Boosting External Quantum Efficiency of Blue Perovskite QLEDs Exceeding 23% by Trifluoroacetate Passivation and Mixed Hole Transportation Design.

Perovskite quantum dot-based light-emitting diodes (QLEDs) have been considered a promising display technology due to their wide color gamut for authentic color expression. Currently, the external quantum efficiency (EQE) for state-of-the-art blue perovskite QLEDs is about 15%, which still lags behind its green and red counterparts (>25%) and blue film-based LEDs. Here, blue perovskite QLEDs that achieve an EQE of 23.5% at 490 nm is presented, to the best knowledge, which is the highest value reported among blue perovskite-based LED fields. This impressive efficiency is achieved through a combination of quantum dot (QD) passivation and optimal device design. First, blue mixed halide perovskite CsPbCl3- xBrx QDs passivated by trifluoroacetate exhibit excellent exciton recombination behavior with a photoluminescence quantum yield of 84% due to reducing uncoordinated Pb surface defects. Furthermore, the device is designed by introducing a mixed hole-transport layer (M-HTL) to increase hole injection and transportation capacity and improve carrier balance. It is further found that M-HTL can decrease carrier leakage and increase radiative recombination in the device, evidenced by the visual electroluminescence spectrum at 2.0 V. The work breaks through the EQE gap of 20% for blue perovskite-based QLEDs and significantly promotes their commercialization process.

Polymer-Surface-Mediated Mechanochemical Reaction for Rapid and Scalable Manufacture of Perovskite QD Phosphors.

Perovskite quantum dots (QDs) have been considered new-generation emitters for lighting and displays due to their high photoluminescence (PL) efficiency, and pure color. However, their commercialization process is currently hindered by the challenge of mass production in a quick and environmentally friendly manner. In this study, a polymer-surface-mediated mechanochemical reaction (PMR) is proposed to prepare perovskite QDs using a high-speed multifunction grinder for the first time. PMR possesses two distinctive features: i) The ultra-high rotating speed (>15 000 rpm) of the grinder facilitates the rapid conversion of the precursor to perovskite; ii) The surface-rich polymer particulate ensures QDs with high dispersity, avoiding QD aggregation-induced PL quenching. Therefore, PMR can successfully manufacture green perovskite QDs with a high PL quantum yield (PLQY) exceeding 90% in a highly material- (100% yield), time- (1 kg min-1), and effort- (solvent-free) efficient manner. Moreover, the PMR demonstrates remarkable versatility, including synthesizing by various polymers and producing diverse colored and Pb-free phosphors. Importantly, these phosphors featuring a combination of polymer and perovskite, are facilely processed into various solid emitters. The proposed rapid, green, and scalable approach has great potential to accelerate the commercialization of perovskite QDs.

A ligand strategy retarding monovalent copper oxidation toward achieving Cs3Cu2I5 perovskite emitters with enhanced stability for lighting.

0D copper-based perovskites (Cs3Cu2I5) have fascinating optical properties, such as strong exciton binding energy, high photoluminescence quantum yield (PLQY) and large Stokes shifts from self-trapped excitons (STEs), which make them highly considerable candidates in the field of lighting. However, the stability of Cs3Cu2I5 is compromised by the oxidation of Cu+ to Cu2+ during the storage or operation process. Here, we proposed a ligand engineering strategy to improve the stability of Cs3Cu2I5via an organic molecule (ethylenediaminetetraacetic acid, EDTA) with multiple functional groups. The strong interaction between carboxyl groups and Cu+ was evidenced through FTIR and XPS, and it could retard monovalent copper oxidation. After storing for 90 days, the EDTA-engineered Cs3Cu2I5 (EDTA-Cs3Cu2I5) maintained its original crystalline structure, while the control Cs3Cu2I5 exhibited an impurity phase. Through quantitative analysis, the content of Cu2+ in EDTA-Cs3Cu2I5 was found to be 83.9% lower than that in control Cs3Cu2I5. Benefiting from the inhibition of Cu+ oxidation, EDTA-Cs3Cu2I5 exhibited improved light emission stability. For example, the optimized EDTA-Cs3Cu2I5 retained 74.7% of the initial photoluminescence (PL) intensity after 90-day storage under ambient conditions, while the pure Cs3Cu2I5 retained only 41.7%. Furthermore, EDTA could passivate defects and enhance the PL properties of the optimized Cs3Cu2I5, which showed a PLQY of 94.7%, much higher than that of 71.4% for pure Cs3Cu2I5. We further constructed a WLED based on the EDTA-engineered Cs3Cu2I5, which showed CIE at (0.3238, 0.3354), a CRI of 91.7, and a T50 of 361 h. The proposed EDTA ligand strategy provides a new way to regulate the light-emitting properties and stabilities of Cs3Cu2I5 for future industrialization.

