All-inorganic Perovskite Quantum Dots Research Articles

Polymer optical fiber amplifier based on all-inorganic perovskite quantum dots

Polymer optical fiber amplifier based on all-inorganic perovskite quantum dots

Sm2O3-doped all-inorganic perovskite nanocrystalline glass induces self-crystallization of CsPbBr3 nanocrystals and is used in WLEDs

All-inorganic perovskite quantum dots (QDs) in glass materials, specifically CsPbX3 (X = Cl, Br, I), are being considered as the next-generation fluorescent materials due to their impressive luminous performance and stability. However, the crystallization process of quantum dots within the glass presents uncontrollable challenge, leading to uneven crystallinity and subsequent reductions in light efficiency, thereby affecting practical applications. In glass ceramics doped with rare-earth oxides, the introduction of rare-earth ions as nucleating agents can promote the self-precipitation of nanocrystalline crystals within the glass. Building upon this principle, we have doped rare-earth ions into borosilicate glass for the first time to induce the self-crystallization of CsPbBr3 QDs. This approach effectively enhances the equilibrium distribution of quantum dots within the glass, resulting in a significant improvement in luminosity. Furthermore, the luminescence spectrum range of quantum dot-shaped luminescent glass materials can be finely tuned through rare-earth ion doping. This finding holds both theoretical and practical significance for their application in the field of lighting.

Rapid room temperature synthesis of Mn-doped perovskite quantum dots for white-light-emitting diodes

All-inorganic perovskite quantum dots (PQDs) have excellent photoelectric performance, such as high photoluminescence quantum yield (PLQY), narrow full width at half-maximum (FWHM), and emission spectra covering the visible light wavelength. The emission color can be tuned over the full visible spectral region making them promising for white-light-emitting diodes (WLEDs). Further control over the optical and magnetic properties of PQDs can be achieved through doping of transition metal ions such as Mn2+ ions. In this paper, a rapid doping method is employed at room temperature by using strong-acid cation-exchange resin during the metal ions doping process, which shortens the doping time, and Mn:CsPb(Cl/Br)3 QDs were obtained. By controlling the reaction time between strong-acid cation-exchange resin and PQDs, we achieve different levels of manganese doping, resulting in a new, to the best of our knowledge, fluorescence peak at 600 nm. The introduction of strong-acid cation-exchange resin preserves the integrity of the PQD structure, while completing the doping within 30 min. Due to the low cost and mild reaction conditions of resin, it is expected that the Mn:CsPb(Cl/Br)3 QDs can be mass-produced in large quantities. In addition, in order to provide high-quality white light emission, and prevent anion exchange reactions when mixed with CsPbBr3 QDs, the CsPbBr3 QDs are coated with silicon. Finally, by combining ultraviolet-light-emitting diodes (UVLEDs) with the aforementioned PQD mixture, this paper successfully fabricates WLEDs and demonstrates its excellent photoelectric performance. The constructed WLEDs produce warm white light with a high color rendering index (CRI) of 91 and a high correlated color temperature (CCT) of 5966 K, and the luminous efficacy (LE) of WLEDs is 41lmW−1.

Remarkable emission enhancement of CsPbBr3 quantum dots based on an Ag nanoparticle-Ag film plasmonic coupling structure.

All-inorganic halide perovskite quantum dots (QDs) have recently received much attention due to their excellent optoelectronic properties. And their emission properties still need to be improved for further applications. Here, we demonstrated a remarkable emission enhancement of the CsPbBr3 QDs based on an Ag nanoparticle-Ag film plasmonic coupling structure. Through precise control of the gap distance between Ag nanoparticle and Ag film, the localized surface plasmon resonance (LSPR) peak was tuned to match the emission wavelength of the CsPbBr3 QDs. We achieved a 30-fold fluorescence intensity enhancement and a lower lasing threshold, which is 25% of that of the CsPbBr3 QDs without plasmonic coupling structure. It is attributed to that the plasmonic coupling structure exhibits an extremely strong local electric field owing to the coupling between LSPR of Ag nanoparticle and surface plasmon polariton of Ag film. This work provides an effective way to enhance the optical emission of perovskite QDs and promotes the further exploration of on-chip light source.

