High Photoluminescence Quantum Yield Research Articles

Strongly-Confined CsPbBr3 Perovskite Quantum Dots with Ultralow Trap Density and Narrow Size Distribution for Efficient Pure-Blue Light-Emitting Diodes.

The development of pure-blue perovskite light-emitting diodes (PeLEDs) faces challenges of spectral stability and low external quantum efficiency (EQE) due to phase separation in mixed halide compositions. Perovskite quantum dots (QDs) with strong confinement effects are promising alternatives to achieve high-quality pure-blue PeLEDs, yet their performance is often hindered by the poor size distribution and high trap density. A strategy combining thermodynamic control with a polishing-driven ligand exchange process to produce high-quality QDs is developed. The strongly-confined pure-blue (≈470nm) CsPbBr3 QDs exhibit narrow size distribution (12% dispersion) and are achieved in Br-rich ion environment based on growth thermodynamic control. Subsequent polishing-driven ligand exchange process removes imperfect surface sites and replaces initial long-chain organic ligands with short-chain benzene ligands. The resulting QDs exhibit high photoluminescence quantum yield (PLQY) to near-unity. The resulting PeLEDs exhibit a pure-blue electroluminescence (EL) emission at 472nm with narrow full-width at half-maximum (FWHM) of 25nm, achieving a maximum EQE of 10.7% and a bright maximum luminance of 7697cdm-2. The pure-blue PeLEDs show ultrahigh spectral stability under high voltage, a low roll-off of EQE, and an operational half-lifetime (T50) of 127min at an initial luminance of 103cdm-2 under continuous operation.

Double Perovskite Single Crystals with High Laser Irradiation Stability for Solid-State Laser Lighting and Anti-counterfeiting.

Laser lighting devices, comprising an ultraviolet (UV) laser chip and a phosphor material, have emerged as a highly efficient approach for generating high-brightness light sources. However, the high power density of laser excitation may exacerbate thermal quenching in conventional polycrystalline or amorphous phosphors, leading to luminous saturation and the eventual failure of the device. Here, for the first time, we raise a single-crystal (SCs) material for laser lighting considering the absence of grain boundaries that scatter electrons and phonons, achieving high thermal conductivity (0.81 W m-1 K-1) and heat-resistance (575 °C). The SCs products exhibit a high photoluminescence quantum yield (89%) as well as excellent stability toward high-power lasers (>12.41 kW/cm2), superior to all previously reported amorphous or polycrystalline matrices. Finally, the laser lighting device was fabricated by assembling the SC with a UV laser chip (50 mW), and the device can maintain its performance even after continuous operation for 4 h. Double perovskite single crystals doped with Yb3+/Er3+ demonstrated multimodal luminescence with the irradiation of 355 and 980 nm lasers, respectively. This characteristic holds significant promise for applications in spectrally tunable laser lighting and multimodal anticounterfeiting.

HCOO- Doping-Induced Multiexciton Emissions in Cs3Cu2I5 Crystals for Efficient X-Ray Scintillation.

Self-trapped exciton (STE) luminescence, typically associated with structural deformation of excited states, has attracted significant attention in metal halide materials recently. However, the mechanism of multiexciton STE emissions in certain metal halide crystals remains largely unexplored. This study investigates dual luminescence emissions in HCOO- doped Cs3Cu2I5 single crystals using transient and steady-state spectroscopy. The dual emissions are attributed to intrinsic STE luminescence originating from the host lattice and extrinsic STE luminescence induced by external dopants, respectively, each of which can be triggered independently at distinct energy levels. Theoretical calculations reveal that multiexciton emission originates from structural distortion of the host and dopant STEs within the 0D lattice in their respective excited states. By meticulously tuning the excitation wavelength and selectively exciting different STEs, the dynamic alteration of color change in Cs3Cu2I5:HCOO- crystals is demonstrated. Ultimately, owing to an extraordinarily high photoluminescence quantum yield (99.01%) and a diminished degree of self-absorption in Cs3Cu2I5:HCOO- crystals, they exhibit remarkable X-ray scintillation characteristics with light yield being improved by 5.4 times as compared to that of pristine Cs3Cu2I5 crystals, opening up exciting avenues for achieving low-dose X-ray detection and imaging.

