Nonradiative Rate Research Articles

Enhanced Fluorescence behavior of Safranine-O by complexing with inorganic clay nanosheets

Our laboratory has been studying the strong enhancement in the fluorescence quantum yield and an excited lifetime of the organic dye molecules on the clay nanosheets and refer to as “Surface-Fixation Induced Emission”. In this study, Safranine-O which is a mono-cationic phenazine-based dye molecule, was used as the organic dye. It has fluorescence enhancement properties on the clay surface due to the suppression of the non-radiative deactivation rate constant (knr) on the clay nanosheets. While Safranine-O in water in the absence of clay nanosheets exhibited the values as 0.068 and 1.09 × 10−9 s for ϕf and τ, those on the clay surface are 0.121 and 1.96 × 10−9 s. knr values in water and on the clay were calculated to be 8.6 × 108s − 1 and 4.5 × 108s − 1, respectively. These results can be explained well by the structure fixing and structure resembling effect. This study helps to explore the possibility of utilizing mono-cationic dye molecules for the realization of desired photo-functional materials and photochemical reactions.

Native defect clustering-induced carrier localization centers leading to a reduction of performance in Ga0.70In0.30N/GaN quantum wells.

In this study, we aimed to better understand the mechanism for creating carrier localization centers (CLCs) in Ga0.70In0.30N/GaN quantum wells (QWs) and examine their impacts on device performance. Particularly, we focused on the incorporation of native defects into the QWs as a main cause of the mechanism behind the CLC creation. For this purpose, we prepared two GaInN-based LED samples with and without pre-trimethylindium (TMIn) flow-treated QWs. Here, the QWs were subjected to a pre-TMIn flow treatment to control the incorporation of defects/impurities in the QWs. In an effort to investigate how the pre-TMIn flow treatment affects the incorporation of native defects into the QWs, we employed steady-state photo-capacitance and photo-assisted capacitance-voltage measurements, and acquired high-resolution micro-charge-coupled device images. The experimental results showed that CLC creation in the QWs during growth is closely related to the native defects, most likely VN-related defects/complexes, since they have a strong affinity to In atoms and the nature of clustering. Moreover, the CLC creation is fatal to the performance of the yellow-red QWs since they simultaneously increase the non-radiative recombination rate, decrease the radiative recombination rate, and increase operating voltage-unlike blue QWs.

YCl3-Substituted CsPbI3 Perovskite Nanorods for Efficient Red-Light-Emitting Diodes.

Cesium lead iodide (CsPbI3) perovskite nanocrystals (NCs) are a promising material for red-light-emitting diodes (LEDs) due to their excellent color purity and high luminous efficiency. However, small-sized CsPbI3 colloidal NCs, such as nanocubes, used in LEDs suffer from confinement effects, negatively impacting their photoluminescence quantum yield (PLQY) and overall efficiency. Here, we introduced YCl3 into the CsPbI3 perovskite, which formed anisotropic, one-dimensional (1D) nanorods. This was achieved by taking advantage of the difference in bond energies among iodide and chloride ions, which caused YCl3 to promote the anisotropic growth of CsPbI3 NCs. The addition of YCl3 significantly improved the PLQY by passivating nonradiative recombination rates. The resulting YCl3-substituted CsPbI3 nanorods were applied to the emissive layer in LEDs, and we achieved an external quantum efficiency of ~3.16%, which is 1.86-fold higher than the pristine CsPbI3 NCs (1.69%) based LED. Notably, the ratio of horizontal transition dipole moments (TDMs) in the anisotropic YCl3:CsPbI3 nanorods was found to be 75%, which is higher than the isotropically-oriented TDMs in CsPbI3 nanocrystals (67%). This increased the TDM ratio and led to higher light outcoupling efficiency in nanorod-based LEDs. Overall, the results suggest that YCl3-substituted CsPbI3 nanorods could be promising for achieving high-performance perovskite LEDs.