APTES and CTAB Synergistic Induce a Heterozygous CsPbBr3/Cs4PbBr6 Perovskite Composite and its Application on the Sensitive Fluorescent Detection of Iodide ions.

Recently, all-inorganic halide perovskite quantum dots (IPQD) as a new fluorescent material with excellent fluorescence properties have attracted wide attention. However, their instability in polar solvents is the main factor hindering their application in analysis. Herein, a heterozygous perovskite (CsPbBr3/Cs4PbBr6) was simultaneously prepared and stabilized by a silylanization strategy using (3-aminopropyl)-triethoxysilane (APTES) and cetyltrimethyl ammonium bromide (CTAB) assisted precipitation encapsulation method. The synthesized CsPbBr3/Cs4PbBr6 emitted an independent fluorescence at 520nm. The obtained CsPbBr3/Cs4PbBr6 exhibited good stability in ethanol/water mixtures. It was used as a fluorescent probe for sensitively detecting iodide ions (I-) by fluorescence quenching mechanism in the concentration range of 1 ~ 70.0 µM with the detection limit (LOD) of 0.83 µM (relative standard deviation (RSD) = 1.33%, n = 20). The simplicity and high selectivity of the proposed fluorescent analysis method were the prominent features. This work could be extended to the other target ion detection by a perovskite fluorescent quenching.

Impact of the Purification Procedure on the Properties of All-inorganic CsPbI3-xBrx Mixed-halide Perovskite Quantum Dots

Impact of the Purification Procedure on the Properties of All-inorganic CsPbI3-xBrx Mixed-halide Perovskite Quantum Dots

Short-chain ligand achieves ultra-stable CsPbX3 perovskite quantum dots for white light-emitting diodes

All-inorganic perovskite quantum dots (PeQDs) have aroused great research interest in white light-emitting diodes (WLED) due to their excellent optoelectronic properties, but the poor stability, caused by dynamically binding long-chain capping ligands, hinders their future practical applications. To address this issue, here, we exploit short-chain butyric acid (BA) to replace long-chain oleic acid (OA) as capping ligand of CsPbX3 PeQDs by a hot-injection method. The addition of BA not only makes the morphology of CsPbBr3 PeQDs uniform and improves the crystallinity but also effectively suppresses nonradiative recombination, achieving a near unit photoluminescence quantum yield of 96%. The BA capped CsPbBr3 PeQDs exhibit high stability up to 180 d stored in ambient environment and also significantly improved resistance against polar solvent, ultra-violet lamp irradiation, and heat, which is rationalized by the strong binding capacity and shortened distance of BA to the PeQDs through ab initio calculations. Furthermore, by combining green-emission CsPbBr3 and red-emission CsPbBr0.8I2.2 PeQDs with blue GaN chip, we achieved WLEDs with excellent luminous properties, showing their great potential in practical application of wide-color-gamut display and lighting.

"Whole-Body" Fluorination for Highly Efficient and Ultra-Stable All-Inorganic Halide Perovskite Quantum Dots.

Inherent "soft" ionic lattice nature of halide perovskite quantum dots (QDs), triggered by the weak Pb-X (X=Cl, Br, I) bond, is recognized as the primary culprit for their serious instability. A promising way is to construct exceedingly strong ionic interaction inside the QDs and increase their crystal cohesive energy by substituting the interior X- with highly electronegative F- , however, which is challenging and hitherto remains unreported. Here, a "whole-body" fluorination strategy is proposed for strengthening the interior bonding architecture of QDs, wherein the F- are uniformly distributed throughout the whole nanocrystal encompassing both the interior lattice and surface, successfully stabilizing their "soft" crystal lattice and passivating surface defects. This approach effectively mitigates their intrinsic instability issues including light-induced phase segregation. As a result, light-emitting devices based on these QDs exhibit exceptional efficiency and remarkable stability.

