Search Results (84)

A tetradentate Pt(II) complex with a 5/6/6 structural backbone, Pt(PhPiPy-O-PytmCz), was synthesized by incorporating two distinct cycloalkyl groups. These structural modifications significantly enhanced the photoluminescence quantum yield and effectively increased the distance between molecules, thereby mitigating undesirable intermolecular interactions and triplet-state quenching. This strategic molecular design resulted in an external quantum efficiency of 11.5% at a wavelength of 539 nm and significantly enhanced operational lifetimes in green phosphorescent organic light-emitting diodes (OLEDs). These findings are expected to inspire the development of new green luminescent materials and innovative strategies in OLED technology. Full article

N-phenyl-1H-Indole-5-carboxamide (Ind-CA) exhibits previously unknown room-temperature phosphorescence (RTP) when immobilized in poly (vinyl alcohol) film (PVA film). High-fluorescence anisotropy of Ind-CA in PVA suggests that the fluorophores are strongly immobilized in a polymer matrix, while a relatively low (ca. 0.1) quantum yield indicates a strong non-radiative singlet excited state deactivation. With an increased triplet-state population, Ind-CA can be used for various phosphorescence studies. The room-temperature phosphorescence (RTP) capability of Ind-CA indicates that there is an intricate balance between RTP and the structure of the indole-containing luminophore, as an isomeric N-1H-indole-5-ylbenzamide (Ind-BA) does not show any appreciable levels of RTP. Moreover, the phosphorescence lifetime of Ind-CA is about two orders of magnitude longer than many other 5-substituted indoles. These results further highlight the prospects for the potential rational designs of small molecules with desired triplet-state configuration and RTP characteristics. Full article

Two-dimensional (2D) metal-halide perovskites with highly efficient room-temperature phosphorescence (RTP) are rare due to their complex structures and intricate intermolecular interactions. In this study, by varying the alkyl chain length in organic amines, we synthesized two 2D metal-halide perovskites, namely 4-POMACC and 4-POEACC, both of which exhibit significant RTP emission. Notably, 4-POMACC demonstrates a stronger green RTP emission with a significantly longer lifetime (254 ms) and a higher photoluminescence quantum yield (9.5%) compared to 4-POEACC. A thorough investigation of structural and optical properties reveals that shorter alkyl chains can enhance the optical performance due to reduced molecular vibrations and more effective exciton recombination. Computational calculations further show that the smaller energy gap between S₁ and T_n in 4-POMA facilitates intersystem crossing, thereby improving RTP performance. Based on their remarkable phosphorescence properties, we demonstrated their applications in information encryption. This work offers a novel design strategy that could inspire the development of next-generation RTP materials. Full article

Triplet–triplet transfer photochemical reactions are essential in many biological, chemical, and photonic applications. Here, the Pd-octaethylporphyrin sensitizer along with triplet–triplet annihilator (TTA) active 9,10-diphenylantracenes (DPA) and the related substituted variants in low concentrations were examined. A full experimental approach is presented for finding the necessary rate parameters with statistical standard deviation parameters. This was achieved by solving the pertinent non-analytical kinetic differential equation and fitting it to the experimental time-resolved photoluminescence of both slow fluorescence and sensitizer phosphorescence. The efficiency of the triplet–triplet energy transfer rate was found to be around 90% in THF but only around 75% in toluene. This appears to follow from the shorter lifetime of the sensitizer triplet in toluene. Moreover, the TTA transfer rate was on average more than 40% in THF toluene whereas a considerably lower value around 20–30% was found for toluene. This originated in an order of magnitude higher solvent quenching rate using toluene, based on the analysis of the delayed fluorescence decay traces. These are also higher than the statistically expected 1/9 TTA efficiency but in accordance with recent results in the literature, that attributed these high values to an inverse intersystem crossing process. In addition, quantum chemical calculations were carried out to reveal the pertinent excited triplet molecular orbitals of the lowest triplet excited state for a series of substituted DPAs, in comparison with the singlet ground state. Conclusively, these states distribute mainly in an anthracene ring in all compounds being in the range 1.64–1.65 eV above the ground state. The TTA efficiency was found to vary depending on the DPA annihilator substitution scheme and found to be smaller in THF. This is likely because the molecular framework over which the T1 excited molecular orbitals distribute is less sensitive for a longer lifetime of the annihilator triplet state. Full article