Bilayer phosphine oxide modification toward efficient and large-area pure-blue perovskite quantum dot light-emitting diodes.

Blue emissive halide perovskite light-emitting diodes (LEDs) are gaining increasing attention. Reducing defects in halide perovskites to improve the performance of the resulting LEDs is a main research direction, but there are limited passivation methods for achieving efficient and spectrally-stable pure-blue LEDs based on mixed-halide perovskites. In this work, double modification layers containing phosphine oxides, i.e., diphenyl[4-(triphenylsilyl)phenyl]phosphine oxide (TSPO1) and 2,7-bis(diphenylphosphoryl)-9,9'-spirobifluorene (SPPO13), are developed to passivate mixed-halide perovskite quantum dot (QD) films. The comprehensive spectroscopic and structural characterization results indicate the presence of strong interactions between TSPO1/SPPO13 and the QDs. Besides, the combination of the bilayer exhibits a synergistic hole-blocking effect, improving the charge balance of the LEDs. LEDs based on the QD/TSPO1/SPPO13 films deliver stable electroluminesence at 469 nm and present a maximum external quantum efficiency (EQE) and luminance of 4.87% and 560 cd m-2, respectively. Benefiting from the uniform QD/TSPO1/SPPO13 film over a large area, LEDs with an area of 64 mm2 show a maximum EQE of 3.91%, which represents the first efficient large-area mixed-halide perovskite LED with stable pure-blue emission. This work provides a method to improve the perovskite QDs-based film quality and optoelectronic properties, and is a step toward the fabrication of highly-efficient large-area blue perovskite LEDs.

Fiber Optic Plate Coupled Pb-Free Perovskite X-ray Camera Featuring Low-Dose-Rate Imaging toward Dental Diagnosis.

Copper-based halide perovskites have been considered as promising scintillators. However, they still cannot meet the requirement of low-dose-rate X-ray imaging in medical diagnosis. Herein, we design a fiber optic plate (FOP) coupled perovskite X-ray camera to reduce the dose rate toward dental X-ray imaging. Tl doped Cs3Cu2I5 prepared via molten salt reaction has a high light yield of 72,000 photons/MeV, resulting from Tl10/Tl20-self-trapped hole emissions. After FOP coupling, the pulp cavity, root canal, dentin and root canal file can be clearly observed under a low dose rate as low as 3 µGyair s-1, which is absolutely lower than the required 5.5 µGyair s-1 for commercial intraoral dental sensors. The realization of such a low dose rate is attributed to the high coupling efficiency of 75% for the FOP and the high brightness of 262 lm m-2 for the scintillation screen. This designed portable X-ray camera shows its huge potential in intraoral dental X-ray imaging.

Recent progress of single-halide perovskite nanocrystals for advanced displays.

Light-emitting diodes based on lead halide perovskite nanocrystals (LHP NCs) have shown an astonishing increase in efficiency in just several years of academic research, reaching high external quantum efficiencies exceeding 20%. The extensive color-tunability and narrow emission bandwidth of LHP NCs, in particular, are of great importance in the creation of the next generation of ultra-high-definition displays, as defined by the Rec. 2020 standard recommendation. In fact, whereas the colour of LHP NCs can be easily tuned by the compositions of halogens, the ion migration in mixed-halide perovskites under the electric field will seriously affect the spectral stability and operational lifetimes of perovskite light-emitting diodes (PeLEDs). Therefore, it is essential to realize efficient colour-saturated PeLEDs based on single-halide perovskite NCs. In this review, we focus on the recent progress in LHP NC-based PeLEDs and highlight the strategy of tuning the spectral emission based on quantum confinement or cation alloying/doping in single-halide perovskite NCs. Finally, we will give an outlook on future research avenues for preparing high-efficiency pure green, red and blue PeLEDs based on single-halide perovskite NCs.

Stabilizing electroluminescence color of blue perovskite LEDs via amine group doping.