Anion exchange as an excellent tool to obtain highly efficient blue-emitting all-inorganic perovskite quantum dots

In this study, we examined the dynamic photoluminescence (PL) characteristics of all-inorganic perovskite quantum dots (QDs) during the anion-exchange process between bromide and chloride ions. CsPbBr3 QDs were synthesized using an ultrasound-induced hot-injection route. These QDs were then treated with TMS-Cl solutions, resulting in the formation of blue-emitting CsPb(Br/Cl)3 QDs with high quantum efficiencies. Even the addition of a small amount of TMS-Cl to the CsPbBr3 solution led to a noticeable blue shift of the emission. Moreover, surface treatment with a small amount of TMS-Cl also resulted in an enhanced PL quantum efficiency (PLQE) owing to surface trap removal. Exposure of the CsPbBr3 perovskite QDs solution to a higher amount of TMS-Cl yielded deep-blue-emitting QDs (412 nm) with a very high PLQE of 57 %.

Aromatic ammonium salts ligand engineering-assisted CsPbBr3 quantum dots enable electroluminescent solar cell

All-inorganic perovskite quantum dots (QDs) have gained significant attention for their excellent optoelectronic properties, making them promising materials for applications in light-emitting diodes (LEDs) and solar cells (SCs), but it is still a challenge to balance colloidal stability of QDs and conductivity of QD films. To address the issue, an effective surface ligand engineering method has been employed by using phenethylammonium bromide (PEABr) to passivate the surface defects of QDs while enhancing the charge transport and injection in QD films. The results indicate that PEABr ligand has successfully been adsorbed onto the surface of CsPbBr3 QDs to passivate the vacancy defects, significantly enhance the electronic coupling between QDs. Systematically experimental studies show that PEABr post-treatment improves the PLQY (85 %) and stability of QDs with enhanced the carrier transport in QD film. Thanks to enhanced optoelectronic performance, the fabricated devices exhibited excellent photovoltaic (PV) and electroluminescent (EL) performance, and the CsPbBr3 QD SC had a PCE of 2.00 % while exhibiting a maximum luminance (Lmax) of 1512 cd cm−2, thus realizing high-performance electroluminescent solar cell.

Ligand-Enhanced Neodymium Doping of Perovskite Quantum Dots for Superior Exciton Confinement.

In this study, all-inorganic perovskite quantum dots (QDs) for pure blue emission are explored for full-color displays. We prepared CsPbBr3 and Cs3NdCl6 QDs via hot injection methods and mixed in various ratios at room temperature for color blending. Nd-doped CsPb(Cl/Br)3 QDs showed a blueshift in emission, and the photoluminescence quantum yields (PLQY, ΦPL) were lower in the 460-470 nm range due to surface halogen and Cs vacancies. To address this, we introduced a silane molecule, APTMS, via a ligand exchange process, effectively repairing these vacancies and enhancing Nd doping into the lattice. This modification promotes the PLQY to 94% at 466 nm. Furthermore, combining these QDs with [1]Benzothieno[3,2-b][1]benzothiophene (BTBT), a conjugated small-molecule semiconductor, in a composite film reduced PLQY loss caused by FRET in solid-state QD films. This approach achieved a wide color gamut of 124% National Television System Committee (NTSC), using a UV LED backlight and RGB perovskite QDs in a BTBT-based organic matrix as the color conversion layer. Significantly, the photostability of this composite was enhanced when used as a color conversion layer (CCL) under blue-LED excitation.

Comprehensive Neurotoxicity of Lead Halide Perovskite Nanocrystals in Nematode Caenorhabditis elegans.