Three cationic Ir(III) complexes, 1, 2, and 3, were successfully synthesized and characterized by tuning the position of a phenyl group at the pyridyl moiety in 2-phenylpyridine. All three complexes exhibited typical aggregation-induced phosphorescence emission (AIPE) properties in CH₃CN/H₂O. The AIPE property was further utilized to achieve the highly sensitive detection of 2,4,6-trinitrophenol (TNP) in aqueous media with low limit of detection (LOD) values of 164, 176, and 331 nM, respectively. This suggests that the different positions of the phenyl group influence the effectiveness of 1, 2, and 3 in the detection of TNP. In addition, 1, 2, and 3 showed superior selectivity and anti-interference properties for the detection of TNP and were observed to have the potential to be used to detect TNP in practical applications. The changes in the luminescence lifetime and UV-Vis absorption spectra of 1, 2, and 3 before and after the addition of TNP indicate that the corresponding quenching process is a combination of static and dynamic quenching. Additionally, the proton nuclear magnetic resonance spectra and results of spectral studies show that the detection mechanism is photo-induced electron transfer (PET). Full article

A cationic Ru(II) complex Ru1 with 5-phenyl-2,2′-bipyridine as ligand was synthesized and fully characterized. Ru1 exhibits significant aggregation-induced phosphorescent emission (AIPE) activity in THF/H₂O. The AIPE property of Ru1 has been successfully used to detect picric acid (PA) in aqueous media. Ru1 exhibits a sensitive luminescence quenching response to PA, with a high quenching constant (K_SV = 2.5 × 10⁴ M⁻¹) and a low limit of detection (LOD = 91 nM). In addition, Ru1 demonstrates high sensitivity and selectivity for detecting PA in different common water samples. The UV-vis absorption spectra and luminescence lifetime of Ru1 show an obvious change after the addition of PA into the Ru1 samples, indicating that the quenching process is a combination of dynamic and static quenching. The density functional theory calculations indicate that the mechanism for the detection of PA is photo-induced electron transfer. Full article

Achieving deep-blue light with high color saturation remains a critical challenge in the development of white light-emitting diode (LED) technology, necessitating luminescent materials that excel in efficiency, low toxicity, and stability. Here, we report the synthesis of [N(C₂H₅)₄]₂Cu₂I₄ (TEA₂Cu₂I₄) single crystals (SCs), which exhibit deep-blue photoluminescence (PL) at 450 nm. These crystals are characterized by a significant Stokes shift of 180 nm, a long lifetime of 1.7 μs, and an impressive photoluminescence quantum yield (PLQY) of 96.7% for SCs and 87.2% for polycrystalline films. The zero-dimensional structure is attributed to the proper spacing of triangular inorganic units [Cu₂I₄]²⁻ by organic cations [N(C₂H₅)₄]⁺. This structural arrangement facilitates broadband deep-blue light emission with phosphorescent characteristics, as evidenced by temperature-dependent PL and time-resolved photoluminescence (TRPL) measurements. The band gap properties of TEA₂Cu₂I₄ were further elucidated through density functional theory (DFT) computations. Notably, the material exhibited minimal PL intensity degradation after continuous UV irradiation and one month of exposure to ambient conditions. Moreover, the polycrystalline film of TEA₂Cu₂I₄ maintained substantial deep-blue emission even after one year of storage. Utilizing TEA₂Cu₂I₄ thin film, we fabricated an electroluminescent device emitting deep-blue light with high color saturation, featuring CIE coordinates (0.143, 0.076) and a brightness of 90 cd/m². The exceptional photophysical properties of TEA₂Cu₂I₄ render it a highly promising candidate for optoelectronic applications. Full article