Observation of two different temperature-dependent behaviors of the defects in III-nitride micro-LEDs

As micro-LED pixel sizes shrink, the volume-to-surface ratio increases, so defect-assisted non-radiative recombination becomes more important for LED pixel efficiency degradation. The donor-type defects on the pixel sidewalls are induced by inductively coupled plasma etching, and the carrier leakage through the sidewalls is determined by the density of surface traps. The defects in quantum wells provide places for the non-radiative recombination of electron–hole pairs, and the recombination rate is related to the thermal velocity of carriers and the trapping cross section of defects. The experimental results indicate that the significant improvement of quantum efficiency from sidewall passivation happens at current densities higher than 400 A/cm2 at an environmental temperature of 300 K. When the temperature decreases to 150 K, the sample with sidewall passivation has 10% higher quantum efficiency at all current ranges. Numerical modeling is applied to evaluate the behaviors of two types of defects at different temperatures. Our observation from modeling reveals that the efficiency drop caused by surface defects is hardly affected by temperature changes, whereas results show that the Shockley–Read–Hall nonradiative recombination rate decreases rapidly at low temperature due to longer carrier lifetime and increased difficulty of electron and hole recombination in traps. Therefore, the significant increase in the efficiency at 150 K, especially in the low current density range, is due to the defects within the quantum well.

Thermally Enhanced and Long Lifetime Red TADF Carbon Dots via Multi-Confinement and Phosphorescence Assisted Energy Transfer.

Thermally activated delayed fluorescence (TADF) materials, which can harvest both singlet and triplet excitons for high-efficiency emission, have attracted widespread concern for their enormous applications. Nevertheless, luminescence thermal quenching severely limits the efficiency and operating stability in TADF materials and devices at high temperature. Herein, a surface engineering strategy is adopted to obtain unique carbon dots (CDs)-based thermally enhanced TADF materials with ≈250% enhancement from 273 to 343K via incorporating seed CDs into ionic crystal network. The rigid crystal network can simultaneously boost reverse intersystem crossing process via enhancing spin-orbit coupling between singlet and triplet states and suppressing non-radiative transition rate, contributing to the thermally enhanced TADF character. Benefiting from efficient energy transfer from triplet states of phosphorescence center to singlet states of CDs, TADF emission at ≈600nm in CDs displays a long lifetime up to 109.6ms, outperforming other red organic TADF materials. Thanks to variable decay rates of the delayed emission centers, time and temperature-dependent delayed emission color has been first realized in CDs-based delayed emission materials. The CDs with thermally enhanced and time-/temperature-dependent emission in one material system can offer new opportunities in information protection and processing.

Excitonic Beam Steering in an Active van der Waals Metasurface.

Two-dimensional transition metal dichalcogenides (2D TMDCs) are promising candidates for ultrathin active nanophotonic elements due to the strong tunable excitonic resonances that dominate their optical response. Here, we demonstrate dynamic beam steering by an active van der Waals metasurface that leverages large complex refractive index tunability near excitonic resonances in monolayer molybdenum diselenide (MoSe2). Through varying the radiative and nonradiative rates of the excitons, we can dynamically control both the reflection amplitude and phase profiles, resulting in an excitonic phased array metasurface. Our experiments show reflected light steering to angles between -30° and 30° at different resonant wavelengths corresponding to the A exciton and B exciton. This active van der Waals metasurface relies solely on the excitonic resonances of the monolayer MoSe2 material rather than geometric resonances of patterned nanostructures, suggesting the potential to harness the tunability of excitonic resonances for wavefront shaping in emerging photonic applications.

