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In this study, we report the successful synthesis and thorough characterization of Eu 3+ -doped Na 3 Ba 2 LaNb 10 O 30 phosphors, targeting their application in white-light-emitting diodes (w-LEDs). The phosphors were synthesized using a high-temperature solid-state method, ensuring robust incorporation of Eu 3+ ions into the host lattice. Comprehensive analyses were performed, including X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray (EDX) spectroscopy, Fourier transform infrared (FT-IR) spectroscopy and Raman spectroscopy, confirming the phase purity, crystallinity, morphology, and elemental composition of the phosphors. We have also studied the electronic structure using diffuse reflectance spectroscopy (DRS). Photoluminescence studies revealed strong red emissions under near-ultraviolet light excitation, with the optimal Eu 3+ doping concentration identified to be 9 mol%. Quantum-yield measurements demonstrated high luminescence efficiency, while chromaticity coordinates indicated excellent color purity suitable for w-LED applications. These findings contribute significantly to the advancement of phosphor materials for solid-state lighting, suggesting promising prospects for their integration into commercial LED devices., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Conventional fluorescent materials frequently exhibit narrow-band emissions with a small full width at half-maximum (fwhm) due to localized-state characteristics, but electroluminescence is less efficient owing to the utilization of only singlet excitons. In this work, taking advantage of naphthalimide (NAI)-acetylide derivatives with a rigid planar structure and localized transition characteristics, we elaborately designed two mononuclear Pt(II) complexes with weak double emissions of fluorescence and phosphorescence. Taking them as synthetic precursors, we prepared three PtAu 2 heteronuclear clusters and successfully attained highly efficient narrow-band red phosphorescence with the fwhm below 30 nm. Both theoretical and experimental results suggest that the phosphorescence of PtAu 2 clusters mainly originates from the naphthalimide-localized 3 IL (intraligand) triplet state. Solution-processed organic light-emitting diodes (OLEDs) achieved highly efficient narrow-band red electroluminescence with an external quantum efficiency (EQE) of 16.7%. The CIE coordinates of the electroluminescence (0.69, 0.31) closely match the standard red emission for ultrahigh-definition display.

Numerous structural and conductive properties of barium cerate (BC) make this material a promising candidate for energy storage applications. In this work, we demonstrated that BC can be proficiently functionalized by incorporating trivalent samarium ions to give rise to optical properties. Single-phased BaCeO 3 :Sm 3+ (BCS) phosphors were synthesized by gel combustion technique followed by calcination. The crystal structure, optical properties, and prospective applications in LEDs were investigated systematically. By linking the information acquired from the diffuse reflectance spectra with that of the PL spectra, we better understood the electronic level structure and energy transfer mechanism. Fine yellow-orange luminescence with 100% color purity (CP) and lower Correlated Color Temperature (CCT) has been achieved via energization at 348 nm wavelength. The x = 0.02 Sm 3+ has been identified as the optimized content for the luminescence with a quantum efficiency of 34.2%. Obtained yellow-orange coordinates (0.564, 0.435) are proximate to commercialized L3 rank amber LED (Nichia corporation). The present results signify that UV light can suitably energize the BCS phosphor to get monochromatic amber light which can be used to guard medications during manufacture and storage., (© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

9,9-Dimethyl-9,10-dihydroacridine (DMAC) is one of the most widely used electron donor for constructing high-performance thermally activated delayed fluorescence (TADF) emitters. However, DMAC-based emitters often suffer from the imperfect color purity, particularly in blue emitters, due to its strong electron-donating capability. To modulate donor strength, 2,7-F-Ph-DMAC and 2,7-CF 3 -Ph-DMAC were designed by introducing the electron-withdrawing 2-fluorophenyl and 2-(trifluoromethyl)phenyl at the 2,7-positions of DMAC. These donors were used, in combination with 2,4,6-triphenyl-1,3,5-triazine (TRZ) acceptor, to develop novel TADF emitters 2,7-F-Ph-DMAC-TRZ and 2,7-CF 3 -Ph-DMAC-TRZ. Compared to the F- or CF 3 -free reference emitter, both two emitters showed hypsochromic effect in fluorescence and comparable photoluminescence quantum yields without sacrificing the reverse intersystem crossing rate constants. In particular, 2,7-CF 3 -Ph-DMAC-TRZ based OLED exhibited a blue shift by up to 39 nm and significantly improved Commission International de l'Éclairage (CIE) coordinates from (0.36, 0.55) to (0.22, 0.41), while the external quantum efficiency kept stable at about 22.5 %. This donor engineering strategy should be valid for improving the color purity of large amount of acridine based TADF emitters. It can be predicted that pure blue TADF emitters should be feasible if these F- or CF 3 -modifed acridine donors are combined with other weaker electron acceptors., (© 2024 Wiley-VCH GmbH.)

Achieving high-luminescence organic light-emitting devices (OLEDs) with narrowband emission and high color purity is important in various optoelectronic fields. Laser displays exhibit outstanding advantages in next-generation display technologies owing to their ultimate visual experience, but this remains a great challenge. Here, we develop a novel OLED based organic single crystals. By strongly coupling the organic exciton state to an optical microcavity, we obtain polariton electroluminescent (EL) emission from the polariton OLEDs (OPLEDs) with high luminance, narrow-band emission, high color purity, high polarization as well as excellent optically pumped polariton laser. Further, we evaluate the potential for electrically pumped polariton laser through theoretical analysis and provide possible solutions. This work provides a powerful strategy with a material-device combination that paves the way for electrically driven organic single-crystal-based polariton luminescent devices and possibly lasers., (© 2024. The Author(s).)

Red fluorescent materials have important application value in the background light and LED lighting fields of displays. In this work, a novel type of rare earth free deep-red phosphor LiMg 4 SbO 7 :Mn 4+ was prepared successfully, and its crystal structure, microstructure, fluorescence spectrum, quantum yield, thermal stability, fluorescence lifetime, color coordinates and color purity were studied in detail. The excitation spectra of LiMg 4 SbO 7 :Mn 4+ phosphors are located at 200-600 nm, which can be matched with ultraviolet, near-ultraviolet, and blue-light chips. The exciting result is that the LiMg 4 SbO 7 :0.002Mn 4+ phosphor exhibits astonishing quantum efficiency, thermal stability and color purity. Finally, the developed LiMg 4 SbO 7 :Mn 4+ and the yellow phosphor Y 3 Al 5 O 12 :Ce 3+ (YAG:Ce 3+ ) were mixed and coated on a blue light chip (460 nm) to produce a w-LED, which exhibited warm white luminescence with color coordinates of (0.3575, 0.3809), correlated colour temperature (CCT) of 4687 K, and color rendering index (CRI) of 83.6. It is reasonable to consider that LiMg 4 SbO 7 :Mn 4+ phosphors with excellent photoluminescence performance have great application value in LED lighting fields.