To date, all-inorganic lead halide perovskite quantum dots have emerged as promising materials for photonic, optoelectronic devices, and biological applications, especially in solar cells, raising numerous concerns about their biosafety. Most of the studies related to the toxicity of perovskite quantum dots (PeQDs) have focused on the potential risks of hybrid perovskites by using zebrafish or human cells. So far, the neurotoxic effects and fundamental mechanisms of PeQDs remain unknown. Herein, a comprehensive methodology is designed to investigate the neurotoxicity of PeQDs by using Caenorhabditis elegans as a model organism. The results show that the accumulation of PeQDs mainly focuses on the alimentary system and head region. Acute exposure to PeQDs results in a decrease in locomotor behaviors and pharyngeal pumping, whereas chronic exposure to PeQDs causes brood decline and shortens lifespan. In addition, some abnormal issues occur in the uterus during reproduction assays, such as vulva protrusion, impaired eggs left in the vulva, and egg hatching inside the mother. Excessive reactive oxygen species formation is also observed. The neurotoxicity of PeQDs is explained by gene expression. This study provides a complete insight into the neurotoxicity of PeQD and encourages the development of novel nontoxic PeQDs.

Green synthesis of highly luminescent CsPbBr3 quantum dots through silica coating and post-treatment with ligands

All-inorganic perovskite quantum dots (PQDs) have received considerable attentions due to their fascinating optical properties. However, the mainstream preparation methods rely on toxic solvents, raising significant environmental and safety concerns. In this work, ethyl acetate was chosen as the environmentally friendly anti-solvent to prepare silica-coated CsPbBr3 PQDs using a aminoalkoxysilane-assisted reprecipitation–encapsulation method. The as-prepared PQDs exhibited tunable emission wavelength and a medium photoluminescence quantum yield (PLQY) of 60%. Furthermore, CsPbBr3 PQDs were post-treated by different ligands with the aim of passivating surface defects. This strategy successfully mitigated the presence of surface defects and minimized non-radiative recombination losses in PQDs. As a result, the PLQY (achieving up to 73%) and stability of PQDs were substantially enhanced (luminescence stability improved by about 40% under the same test conditions). Our studies offer a novel approach for the environmentally friendly large-scale production of PQDs, opening up new possibilities for their practical applications.

Improvement of the Stability and Optical Properties of CsPbBr3 QDs.

All-inorganic perovskite quantum dots (CsPbX3 QDs) (X = Cl, Br, I) have the advantages of adjustable emission position, narrow emission spectrum, high fluorescence quantum efficiency (PLQY), easy preparation, and elevated defect tolerance; therefore, they are widely used in optoelectronic devices, such as solar cells, light-emitting diodes, and lasers. However, their stability still constrains their development due to their intrinsic crystal structure, ionic exchange of surface ligands, and exceptional sensitivity to environmental factors, such as light, water, oxygen, and heat. Therefore, in this paper, we investigate the stability improvement of CsPbX3 QDs and apply fabricated high-efficiency, stable perovskite QDs to solar cells to improve the performance of the cells further. In this paper, we focus on CsPbBr3 QDs with intrinsic extreme stability and optimize CsPbBr3 QDs using strategies, such as Mn+ doping, ligand regulation, and polymer encapsulation, which can improve optical properties while ensuring their stability. The test results show that the above five methods can improve the strength and luminescence performance of QDs, with the best stability achieved when PMMA encapsulates QDs with a ratio of PMMA = 2:1 and PLQY increases from 60.2% to 90.1%.

