ electroluminescence (EL) intensity needs to be further improved for device applications. Herein, an efficient 1.5-µm OLED made from a sensitized organic Er3+ co-doped system is realized, where a “traditional” organic phosphorescent molecule with minimal triplet–triplet annihilation is used as a chromophore sensitizer. The chromophore provides efficient sensitization to a co-doped organic Er3+ complex with a perfluorinated-ligand shell. The large volume can protect the Er3+ 1.5-µm luminescence from vibrational quenching. The average lifetime of the sensitized Er3+ 1.5-µm luminescence reaches ~0.86 ms, with a lifetime component of 2.65 ms, which is by far the longest Er3+ lifetime in a hydrogen-abundant organic environment and can even compete with that obtained in the fully fluorinated organic Er3+ system. The optimal sensitization enhances the Er3+ luminescence by a factor of 1600 even with a high concentration of the phosphorescent molecule, and bright 1.5-µm OLEDs are obtained., Light emission: Erbium and iridium make a powerful combination Light emission from ions of the element erbium, for use in electrically driven light-emitting devices, can be significantly enhanced by adding sensitizer materials containing iridium ions. The potential of erbium for cost-effective light emission in photonics applications is well-recognized, but methods to increase the power efficiency of the devices are keenly sought. Hong-Fei Li and colleagues at Queen Mary University of London, UK, and Northeast Normal University in Changchun, China, found that a phosphorescent iridium complex enhanced the emission from an erbium complex by a factor of up to 1600. The dramatic effect of the iridium sensitizer was demonstrated in an organic (carbon-based) light-emitting diode. This innovation emphasizes the potential advantages of exploring combinations of molecular complexes in light-emitting devices, rather than seeking a single light-emitting molecule possessing all of the properties required.

Polaritons are quasi-particles composed of a superposition of excitons and photons that can be created within a strongly coupled optical microcavity. Here, we describe a structure in which a strongly coupled microcavity containing an organic semiconductor is coupled to a second microcavity containing a series of weakly coupled inorganic quantum wells. We show that optical hybridisation occurs between the optical modes of the two cavities, creating a delocalised polaritonic state. By electrically injecting electron–hole pairs into the inorganic quantum-well system, we are able to transfer energy between the cavities and populate organic-exciton polaritons. Our approach represents a new strategy to create highly efficient devices for emerging ‘polaritonic’ technologies., Microcavities: Hybrid semiconductors team up for a quantum LED Researchers have optically connected organic semiconductors and inorganic thin films to produce a light-emitting diode powered by quasi-particles that are part light and part matter. Polaritons, which form when electron–hole pairs in a semiconductor interact with photons, can be energy efficient sources of coherent light. Rahul Jayaprakash from the University of Sheffield in the United Kingdom and co-workers have now developed a device that generates electron-hole pairs inside a reflective microcavity filled with gallium–indium–phosphorus thin films. Then, they coupled the chamber’s optical resonance to a second microcavity containing light-absorbing phthalocyanine dye molecules. Time-resolved spectroscopy revealed that energy transfer from the inorganic to the organic microcavity creates sufficient polaritons densities for a visible-light LED, thanks to a delocalized quantum state that forms over both chambers.

It is commonly accepted that a full bandgap voltage is required to achieving efficient electroluminescence (EL) in organic light-emitting diodes. In this work, we demonstrated organic molecules with a large singlet-triplet splitting can achieve efficient EL at voltages below the bandgap voltage. The EL originates from delayed fluorescence due to triplet fusion. Finally, in spite of a lower quantum efficiency, a blue fluorescent organic light-emitting diode having a power efficiency higher than some of the best thermally activated delayed fluorescent and phosphorescent blue organic light-emitting diodes is demonstrated. The current findings suggest that leveraging triplet fusion from purely organic molecules in organic light-emitting diode materials offers an alternative route to achieve stable and high efficiency blue organic light-emitting diodes., Though organic light-emitting diodes (OLEDs) with electroluminescence at sub-bandgap voltages have been reported, realizing high efficiency in such a device is difficult. Here, the authors report high efficiency sub-bandgap OLEDs featuring organic molecules with large singlet-triplet splitting.

The emerging thermally activated delayed fluorescence materials have great potential for efficiencies in organic light-emitting diodes by optimizing molecular structures of the emitter system. However, it is still challenging in the device structural design to achieve high efficiency and stable device operation in white organic light-emitting diodes. Here we propose a universal design strategy for thermally activated delayed fluorescence emitter-based fluorescent white organic light-emitting diodes, establishing an advanced system of “orange thermally activated delayed fluorescence emitter sensitized by blue thermally activated delayed fluorescence host” combined with an effective exciton-confined emissive layer. Compared to reference single-layer and double-layer emissive devices, the external quantum efficiency improves by 31 and 45%, respectively, and device operational stability also shows nearly fivefold increase. Additionally, a detailed optical simulation for the present structure is made, indicating the validity of the design strategy in the fluorescent white organic light-emitting diodes., Demonstrating white organic light-emitting diodes (OLEDs) based on thermally activated delayed fluorescence (TADF) emitters with high performance and operational stability remains a challenge. Here, the authors show efficient and stable white OLEDs based on a double-dopant TADF system.