Two new Tb(III) metal–organic frameworks based on 4,7-dimethylphenanthroline (dmphen) and flexible ligand trans-1,4-cyclohexanedicarboxylate (chdc²⁻) were synthesized and characterized. Their crystallographic formulae are [Tb₂(dmphen)₂(H₂O)₂(chdc)₃]·2DMF (1; DMF = N,N-dimethylformamide) and [Tb₂(dmphen)₂(NO₃)₂(chdc)₂]·2DMF (2). Among some differences in their synthetic conditions, the most important one is apparently the using of terbium(III) nitrate instead of terbium(III) chloride as a metal precursor in the synthesis of 2, providing a nitrate coordination to Tb³⁺, and its subsequent notable structural differences to 1. Compound 1 was found to have a layered hcb structure with intralayer windows ca. 10 × 8 Ų in size. Its layer-to-layer packing leaves narrow channels running across these windows, with 18% as a total solvent-accessible volume in the coordination structure. Compound 2 was found to have a layered sql structure with smaller intralayer windows of ca. 8 × 6 Ų in size. Methyl substituents on the phen ligands do not affect the topology of the framework but seem to have a substantial effect on the packing density, as well as the pore volume of the resulting MOF. A high 18.4% luminescence quantum yield was found for 2. Its emission lifetime of 0.695(12) ms belongs to a typical range for phosphorescent Tb(III)-carboxylate complexes. A quenching of its emission by different nitroaromatic molecules was found. A linear concentration dependence on 3-nitrotoluene and 4-nitro-m-xylene at micromolar concentrations was found during luminescent titration experiments (LOD values ca. 350 nM), suggesting this MOF to be a viable and highly sensitive luminescent sensor for such substrates. Full article

A synthetic approach to prepare boron-enriched π-conjugated photoactive molecular systems based on ortho-carborane using the Cu(I)-catalyzed Sonogashira-type coupling reaction has been developed. The obtained luminophores have been found to possess absorption in the range of 300 to 400 nm, emission of up to 700 nm, and photoluminescence quantum yields of up to 99% in non-polar solvents. TD-DFT calculations have demonstrated that the luminophores are characterized by phosphorescent emission behavior with a lifetime of about 7 μs. In addition, the rigidochromism for the synthesized compounds has been revealed; particularly, the transition electronic state and bathochromic shift have been elucidated in the emission spectra. The exhibited luminescent characteristics indicate that the elaborated vinylcarborane fluorophores could be considered as promising building blocks in the design of advanced photofunctional materials for molecular electronics. Full article

Organic light-emitting diode (OLED) technology has rapidly emerged in the display and lighting sectors due to its high contrast ratio, wide viewing angle, and sleek design. Beyond these attributes, OLEDs have also demonstrated crucial applications in medicine, fashion, sports, and more, leveraging their emissive properties and flexible design. As the cornerstone of full-color displays, blue OLEDs, whose performance directly impacts color rendition and saturation, have garnered significant attention from both scientific researchers and industrial practitioners. Despite the numerous advantages of OLED technology, blue OLEDs still confront formidable challenges in terms of luminous efficiency, durability, and material stability. This review examines the evolution of blue OLED materials over recent years, specifically focusing on three generations: fluorescent, phosphorescent, and thermally activated delayed fluorescence (TADF). Through molecular design, device structure optimization, and the application of innovative technologies, remarkable advancements have been achieved in enhancing the luminous efficiency, lifetime, and color purity of blue OLEDs. However, to advance commercialization, future efforts must not only ensure high efficiency and long lifetime but also improve material stability, environmental sustainability, and reduce development costs. Emerging materials such as thermally activated exciton materials and the application of hyperfluorescent (HF) OLED technology represent vital driving forces for the continuous advancement of blue OLED technology. It is anticipated that significant milestones will continue to be achieved in the development of highly efficient blue OLEDs in the future. Full article