We present quad-layered reflective structural color filters generating vivid additive primary colors by controlling a mode number in a Fabry-Perot (FP) cavity and an anti-reflective (AR) coating layer, thus accomplishing high spectral contrast which is highly demanded in creating sharp colors. The reflection brightness of fabricated structural color filters is over 78% and a color gamut is comparable to the standard color gamut (sRGB). Higher-order resonant modes are exploited yielding a narrow passband with strong suppression of the reflection at shorter and longer wavelength ranges for a green color, while red and blue colors are produced by employing fundamental resonant modes. Besides, the structural color filters maintain both high brightness and high color purity at oblique incidence angles up to 40° due to a small angle of refraction by a cavity medium with high refractive index. Moreover, a large-scale fabrication is enabled owing to the simplicity of a device structure, where thin film deposition is used. The scheme presented in this work may open the door to a number of applications, such as reflective displays, imaging devices, colored photovoltaics, and decorations., (© 2024. The Author(s).)

Inkjet printing technology offers a unique approach to producing direct-patterned pixels without fine metal masks for active matrix displays. Organic light-emitting diodes (OLEDs) consisting of thermally activated delayed fluorescence (TADF) emitters facilitate efficient light emission without heavy metals, such as platinum and iridium. Multi-resonance TADF molecules, characterized by their small full width at half maxima (FWHM), are highly suitable for the requirements of wide color-gamut displays. Herein, host-free TADF inks with a low concentration of 1 mg/mL were developed and inkjet-printed onto a seeding layer, concurrently serving as the hole-transporting layer. Attributed to the proof-of-concept of host-free inks printed on a mixed seeding layer, a maximum external quantum efficiency of 13.1% (improved by a factor of 21.8) was achieved in the inkjet-printed OLED, with a remarkably narrow FWHM of only 32 nm. Highly efficient energy transfer was facilitated by the effective dispersion of the sensitizer around the terminal emitters.

Two blue-emitting materials, 4-(12-([1,1':3',1″-terphenyl]-5'-yl)chrysen-6-yl)-N,N-diphenylaniline (TPA-C-TP) and 6-([1,1':3',1″-terphenyl]-5'-yl)-12-(4-(1,2,2-triphenylvinyl)phenyl)chrysene (TPE-C-TP), were prepared with the composition of a chrysene core moiety and terphenyl (TP), triphenyl amine (TPA), and tetraphenylethylene (TPE) moieties as side groups. The maximum photoluminescence (PL) emission wavelengths of TPA-C-TP and TPE-C-TP were 435 and 369 nm in the solution state and 444 and 471 nm in the film state. TPA-C-TP effectively prevented intermolecular packing through the introduction of TPA, a bulky aromatic amine group, and it showed an excellent photoluminescence quantum yield (PLQY) of 86% in the film state. TPE-C-TP exhibited aggregation-induced emission; the PLQY increased dramatically from 0.1% to 78% from the solution state to the film state. The two synthesized materials had excellent thermal stability, with a high decomposition temperature exceeding 460 °C. The two compounds were used as emitting layers in a non-doped device. The TPA-C-TP device achieved excellent electroluminescence (EL) performance, with Commission Internationale de L'Eclairage co-ordinates of (0.15, 0.07) and an external quantum efficiency of 4.13%, corresponding to an EL peak wavelength of 439 nm.

Production of color-tunable emission via simple method for upcoming displays and lighting technologies, and their exceptional luminescence provide considerable potential in sensing application. As environmental pollution and diseases brought by cadmium have always been global issues, therefore, it is imperative to develop an inexpensive, quick, easy, and selective approach for detecting trace cadmium. Herein, we describe the preperation of ZnO/carbon quantum dots (ZnO/CQDs) nanocomposite that emits strongly in the yellow-orange zone with the chromaticity coordinates (0.51, 0.47) and a high color purity (CP) value of 94.3%. The as-produced ZnO/CQDs are used as a fluorescence sensor for Cd 2+ via quenching mechanism due to competitive coordination between ZnO/CQDs and Cd 2+ with the limit of detection (LOD) of 0.14 μM. Additionally, the suggested method can successfully detect Cd 2+ in water samples, demonstrating the feasibility and potential uses of the sensing platform. This study may pave the way for the development of environmentally safe, high-performing, and inexpensive color-tunable phosphor for white LEDs and sensing applications., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

High color purity blue quantum dot light-emitting diodes (QLEDs) have great potential applications in the field of ultra-high-definition display. However, the realization of eco-friendly pure-blue QLEDs with a narrow emission linewidth for high color purity remains a significant challenge. Herein, a strategy for fabricating high color purity and efficient pure-blue QLEDs based on ZnSeTe/ZnSe/ZnS quantum dots (QDs) is presented. It is found that by finely controlling the internal ZnSe shell thickness of the QDs, the emission linewidth can be narrowed by reducing the exciton-longitudinal optical phonon coupling and trap states in the QDs. Additionally, the regulation of the QD shell thickness can suppress the Förster energy transfer between QDs in the QLED emission layer, which will help to reduce the emission linewidth of the device. As a result, the fabricated pure-blue (452 nm) ZnSeTe QLED with ultra-narrow electroluminescence linewidth (22 nm) exhibit high color purity with the Commission Internationale de l'Eclairage chromatic coordinates of (0.148, 0.042) and considerable external quantum efficiency (18%). This work provides a demonstration of the preparation of pure-blue eco-friendly QLEDs with both high color purity and efficiency, and it is believed that it will accelerate the application process of eco-friendly QLEDs in ultra-high-definition displays., (© 2023 Wiley-VCH GmbH.)

The emerging nitrogen-embedded multiple resonance (MR) emitters with an indolo[3,2,1- jk ] carbazole (ICz) unit have exhibited promising performance for high-resolution organic light-emitting diode (OLED) devices, while the underlying photophysics has been rarely reported. In this work, the optical spectra, color purity, and emitting efficiency of ICz-based MR emitters were investigated by using electronic structure and thermal vibration correlation function (TVCF) calculations. Unlike B-N MR emitters, the high color purity of investigated ICz-based MR emitters was mainly contributed by considerable structural rigidity, which also greatly affects the radiative decay rate and fluorescence quantum yield of the S 1 state. For the majority of investigated emitters, potential reverse intersystem crossing (RISC) channels (T 1 → S 1 and T 2 → S 1 ) are limited by thermally inaccessible Δ E ST * or insufficient spin-orbital coupling (SOC), which can be distinguished by the calculated temperature-dependent RISC rate pattern. We provided a systematic photophysical picture for ICz-based MR emitters that might be interesting for the OLED design and application community.

