Stable Electroluminescence Spectra Research Articles

Efficient and Stable Blue Perovskite Light‐Emitting Diodes Enabled by Effective Hydrolysis of Dichloride

AbstractDespite the substantial progress in sky‐blue (480−495 nm) perovskite light‐emitting diodes (PeLEDs), the pure‐blue PeLEDs (<480 nm) merely show moderate performances. As a straightforward and effective facile way to obtain pure‐blue emission, the bromide‐chloride mixed perovskites have received considerable attention. However, the tricky issue of halide migration in the mixed halide perovskites makes a tough challenge to achieve efficient PeLEDs with stable electroluminescence (EL) spectra. Herein, the in situ treatment of Cl‐rich benzene phosphorus oxydichloride (BPOD) is proposed to achieve high‐quality pure‐blue perovskites by simultaneously enlarging the perovskite bandgap, passivating the halide vacancy defects, and immobilizing the halide ions through the hydrolysis products of chloride ions and phenylphosphonic acid. As a result, highly‐performed pure‐blue PeLEDs with a maximum external quantum efficiency (EQE) of 9.3% at 477 nm, an impressive lifetime of 34.7 min at 104 cd m−2, and very stable EL spectra are achieved, which are superior to the conventional mixed halide PeLEDs based on lead‐chloride precursor, representing one of the best performances for mixed halide pure‐blue PeLEDs. Therefore, this work contributes a feasible and effective method for efficient and stable pure‐blue PeLEDs.

Highly Horizontal Oriented Tricomponent Exciplex Host with Multiple Reverse Intersystem Crossing Channels for High-Performance Narrowband Electroluminescence and Eye-Protection White Organic Light-Emitting Diodes.

Despite multiple-resonance thermally activated delayed fluorescence (MR-TADF) emitters with small full-width at half maximum are attractive for wide color-gamut display and eye-protection lighting applications, their inefficient reverse intersystem crossing (RISC) process and long exciton lifetime induce serious efficiency roll-off, which significantly limits their development. Herein, a novel device concept of building highly efficient tricomponent exciplex with multiple RISC channels is proposed to realize reduced exciton quenching and enhanced upconversion of nonradiative triplet excitons, and subsequently used as a host for high-performance MR-TADF organic light-emitting diodes (OLEDs). Compared with traditional binary exciplex, the tricomponent exciplex exhibits obviously improved photoluminescence quantum yield, emitting dipole orientation and RISC rate constant, and a record-breaking external quantum efficiency (EQE) of 30.4% is achieved for tricomponent exciplex p-PhBCzPh: PO-T2T: DspiroAc-TRZ (50: 20: 30) based OLED. Remarkably, maximum EQEs of 36.2% and 40.3% and ultralow efficiency roll-off with EQEs of 26.1% and 30.0% at 1000cd m-2 are respectively achieved for its sky-blue and pure-green MR-TADF doped OLEDs. Additionally, the blue emission unit hosted by tricomponent exciplex is combined with an orange-red TADF emission unit to achieve a double-emission-layer blue-hazard-free warm white OLED with an EQEmax of 30.3% and stable electroluminescence spectra over a wide brightness range.

All-fluorescent white organic light-emitting diodes employing a deep-blue HLCT material simultaneously as emitter and host achieving excellent electroluminescence performance with efficiency roll-off