We designed and synthesized new indolocarbazole-triazine derivatives, 9-di-tert-butyl-5,7-bis(4-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-5,7-dihydroindolo[2,3-b]carbazole (2TRZ-P-ICz) and 3,9-di-tert-butyl-5,7-bis(5′-(4,6-diphenyl-1,3,5-triazin-2-yl)-[1,1′:3′,1″-terphenyl]-2′-yl)-5,7-dihydroindolo[2,3-b]carbazole (2TRZ-TP-ICz), as new bipolar host materials for red phosphorescent OLEDs. In the film state, 2TRZ-P-ICz and 2TRZ-TP-ICz exhibited photoluminescence maxima at 480 nm and 488 nm, respectively. The dipole moment characteristics of the new compounds under various solvent conditions were investigated using the Lippert–Mataga equation. The results showed that the dipole moment of 2TRZ-P-ICz is 26.9D, while that of 2TRZ-TP-ICz is 21.3D. The delayed fluorescence lifetimes were 0.188 μs for 2TRZ-P-ICz and 2.080 μs for 2TRZ-TP-ICz, with 2TRZ-TP-ICz showing TADF characteristics. Additionally, 2TRZ-TP-ICz was found to have a ΔEST of less than 0.2 eV. The triplet energy levels of the newly synthesized bipolar host materials were found to be 2.72 and 2.75 eV, confirming their suitability for use in red phosphorescent OLEDs. To investigate the carrier mobility of the synthesized materials, hole-only devices and electron-only devices were fabricated and tested. The hole mobility value at 1V was found to be 3.43 × 10⁻³ cm²/Vs for 2TRZ-P-ICz and 2.16 × 10⁻³ cm²/Vs for 2TRZ-TP-ICz. For electron mobility at 1V, 2TRZ-P-ICz showed a value of 4.41 × 10⁻⁹ cm²/Vs, while 2TRZ-TP-ICz exhibited a value of 9.13 × 10⁻⁹ cm²/Vs. As a result, when the new material was used as a host in red phosphorescent OLEDs, 2TRZ-TP-ICz achieved a current efficiency of 9.92 cd/A, an external quantum efficiency of 13.7%, CIE coordinates of (0.679, 0.319), and an electroluminescence maximum wavelength of 626 nm. Full article

The tetradentate ligand, merging a carbazole unit with high triplet energy and dimethoxy bipyridine, renowned for its exceptional quantum efficiency in coordination with metals like Pt, is expected to demonstrate remarkable luminescent properties. However, instances of tetradentate ligands such as bipyridine-based pyridylcarbazole derivatives remain exceptionally scarce in the current literature. In this study, we developed a tetradentate ligand based on carbazole and 2,3′-bipyridine and successfully complexed it with Pt(II) ions. This novel compound (1) serves as a sky-blue phosphorescent material for use in light-emitting diodes. Based on single-crystal X-ray analysis, compound 1 has a distorted square-planar geometry with a 5/6/6 backbone around the Pt(II) core. Bright sky-blue emissions were observed at 488 and 516 nm with photoluminescent quantum yields of 34% and a luminescent lifetime of 2.6 μs. TD-DFT calculations for 1 revealed that the electronic transition was mostly attributed to the ligand-centered (LC) charge transfer transition with a small contribution from the metal-to-ligand charge transfer transition (MLCT, ~14%). A phosphorescent organic light-emitting device was successfully fabricated using this material as a dopant, along with 3′-di(9H-carbazol-9-yl)-1,1′-biphenyl (mCBP) and 9-(3′-carbazol-9-yl-5-cyano-biphenyl-3-yl)-9H-carbazole-3-carbonitrile (CNmCBPCN) as mixed hosts. A maximum quantum efficiency of 5.2% and a current efficiency of 15.5 cd/A were obtained at a doping level of 5%. Full article