In this study, Eu 3+ and K + co-doped Ca 3 WO 6 double perovskite, a high-color-purity red phosphor, is quantitatively investigated using synchrotron X-ray diffraction Rietveld refinement, energy dispersive X-ray spectroscopy, and high-resolution PL spectroscopy. The Eu 3+ fluorescence line-narrowing (FLN) results, used to estimate the Eu 3+ occupation at given sites (so-called A and B sites) in the host crystal (A 2 BMO 6 ; A, B = Ca; M = W), reveal that the Eu 3+ ions have a twin distribution in both the A and B sites with high asymmetry ratios of Λ A  = 9.7 and Λ B  = 10.7, respectively. More interestingly, at lower Eu 3+ doping levels, the ions are predominantly located at the B sites (≈75%), indicating that the high color purity of Ca 3 WO 6 :(Eu 3+ , K + ) is mainly caused by the high asymmetry ratios of the Eu 3+ sites. Rietveld refinement combined with the FLN technique provides more reliable results for increasing the Eu 3+ substitution at the A site with Eu 3+ and K + doping concentrations, which lower the lattice energy of Ca 3 WO 6 :(Eu 3+ , K + ). The structural distortions owing to K + co-doping in terms of the quadratic elongation and bond-angle variance exhibit good correlations with the Ca(Eu)O 12 A-site cuboctahedra and Ca(Eu)O 6 B-site octahedra, partially accounting for the higher Λ values., (© 2023 The Authors. Advanced Science published by Wiley-VCH GmbH.)

Cross-linkable hole transport materials (HTMs) are ideal for improving the performance of solution-processed quantum dot light-emitting diodes (QLEDs) and phosphorescent light-emitting diodes (OLEDs). However, previously developed cross-linkable HTMs possessed poor hole transport properties, high cross-linking temperatures, and long curing times. To achieve efficient cross-linkable HTMs with high mobility, low cross-linking temperature, and short curing time, we designed and synthesized a series of low-temperature cross-linkable HTMs comprising dibenzofuran (DBF) and 4-divinyltriphenylamine (TPA) segments for highly efficient solution-processed QLEDs and OLEDs. The introduction of divinyl-functionalized TPA in various positions of the DBF core remarkably affected their chemical, physical, and electrochemical properties. In particular, cross-linked 4-(dibenzo[ b , d ]furan-3-yl)- N , N -bis(4-vinylphenyl)aniline (3-CDTPA) exhibited a deep highest occupied molecular orbital energy level (5.50 eV), high hole mobility (2.44 × 10 -4 cm 2 V -1 s -1 ), low cross-linking temperature (150 °C), and short curing time (30 min). Furthermore, a green QLED with 3-CDTPA as the hole transport layer (HTL) exhibited a notable maximum external quantum efficiency (EQE max ) of 18.59% with a remarkable maximum current efficiency (CE max ) of 78.48 cd A -1 . In addition, solution-processed green OLEDs with 3-CDTPA showed excellent device performance with an EQE max of 15.61%, a CE max of 52.51 cd A -1 , and outstanding CIE( x , y ) color coordinates of (0.29, 0.61). This is one of the highest reported EQEs and CEs with high color purity for green solution-processed QLEDs and OLEDs using a divinyl-functionalized cross-linked HTM as the HTL. We believe that this study provides a new strategy for designing and synthesizing practical cross-linakable HTMs with enhanced performance for highly efficient solution-processed QLEDs and OLEDs.

Eu 3+ -doped phosphors have been much attractive owing to their narrow-band red emission peak at 610-630 nm with high color purity; however, the weak and narrow absorption band in the NUV region limits their applications. Doping a higher amount of Eu 3+ ions into a non-concentration quenching host could be key to enhancing the efficiency of the absorption value and emission intensity. Hence, the design of Eu 3+ -heavily doped phosphors with a suitable host lattice is key for applications. In this study, red-emitting Eu 3+ -doped Gd(BO 2 ) 3 -Y 3 BO 6 -GdBO 3 (GdYGd:Eu 3+ ) phosphor with a high quantum efficiency of 58.4% and excellent color purity of 99.5% is reported for the first time. The phosphor is efficiently excited by NUV light at 394 nm and emits a strong red emission band in the 590-710 nm range, peaking at 612 nm. The optimal annealing temperature and Eu 3+ doping content to obtain the strongest PL intensity are 1100 °C and 20 mol%, respectively. The optimized GdYGd:Eu 3+ phosphor possesses a high activation energy of 0.319 eV and a lifetime of 1.14 ms. An illustration of phosphor-coated NUV LED with chromaticity coordinates ( x = 0.5636, y = 0.2961) was successfully synthesized, demonstrating the great potential of GdYGd:Eu 3+ phosphor for NUV-pumped WLED applications., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Advanced multiple resonance induced thermally activated delayed fluorescence (MR-TADF) emitters have emerged as a privileged motif for applications in organic light-emitting diodes (OLEDs), because they furnish highly tunable TADF characteristics and high color purity emission. Herein, based on the unique nitrogen-atom embedding molecular engineering (NEME) strategy, a series of compounds BN-TP-Nx (x=1, 2, 3, 4) have been customized. The nitrogen-atom anchored at different position of triphenylene hexagonal lattice entails varying degrees of perturbation to the electronic structure. The newly-constructed emitters have demonstrated the precise regulation of emission maxima of MR-TADF emitters to meet the actual industrial demand, and further enormously enriched the MR-TADF molecular reservoir. The BN-TP-N3-based OLED exhibits ultrapure green emission, with peak of 524 nm, full-width at half-maximum (FWHM) of 33 nm, Commission Internationale de L'Eclairage (CIE) coordinates of (0.23, 0.71), and maximum external quantum efficiency (EQE) of 37.3 %., (© 2023 Wiley-VCH GmbH.)

Materials with tunable emission colors has attracted increasing interest in both fundamental research and applications. As a key member of light-emitting materials family, lanthanide doped upconversion nanoparticles (UCNPs) have been intensively demonstrated to emit light in any color upon near-infrared excitation. However, realizing the trichromatic emission in UCNPs with a fixed composition remains a great challenge. Here, without excitation pulsed modulation and three different near-infrared pumping, we report an experimental design to fine-control emission in the full color gamut from core-shell-structured UCNPs by manipulating the energy migration through dual-channel pump scheme. We also demonstrate their potential application in full-color display. These findings may benefit the future development of convenient and versatile optical methos for multicolor tuning and open up the possibility of constructing full-color volumetric display systems with high spatiotemporal resolution., (© 2023 Wiley-VCH GmbH.)