International audience; This paper evaluates the effect of training algorithms in an artificial neural network (ANN) equalizer for a feedforward multi-layer perceptron configuration in visible light communication systems using a low bandwidth organic light source. We test the scaled conjugate-gradient, conjugate-gradient backpropagation and Levenberg-Marquardt back propagation (LM) algorithms with 5, 10, 20, 30, and 40 neurons. We show that, LM offers superior bit error rate performance in comparison to other training algorithms based on the mean square error. The training methods can be selected based on the trade-off between complexity and performance.

Organic light-emitting diodes (OLEDs) suffer from notorious light trapping, resulting in only moderate external quantum efficiencies. Here, we report a facile, scalable, lithography-free method to generate controllable nanostructures with directional randomness and dimensional order, significantly boosting the efficiency of white OLEDs. Mechanical deformations form on the surface of poly(dimethylsiloxane) in response to compressive stress release, initialized by reactive ions etching with periodicity and depth distribution ranging from dozens of nanometers to micrometers. We demonstrate the possibility of independently tuning the average depth and the dominant periodicity. Integrating these nanostructures into a two-unit tandem white organic light-emitting diode, a maximum external quantum efficiency of 76.3% and a luminous efficacy of 95.7 lm W−1 are achieved with extracted substrate modes. The enhancement factor of 1.53 ± 0.12 at 10,000 cd m−2 is obtained. An optical model is built by considering the dipole orientation, emitting wavelength, and the dipole position on the sinusoidal nanotexture., For organic light-emitting diodes (OLEDs) to reach their potential for lighting applications, improved light out-coupling using industry-compatible methods are required. Here, the authors report reactive ion etching-induced quasi-periodic nanostructures for improved light extraction in white OLEDs.

Funding: Leverhulme Trust (Grant Number(s): RPG-2017-231); Alexander von Humboldt-Stiftung; Engineering and Physical Sciences Research Council (Grant Number(s): EP/R010595/1); Division of Chemical, Bioengineering, Environmental, and Transport Systems (Grant Number(s): 1706207) As solid‐state light sources based on amorphous organic semiconductors, organic light‐emitting diodes (OLEDs) are widely used in modern smartphone displays and TVs. Due to the dramatic improvements in stability, efficiency, and brightness achieved over the last three decades, OLEDs have also become attractive light sources for compact and “imperceptible” biomedical devices that use light to probe, image, manipulate, or treat biological matter. The inherent mechanical flexibility of OLEDs and their compatibility with a wide range of substrates and geometries are of particular benefit in this context. Here, recent progress in the development and use of OLEDs for biomedical applications is reviewed. The specific requirements that this poses are described and compared to the current state of the art, in particular in terms of the brightness, patterning, stability, and encapsulation of OLEDs. Examples from several main areas are then discussed in some detail: on‐chip sensing and integration with microfluidics, wearable devices for optical monitoring, therapeutic devices, and the emerging use in neuroscience for targeted photostimulation via optogenetics. The review closes with a brief outlook on future avenues to scale the manufacturing of OLED‐based devices for biomedical use. Publisher PDF

Efficient conjugated polymer optoelectronic devices benefit from concomitantly high luminescence and high charge carrier mobility. This is difficult to achieve, as interchain interactions, which are needed to ensure efficient charge transport, tend also to reduce radiative recombination and lead to solid-state quenching effects. Many studies detail strategies for reducing these interactions to increase luminescence, or modifying chain packing motifs to improve percolation charge transport; however achieving these properties together has proved elusive. Here, we show that properly designed amorphous donor-alt-acceptor conjugated polymers can circumvent this problem; combining a tuneable energy gap, fast radiative recombination rates and luminescence quantum efficiencies >15% with high carrier mobilities exceeding 2.4 cm2/Vs. We use photoluminescence from exciton states pinned to close-crossing points to study the interplay between mobility and luminescence. These materials show promise towards realising advanced optoelectronic devices based on conjugated polymers, including electrically-driven polymer lasers., Designing conjugated polymers with high charge carrier mobility and fluorescence quantum efficiency, though attractive for optoelectronics, remains challenging. Here, the authors report a strategy for designing donor-acceptor copolymers whose optoelectronic properties exceed the state-of-the-art.