In order to improve the data productivity of a wind tunnel test, the model under investigation in the wind tunnel is moved continuously with a predetermined constant angular speed in the so-called pitch–traverse mode. Alternatively, the wind tunnel model can be moved in the so-called pitch–pause mode, in which it keeps its position for a certain (measurement) time at a fixed pitch position, after which it is moved to the next pitch position. The latter procedure is more time-consuming, so, for the same time interval, the number of measured data points taken in the pitch–pause mode is less than that for the pitch–traverse mode. Since wind tunnel test time can be quite expensive, in most wind tunnel tests where only conventional forces and pressures are recorded with conventional measuring systems, the wind tunnel model is moved in the pitch–traverse mode in order to obtain as much aerodynamic data as possible during the tunnel runtime. The application of the Pressure-Sensitive Paint (PSP) technique has been widely used in wind tunnel testing for the purpose of providing pressure data on wind tunnel models with high spatial resolution. The lifetime-based PSP method has several advantages over the intensity-based method since it often has higher accuracy. Up until now, the lifetime-based PSP technique has mainly been used for wind tunnel testing, where the test model has been moved to the pitch–pause mode. The traditional lifetime method using on-chip accumulation requires multiple (~1000) excitation light pulses to accumulate enough luminescence (fluorescence or phosphorescence) photons on the camera sensor to provide acceptable signal-to-noise ratios and, therefore, it may seem to be not compatible with a continuously moving wind tunnel model. Nevertheless, the present study verifies the application of lifetime-based PSP utilizing on-chip accumulation with a continuously moving wind tunnel model which would make the entire PSP data acquisition compatible with that of the conventional measurements (forces and pressures), as mentioned above. In this paper, the applicability of the lifetime-based PSP technique to a continuously moving wind tunnel model (in pitch–traverse mode) is investigated with the help of measurements in the transonic wind tunnel in Göttingen (TWG). For this investigation, PSP was applied on the delta-wing model DLR-F22, which is to be tested in TWG. The pressure distribution on the wind tunnel model was measured using the PSP lifetime method for both model movement modes (pitch–pause and pitch–traverse mode) so that the corresponding PSP results could be directly compared with each other. In addition, an error analysis of the PSP results was carried out and compared with the conventional pressure measurement results, hence providing an assessment of the accuracy of the PSP results; finally, a recommendation for future PSP measurements could be given. Full article

The ever-growing prominence and widespread acceptance of organic light-emitting diodes (OLEDs), particularly those employing thermally activated delayed fluorescence (TADF), have firmly established them as formidable contenders in the field of lighting technology. TADF enables achieving a 100% utilization rate and efficient luminescence through reverse intersystem crossing (RISC). However, the effectiveness of TADF-OLEDs is influenced by their high current density and limited device lifetime, which result in a significant reduction in efficiency. This comprehensive review introduces the TADF mechanism and provides a detailed overview of recent advancements in the development of host-free white OLEDs (WOLEDs) utilizing TADF. This review specifically scrutinizes advancements from three distinct perspectives: TADF fluorescence, TADF phosphorescence and all-TADF materials in host-free WOLEDs. By presenting the latest research findings, this review contributes to the understanding of the current state of host-free WOLEDs, employing TADF and underscoring promising avenues for future investigations. It aims to serve as a valuable resource for newcomers seeking an entry point into the field as well as for established members of the WOLEDs community, offering them insightful perspectives on imminent advancements. Full article

Narrowband afterglow materials display interesting functions in high-quality anti-counterfeiting and multiplexed bioimaging. However, there is still a limited exploration of these afterglow materials, especially for those with a full width at half maxima (FWHM) around 30 nm. Here, we report the fabrication of narrowband organic/inorganic hybrid afterglow materials via energy transfer technology. Coronene (Cor) with a long phosphorescence feature and broad phosphorescence band is selected as the donor for energy transfer, and inorganic quantum dots (QDs) of CdSe/ZnS with a narrowband emission are used as acceptors. Upon doping into the organic matrix, the resultant three-component materials exhibit a narrowband afterglow with an afterglow lifetime of approximately 3.4 s and an FWHM of 31 nm. The afterglow wavelength of the afterglow materials can be controlled by the QDs. This work based on organic/inorganic hybrids provides a facile approach for developing multicolor and narrowband afterglow materials, as well as opens a new way for expanding the features of organic afterglow for multifunctional applications. It is expected to rely on narrowband afterglow emitters to solve the “spectrum congestion” problem of high-density information storage in optical anti-counterfeiting and information encryption. Full article