Simultaneously achieving high efficiency and small efficiency roll-off remains a huge challenge for white organic light-emitting diodes (OLEDs), which greatly restricts their industrial application in the lighting field. Recently developed hybridized local and charge transfer (HLCT) materials have a “hot exciton” channel, which can maximize the utilization rate of excitons and suppress efficiency roll-off via rapid reverse intersystem crossing (RISC) from high-lying triplet state (Tn, n ≥ 2) to singlet state (S1). In this work, employing blue HLCT material pCzAnN as the sensitizing host, by precise concentration management, the traditional fluorescent C545T- and DCJTB-based green and orange-red OLEDs are first fabricated, which achieve the maximum external quantum efficiency (EQE) exceeding the theoretical limit of 5 %, reaching 8.51 % and 6.64 %, respectively. On this basis, by strategic device structure design, all-fluorescent two- and three-color white OLEDs are demonstrated having pCzAnN simultaneously as blue emitter and sensitizing host of C545T and DCJTB. The resulting two- and three-color white devices obtain maximum EQE beyond 5 %. What's more, all three-color white devices exhibit extremely small efficiency roll-off, where the efficiency drops are less than 1 % at a practical luminance of 1000 cd/m2, which is comparable to the best works reported in the literatures. At the same time, the optimized three-color white device realizes ideal white emission, in which the electroluminescence (EL) spectra contain three almost equal intensity emission wavebands accompanied by a high color rendering index of 87. Stable EL spectra under a wide luminance range (3863 ∼ 27710 cd/m2) indicate a huge potential application. We believe this work can provide new idea for developing high-efficiency and low roll-off white OLEDs in the future.

Phase Engineering Reinforced Energy Transfer for High-Performance Blue Perovskite Light-Emitting Diodes.

Layered metal-halide perovskites, a category of self-assembled quantum wells, are of paramount importance in emerging photonic sources, such as lasers and light-emitting diodes (LEDs). Despite high trap density in two-dimensional (2D)perovskites, efficient non-radiative energy funneling from wide- to narrow-bandgap components, sustained by the Förster resonance energy transfer (FRET) mechanism, contributes to efficient luminescence by light or electrical injection. Herein, it is demonstrated that bandgap extension of layered perovskites to the blue-emitting regime will cause sluggish and inefficient FRET, stemming from the tiny spectral overlap between different phases. Motivated by the importance of blue LEDs and inefficient energy transfer in materials with phase polydispersity, wide-bandgap quasi-2D perovskites with narrow phase distribution, improved crystallinity, and the pure crystal orientation perpendicular to the charge transport layer are developed. Based on this emitter, high-performance blue perovskite LEDs with improved electroluminescence (EL) external quantum efficiency (EQE) of 7.9% at 478nm, a narrow full width at half-maximum (FWHM) of 22nm and a more stable EL spectra are achieved. These results provide an important insight into spectrally stable and efficient blue emitters and EL devices based on perovskites.

Nucleophilic Reaction‐Enabled Chloride Modification on CsPbI3 Quantum Dots for Pure Red Light‐Emitting Diodes with Efficiency Exceeding 26 %

AbstractHigh‐performance pure red perovskite light‐emitting diodes (PeLEDs) with an emission wavelength shorter than 650 nm are ideal for wide‐color‐gamut displays, yet remain an unprecedented challenge to progress. Mixed‐halide CsPb(Br/I)3 emitter‐based PeLEDs suffer spectral stability induced by halide phase segregation and CsPbI3 quantum dots (QDs) suffer from a compromise between emission wavelength and electroluminescence efficiency. Here, we demonstrate efficient pure red PeLEDs with an emission centered at 638 nm based on PbClx‐modified CsPbI3 QDs. A nucleophilic reaction that releases chloride ions and manipulates the ligand equilibrium of the colloidal system is developed to synthesize the pure red emission QDs. The comprehensive structural and spectroscopic characterizations evidence the formation of PbClx outside the CsPbI3 QDs, which regulates exciton recombination and prevents the exciton from dissociation induced by surface defects. In consequence, PeLEDs based on PbClx‐modified CsPbI3 QDs with superior optoelectronic properties demonstrate stable electroluminescence spectra at high driving voltages, a record external quantum efficiency of 26.1 %, optimal efficiency roll‐off of 16.0 % at 1000 cd m−2, and a half lifetime of 7.5 hours at 100 cd m−2, representing the state‐of‐the‐art pure red PeLEDs. This work provides new insight into constructing the carrier‐confined structure on perovskite QDs for high‐performance PeLEDs.