Voltage loading-induced change in the electroluminescence (EL) wavelength of mixed halide perovskite light-emitting diodes (PeLEDs), so-called color-shift, has become an inevitable phenomenon, which is seriously unfavorable to their applications in lighting and display. Here, we achieve color-stable blue PeLEDs via a hydrogen-bonded amine-group doping strategy. Selecting guanidine (GA) or formamidinium (FA) as amine-group (-NH2) doping source for CsPbBrxCl3-x quantum dots (QDs), experimental and theoretical results reveal that the strong N-H⋯X (X = Br/Cl) bonding can be produced between -NH2 dopants and Pb-X lattices, thereby increasing the migration barrier of halide anions. Resultantly, color-stable sky-blue devices were realized with emission peaks fixed at 490.5 (GA) and 492.5 (FA) nm without any obvious shift as the voltage increases, in sharp contrast devices without N-H⋯X producing a 15 nm red-shift from 487 to 502 nm. Not only that, maximum external quantum efficiency is improved to 3.02% and 4.14% from the initial 1.3%. This finding offers a convenient boulevard to achieve color-stable PeLEDs with high efficiency.

Perovskite QLED with an external quantum efficiency of over 21% by modulating electronic transport.

Perovskite quantum-dot-based light-emitting diodes (QLEDs) are highly promising for future solid-state lightings and high-definition displays due to their excellent color purity. However, their device performance is easily affected by charge accumulation induced luminescence quenching due to imbalanced charge injection in the devices. Here we report green perovskite QLEDs with simultaneously improved efficiency and operational lifetime through balancing the charge injection with the employment of a bilayered electron transport structure. The charge-balanced QLEDs exhibit a color-saturated green emission with a full-width at half-maximum (FWHM) of 18 nm and a peak at 520 nm, a low turn-on voltage of 2.0 V and a champion external quantum efficiency (EQE) of 21.63%, representing one of the most efficient perovskite QLEDs so far. In addition, the devices with modulated charge balance demonstrate a nearly 20-fold improvement in the operational lifetime compared to the control device. Our results demonstrate the great potential of further improving the device performance of perovskite QLEDs toward practical applications in lightings and displays via rational device engineering.

Perovskite light-emitting/detecting bifunctional fibres for wearable LiFi communication.

Light fidelity (LiFi), which is emerging as a compelling technology paradigm shifting the common means of high-capacity wireless communication technologies, requires wearable and full-duplex compact design because of its great significance in smart wearables as well as the 'Internet of Things'. However, the construction of the key component of wearable full-duplex LiFi, light-emitting/detecting bifunctional fibres, is still challenging because of the conflicting process between carrier separation and recombination, as well as the highly dynamic film-forming process. Here, we demonstrate light-emitting/detecting bifunctional fibres enabled by perovskite QDs with hybrid components. The hybrid perovskite inks endow fibres with super-smooth QD films. This, combined with the small exciton binding energy and high carrier mobility of perovskite QDs, enables successful integration of electroluminescence and photodetection into monofilaments. The bifunctional fibres possess the narrowest electroluminescence full width at half maximum of ~19 nm and, more importantly, the capability for simultaneously transmitting and receiving information. The successful fabrication of narrow emission full-duplex LiFi fibres paves the way for the fabrication and integration of low crosstalk interoperable smart wearables.

A bilateral interfacial passivation strategy promoting efficiency and stability of perovskite quantum dot light-emitting diodes.

Perovskite quantum-dot-based light-emitting diodes (QLEDs) possess the features of wide gamut and real color expression, which have been considered as candidates for high-quality lightings and displays. However, massive defects are prone to be reproduced during the quantum dot (QD) film assembly, which would sorely affect carrier injection, transportation and recombination, and finally degrade QLED performances. Here, we propose a bilateral passivation strategy through passivating both top and bottom interfaces of QD film with organic molecules, which has drastically enhanced the efficiency and stability of perovskite QLEDs. Various molecules were applied, and comparison experiments were conducted to verify the necessity of passivation on both interfaces. Eventually, the passivated device achieves a maximum external quantum efficiency (EQE) of 18.7% and current efficiency of 75 cd A-1. Moreover, the operational lifetime of QLEDs is enhanced by 20-fold, reaching 15.8 h. These findings highlight the importance of interface passivation for efficient and stable QD-based optoelectronic devices.