Excitation Intensity-Dependent Quantum Yield of Semiconductor Nanocrystals

One of the key phenomena that determine the fluorescence of nanocrystals is the nonradiative Auger-Meitner recombination of excitons. This nonradiative rate affects the nanocrystals' fluorescence intensity, excited state lifetime, and quantum yield. Whereas most of the above properties can be directly measured, the quantum yield is the most difficult to assess. Here we place semiconductor nanocrystals inside a tunable plasmonic nanocavity with subwavelength spacing and modulate their radiative de-excitation rate by changing the cavity size. This allows us to determine absolute values of their fluorescence quantum yield under specific excitation conditions. Moreover, as expected considering the enhanced Auger-Meitner rate for higher multiple excited states, increasing the excitation rate reduces the quantum yield of the nanocrystals.

Efficient Near-Infrared Luminescence of Self-Assembled Platinum(II) Complexes: From Fundamentals to Applications.

ConspectusDesigning bright and efficient near-infrared (NIR) emitters has drawn much attention due to numerous applications ranging from biological imaging, medical therapy, optical communication, and night-vision devices. However, polyatomic organic and organometallic molecules with energy gaps close to the deep red and NIR regime are subject to dominant nonradiative internal conversion (IC) processes, which drastically reduces the emission intensity and exciton diffusion length of organic materials and hence hampers the optoelectronic performances. To suppress nonradiative IC rates, we suggested two complementary approaches to solve the issues: exciton delocalization and molecular deuteration. First, exciton delocalization efficiently suppresses the molecular reorganization energy through partitioning to all aggregated molecules. According to the IC theory together with the effect of exciton delocalization, the simulated nonradiative rates with the energy gap ΔE = 104 cm-1 decrease by around 104 fold when the exciton delocalization length equals 5 (promoting vibronic frequency ωl = 1500 cm-1). Second, molecular deuterations reduce Franck-Condon vibrational overlaps and vibrational frequencies of promoting modes, which decreases IC rates by 1 order of magnitude in comparison to the rates of nondeuterated molecules under ΔE of 104 cm-1. Although deuteration of molecules has long been attempted to increase emission intensity, the results have been mixed. Here, we provide a robust derivation of the IC theory to demonstrate its validity, especially to emission in the NIR region.The concepts are experimentally verified by the strategic design and synthesis of a class of square-planar Pt(II) complexes, which form crystalline aggregates in vapor deposited thin films. The packing geometries are well characterized by the grazing angle X-ray diffraction (GIXD), showing domino-like packing arrangements with the short ππ separation of 3.4-3.7 Å. Upon photoexcitation, such closely packed assemblies exhibit intense NIR emission maximized in the 740-970 nm region through metal-metal-to-ligand charge transfer (MMLCT) transition with unprecedented photoluminescent quantum yield (PLQY) of 8-82%. To validate the existence of exciton delocalization, we applied time-resolved step-scan Fourier transform UV-vis spectroscopy to probe the exciton delocalization length of Pt(II) aggregates, which is 5-9 molecules (2.1-4.5 nm) assuming that excitons mainly delocalized along the direction of ππ stacking. According to the dependence of delocalization length vs simulated IC rates, we verify that the observed delocalization lengths contribute to the high NIR PLQY of the aggregated Pt(II) complexes. To probe the isotope effect, both partially and completely deuterated Pt(II) complexes were synthesized. For the case of the 970 nm Pt(II) emitter, the vapor deposited films of per-deuterated Pt(II) complexes exhibit the same emission peak as that of the nondeuterated one, whereas PLQY increases ∼50%. To put the fundamental studies into practice, organic light-emitting diodes (OLEDs) were fabricated with a variety of NIR Pt(II) complexes as the emitting layer, showing the outstanding external quantum efficiencies (EQEs) of 2-25% and the remarkable radiances 10-40 W sr-1 m-2 at 740-1002 nm. The prominent device performances not only successfully prove our designed concept but also reach a new milestone for highly efficient NIR OLED devices.This Account thus summarizes our approaches about how to boost the efficiency of the NIR emission of organic molecules from an in-depth fundamental basis, i.e., molecular design, photophysical characterization, and device fabrication. The concept of the exciton delocalization and molecular deuteration may also be applicable to a single molecular system to achieve efficient NIR radiance, which is worth further investigation in the future.