Modified t-butyl in tetradentate platinum (II) complexes enables exceptional lifetime for blue-phosphorescent organic light-emitting diodes

In blue phosphorescent dopants, the tetradentate platinum(II) complex is a promising material showing high efficiency and stability in devices. However, metal-metal-to-ligand charge transfer (MMLCT) formation leads to low photo-luminescence quantum yields (PLQYs), wide spectra, and intermolecular interaction. To suppress MMLCT, PtON-tb-TTB and PtON-tb-DTB are designed using theoretical simulation by modifying t-butyl in PtON-TBBI. Both materials effectively suppress MMLCT and exhibit high PLQYs of 99% and 78% in 5 wt% doped film, respectively. The PtON-tb-TTB and PtON-tb-DTB devices have maximum external quantum efficiencies of 26.3% and 20.9%, respectively. Additionally, the PtON-tb-DTB device has an extended lifetime of 169.3 h with an initial luminescence of 1200 nit, which is 8.5 times greater than the PtON-TBBI device. Extended lifetime because of suppressed MMLCT and smaller displacement between the lowest triplet and triplet metal-centered states compared to other dopants. The study provides an effective approach to designing platinum(II) complexes for long device lifetimes.

Engineering Highly Emissive Tetra(t‐Butyl)rubrene/off‐Stoichiometry Thiol‐Ene Hybrids Toward Flexible Luminescent Solar Concentrator‐Integrated Photovoltaics with Excellent Stability

Luminescent solar concentrators (LSCs) are highly valued in transparent photovoltaics for their versatility and adaptability as effective large‐area sunlight collectors. However, constructing LSCs as efficient, long‐term stable, and easily malleable power‐generating units still remains a challenge. Herein, high photostability, high photoluminescence quantum yield (ΦPL), and Stokes‐shifted emission are achieved in tetra(t‐butyl)rubrene/off‐stoichiometry thiol‐ene (TBRb/OSTE) hybrids by incorporating TBRb molecules into OSTE polymers. To demonstrate their potentials in LSCs, a luminescent solar concentrator integrated photovoltaics (LSCIPV) is created using a one‐step synthesis that combines the preparation of TBRb/OSTE hybrids, coupling with the silicon solar cell, and the encapsulation of both components. The LSCIPV demonstrates remarkable flexibility and the integration of an ethylene tetrafluoroethylene film contributes to a hydrophobic surface and antireflection effect, resulting in an external photon efficiency (ηext) of 4.9% and a power conversion efficiency of 1.04% for the 100 cm2 device. The LSCIPV exhibits good photostability over 800 h of UV light exposure. Monte Carlo ray‐tracing simulations indicate that an optimized TBRb‐based LSCIPV can potentially achieve an ηext of 1.3%, even for a large device with an area of 1 m2.

A Boron, Nitrogen, and Oxygen Doped π-Extended Helical Pure Blue Multiresonant Thermally Activated Delayed Fluorescent Emitter for Organic Light Emitting Diodes That Shows Fast kRISC Without the Use of Heavy Atoms.

Narrowband emissive multiresonant thermally activated delayed fluorescence (MR-TADF) emitters are a promising solution to achieve the current industry targeted color standard, BT.2020, for blue color without using optical filters, aiming for high efficiency organic light-emitting diodes (OLEDs). However, their long triplet lifetimes, largely affected by their slow reverse intersystem crossing rates, adversely affect device stability. In this study, a helical MR-TADF emitter (f-DOABNA) has been designed and synthesized. Because of its π-delocalized structure, f-DOABNA possesses a small singlet-triplet gap, ΔEST, and displays simultaneously an exceptionally faster reverse intersystem crossing rate constant, kRISC, of up to 2 × 106 s-1 and a very high photoluminescence quantum yield, ΦPL, of over 90% in both solution and doped films. The OLED with f-DOABNA as the emitter achieved a narrow deep-blue emission at 445nm (full width at half-maximum of 24nm) associated with CIE coordinates of 0.150, 0.041, and showed a high maximum external quantum efficiency, EQEmax, of ∼20%. This article is protected by copyright. All rights reserved.