Here, we develop an in situ photoluminescence (PL) system to monitor the nucleation and growth of perovskite nanocrystals and control the monomer supply rate to achieve strongly confined and monodispersed quantum dots (QDs) with average size of 3.4 nm. Pure-blue (460 nm wavelength) CsPbBr 3 QDs with near unity PL quantum yield and narrow size distribution (small size dispersion of 9.6%) were thus produced. Light-emitting diodes (LEDs) based on these QDs were prepared by using an all-solution processing route, which showed narrow electroluminescence with full width at half-maximum of 20 nm and a high color purity of 97.3%. The device also had a high external quantum efficiency of 10.1%, maximum luminance of 11 610 cd m -2 , and continuous operation lifetime of 21 h at the initial luminance of 102 cd m -2 , corresponding to the state-of-art for pure-blue perovskite LEDs.

The chemical diversity and structural flexibility of lead halide perovskites (LHPs) offer tremendous opportunities to tune their optical properties through internal molecular engineering and external stimuli. Herein, we report the wide-range and ultrapure photoluminescence emissions in a family of homologous 2D LHPs, [MeOPEA] 2 PbBr 4-4x I 4x (MeOPEA=4-methoxyphenethylammonium; x=0, 0.2, 0.425, 0.575, 1) enabled through internal chemical pressure and external hydrostatic pressure. The chemical pressure, induced by the C-H⋅⋅⋅π interactions and halogen doping/substitution strengthens the structural rigidity to give sustained narrow emissions, and regulates the emission energy, respectively. Further manipulation of physical pressure leads to wide-range emission tuning from 412 to 647 nm in a continuous and reversible manner. This work could open up new pathways for developing 2D LHP emitters with ultra-wide color gamut and high color purity which are highly useful for pressure sensing., (© 2023 Wiley-VCH GmbH.)

Stable deep blue multiresonance emitters with small full width at half maximum (FWHM) are attractive for wide color-gamut organic light-emitting diodes (OLEDs). However, the steric repulsion from the spatially close hydrogens would twist the multiresonance skeletons, causing spectral broadening and molecular instability issues. Here, we strategically introduce a mesitylboron locking unit into a carbazole-embedded multiresonance model emitter, alleviating the hydrogen repulsions and also strengthening the para-positioned weak carbon-nitrogen bond in anionic states. An emission peaking at 452 nm with an FWHM of merely 14 nm and nearly BT.2020 blue chromaticity coordinates are obtained in toluene, affording a high maximum external quantum efficiency of 33.9% in a sensitizing device. Moreover, an impressive LT97 (time to decay to 97% of the initial luminance) of 178 hours at a constant current density of 12 mA/cm 2 was achieved in a stable device with a small y coordinate of 0.057, nearly 20 times longer than the model emitter with even a substantially red-shifted emission.

A sequence of quantum chemical computations of increasing accuracy was used in this work to identify molecules with small exciton reorganization energy (exciton-vibration coupling), of interest for light emitting devices and coherent exciton transport, starting from a set of ∼4500 known molecules. We validated an approximate computational approach based on single-point calculations of the force in the excited state, which was shown to be very efficient in identifying the most promising candidates. We showed that a simple descriptor based on the bond order could be used to find molecules with potentially small exciton reorganization energies without performing excited state calculations. A small set of chemically diverse molecules with a small exciton reorganization energy was analyzed in greater detail to identify common features leading to this property. Many such molecules display an A-B-A structure where the bonding/antibonding patterns in the fragments A are similar in HOMO and LUMO. Another group of molecules with small reorganization energy displays instead HOMO and LUMO with a strong nonbonding character.

A common full-color method involves combining micro-light-emitting diodes (LEDs) chips with color conversion materials such as quantum dots (QDs) to achieve full color. However, during color conversion between micro-LEDs and QDs, QDs cannot completely absorb incident wavelengths cause the emission wavelengths that including incident wavelengths and converted wavelength through QDs, which compromises color purity. The present paper proposes the use of a recycling-reflection color-purity-enhancement film (RCPEF) to reflect the incident wavelength multiple times and, consequently, prevent wavelength mixing after QDs conversion. This RCPEF only allows the light of a specific wavelength to pass through it, exciting blue light is reflected back to the red and green QDs layer. The prototype experiment indicated that with an excitation light source wavelength of 445.5 nm, the use of green QDs and RCPEFs increased color purity from 77.2% to 97.49% and light conversion efficiency by 1.97 times and the use of red QDs and RCPEFs increased color purity to 94.68% and light conversion efficiency by 1.46 times. Thus, high efficiency and color purity were achieved for micro-LEDs displays., (© 2021. The Author(s).)

In this study, we synthesized and characterized multiresonant thermally activated delayed fluorescent (TADF) materials embedded with nitrogen-boron-oxygen (N-B-O), exhibiting color-tunability between blue and green, namely NBO, m-DiNBO, and p-DiNBO. The three emitter materials showed a high photoluminescence quantum yield (PLQY) and a state-of-the-art narrow full width at half maximum (FWHM) of 96 %/25 nm, 87 %/17 nm, and 99 %/19 nm, respectively. For m-DiNBO and p-DiNBO, the emission color could be tuned from blue to green by regulating the nonbonding/bonding molecular orbital characters. Owing to the expanded planar molecular structure, m-DiNBO and p-DiNBO showed high horizontal dipole ratio (Θ) of 88 % and 92 %, respectively. OLEDs were prepared with NBO, m-DiNBO, and p-DiNBO, exhibiting high external quantum efficiencies of 16.8 %, 24.2 %, and 21.6 %, respectively. NBO and m-DiNBO exhibited pure-blue emission with CIE coordinates of (0.137, 0.142) and (0.126, 0.098), respectively. p-DiNBO showed pure-green emission with a CIE coordinate of (0.258, 0.665)., (© 2022 Wiley-VCH GmbH.)

Invited for the cover of this issue is the group of H. Sasabe and J. Kido at Yamagata University in Japan. The image depicts the molecular structures of N-B-O embedded multi-resonant thermally activated delayed fluorescent (MR-TADF) emitters, which achieved ultra-pure deep-blue/green emission with high efficiency in OLEDs. Read the full text of the article at 10.1002/chem.202201605., (© 2022 Wiley-VCH GmbH.)