Anomalous thickness dependence of photoluminescence quantum yield in black phosphorous

Black phosphorus has emerged as a unique optoelectronic material, exhibiting tunable and high device performance from mid-infrared to visible wavelengths. Understanding the photophysics of this system is of interest to further advance device technologies based on it. Here we report the thickness dependence of the photoluminescence quantum yield at room temperature in black phosphorus while measuring the various radiative and non-radiative recombination rates. As the thickness decreases from bulk to ~4 nm, a drop in the photoluminescence quantum yield is initially observed due to enhanced surface carrier recombination, followed by an unexpectedly sharp increase in photoluminescence quantum yield with further thickness scaling, with an average value of ~30% for monolayers. This trend arises from the free-carrier to excitonic transition in black phosphorus thin films, and differs from the behaviour of conventional semiconductors, where photoluminescence quantum yield monotonically deteriorates with decreasing thickness. Furthermore, we find that the surface carrier recombination velocity of black phosphorus is two orders of magnitude lower than the lowest value reported in the literature for any semiconductor with or without passivation; this is due to the presence of self-terminated surface bonds in black phosphorus.

Fluoro substitution effect on 2,1,3-benzothiadiazole-based hybridized local and charge transfer state fluorophores for high-performance organic light-emitting diodes

Fluoro substitution of organic semiconductors is an effective way to improve some related performance of the materials, such as the carrier mobility in organic photovoltaics (OPVs) and organic field-effect transistors (OFETs) applications. However, the influence of fluoro substitution for fluorophores in organic light-emitting diodes (OLEDs) applications is rarely reported. Here, with fluorinated electron-deficient 2,1,3-benzothiadiazole (BT) unit as the acceptor and triphenylamine (TPA) as the donor, we construct two new D-A-type fluorophores DTPA-fBT and DTPA-ffBT. Theoretical calculations and experimental results reveal that the lowest excited states (S1) of the materials are characterized by hybridized local and charge-transfer (HLCT) properties, in which the fluorine substitution will increase the proportion of the charge-transfer (CT) component. Due to the introduction of fluoro substitution, multiple fluorine hydrogen bonds are formed, which endow the molecules with more rigid conformation, leading to lower non-radiative rates and higher photoluminescence quantum yield (PLQY) in solution and doped film, as well as improved thermal stability in the solid state. As a result, the two fluorinated DTPA-ffBT demonstrate significantly improved performance in OLEDs with a maximum external quantum efficiency (EQE) of 7.25% (5.90% for fluorine-free counterpart) and very low-efficiency roll-off (roll-off <7% at 10,000 cd m−2).

Quantum Efficiency Improvement of InGaN Near Ultraviolet LED Design by Genetic Algorithm

A near-ultraviolet (367-nm) InGaN light-emitting diode (LED) with 5.75 nm quantum well depth was designed and both internal/external quantum efficiency (IQE/EQE) values were optimized considering the effects of non-radiative recombination rates and possible fabrica-tion errors. Firstly, the IQE of the design was enhanced by a genetic algorithm code which was developed particularly for this study. Distributed Bragg Reflectors and optional ultra-thin 1nm AlN interlayer were also used to increase overall light extraction efficiency. Then, alloy and doping concentration effects on wavelength-dependent optical and structural parameters were analyzed via the CASTEP software package based on density functional theory to pre-sent a more detailed and realistic optimization. The relatively great values of 42.6% IQE and 90.2% LEE were achieved. The final structure with 1.00 mm × 1.00 mm surface area requires only 200 mW input power to operate at 3.75 V.

Computational and optoelectronic quantification of semi-conducting, warm ruby red color emanating Eu3+ complexes with hetro-cyclic ligands.