Regulating photoluminescence through single-crystal-to-single-crystal transformation of solvent-containing zero-dimensional hybrid metal halide isomers

Regulating photoluminescence (PL) properties induced by single-crystal-to-single-crystal (SCSC) transformation has sparked significant interest in the research of zero-dimensional organic–inorganic metal halides (0-D OIMHs). To best of our knowledge, the SCSC transformation of solvent-containing 0-D OIMH isomers hasn’t been reported yet. In this work, we report the first example of SCSC transformation between two isomers containing lattice solvent molecules, namely α- and β-[EtPPh3]2[SbCl5]·MeCN (α- and β-1·MeCN; EtPPh3 = ethyltriphenylphosphonium; MeCN = acetonitrile). Differential scanning calorimetry (DSC) results show that the SCSC transformation from α- to β-1·MeCN is an exothermic process, implying that β-1·MeCN is a more stable phase than α-1·MeCN. Moreover, α- and β-1·MeCN exhibit bright orange (emission peak: 610 nm) and red (emission peak: 635 nm) emission under 360/365 nm excitation, respectively. DFT calculations suggest that the negligible self-absorption and a strong exciton confinement contribute to their effective PL emission. By analyzing temperature-dependent PL spectra, β-1·MeCN has been found to exhibit stronger electron-phonon coupling under excitation than α-1·MeCN. Thus, the broader emission with full width at half maximum (FWHM: 134 vs. 147 nm) and the higher photoluminescence quantum yield (PLQY: 40.37% vs. 70.50%) have been realized by SCSC transformation from α- to β-1·MeCN by heating at 92 °C. Benefitting from the regulation of PL performances brought by SCSC transformation, the white light-emitting-diode (LED) devices assembled by using β-1·MeCN as red phosphor could be optimized, and the CRI reaches as high as 95.3.

Tuneable Efficient White Emission of Sb3+/Mn2+ Co-Doped Lead-Free Perovskites for Single-Component White Light-Emitting Diodes.

Inorganic lead-free perovskite nanocrystals (NCs) with broadband self-trapped exciton (STEs) emission and low toxicity have shown enormous application prospects in the field of display and lighting. However, white light-emitting diodes (WLEDs) based on a single-component material with high photoluminescence quantum yield (PLQY) remain challenging. Here, we demonstrate a novel codoping strategy by introducing Sb3+/Mn2+ ions to achieve the tuneable dual emission in lead-free perovskite Cs3InCl6 NCs. The PLQY increases to 59.64% after doping with Sb3+. The codoped Cs3InCl6 NCs exhibit efficient white light emission due to the energy transfer channel from STEs to Mn2+ ions with PLQY of 51.38%. Density functional theory (DFT) calculations have been used to verify deeply the effects of Sb3+/Mn2+ doping. WLEDs based on Sb3+/Mn2+-codoped Cs3InCl6 NCs are explored with color rendering index of 85.5 and color coordinate of (0.398, 0.445), which have been successfully applied as photodetector lighting sources. This work provides a new perspective for designing novel lead-free perovskites to achieve single-component WLEDs.

High-Color-Rendition White QLEDs by Balancing Red, Green and Blue Centres in Eco-Friendly ZnCuGaS:In@ZnS Quantum Dots.