Delayed fluorescence (DF) emitters with high color purity are of high interest for applications in high-resolution displays. However, the charge transfer required by high emitting efficiency usually conflicts with the expected color purity. In this work, we investigated the S 1 /S 0 conformational relaxation, spin-orbital coupling (SOC), and vibronic coupling of hot-exciton emitters while hybrid local and charge transfer (HLCT) state tuning was achieved by a structural meta -effect. The meta- linkage leads to suppressed S 1 /S 0 conformational relaxation and weakened vibronic coupling, while the unsacrificed emitting efficiency is largely ensured by multiple rISC channels (T n → S m ) with thermally accessible triplet-singlet energy gap (Δ E ) and effective SOC. We demonstrated that the unique excited-state mechanism provides opportunities to improve the emitting color purity of hot-exciton emitters without sacrificing emitting efficiency by HLCT state tuning with simple chemical structural modification, for which hot-exciton emitters might play a more important role for high-resolution organic light-emitting diode displays.ST ) and effective SOC. We demonstrated that the unique excited-state mechanism provides opportunities to improve the emitting color purity of hot-exciton emitters without sacrificing emitting efficiency by HLCT state tuning with simple chemical structural modification, for which hot-exciton emitters might play a more important role for high-resolution organic light-emitting diode displays.

Multiple resonance thermally activated delayed fluorescence (MR-TADF) compounds have set off an upsurge of research because of their tremendous application prospects in the field of wide color gamut display. Herein, we propose a novel MR-TADF molecular construction paradigm based on polycyclization of the multiple resonance parent core, and construct a representative multiple resonance polycyclic aromatic hydrocarbon (MR-PAH) based on the para-alignment of boron and nitrogen atoms into a six-membered ring (p-BNR). Through the retrosynthesis analysis, a concise synthesis strategy with wide applicability has been proposed, encompassing programmed sequential boron esterification, Suzuki coupling and Scholl oxidative coupling. The target model molecule BN-TP shows green fluorescence with an emission peak at 523 nm and a narrow full-width at half-maximum (FWHM) of 34 nm. The organic light-emitting diode (OLED) employing BN-TP as an emitter exhibits ultrapure green emission with Commission Internationale de L'Eclairage (CIE) coordinates of (0.26, 0.70), and achieves a maximum external quantum efficiency (EQE) of 35.1 %., (© 2022 Wiley-VCH GmbH.)

Organic light-emitting diodes (OLEDs) have been widely used, particularly in display applications. OLEDs are easily degraded without stringent encapsulation owing to their susceptibility to water vapor and oxygen. Therefore, establishing an effective protection method for these devices is essential. In this study, we demonstrate the device protection performance and improvement in color purity by introducing CaF 2 /ZnS multilayered films on a top-emitting inverted-type OLED (iOLED), which was originally intended to act as a distributed Bragg reflector (DBR). To test the protection performance of each dielectric layer, conventional bottom-emitting OLEDs (cOLEDs) with and without single layers of CaF 2 and ZnS were investigated for comparison. All OLEDs were stored in an atmosphere without stringent encapsulation, such as a cover glass. The luminescence area of cOLEDs without the dielectric film decreased by more than 90% after 3 days of fabrication. In contrast, the dark-spot formation was moderated after the same period for the dielectric single-layer deposited cOLEDs. Notably, the iOLED with DBR completely preserved the emitting area even after 2 months of fabrication. This suggests that DBR acted as a protective film for the organic layer, whereas the inverted structure also contributed to reducing the degradation of air- and moisture-sensitive materials., Competing Interests: The authors declare no competing financial interest., (© 2022 The Authors. Published by American Chemical Society.)

Structural colors have been reported instead of conventional dye- or pigment-based color filters. Color selectivity can degrade as structure-based optical resonances are accompanied by several resonance modes. In this work, we suggest a simple and effective design of the plasmonic color filter (PCF) that integrated the PCF with the one-dimensional (1D) photonic crystal (PhC). The introduced PhC creates an optical band gap and suppresses undesired peaks of the PCF caused by the high-order resonance mode. Finally, the suggested structure provides a high color purity. This study can be a guideline for technology that replaces conventional color filters.

We present an improved color purity of additive transmissive structural color filters by controlling a resonance order and by inserting a highly absorbing material. The proposed structure consists of a single metal sandwiched by two transparent dielectric media serving as a cavity to minimize the ohmic loss in the metal mirrors, which is distinctly different from a conventional Fabry-Perot (FP) cavity that is in general designed to have two metal mirrors. Low reflections at an air-dielectric interface cause a quality-factor of a resonance to be reduced, causing a degraded color purity, which can be improved by employing a 1st order resonance that exhibits a narrower bandwidth than a fundamental FP resonant mode (0th order). For a red color with the improved purity, introducing an ultrathin absorbing layer in the middle of a top cavity enables the 1st resonance to be trivially influenced while selectively suppressing a 2nd order resonance appearing at the shorter wavelength region. Moreover, angle-insensitive performances up to 60° are attained by utilizing a cavity material with high index of refraction. Besides, the fabrication of the structural coloring devices involves a few deposition steps, thus rendering the approach suitable for applications over the large area. The described concept could be applied to diverse applications, such as colored solar panels, sensors, imaging devices, and decorations.

In this work, a novel red-emitting oxyfluoride phosphor Na 2 NbOF 5 :Mn 4+ with an ultra-intense zero-phonon line (ZPL) was successfully synthesized by hydrothermal method. The phase composition and luminescent properties of Na 2 NbOF 5 :Mn 4+ were studied in detail. The photoluminescence excitation spectrum contains two intense excitation bands centered at 369 and 470 nm, which match well with commercial UV and blue light-emitting diode (LED) chips. When excited by 470 nm blue light, Na 2 NbOF 5 :Mn 4+ exhibits red light emission dominated by ZPL. Notably, the color purity of the Na 2 NbOF 5 :Mn 4+ red phosphor can reach 99.9%. Meanwhile, the Na 2 NbOF 5 :Mn 4+ phosphor has a shorter fluorescence decay time than commercial K 2 SiF 6 :Mn 4+ , which is conducive to fast switching of images in display applications. Profiting from the intense ZPL, white light-emitting diode (WLED) with high color rendering index of Ra = 86.2 and low correlated color temperature of T c = 3133 K is realized using yellow YAG:Ce 3+ and red Na 2 NbOF 5 :Mn 4+ phosphor. The WLED fabricated using CsPbBr 3 quantum dots (QDs) and red Na 2 NbOF 5 :Mn 4+ phosphor shows a wide color gamut of 127.56% NTSC (National Television Standard Committee). The results show that red-emitting Na 2 NbOF 5 :Mn 4+ phosphor has potential application prospects in WLED lighting and display backlight.