Ultrastable emissive perovskite nanocomposite via dual protection of polymer-grafted TS-1 zeolite for backlight display application

Instability of all-inorganic perovskite quantum dots (PQDs) driven by the inherent ionic nature poses a grand challenge towards their long-term stability in optoelectronic devices. Herein, we report the crafting of a highly stable dual-protected CsPbBr3 perovskite nanocomposite by capitalizing on the encapsulation of a hydrophobic Styrene-Divinylbenzene (St-Dvb) copolymer grafted hierarchical titanium silicalite-1 (TS-1) zeolite shell. Firstly, an optimal hot injection method was used to accommodate CsPbBr3 PQDs into hierarchical TS-1 zeolite. After the modification of terminated Si-OH groups on the surface of TS-1 by phenyltriethoxysilane (PTES), a subsequent polymerization of St and Dvb was implemented using azobisisobutyronitrile (AIBN) as initiator to result in the highly emissive CsPbBr3-TS@St-Dvb nanocomposite, exhibiting outstanding luminescent stability against heat, polar solvents, and UV light irradiation. The as-prepared CsPbBr3-TS@St-Dvb nanocomposite also showed strongly suppressed anion exchange and high compatibility in polymer matrix, enabling improved applicability for versatile lighting and optical display applications. Ultimately, a white light-emitting diode (WLED) composed of green-emitting CsPbBr3-TS@St-Dvb and red-emitting K2SiF6:Mn4+ phosphor onto a commercial blue InGaN LED chip with wide color gamut and excellent stability is demonstrated. This work highlights a judiciously-designed and hard-soft dual-protected strategy to produce ultrastable perovskite nanomaterials with high brightness and durability for backlight display application.

Effect of silica encapsulation on the stability and photoluminescence emission of FAxCs1-xPbX3 quantum dots for white mini light emitting diodes

Development of wide-color gamut white light-emitting diodes (WLEDs) for displays, with nitride-based phosphors and conventional core-shell quantum dots (QDs) such as InP, CdSe, and all-inorganic CsPbI3 perovskite quantum dots due to their excellent optoelectronic properties performance, is an excellent candidate for new optoelectronic applications.However, in backlight applications, the color gamut of perovskite quantum dots will be reduced due to the matching degree of color filter, which will limit its application in wide color gamut. To address these issues, in this paper, we propose a novel approach, namely, formamidine acetate (FA+) cationic doping, in CsPbI3 system synthesized at room temperature by organic-inorganic ligand passivation method which can effectively maintain structural stability. At the same time, the PL emission band of CsPbI3 is increased by doping FA + cations and the color gamut range is improved. We will discuss this change in detail, and quantum dot films using spin coating method can be maintained for a month in atmospheric conditions. For practical applications, the color gamut range can reach 133%. Therefore, our proposed perovskite quantum dots, FAxCs1-xPbI3, have great potential for application in wide color gamut displays.

An innovative strategy: ultra-stable alkaline earth modified CsPbBr3 quantum dots glass was prepared by washing-heat cycle for high definition backlight display

All-inorganic perovskite quantum dots (QDs) as high-quality materials for backlight display are still limited by their own low stability. Herein, the crystallization of CsPbBr3 (CPB) QDs in a glass matrix was promoted by modifying the glass network structure with alkaline earth metals (Mg, Ca, Sr, Ba). What's more, a washing-heat treatment cycle strategy was used to optimize the best-modified sample (CPB–Mg). Among them, CPB-12Mg (add 12% MgO) showed a high photoluminescence quantum yield (PLQY = 62%) after the cycling process. More surprisingly, the six-step washing-heat treated-sample (CPB–12Mg-6) showed excellent stability. When CPB-12Mg-6 was irradiated for 240 h at 60°C, 90% relative humidity (RH), and 880 W/m2 blue light power (60°C, 90% RH, 880 W/m2), the original 90% fluorescence emission could still be maintained. Subsequently, a series of CPB-12Mg-6/CsPbBr1.5I1.5@PS light conversion films were prepared by the master batch blending method. The backlight conversion film for liquid crystal display (LCD) achieves a wide color gamut that covers 126% of the NTSC 1953 and 93.6% of the Rec.2020 standard. This innovative washing-heat treatment cycle strategy provides a new idea for improving the stability of perovskite quantum dots.