Six Eu3+ complexes were synthesised with β-keto acid as main ligand and secondary ligands through liquid assisted grinding method. These complexes were characterised by various techniques such as spectroscopic technique, XRD, EDAX, SEM analysis, thermal technique, Urbach energy and optical band gap investigation. The luminous photophysical properties were studied by PL spectroscopy in solid as well as solution phase and some theoretical calculation was done to investigate the radiative (Arad) & non-radiative (Anrad) transition rate, quantum efficiency (ɸ), Judd Ofelt parameters for 5D0 → 7F2,4 transitions in both states. Judd Ofelt parameters were also calculated by the JOES software and the outcomes are well harmonised with theoretical values. The complexes have CIE color coordinate value in ruby red region and above 88.65% color purity in both phases, which made them attractive candidates for red light-emitting displays. 5D0 → 7F2 transition was proposed as a laser emission transition owing to their high branching ratio (67.18-74.24%) in solid and (60.09-74.40%) in solution phase. Computational methods were employed to determine the structure and energy of various molecular orbitals. Antimicrobial assay of complexes was also rationalised and found that the complexes are pertinent as good bactericidal and fungicidal agents in pharmaceutical industry.

Effect of electrosteric stabilization of TiO2 nanoparticles on photophysical properties of organic/inorganic hybrid nanocomposite

Hybrid organic/inorganic nanocomposites are considered one of the most significant research areas due to their enhanced optoelectronic properties. This article is a detailed investigation of the effect of stabilization and dispersion of titanium dioxide (TiO2) nanoparticles on the photophysical properties of the conjugated polymer, (poly(2-methoxy-5-(2-ethylhexyloxy)1,4-phenylenevinylene (MEH-PPV). To obtain a colloidally stable nanoparticle dispersion, electrosteric stabilization of TiO2 in the MEH-PPV matrix is attempted. This work demonstrates the efficient electrostatic stabilization of TiO2 nanoparticle dispersion based on pH, zeta potential, and synthesis route. Further steric stabilization was achieved through in situ polymerization of MEH-PPV on the surface of TiO2 nanoparticles, which further reduced the van der Waal force of attraction (VFA). As a result of the combination of electrostatic and steric (electrosteric) stabilization, MEH-PPV: TiO2 hybrid nanocomposites with reduced polymer defects were successfully produced, resulting in improved absorbance, reduced non-radiative recombination rates, and long-term stability.

Crosslinking and densification by plasma-enhanced molecular layer deposition for hermetic seal of flexible perovskite solar cells

Flexible perovskite solar cells are new energy devices with a promising future due to their numerous advantages, such as high defect tolerance, strong solar absorption and low non-radiative carrier recombination rates. However, their operational stability is still an ongoing challenge during upgrading, and their inferior moisture corrosion resistance is still a major issue for better performances. Thin-film encapsulation could effectively enhance the operational stability of perovskite solar cells but obtaining encapsulation films with excellent barrier performance always come at the expense of poor flexibility. Therefore, the development of novel encapsulation materials with both barrier performance and flexibility is urgent for the compatibility of flexible applications. In this work, "Plasma-Enhanced Molecular Layer Deposition" was used for the first time to prepare a highly cross-linked, densified flexible encapsulation material AlOC at 40 ℃ to break through the traditional technology. The resulting encapsulation material can be applied to flexible perovskite solar cells as a barrier film without any damage. The as-obtained encapsulation film exhibited a water vapor transmittance rate of 1.44 × 10−5 g m−2 day−1 and preserved 95 % of its initial barrier performance after 10,000 bends with a 3 mm bend radius. Such performance was the best among the reported thin-film encapsulation layers of flexible perovskite solar cells.

Photophysical Rate Constants and Oxygen Dependence for Si and Ge Rhodamine Zwitterions.