Borate oxyfluoride glasses are transparent in the infrared, ultraviolet and visible regions and represent an ideal host matrix for optically active dopants. Due to their lower phonon energies compared to a silicate glass matrix, non-radiative transitions are suppressed and high luminescence efficiency is expected. This work reports on a complete upconversion (UC) luminescence study of the optically active B 2 O 3 -Al 2 O 3 -KF-LiO (BAKL) glass-ceramics incorporated with Er 3+ /Yb 3+ ions. The triclinic BAKL:Er 3+ /Yb 3+ glass-ceramic (GC) phosphor was synthesized using the conventional melt-quenching technique and the subsequent heat treatment of the precursor glass. The successful synthesis of BAKL:Er 3+ /Yb 3+ GCs was confirmed by X-ray diffraction, Fourier transform infra-red and differential thermal analysis measurements. The glasses were crystallized under controlled conditions, and the influence of phase composition (glass-to-crystalline phase ratio) on the wavelength and UC luminescence was thoroughly studied under 980 nm excitation. Interesting color tuning properties (white to intense green emission) of the sample were observed with laser pump power increment. The color tuning properties were explained using a new strategy i.e. the energy bridging mechanism between Er 3+ ion clusters through an intermediate Yb 3+ level. Moreover, their high color purity is well retained by varying the NIR excitation pump power densities and photometric characterization indicated the suitability in light emitting diodes and Er 3+ doped fiber amplifier applications.

Trivalent europium-based monochromatic red light-emitting phosphors are an essential component to realize high-performance smart lighting devices; however, the concentration and thermal quenching restrict their usage. Here, we report a series of efficient Eu 3+ -substituted Li 3 Y 3 BaSr(MoO 4 ) 8 red-emitting phosphors based on a stratified scheelite structure with negligible concentration and thermal quenching. All of the host and phosphor compositions crystallize in monoclinic crystal structure (space group C 2/ c ). All of the phosphor compositions produce narrow-band red emission (FWHM ∼6 nm), which is highly apparent to the human eyes, and lead to exceptional chromatic saturation of the red spectral window. Concurrently, detailed investigations were carried out to comprehend the concentration and thermal quenching mechanism. Absolute quantum yields as high as 88.5% were obtained for Li 3 Y 0.3 Eu 2.7 BaSr(MoO 4 ) 8 phosphor with virtuous thermal stability (at 400 K, retaining 87% of its emission intensity). The light-emitting diodes were constructed by coupling Li 3 BaSrY 0.3 Eu 2.7 (MoO 4 ) 8 red phosphor with a near-UV LED chip (395 nm) operated at 20 mA forward bias, and the hybrid white LED (an organic yellow dye + red Li 3 Y 3 BaSr(MoO 4 ) 8 :Eu 3+ phosphor integrated with an NUV LED chip) showed a low CCT (6645 K), high CRI (83) values, and CIE values of x = 0.303; y = 0.368, which indicated that the synthesized phosphors can be a suitable red component for white LEDs. In addition, we have systematically investigated the Sm 3+ and Sm 3+ , Eu 3+ activation in Li 3 Y 3 BaSr(MoO 4 ) 8 to display the latent use of the system in plant growth applications and establish that the phosphor exhibits orange red emission with an intense deep-red emission (645 nm ( 4 G 5/2 → 6 H 9/2 )). The phytochrome (Pr) absorption spectrum well matched the fabricated deep-red LED (by integrating a NUV LED + Li 3 Y 3 BaSr(MoO 4 ) 8 :Sm 3+ and Eu 3+ phosphor) spectral lines.

Eu(iii) complexes emit red light with a high color purity and have consequently attracted attention for development toward display and physical sensing applications. The characteristic pure color emission originates from the intra-4f-4f transition, and the brightness strongly depends on the electronic and steric structures of organic ligands. A large π-conjugated ligand design with a large absorption coefficient has been actively studied for achieving bright emission. The π-conjugated Eu(iii) luminophores also provide oxygen and temperature sensing properties by controlling their excited state dynamics based on π-electron systems. A comprehensive understanding of the design strategy of large π-conjugated ligands is crucial for the further development of luminescent Eu(iii) complexes. In this review, we summarize the research progress on π-conjugated Eu(iii) luminophores exhibiting bright emission and their physical sensing applications., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Lead halide perovskite nanocrystals (PNCs) are emerging as promising light emitters to be actively explored for high color purity and efficient light-emitting diodes. However, the most reported lead halide perovskite nanocrystal light-emitting diodes (PNCLEDs) encountered issues of emission line width broadening and operation voltage elevating caused by the quantum confinement effect. Here, we report a new type of PNCLED using large-size CsPbBr 3 PNCs overly exceeding the Bohr exciton diameter, achieving ultranarrow emission line width and rapid brightness rise around the turn-on voltage. We adopt calcium-tributylphosphine oxide hybrid ligand passivation to produce highly dispersed large-size colloidal CsPbBr 3 PNCs with a weak size confinement effect and also high photoluminescence quantum yield (∼85%). Utilizing these large-size PNCs as emitters, we manifest that the detrimental effects caused by the quantum confinement effect can be avoided in the device, thereby realizing the highest color purity in green PNCLED, with a narrow full width at half-maximum of 16.4 nm and a high corrected maximum external quantum efficiency of 17.85%. Moreover, the operation half-life time of the large-size PNCLED is 5-fold of that based on smaller-size PNCs. Our work provides a new avenue for improving the performance of PNCLEDs based on unconventional large-size effects.

Inorganic electrochromic (EC) materials with vibrant multicolor change that are compatible with large-scale processing have been at the forefront of EC technology and are crucial in a wide range of applications, such as displays and camouflage. However, limited strategies are available to realize such inorganic materials, and challenges such as low color purity are yet to be overcome. Here, we demonstrate multilayered metal-dielectric metamaterials (MMDMs) as a new family of inorganics-based EC materials to achieve dynamic alternation among multicolors with high contrast and high color purity, which are structurally realized by significantly enhancing the confinement of the incident light in specific optical frequencies. This multilayer structure renders high reflectivity (75%), high quality factor (7.4), and a full width at half-maximum of 60 nm before coloration and presents a color gamut at least 40% wider than that of previously reported metamaterials after coloration, indicating good color quality.

The key factors determining the emission bandwidth of thermally activated delayed fluorescence (TADF) are investigated by combining computational and experimental approaches. To achieve high internal quantum efficiencies in a metal-free organic light-emitting diode via TADF, the first triplet (T 1 ) to first singlet (S 1 ) reverse intersystem crossing is promoted by configuring molecules in an electron donor-acceptor (D-A) alternation with a large dihedral angle, which results in a small energy gap (Δ E ST ) between S 1 and T 1 levels. This allows for effective non-radiative up-conversion of triplet excitons to singlet excitons that fluoresce. However, this traditional molecular design of TADF results in broad emission spectral bands (full-width at half-maximum = 70-100 nm). Despite reports suggesting that suppressing the D-A dihedral rotation narrows the emission band, the origin of emission broadening remains elusive. Indeed, our results suggest that the intrinsic TADF emission bandwidth is primarily determined by the charge transfer character of the molecule, rather than its propensity for rotational motion, which offers a renewed perspective on the rational molecular design of organic emitters exhibiting sharp emission spectra.