International audience; Visible light communication (VLC) employs light emitting diodes (LEDs) to provide illumination and data communications simultaneously. Organic LEDs (OLEDs) employing small molecules and long-chain polymers PLEDs, have been gaining attention within the VLC research community due to their inherent advantages such as flexible substrates and low-cost manufacturing. However, the carrier mobility of organic semiconductors is much slower than the devices composed of metal alloys, such as gallium nitride, thus leading to a restriction in the OLED modulation bandwidth. The manufacturing processes, materials and the photoactive size of the devices can affect the raw bandwidth of OLEDs. To increase the transmission speeds, novel approaches have been proposed including equalization techniques, signalling schemes and the optimum driver circuits. The paper provides a survey on the evolution of OLED-based VLC systems, and the respective challenges and recent progresses.

Today the high demand for electronics leads to massive production of waste, thus green materials based electronic devices are becoming more important for environmental protection and sustainability. The biomaterial based hydrogels are widely used in tissue engineering, but their uses in photonics are limited. In this study, silk fibroin protein in hydrogel form is explored as a bio-friendly alternative to conventional polymers for lens applications in light-emitting diodes. The concentration of silk fibroin protein and crosslinking agent had direct effects on optical properties of silk hydrogel. The spatial radiation intensity distribution was controlled via dome- and crater-type silk-hydrogel lenses. The hydrogel lens showed a light extraction efficiency over 0.95 on a warm white LED. The stability of silk hydrogel lens is enhanced approximately three-folds by using a biocompatible/biodegradable poly(ester-urethane) coating and more than three orders of magnitude by using an edible paraffin wax coating. Therefore, biomaterial lenses show promise for green optoelectronic applications., Marie Curie Career Integration Grant (PROTEINLED); Turkish Academy of Sciences; Scientific and Technological Research Council of Turkey (TÜBİTAK)

Photolithography has been a major enabling tool for miniaturisation of silicon devices that underpinned the electronics revolution. Rapid, high-resolution patterning of key material characteristics would, similarly, accelerate the advent of molecular electronics and photonics. Here we advance a versatile approach employing local diffusion of functional small-molecular compounds through a solution-processed ‘molecular gate’ interlayer. Diffusion is activated using laser light or solvent vapour jets―a process that can be finely modulated down to molecule-on-demand deposition precision with almost photolithographic resolution (3 S cm–1 for improved electronic devices. Finally, we demonstrate the unique capability for one-step patterning of multiple functionalities by spatially modulating composition in ternary blends, leading to locally tunable photoluminescence from blue to red., We are indebted to Enrique Pascual (ICMAB-CSIC) for providing insights into laser patterning and Lou Kiss (Middlesex University) for freely shared advice on the preparation of the graphics. We express our deepest gratitude to Paul Smith (ETH Zürich) for critically reviewing the manuscript. We thank Miquel Casademont-Viñas (ICMAB-CSIC) for invaluable contribution to exploring the limits of the method, and Agustín Mihi and Andrés Gómez (ICMAB-CSIC) for assistance with optical spectroscopy and AFM analysis. We also thank Daniel Kremer and Hans-Werner Schmidt (Universität Bayreuth) for their customary hospitality and assistance with DSC measurements. We further acknowledge financial support from the Spanish Ministry of Economy, Industry and Competitiveness through the “Severo Ochoa” Programme for Centers of Excellence in R&D (SEV-2015-0496) and project reference PGC2018-095411-B-I00, as well as the European Research Council (ERC) under grant agreement number 648901.

The energy gap law (EG-law) and aggregation quenching are the main limitations to overcome in the design of near-infrared (NIR) organic emitters. Here, we achieve unprecedented results by synergistically addressing both of these limitations. First, we propose porphyrin oligomers with increasing length to attenuate the effects of the EG -law by suppressing the non-radiative rate growth, and to increase the radiative rate via enhancement of the oscillator strength. Second, we design side chains to suppress aggregation quenching. We find that the logarithmic rate of variation in the non-radiative rate vs. EG is suppressed by an order of magnitude with respect to previous studies, and we complement this breakthrough by demonstrating organic light-emitting diodes with an average external quantum efficiency of ~1.1%, which is very promising for a heavy-metal-free 850 nm emitter. We also present a novel quantitative model of the internal quantum efficiency for active layers supporting triplet-to-singlet conversion. These results provide a general strategy for designing high-luminance NIR emitters., Light-emitting diodes: Near-infrared fluorescence from organic molecules Organic (carbon-based) light-emitting diodes (LEDs) that emit near-infrared light can be built by linking together large organic molecules called porphyrins, offering many potential industrial and medical applications. Organic near-infrared LEDs have several advantages over conventional LEDs based on inorganic semiconductors, including mechanical flexibility, biocompatibility and the absence of polluting heavy metals. Researchers in the UK and Italy led by Harry Anderson at the University of Oxford and Franco Cacialli at University College London explored the potential of linked porphyrin structures that fluoresce at near-infrared wavelengths. The optical properties of the materials are improved by engineering the molecular structure and a quantitative model is presented to explain the efficient emission. This research provides understanding of exciton dynamics and points towards innovative uses of near-infrared light in applications including light therapy, optical communications, biosensors and biometric systems.