The family of group XIV rhodamine zwitterions are fluorescence probes with carbon, silicon, germanium, or tin substituted in the 10-position of the xanthene ring. Because of their inherent near-infrared fluorescence, photostability and high quantum yields in aqueous solutions, the Si and Ge containing fluorophores in this class have become increasingly important for fluorescent labeling of proteins and biological molecules. This study fully characterizes photophysical rates derived from a model consisting of a singlet ground state, the lowest singlet excited state, and the lowest triplet excited state for two exemplar group XIV rhodamine zwitterions, one containing Si and the other Ge. Within a simple Jablonski diagram, all radiative and non-radiative rates, including intersystem crossing and triplet depopulation rates, were measured as a function of oxygen concentration. It was shown that the triplet depopulation rates are intrinsically fast in comparison with traditional xanthene containing fluorophores, probably due to the increased spin-obit coupling from the Si and Ge substitution in the xanthene ring. Dissolved oxygen increases both the intersystem crossing and triplet depopulation rates. Stern-Volmer analysis was conducted to estimate rates of quenching by oxygen. The experimental data was used to estimate the initial rates for reactive oxygen production by Si and Ge containing fluorophores in aqueous solutions containing different concentrations of dissolved O2. These estimates showed a significantly slower initial rate of reactive oxygen production in comparison with rhodamine 6G. This goes a long way to explaining their inherent photostability. Spectroscopic experiments were also conducted in 77 K viscous aqueous glasses where it was observed that the fluorescence spectra remained unchanged, and the quantum yields increased from 0.53 to 0.84 and from 0.52 to 0.89 for the Si and Ge containing fluorophores respectively; no phosphorescence was observed. All intersystem crossing and triplet depopulation rates were measured using fluorescence correlation spectroscopy (FCS) and analyzed using a new method that extrapolated the power dependence of the FCS curves to optical saturation. This method was verified using published data.

Internal conversion rates from the extended thawed Gaussian approximation: Theory and validation.

The theoretical prediction of the rates of nonradiative processes in molecules is fundamental in assessing their emissive properties. In this context, global harmonic models have been widely used to simulate vibronic spectra as well as internal conversion rates and to predict photoluminescence quantum yields. However, these simplified models suffer from the limitations that are inherent to the harmonic approximation and can have a severe effect on the calculated internal conversion rates. Therefore, the development of more accurate semiclassical methods is highly desirable. Here, we introduce a procedure for the calculation of nonradiative rates in the framework of the time-dependent semi-classical Extended Thawed Gaussian Approximation (ETGA). We systematically investigate the performance of the ETGA method by comparing it to the adiabatic and vertical harmonic methods, which belong to the class of widely used global harmonic models. Its performance is tested in potentials that cannot be treated adequately by global harmonic models, beginning with Morse potentials of varying anharmonicity followed by a double well potential. The calculated radiative and nonradiative internal conversion rates are compared to reference values based on exact quantum dynamics. We find that the ETGA has the capability to predict internal conversion rates in anharmonic systems with an appreciable energy gap, whereas the global harmonic models prove to be insufficient.

The location of benzothiazole on the skeleton of rofecoxib defines an AIEgen and its potential application as multifunctional materials

Aggregation-induced emission (AIE) fluorescent molecules with unique photoelectric properties have received extensive attention due to the wide range of applications. In this study, a novel benzothiazole-rofecoxib-based luminogen, o-RBZ, was constructed by integrating the benzothiazole unit into the rofecoxib scaffold. It showed an obvious AIE property, which was investigated and elucidated clearly by systematic experimental and theoretical research. According to single-crystal X-ray and Hirshfeld surface analysis, the highly twisted structure of o-RBZ and restricted-stacking may allow for bright emission in the solid state. Meanwhile, the theoretical calculation revealed that small oscillator strengths (f = 0.06) and a large root mean square deviation (RMSD) were mainly responsible for the large non-radiative transition rate and the suppression of luminous efficacy in DMSO. Furthermore, o-RBZ displayed apparent solvatochromism, mechanochromism, and lipid droplets-specific imaging properties (Pearson's correlative coefficient value of 0.94, low cell cytotoxicity). These findings suggest that AIE-active o-RBZ has the potential to be developed as a multi-functional material for mechanical-force sensors and lipid droplets imaging probes.