White light-emitting diodes (WLEDs) are the key components in the next-generation lighting and display devices. The inherent toxicity of Cd/Pb-based quantum dots (QDs) limits the further application in WLEDs. Recently, more attention is focused on eco-friendly QDs and their WLEDs, especially the phosphor-free WLEDs based on mono-component, which profits from bias-insensitive color stability. However, the imbalanced carrier distribution between red-green-blue luminescent centers, even the absence of a certain luminescent center, hinders their balanced and stable photoluminescence/electroluminescence (PL/EL). Here, an In3+-doped strategy in Zn-Cu-Ga-S@ZnS QDs is first proposed, and the balanced carrier distribution is realized by non-equivalent substitution and In3+ doping concentration modulation. The alleviation of the green emitter by the In3+-related red emitter and the compensation of blue emitter by the Zn-related electronic states contribute to the balanced red-green-blue emitting with high PL quantum yield (PLQY) of 95.3% and long lifetime (T90) of over 1100 h in atmospheric conditions. Thus, the In3+-doped WLEDs can achieve exceedingly slight proportional variations between red-green-blue EL intensity over time (∆CIE = (0.007, 0.009)), and high champion CRI of 94.9. This study proposes a single-component QD with balanced and stable red-green-blue PL/EL spectrum, meeting the requirements of lighting and display.

High‐Performance White Emission from Cu‐Based Perovskite Compound

AbstractThe white emissions based on lead‐free perovskites with broadband emission due to self‐trapped excitons (STEs) are considered as an ideal candidate for next‐generation white light‐emitting diodes (WLEDs). Recently, copper‐based halide perovskites Cs3Cu2I5@CsCu2I3 composites films with a high color‐rendering index (CRI) have been developed for WLEDs. However, the Cs3Cu2I5@CsCu2I3 composites generally exhibit a relatively low photoluminescence quantum yield (PLQY). Herein, a high PLQY up to 86.75% copper‐based perovskite Gua3Cu2I5 (Gua = guanidine) films with a broadband strong yellow STEs emission centered at 544 nm is synthesized. By combining with efficient blue STEs emission Cs3Cu2I5 component via composition engineering of Cs3Cu2I5@Gua3Cu2I5, a high PLQY of up to 96.1% is achieved on the white emission composites films. Moreover, a high CRI of 93 WLEDs is achieved by integrating Cs3Cu2I5@Gua3Cu2I5 composites film onto a UV LED chip. These findings provide a simple and effective strategy for designing highly efficient white light‐emitting diodes.

Controlling Interfacial Amidation Reaction Rate to Regulate Crystal Growth toward High-Performance FAPbBr3-Based Inverted Light-Emitting Diodes.

Controlling interfacial reactions is critical for zinc oxide (ZnO)-based inverted perovskite light-emitting diodes (PeLEDs), boosting the external quantum efficiency (EQE) of the near-infrared device to above 20%. However, violent interfacial reactions between the bromine-based perovskites and ZnO-based films severely limit the performance of inverted green PeLEDs, whose efficiency and stability lag far behind those of their near-infrared counterparts. Here, a controllable interfacial amidation between the bromine-based perovskites and magnesium-doped ZnO (ZnMgO) film utilizing caprylyl sulfobetaine (SFB) is realized. The SFB molecules strongly interact with formamidinium bromide, decelerating the amidation reaction between formamidinium and carboxylate groups on the ZnMgO film, thus regulating the crystallization of FAPbBr3. Combined with the passivation of benzylamine, a FAPbBr3 bulk film directly deposited on a ZnMgO substrate with single-crystal characteristics is obtained, exhibiting a high photoluminescence quantum yield of above 80%. The resultant PeLEDs demonstrate a peak EQE of exceeding 20% at a high luminance of 120,000 cd m-2 and a half lifetime of 26 min at 11,000 cd m-2, representing the state-of-the-art inverted green electroluminescence. This work resolves the crucial issues of violent interfacial reactions and provides a strategy toward inverted green PeLEDs with outstanding performance.

Epitaxial Growth of CsPbBr3 Pyramids/CdS Nanobelt Heterostructures for High-Performance Photodetectors.