Novel Lewis Base Cyclam Self-Passivation of Perovskites without an Anti-Solvent Process for Efficient Light-Emitting Diodes.

Metal halide perovskites have been focused as a candidate applied as a promising luminescent material for next-generation high-quality lighting and high-definition display. However, as perovskite films formed, high density of defects would be produced in solution processing inevitably, leading to low exciton recombination efficiency in light-emitting diodes (LEDs). Herein, a facile and novel self-passivation strategy to inhibit defect formation in perovskite films for constructing high-performance LEDs is developed. For the first time, we introduce 1,4,8,11-tetraazacyclotetradecane (cyclam) in perovskite precursor solution, and it spontaneously passivates defect states of CsPbBr3-based perovskites by coaction between amine and uncoordinated lead ions during spin-coating without an anti-solvent process. Furthermore, as a delocalized system, cyclam also possesses chemical properties that facilitate exciton transportation. The proposed passivation strategy boosts the external quantum efficiency from 1.25% (control device) to 16.24% (cyclam-passivated device). Furthermore, defect passivation is also conductive to reduce LED degradation paths and improve device stability as the extrapolated lifetime (T50) of LEDs at an initial brightness of 100 cd/m2 is increased from 0.9 to 127 h. These findings indicate that the introduction of cyclam is highly effective to enhance the performance of LEDs, and such a strategy in effectively reducing the defects could be also applied in other perovskite-based devices, such as lasers, solar cells, and photodetectors.

Predictive Value of Fissured Tongue in Functional Dyspepsia Combined with Depression.

Anxiety and depression are common in functional dyspepsia (FD) patients. Although fissured tongue (FT) is often observed in FD, its clinical value in such patients is rarely reported. We analyzed clinical data of FD patients with FT with the aim of elucidating the clinical value of FT in FD. This study suggests FD patients with different types of FT with the course of disease and the 9-item Patient Health Questionnaire (PHQ9) showed a significant difference. The PHQ9, course of disease, and self-rated dyspepsia symptoms (SRDS) correlated positively with the types of FT by the Spearman rank analysis. Epigastric pain, bloating, nausea, and SRDS showed a significant difference between FT-FD and nonfissured tongue- (NFT-) FD as well as between FD patients with and without symptoms of depression. Many FD patients also have FT, which may be associated with depressive symptoms. The longer the course of disease, the more serious the fissured tongue; thus, it may provide a predictive value for the diagnosis of depressive symptoms in FD patients.

Self-template Synthesis of Metal Halide Perovskite Nanotubes as Functional Cavities for Tailored Optoelectronic Devices.

Intriguing optoelectronic features of low-dimensional perovskites drive researchers to develop novel nanostructures for exploring new photophysical properties and meeting the requirements of future practical applications. Here, we report the facile and universal synthesis of metal halide perovskite nanotubes (NTs) in a micro alkylammonium emulsion system for the first time. The [PbBr6]4--based NTs with a diameter of 300 nm and length of 100 µm were synthesized through the reaction of PbBr2 and long-chain bromide in advance, which can be controllably converted into general metal halide perovskite APbBr3 (A = Cs, FA, MA) with preserved tubular morphology by introducing the Cs+, MA+, and FA+ cations. Importantly, the NTs can readily couple with other nanofillers exhibiting tunable and novel optoelectronic properties demonstrated by the photodetectors. The device performance can be significantly improved and broadened to infrared photoresponse through the introduction of Au nanocrystal (NC) plasma and PbS NCs, respectively. These results demonstrate that the metal halide perovskite NTs are expected to enrich the diversity of nanostructures and have a huge potential in the fabrication of integrated, light-manipulated, and miniaturized electronic and photonic devices.

Synthesis of stable and phase-adjustable CsPbBr3@Cs4PbBr6 nanocrystals via novel anion-cation reactions.