Due to complex structure and surface functionalities, photoluminescence mechanisms of Carbon Dots are unknown, and it is challenging to synthesize Carbon Dots to achieve the desired optical properties. Herein, Carbon Dots simultaneously exhibiting high-color-purity (FWHM~24 nm) long wavelength one-photon fluorescence emission at 620 nm and NIR induced two-photon fluorescence emission at 630 and 680 nm are prepared by edge amino protonation treatment. Systematic analysis reveals that the protonation of 2,3-diaminophenazine changes the molecular state of Carbon Dots, decreases the photon transition band gap, and triggers red fluorescence emission with the dramatically narrowed peak width. As the oxidation products of reactant o-phenylendiamine, the emergence of 2,3-diaminophenazine as a photoluminescence determiner suggests that fluorophore products of precursor conversion are viable determinants of the desired luminescence properties of Carbon Dots. This work shows a new way for predicting and controlling photoluminescence properties of Carbon Dots, and may guide the development of tunable Carbon Dots for a broad range of applications., (© 2021. The Author(s).)

Layered rare-earth hydroxides (LREHs) are promising optical and magnetic materials, while it is hard to obtain monolayer nanosheets through a direct exfoliation. In this study, organic dodecyl sulfate (C 12 H 25 SO 4 - , DS - ) was used to prepare LREHs. In-plane lattice parameters of the LREHs decreased from Sm 3+ to Er 3+ contents. By a direct sonication of the LREHs in formamide, nanosheets were obtained with a thickness of ∼1 nm and size of ∼500 nm. Compared to the bulk crystals, exfoliation resulted in a slight elongation of in-plane lattice constants and a more asymmetric coordination environment. The suspension of europium hydroxide nanosheets exhibited a remarkably high red-light emission purity (91.4%). This work demonstrated an important strategy toward an efficient synthesis of well-defined LREH nanosheets with high color purity.- contents. By a direct sonication of the LREHs in formamide, nanosheets were obtained with a thickness of ∼1 nm and size of ∼500 nm. Compared to the bulk crystals, exfoliation resulted in a slight elongation of in-plane lattice constants and a more asymmetric coordination environment. The suspension of europium hydroxide nanosheets exhibited a remarkably high red-light emission purity (91.4%). This work demonstrated an important strategy toward an efficient synthesis of well-defined LREH nanosheets with high color purity.

The discovery of high color purity red-emitting phosphors is a major challenge for solid-state lighting materials. Benefitting from highly condensed and flexible framework structure of β-Ca 3 (PO 4 ) 2 -type compounds, we have successfully prepared three different kinds of novel high color purity red-emitting phosphors Sr 19 Mg 2 (PO 4 ) 14 : Re 3+ (Re 3+ = Eu 3+ , Sm 3+ , Pr 3+ ) by using traditional sintering method. Rietveld refinement, SEM measurement, absorption spectra, emission/excitation spectra, fluorescence decay analysis and emission spectra in terms of different temperature were investigated and discussed clearly. The matrix optical band gap was calculated to be 4.5 eV by reflection data, which indicated the suitable host for rare earth doping. The single doped Eu 3+ , Sm 3+ and Pr 3+ phosphors could respectively exhibit characteristic and strong red emission peaks at 614 nm, 598 nm and 642 nm when excited by (near) ultraviolet radiation. Excitingly, all samples could obtain high color purity with the value of 91.6%, 90.6% and 84.8% for Eu 3+ , Sm 3+ , Pr 3+ ions, respectively. Moreover, the thermal stability can stay strong which still keep over 75% at 150℃ when comparing with that at atmospheric temperature. The quantum efficiency (QE) is another important parameter for phosphors which were measured to be 46.6% for Eu 3+ , 53.1% for Sm 3+ and 10.3% for Pr 3+ . The present work indicates that the Sr 19 Mg 2 (PO 4 ) 14 : Re 3+ phosphors are efficient red components with extraordinary color purity and high quantum efficiency for industrial applications as solid-state lighting materials., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Environment-friendly high color purity blue zinc selenide (ZnSe) quantum dot-based light-emitting diodes (QLEDs) are promising candidates in next-generation display applications. However, due to the large bandgap of ZnSe (2.7 eV), the reported electroluminescence (EL) wavelengths of ZnSe QLEDs are mainly located within the range from purple to violet blue, and preparing blue emitting (>445 nm) ZnSe QLEDs remains challenging. Herein, we report a seed-mediated and double shell strategy to synthesize large-sized blue ZnSe/ZnS/ZnS core/shell/shell quantum dots (QDs). The as-prepared QDs possess excellent features including narrow full widths at half-maximum (11-19 nm), tunable emission wavelengths (410-451 nm), and high photoluminescence quantum yields (≥50%). Using ZnSe/ZnS/ZnS QDs as emitters in an inverted device, a color saturated blue QLED with an EL wavelength of 446 nm, a maximum luminance of 106 cd m -2 , a current efficiency of 0.94 cd A -1 , and an EQE of 2.62% is successfully fabricated. These results indicate that blue ZnSe QLEDs have great potential for future display technologies.

The Eu 3+ -doped Sr 2 InTaO 6 phosphors were obtained by solid-state reaction method and the phase purity of Sr 2 InTaO 6 :Eu 3+ samples were investigated by the XRD patterns. The Rietveld refinements were conducted to further obtain crystal structure information and the results indicate Sr 2 InTaO 6 :Eu 3+ samples crystallized in the monoclinic system with a P 121 space group. The optical band gap of Sr 2 InTaO 6 was calculated to be 3.84 eV by the diffuse reflectance spectra, which are consistent with the result (3.823 eV) of density functional theory. Under 396 nm excitation, the Sr 2 InTaO 6 :Eu 3+ phosphor showed a red photoluminescence band centered at about 624 nm due to the 5 D 0 → 7 F 2 transition. Monitored at 624 nm, the phosphors showed two wide bands from 200 nm to 500 nm, which originated from the charge-transfer band of Eu 3+ -O 2- and f-f transitions of Eu 3+ ions. The optimum luminous concentration is 0.12 because of the concentration quenching determined to be a quadrupole-quadrupole interaction. The luminescence decay lifetimes of the Sr 2 InTaO 6 :Eu 3+ phosphors were milliseconds. Significantly, the temperature-dependent emission spectra of Sr 2 InTaO 6 :0.12Eu 3+ phosphors exhibited good thermal stability and the CIE chromaticity coordinates of Sr 2 InTaO 6 were (0.6265, 0.3693) with high color purity. The present work demonstrated that the Sr 3+ were (0.6265, 0.3693) with high color purity. The present work demonstrated that the Sr 2 InTaO 6 :Eu 3+ red-emitting phosphors show great application in lighting technology., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Pure sky-blue fluorescence (FWHM: 50 nm) from lutetium-based coordination polymer with diphenyl-anthracene derivative is demonstrated for the first time. The observed high color purity is based on the tightly packed crystal structure of the coordination polymer with multiple CH-F interactions., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Development of multicolor-emitting upconversion nanoparticles (UCNPs) is of significant importance for applications in optical encoding, anti-counterfeiting, display, and bioimaging. However, realizing the orthogonal three-primary color (TPC) upconversion luminescence in a single nanoparticle remains a huge challenge. Herein, we have rationally designed core-multishell-structured NaYF 4 UCNPs through regulating the dopant concentration, composition of luminescent layers, and shell position and thickness, which are capable of emitting red, green, and blue luminescence with high color purity in response to ternary near-infrared quadrature excitations (1560/808/980 nm). Moreover, their high color purity is well retained with varying excitation power densities. This orthogonal TPC emissions property of such UCNPs endows them with great promise in the field of security. As a proof-of-concept, we have demonstrated the feasibility of combining such UCNPs with MnO 2 nanosheets for information encryption and decryption. This work not only offers a new way to achieve TPC upconversion luminescence at a single nanoparticle level but also broadens the scope of application for security protection.