Perovskites have great potential for optoelectronic applications due to their high photoluminescence quantum yield, large absorption coefficient, great defect tolerance, and adjustable band gap. Perovskite heterostructures may further enhance the performance of optoelectronic devices. So far, however, most of perovskite heterostructures are fabricated by mechanical stacking or spin coating, which could introduce a large number of defects or impurities at the heterointerface owing to the random stacking process. Herein, we report the epitaxial growth of CsPbBr3 pyramids/CdS nanobelt heterostructures via a 2-step vapor deposition route. The CsPbBr3 triangular pyramids are well aligned on the surface of CdS nanobelts with the epitaxial relationships of (0-22)CsPbBr3||(1-20)CdS and (-211)CsPbBr3||(002)CdS. Time-resolved photoluminescence results reveal that effective charge transfer occurred at the heterointerface, which can be attributed to the type-II band arrangement. Theoretical simulations reveal that the unique CsPbBr3 pyramids/CdS nanobelt structure facilitates diminishing the reflection losses and enhancing the light absorption. The photodetector based on these CsPbBr3 pyramids/CdS nanobelt heterostructures exhibited an ultrahigh photoswitching ratio of 2.14 × 105, a high responsivity up to 4.07 × 104 A/W, a high detectivity reaching 1.36 × 1013 Jones, fast photoresponses (τrise = 472 μs and τdecay = 894 μs), low dark current, and suppressed hysteresis.

Effective exciplex host for solution-processed narrowband blue TADF-OLEDs using a 9-(dibenzo[b,d]thiophen-2-yl)-9H-carbazole analogue with an adamantane substituent

Implementing an exciplex host system in the emitting layer is crucial for achieving highly efficient thermally activated delayed fluorescence (TADF) and phosphorescent organic light-emitting diodes (OLEDs). In this study, we successfully designed and synthesized 3-((3r,5r,7r)-adamantan-1-yl)-9-(dibenzo[b,d]thiophen-2-yl)-9H-carbazole (AdCz-DBT) and 9-(dibenzo[b,d]thiophen-2-yl)-9H-carbazole (Cz-DBT) as p-type hosts for the exciplex host implementation, and 7-(4-(tert-butyl)phenyl)-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene (tPDBA) as an n-type host. The AdCz-DBT host incorporates a large and robust adamantane group into Cz-DBT, increasing molecular weight, film-forming properties and thermal stability. Additionally, AdCz-DBT maintains energy levels and photophysical properties similar to those of adamantane-free Cz-DBT. Efficient exciplex emission was observed in the blend film due to well-matched energy levels of the synthesized p- and n-type hosts. The introduction of adamantane into Cz-DBT did not hinder exciplex formation, resulting in a relatively high photoluminescence quantum yield and improved charge balance in the mixed host with tPDBA.Ultimately, the solution-processed blue TADF-OLED with the AdCz-DBT:tPDBA blend host demonstrated a relatively high external quantum efficiency of 8.00% and a long operational lifetime, exhibiting excellent performance compared to devices using the Cz-DBT:tPDBA blend host.

TADF deep-blue OLED with color index approaching Rec.2020 standard blue gamut achieved by a boron-based D–A type molecular skeleton

The ultra-high definition (UHD) displays in the market require organic light-emitting diodes (OLEDs) to meet the Rec.2020 color gamut standard, while it is still challenging to exploit ultra-deep-blue emitters that satisfy such blue standard. Herein, by substituting tCz (3,6-di(tert-butyl)carbazole) donor unit on the robust BOC (8,8,12,12-tetramethyl-8,12-dihydro-4-oxa-3a2-boradibenzo[cd,mn]pyrene) acceptor unit with high structural rigidity and appropriate energy levels, a novel boron-based D–A type thermally activated delayed fluorescence (TADF) ultra-deep-blue emitter, namely, tCz-BOC, was readily designed and synthesized. Inheriting from its rigid organoboron core, the emitter presents ultra-deep-blue emission with narrow spectral full width at half maximum (FWHM) of 54 nm and high photoluminescence quantum yield up to 73.7%. Additionally, tCz-BOC can effectively harvest T1 excitons through high-lying T2 mediated reverse intersystem crossing process. As a consequence, the fabricated OLED based on tCz-BOC exhibits a satisfactory ultra-deep-blue emission with λEL of 424 nm, narrow emission bandwidth with FWHM of 47 nm, excellent maximum external quantum efficiency (EQEmax) of 13.9%, as well as the CIEy coordinate of 0.047, which is fairly close to the Rec.2020 blue color gamut.