All-inorganic cesium lead halide perovskites have emerged as promising semiconductor materials due to their preeminent performance in lighting, display, light detecting, and laser fields. However, the applications of lead halide perovskites are limited by the dissatisfactory stability owing to their fragile ionic crystal characteristics and highly dynamic surface-coordinated states. The in situ diphase structure passivation possessing the same chemical constituents (such as passivating CsPbBr3 with Cs4PbBr6) has been proven to be an effective way to improve the stabilities and simultaneously maintain the highly efficient luminescence properties. Herein, for the first time, we report a novel anion-cation reaction method to synthesize the lead halide perovskite NCs with diphase CsPbBr3@Cs4PbBr6 structure. Moreover, we have found that the phase transformation between CsPbBr3 and Cs4PbBr6 is temperature dependent. Thus, we could control the relative composition of the diphase CsPbBr3@Cs4PbBr6 composite by adjusting the temperature. The optimized CsPbBr3@Cs4PbBr6 composite NCs achieve highly light emissive performance and stabilities against atmosphere, moisture and heating. Furthermore, we could obtain 135% of the NTSC color gamut through anion exchange. These highly emissive composite NCs with improved stabilities exhibit great potential in future optoelectronic fields.

Narrowband Perovskite Photodetector-Based Image Array for Potential Application in Artificial Vision.

Image sensor arrays are widely used in digital cameras, smartphones, and biorobots. However, most commercial image arrays rely on the dichroic prisms or a set of interference filters to distinguish characteristic color spectrum, which significantly increases the cost and fabrication processing complexity. In this work, an ultranarrow response photodetector with full-width at half-maximum being ∼12 nm and specific detectivity over 1011 Jones at 545 nm are successfully achieved in CsPbBr3 polycrystalline films using freeze-drying casting method to adjust the surface-charge recombination. To our best knowledge, this is the narrowest spectrum response for perovskite photodetectors in the visible light waveband. More importantly, a series of narrowband photodetectors are developed to enhance diverse selectivity for target signals covering from blue light to red light via bandgap tuning in CsPbX3 by tailoring the halide component. Finally, an integrated sensing array with CsPbX3 (X = Cl, Br, I) narrowband photodetectors acting as color recognition cones is constructed, which presents clear color and shape recognition paving the way for commercialization of perovskite photodetector in artificial vision.

Organic-Inorganic Hybrid Passivation Enables Perovskite QLEDs with an EQE of 16.48.

Perovskite quantum dots (QDs) with high photoluminescence quantum yields (PLQYs) and narrow emission peak hold promise for next-generation flexible and high-definition displays. However, perovskite QD films often suffer from low PLQYs due to the dynamic characteristics between the QD's surface and organic ligands and inefficient electrical transportation resulting from long hydrocarbon organic ligands as highly insulating barrier, which impair the ensuing device performance. Here, a general organic-inorganic hybrid ligand (OIHL) strategy is reported on to passivate perovskite QDs for highly efficient electroluminescent devices. Films based on QDs through OIHLs exhibit enhanced radiative recombination and effective electrical transportation properties compared to the primal QDs. After the OIHL passivation, QD-based light-emitting diodes (QLEDs) exhibit a maximum peak external quantum efficiency (EQE) of 16.48%, which is the most efficient electroluminescent device in the field of perovskite-based LEDs up to date. The proposed OIHL passivation strategy positions perovskite QDs as an extremely promising prospect in future applications of high-definition displays, high-quality lightings, as well as solar cells.

Proliferation Potential-Related Protein Promotes the Esophageal Cancer Cell Proliferation, Migration and Suppresses Apoptosis by Mediating the Expression of p53 and Interleukin-17.

OBJECTIVE: This study aims to investigate the mechanism of proliferation potential-related protein (PP-RP) in influencing the proliferation, migration, and apoptosis of esophageal cancer cells. METHODS: Quantitative real-time PCR and western blotting were performed to analyze the expression of PP-RP gene, p53, and interleukin (IL)-17 in human normal tissues and tumor tissues, as well as the expression of p53 and IL-17 in Eca109 and TE3 cells. The esophageal cancer cell proliferation was detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), cell apoptosis was detected by flow cytometry, and cell migration was detected by transwell migration. RESULTS: PP-RP expressed highly in tumor tissue and Eca109 and TE3 cells, PP-RP overexpression inhibited the expression of p53 and promoted the expression of IL-17 in Eca109 and TE3 cells. PP-RP overexpression increased the expression of F-actin, promoted cell proliferation, and migration and suppressed cell apoptosis. Cell proliferation ability and cell migration ability were significantly strengthened while apoptosis was suppressed by PP-RP + pyruvate carboxylase deoxyribonucleic acid (PCDNA)-p53 group and PP-RP + IL-17 siRNA group in TE3 cells. CONCLUSION: Our data suggest that PP-RP promotes esophageal cancer cell proliferation and migration, and suppresses apoptosis by mediating the expression of p53 and IL-17.