Highly Stable CsPbI3 Perovskite Quantum Dots Enabled by Single SiO2 Coating toward Down-Conversion Light-Emitting Diodes

All-inorganic CsPbI3 perovskite quantum dots (PeQDs) have sparked widespread research due to their excellent optoelectronic properties and facile synthesis. However, attaining highly stable CsPbI3 perovskite quantum dots (PeQDs) against heat and polar solvents still remains a challenge and hinders any further practical application. Here, by exploiting (3-aminopropyl) triethoxysilane (APTES) as the sole silica (SiO2) precursor, we report a one-step in situ synthesis of single SiO2-coated CsPbI3 (SiO2-CsPbI3) PeQDs, namely that one SiO2 particle only contains one CsPbI3 PeQD particle. The obtained SiO2-CsPbI3 PeQDs are cubic in shape, have a more uniform size distribution, and possess narrow emission, with near unit photoluminescence quantum yields of up to 97.5%. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy confirm the formation of SiO2 through the hydrolysis of APTES on the CsPbI3 PeQDs surface. Furthermore, they have a significantly improved stability against storage, heat, and ethanol. By combining purple-emission GaN light-emitting diodes, the SiO2-CsPbI3 PeQDs were successfully employed as down-conversion emitters and exhibited considerable enhanced luminous performance and excellent stability, demonstrating their promising future in the practical application of solid-state lighting fields.

Bionic optic nerve based on perovskite (CsPbBr 3) quantum-dots

The bionic optic nerve can mimic human visual physiology and is a future treatment for visual disorders. Photosynaptic devices could respond to light stimuli and mimic normal optic nerve function. By modifying (Poly(3,4-ethylenedioxythio-phene):poly (styrenesulfonate)) active layers with all-inorganic perovskite quantum dots, with an aqueous solution as the dielectric layer in this paper, we developed a photosynaptic device based on an organic electrochemical transistor (OECT). The optical switching response time of OECT was 3.7 s. To improve the optical response of the device, a 365 nm, 300 mW·cm -2 UV light source was used. Basic synaptic behaviors such as postsynaptic currents (0.225 mA) at a light pulse duration of 4 s and double pulse facilitation at a light pulse duration of 1 s and pulse interval of 1 s were simulated. By changing the way light stimulates, for example, by adjusting the intensity of the light pulses from 180 to 540 mW·cm -2, the duration from 1 to 20 s, and the number of light pulses from 1 to 20, the postsynaptic currents were increased by 0.350 mA, 0.420 mA, and 0.466 mA, respectively. As such, we realized the effective shift from short-term synaptic plasticity (100 s recovery of initial value) to long-term synaptic plasticity (84.3% of 250 s decay maximum). This optical synapse has a high potential for simulating the human optic nerve.

Capping Ligand Engineering Enables Stable CsPbBr3 Perovskite Quantum Dots toward White-Light-Emitting Diodes.

All-inorganic perovskite quantum dots (PeQDs) have sparked extensive research focus on white-light-emitting diodes (WLEDs), but stability and photoluminescence efficiency issues are still remain obstacles impeding their practical application. Here, we reported a facile one-step method to synthesize CsPbBr3 PeQDs at room temperature using branched didodecyldimethylammonium fluoride (DDAF) and short-chain-length octanoic acid as capping ligands. The obtained CsPbBr3 PeQDs have a near-unity photoluminescence quantum yield of 97% due to the effective passivation of DDAF. More importantly, they exhibit much improved stability against air, heat, and polar solvents, maintaining >70% of initial PL intensity. Making use of these excellent optoelectronic properties, WLEDs based on CsPbBr3 PeQDs, CsPbBr1.2I1.8 PeQDs, and blue LEDs were fabricated, which show a color gamut of 122.7% of the National Television System Committee standard, a luminous efficacy of 17.1 lm/W, with a color temperature of 5890 K, and CIE coordinates of (0.32, 0.35). These results indicate that the CsPbBr3 PeQDs have great practical potential in wide-color-gamut displays.