Efficient non-doped cluster light-emitting diodes based on semiconducting copper iodide hybrids

Copper iodide hybrid clusters have attracted lots of interest in solution-processed light-emitting diodes (LEDs) for solid-state lighting and display in recent years, benefiting from their simple synthesis, structural diversity, high photoluminescence quantum yield (PLQY), and non-toxicity. However, most efficient copper iodide cluster LEDs are made by host-guest doped emitters and thus suffer from cumbersome synthesis and increased costs from the expensive hosts. Here, we report a non-doped cluster LED based on a novel copper iodine hybrid [35DPPy]4Cu2I2 (35DPPy: 3,5-diphenylpyridine) with high PLQY and decent charge transport characteristic. The non-doped [35DPPy]4Cu2I2 film synthesized by a one-step spin-coating approach possess the flat and compact morphology, high PLQY of 59.6%, and excellent heat/ultraviolet (UV) light/moisture/oxygen stability. The efficient green PL of [35DPPy]4Cu2I2 is proved to originate from the synergistic contribution from thermally activated delayed fluorescence and phosphorescence. A non-doped green LED based on [35DPPy]4Cu2I2 emitters is fabricated, achieving a peak external quantum efficiency of 4.8% and a maximum luminance of 3895 cd/m2. More importantly, large-area LEDs with an emitting area of 4.00 cm2 are realized with homogeneous and bright electroluminescence, showing their attractive potentials as novel electroluminescent emitters in the application of non-doped cluster LEDs.

Solvent-Induced Bright Emission in Lead-Free Organic-Inorganic Antimony Bromides with Reversible Transformation.

Lead-free low-dimensional organic-inorganic metal halides have gained increasing attention in a wide range of applications due to their low toxicity, outstanding optical performance, and structural tunability. In this work, a general method of incorporating organic molecule into sodium antimony bromides is introduced. The 1D Na3SbBr6(C2H6OS)6 and Na3SbBr6(C4H8OS)6 single crystals exhibit bright yellow and orange emission with PL peaks at 610 and 664nm, and high photoluminescence quantum yields (PLQYs) of 85% and 60%, respectively. These two compounds can be reversibly converted into each other by the removal and addition of the organic components. Their exceptional luminescent performance enables them to be used as solid-state phosphors for the fabrication of yellow and orange down-conversion LEDs. A white LED with a high color rendering index (CRI) of 95 is also fabricated by using Na3SbBr6(C2H6OS)6 as the yellow phosphor. The universality of this method is demonstrated by synthesizing other members of this family with diverse A-groups, including methylammonium (MA) and formamidinium (FA). This work provides an effective strategy for the development of diverse lead-free and high-performance organic-inorganic hybrid materials and indicates these organic-inorganic hybrid compounds are promising luminescent materials for lighting or displays.

Superior electron mobility, red electroluminescence with high quantum efficiency from printable room temperature columnar liquid crystalline perylene bisimide

Synthesis of highly fluorescent compounds is currently a critical requirement to facilitate the economical and metal-independent manufacture of organic light-emitting diodes (OLEDs) on a large scale. This study presents a highly soluble, swallow tail based electron deficient perylene bisimide (PBIST) exhibiting room temperature columnar oblique (Colob) liquid crystalline behavior along with a high photoluminescence quantum yield, positioning itself as a promising candidate for efficient OLEDs. Incorporation of swallow tails helped in enhancing the solubility and reduction of the clearing points. This unique tailor-made molecular design with the liquid crystalline phase allowed a demonstration of n-type field effect mobility of 0.008 cm2 V−1s−1 when annealed in the liquid crystalline mesophase range (at 70 °C) which can be exploited in the fabrication of printable electronic devices. Capitalizing on the high charge transport and luminescence attributes of PBIST, a series of devices were fabricated by utilizing PBIST as a single emitter and dispersed at different concentrations of 0.3, 0.5 and 1 wt% in host material CBP. Impressively, doped devices featuring the CBP as a host at a 0.5 wt% PBIST concentration exhibited an external quantum efficiency (EQE) as high as 7 %, accompanied by a luminance of 1787 cd/m2. The high EQE is attributed mainly to the triplet–triplet annihilation (TTA) process. This notable EQE enhancement signifies a substantial stride towards expanding the utility of multifunctional columnar self-assembled materials for the advancement of OLEDs.