Room-Temperature Triple-Ligand Surface Engineering Synergistically Boosts Ink Stability, Recombination Dynamics, and Charge Injection toward EQE-11.6% Perovskite QLEDs.

Developing low-cost and high-quality quantum dots (QDs) or nanocrystals (NCs) and their corresponding efficient light-emitting diodes (LEDs) is crucial for the next-generation ultra-high-definition flexible displays. Here, there is a report on a room-temperature triple-ligand surface engineering strategy to play the synergistic role of short ligands of tetraoctylammonium bromide (TOAB), didodecyldimethylammonium bromide (DDAB), and octanoic acid (OTAc) toward "ideal" perovskite QDs with a high photoluminescence quantum yield (PLQY) of >90%, unity radiative decay in its intrinsic channel, stable ink characteristics, and effective charge injection and transportation in QD films, resulting in the highly efficient QD-based LEDs (QLEDs). Furthermore, the QD films with less nonradiative recombination centers exhibit improved PL properties with a PLQY of 61% through dopant engineering in A-site. The robustness of such properties is demonstrated by the fabrication of green electroluminescent LEDs based on CsPbBr3 QDs with the peak external quantum efficiency (EQE) of 11.6%, and the corresponding peak internal quantum efficiency (IQE) and power efficiency are 52.2% and 44.65 lm W-1 , respectively, which are the most-efficient perovskite QLEDs with colloidal CsPbBr3 QDs as emitters up to now. These results demonstrate that the as-obtained QD inks have a wide range application in future high-definition QD displays and high-quality lightings.

A Voltage-Boosting Strategy Enabling a Low-Frequency, Flexible Electromagnetic Wave Absorption Device.

Nowadays, low-frequency electromagnetic interference (<2.0 GHz) remains a key core issue that plagues the effective attenuation performance of conventional absorption devices prepared via the component-morphology method (Strategy I). According to theoretical calculations, one fundamental solution is to develop a material that possesses a high ε' but lower ε″. Thus, it is attempted to control the dielectric values via applying an external electrical field, which inducts changes in the macrostructure toward a performance improvement (Strategy II). A sandwich-structured flexible electronic absorption device is designed using a carbon film electrode to conduct an external current. Simultaneously, an absorption layer that is highly responsive to an external voltage is selected via Strategy I. Relying on the synergistic effects from Strategies I and II, this device demonstrates an absorption value of more than 85% at 1.5-2.0 GHz with an applied voltage of 16 V while reducing the thickness to ≈5 mm. In addition, the device also shows a good absorption property at 25-150 °C. The method of utilizing an external voltage to break the intrinsic dielectric feature by modifying a traditional electronic absorption device is demonstrated for the first time and has great significance in solving the low-frequency electromagnetic interference issue.

Ce3+-Doping to Modulate Photoluminescence Kinetics for Efficient CsPbBr3 Nanocrystals Based Light-Emitting Diodes.

Inorganic perovskite CsPbBr3 nanocrystals (NCs) are emerging, highly attractive light emitters with high color purity and good thermal stability for light-emitting diodes (LEDs). Their high photo/electroluminescence efficiencies are very important for fabricating efficient LEDs. Here, we propose a novel strategy to enhance the photo/electroluminescence efficiency of CsPbBr3 NCs through doping of heterovalent Ce3+ ions via a facile hot-injection method. The Ce3+ cation was chosen as the dopant for CsPbBr3 NCs by virtue of its similar ion radius and formation of higher energy level of conduction band with bromine in comparison with the Pb2+ cation to maintain the integrity of perovskite structure without introducing additional trap states. It was found that by increasing the doping amount of Ce3+ in CsPbBr3 NCs to 2.88% (atomic percentage of Ce compared to Pb) the photoluminescence quantum yield (PLQY) of CsPbBr3 NCs reached up to 89%, a factor of 2 increase in comparison with the native, undoped ones. The ultrafast transient absorption and time-resolved photoluminescence (PL) spectroscopy revealed that Ce3+-doping can significantly modulate the PL kinetics to enhance the PL efficiency of doped CsPbBr3 NCs. As a result, the LED device fabricated by adopting Ce3+-doped CsPbBr3 NCs as the emitting layers exhibited a pronounced improvement of electroluminescence with external quantum efficiency (EQE) from 1.6 to 4.4% via Ce3+-doping.