The design and synthesis of organic materials with a narrow emission band in the longer wavelength region beyond 510 nm remain a great challenge. For constructing narrowband green emitters, we propose a unique molecular design strategy based on frontier molecular orbital engineering (FMOE), which can integrate the advantages of a twisted donor-acceptor (D-A) structure and a multiple resonance (MR) delayed fluorescence skeleton. Attaching an auxiliary donor to a MR skeleton leads to a novel molecule with twisted D-A and MR structure characteristics. Importantly, a remarkable red-shift of the emission maximum and a narrowband spectrum are achieved simultaneously. The target molecule has been employed as an emitter to fabricate green organic light-emitting diodes (OLEDs) with Commission Internationale de L'Eclairage (CIE) coordinates of (0.23, 0.69) and a maximum external quantum efficiency (EQE) of 27.0 %., (© 2020 Wiley-VCH GmbH.)

Thermally activated delayed fluorescence (TADF) sensitization of fluorescence is a promising strategy to improve the color purity and operational lifetime of conventional TADF organic light-emitting diodes (OLEDs). Here, we propose a new design strategy for TADF-sensitized fluorescence based on acrylic polymers with a pendant energy-harvesting host, a TADF sensitizer, and fluorescent emitter monomers. Fluorescent emitters were rationally designed from a series of homologous polycyclic aromatic amines, resulting in efficient and color-pure polymeric fluorophores capable of harvesting both singlet and triplet excitons. Macromolecular analogues of blue, green, and yellow fourth-generation OLED emissive layers were prepared in a facile manner by Cu(0) reversible deactivation radical polymerization, with emission quantum yields up to 0.83 in air and narrow emission bands with full width at half-maximum as low as 57 nm. White-light emission can easily be achieved by enforcing incomplete energy transfer between a deep blue TADF sensitizer and yellow fluorophore to yield a single white-emissive polymer with CIE coordinates (0.33, 0.39) and quantum yield 0.77. Energy transfer to the fluorescent emitters occurs at rates of 1-4 × 10 8 s -1 , significantly faster than deactivation caused by internal conversion or intersystem crossing. Rapid energy transfer facilitates high triplet exciton utilization and efficient sensitized emission, even when TADF emitters with a low quantum yield are used as photosensitizers. Our results indicate that a broad library of untapped polymers exhibiting efficient TADF-sensitized fluorescence should be readily accessible from known TADF materials, including many monomers previously thought unsuitable for use in OLEDs.

The class of organic-inorganic lead halides with perovskite crystal structures has recently emerged as promising materials for a variety of practical optoelectronic applications. In particular, hybrid halide perovskite quantum dots possess excellent intrinsic optoelectronic properties such as high color purity (full width at half-maximum of 24.59 nm) and photoluminescence quantum yields (92.7%). In this work, we demonstrate the use of perovskite quantum dot materials as an emissive layer of hybrid light-emitting transistors. To investigate the working mechanism of perovskite quantum dots in light-emitting transistors, we investigated the electrical and optical characteristics under both p-channel and n-channel operation. Using these materials, we have achieved perovskite quantum dot light-emitting transistors with high electron mobilities of up to 12.06 cm 2 ·V -1 s -1 , high brightness of up to 1.41 × 10 4 cd m -2 , and enhanced external quantum efficiencies of up to 1.79% operating at a source-drain potential of 40 V.

The creation of white and multicoloured 3D-printed objects with high color fidelity via powder sintering processes is currently limited by discolouration from thermal sensitizers used in the printing process. Here, we circumvent this problem by using switchable, photochromic tungsten oxide nanoparticles, which are colorless even at high concentrations. Upon ultraviolet illumination, the tungsten oxide nanoparticles can be reversibly activated, making them highly absorbing in the infrared. Their strong infrared absorption upon activation renders them efficient photothermal sensitizers that can act as fusing agents for polymer powders in sintering-based 3D printing. The WO 3 nanoparticles show fast activation times, and when mixed with polyamide powders, they exhibit a heating-to-color-change ratio greatly exceeding other sensitizers in the literature. Upon mixing with colored inks, powders containing WO 3 display identical coloration to a pristine powder. This demonstrates the potential of WO 3, and photochromic nanoparticles in general as a new class of material for advanced manufacturing.

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.

Perovskite-based light-emitting diodes (PeLEDs) are now approaching the upper limits of external quantum efficiency (EQE); however, their application is currently limited by reliance on lead and by inadequate color purity. The Rec. 2020 requires Commission Internationale de l'Eclairage coordinates of (0.708, 0.292) for red emitters, but present-day perovskite devices only achieve (0.71, 0.28). Here, lead-free PeLEDs are reported with color coordinates of (0.706, 0.294)-the highest purity reported among red PeLEDs. The variation of the emission spectrum is also evaluated as a function of temperature and applied potential, finding that emission redshifts by <3 nm under low temperature and by <0.3 nm V -1 with operating voltage. The prominent oxidation pathway of Sn is identified and this is suppressed with the aid of H 3 PO 2 . This strategy prevents the oxidation of the constituent precursors, through both its moderate reducing properties and through its forming complexes with the perovskite that increase the energetic barrier toward Sn oxidation. The H 3 PO 2 additionally seeds crystal growth during film formation, improving film quality. PeLEDs are reported with an EQE of 0.3% and a brightness of 70 cd m -2 ; this is the record among reported red-emitting, lead-free PeLEDs., Competing Interests: The authors declare no conflict of interest., (© 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim.)