Photoluminescence Enhancement for Efficient Mixed‐Halide Blue Perovskite Light‐Emitting Diodes

AbstractThe development of highly efficient blue perovskite light‐emitting diodes (PeLEDs) remains a big challenge, requiring more fundamental investigations. In this work, significant photoluminescence enhancement in mixed halide blue perovskite films is demonstrated by using a molecule, benzylphosphonic acid, which eventually doubles the external quantum efficiency to 6.3% in sky‐blue PeLEDs. The photoluminescence enhancement is achieved by forming an oxide‐bonded perovskite surface at grain boundaries and suppressing electron–phonon interaction, which enhances the radiative recombination rate and reduces the nonradiative recombination rate, respectively. Moreover, severe thermal quenching is observed in the blue perovskite films, which can be explained by a two‐step mechanism involving exciton dissociation and electron–phonon interaction. The results suggest that enhancing the radiative recombination rate and reducing the electron–phonon interaction‐induced nonradiative recombination rate are crucial for achieving blue perovskite films with strong emission at or above room temperature.

Performance enhancement in thermally activated delayed fluorescence emitters by multi-fold layout

A series of thermally activated delayed fluorescence (TADF) materials, namely o-Ac2BBP, o-Px2BBP, D-BP-DMAC and D-BP-PXZ, were designed with double acridine (DMAC) or phenoxazine (PXZ) donors and double carbonyl acceptors. Phenylene and biphenylene were selected as the central bridges for these emitters, and each benzene ring on the central bridge was substituted at ortho-sites. The biphenylene bridge based D-BP-DMAC and D-BP-PXZ show 3D dimensional non-planar conformations and multi-fold layout, which result in multiple intramolecular interactions including C–H⋯O hydrogen bonds and C–H···π interactions and finally strongly stabilized and rigidified the whole molecular structures by locking the molecular geometry. As a result, the nonradiative transition rates (knr) were effectively suppressed by 5 times in comparison with the corresponding phenylene bridged analogues, and the photoluminescence quantum yields were increased to over 95%. The green and yellow OLEDs with D-BP-DMAC and D-BP-PXZ as doped emitters exhibited the maximum external quantum efficiencies (EQE) of 24.3% and 17.3%, which are almost double of the corresponding values (13.1% and 9.3%) of the phenylene bridged analogues o-Ac2BBP and o-Px2BBP. These results indicate that to increase molecular rigidity by multi-fold-layout is an effective design strategy to enhance the performance of TADF materials and OLEDs.

Achieving bright green emission in Tb3+ doped ternary yttrate-based nanocrystalline powder for solid-state illumination applications

Tb3+ activated ternary yttrate-based nanophosphor series was fabricated via a simple solution combustion (SC) methodology. An orthorhombic crystal lattice havingspace group Pnma (62) with irregularly shaped particles with sizes between 32 and 54 nm was formed. Morphological features and elemental analysis were examined via TEM, SEM, and EDAX techniques, respectively. On near-ultraviolet (NUV) stimulation, luminescence spectra presented a bright green emission at 18315 cm−1 wavenumbers consistent with the electronic transition 5D4→7F5. The decay lifetimes, quantum efficiency, and non-radiative rates were also examined. The critical distance (Rc) originated to be 20.21 Å inducing the multipolar interrelations as the probable route for concentration quenching. The energy bandgap was examined via Diffuse Reflectance Spectroscopy (DRS). A brilliant luminescence profile is also replicated in green coordinates (0.2531, 0.4998) and 7479 K (color temperature), which has been committed to typical television, European-Broadcasting-Union (EBU), NICHIA-LED green coordinates, pc-WLEDs, and another solid-state lighting (SSL) applications.