Efficient narrowband organic light-emitting diodes based on B,O embedded multi-resonance emitters containing B-N covalent bonds

Multi-resonance (MR) thermally activated delayed fluorescence (TADF) materials emerge rapidly in recent years, and are expected to be an effective solution for ultra-high-resolution displays. Solving the main issues of low yield and dangerous lithium reagent for synthesis, extending the material diversity and figuring out the structure–activity relationship would all be beneficial to promote their commercialization. Herein, two easy-to-access MR-TADF emitters, BO-N1 and BO-N2, are constructed by integrating B,O-based MR polycyclic aromatic with B-N covalent bonds. The B-N covalent bonds are formed through simple amine-directed borylation with high yield over 90 %, which significantly improves yield, simplifies procedure and effectively avoids hazardous lithiation compared to the traditional methods. Two emitters exhibit bright green emissions in doped films with full width at half maximum (FWHM) of 28 and 24 nm, and high photoluminescence quantum yields (PLQY) of 85 % and 90 %. The green electroluminescent device of BO-N2 achieves narrow-band spectrum with FWHM of 29 nm, maximum brightness of 10480 cd m−2 and external quantum efficiency (EQE) of 20.1 %.

Photoluminescence and thermally stimulated luminescence properties of undoped and Tb-doped Sr3Gd(PO4)3 single crystals

Using the floating zone method, undoped and 0.5, 1, and 5% Tb-doped Sr3Gd(PO4)3 (SGPO) single crystals were synthesized. Investigations were conducted on the photoluminescence (PL) and thermally stimulated luminescence (TSL) of all the SGPO single crystals. The highest PL quantum yield was shown in the 5% Tb-doped single crystal among the synthesized SGPO single crystals. The undoped SGPO single crystal displayed an emission peak in both TSL and PL at 310 nm owing to the Gd3+ 4f–4f transition. In the Tb-doped SGPO single crystals, emission peaks in PL and TSL at 310–620 nm were caused by the 4f–4f transitions of Tb3+ in addition to Gd3+. In the TSL dose response function, the 1% Tb-doped SGPO single crystal exhibited the highest TSL intensity, and the TSL signal could be detected at least 0.01 mGy.

Harnessing the Synergetic Effects of Ag, Mn Dopants in Eco-Friendly Ultraviolet Selective Quantum Dots for Luminescent Solar Concentrators.

Quantum dots (QDs) are promising building blocks for luminescent solar concentrators (LSCs), yet most QD-based LSCs suffer from toxic metal composition and color tinting. UV-selective harvesting QDs can enable visible transparency, but their development is restricted by large reabsorption losses and low photoluminescence quantum yield (PLQY). The developed here Ag, Mn: ZnInS2/ZnS QDs show a high PLQY of 53% due to the passivating effect of ZnS shell. These QDs selectively absorb UV light and emit orange-red light with a large Stokes shift of 180nm. A LSC of 5×5×0.2cm3, fabricated using a poly(lauryl methacrylate) (PLMA) as a matrix, maintains 87% of integrated PL after 7h of UV exposure. The QD-PLMA achieved 90.7% average visible transparency (AVT) and a color rendering index (CRI) of 95.8, which is close to plain PLMA (AVT=90.8%; CRI=99.5), yielding excellent visible light transparency. Incorporating Si-PVs at LSC edges, the Ag, Mn: ZIS/ZnS QD-LSC achieved an optical efficiency of 1.42%, ranking competitively among high-performing UV-harvesting LSCs.