Nucleophilic Reaction-Enabled Chloride Modification on CsPbI3 Quantum Dots for Pure Red Light-Emitting Diodes with Efficiency Exceeding 26 .

High-performance pure red perovskite light-emitting diodes (PeLEDs) with an emission wavelength shorter than 650 nm are ideal for wide-color-gamut displays, yet remain an unprecedented challenge to progress. Mixed-halide CsPb(Br/I)3 emitter-based PeLEDs suffer spectral stability induced by halide phase segregation and CsPbI3 quantum dots (QDs) suffer from a compromise between emission wavelength and electroluminescence efficiency. Here, we demonstrate efficient pure red PeLEDs with an emission centered at 638 nm based on PbClx -modified CsPbI3 QDs. A nucleophilic reaction that releases chloride ions and manipulates the ligand equilibrium of the colloidal system is developed to synthesize the pure red emission QDs. The comprehensive structural and spectroscopic characterizations evidence the formation of PbClx outside the CsPbI3 QDs, which regulates exciton recombination and prevents the exciton from dissociation induced by surface defects. In consequence, PeLEDs based on PbClx -modified CsPbI3 QDs with superior optoelectronic properties demonstrate stable electroluminescence spectra at high driving voltages, a record external quantum efficiency of 26.1 %, optimal efficiency roll-off of 16.0 % at 1000 cd m-2 , and a half lifetime of 7.5 hours at 100 cd m-2 , representing the state-of-the-art pure red PeLEDs. This work provides new insight into constructing the carrier-confined structure on perovskite QDs for high-performance PeLEDs.

Efficient all-fluorescence white organic light-emitting diodes with superior color stability and low efficiency roll-off employing matrix-free blue emitting layers

All-fluorescence WOLEDs comprising a matrix-free TADF blue emitting layer simultaneously reach low efficiency roll-off and extremely color stable electroluminescence spectra.

Naphthalene Embedded Multi-Resonance Emitters Enabling Efficient Narrow Emissive Blue OLEDs.

Achieving high color purity for blue emitters remains a challenge in organic light emitting diodes. In this study, we have designed and synthesized three naphthalene (NA) embedded multi-resonance (MR) emitters, named SNA, SNB and SNB1, based on N-B-O frameworks with isomer variations for finely adjusting the photophysical properties. These emitters show tunable blue emission with emission peaks of 450-470 nm. Small full width of half maximumof 25-29 nm are achieved in these emitters, indicating the well maintaining of molecular rigidity and MR effect with NA extension. Such design also ensures a fast radiative decay. No obvious delayed fluorescence is observed in all three emitters due to the relatively large energy differences between the first singlet and triplet excited states. Both SNA and SNB enable high electroluminescent (EL) performance in doped devices with external quantum efficiency (EQE) of 7.2% and 7.9%, respectively. When applying the sensitized strategy, devices based on SNA and SNB show huge improvement with EQE of 29.3% and 29.1%. More importantly, SNB with twist geometry enables stable EL spectra with almost unchanged FWHM under different doping concentrations. This work demonstrates the potential of NA extension design in constructing narrowband emissive blue emitters.

Spectrally Stable Deep‐Blue Perovskite Light‐Emitting Diodes Enabled by a Deep Eutectic Solvent

AbstractFull‐color LED display requires Commission Internationale de l'Eclairage (CIE) 1931 coordinates of (0.14, 0.08), based on the National Television Standards Committee (NTSC) blue standard. However, such deep‐blue perovskite light‐emitting diodes (PeLEDs) still lag far behind in terms of device efficiency. Moreover, spectral stability remains a big challenge. To settle these issues, a kind of deep eutectic solvent (DES) is introduced as the perovskite precursor solvent additive, which is formed from a hydrogen bond acceptor (HBA) choline chloride and a hydrogen bond donor (HBD) urea via the hydrogen bond interaction. The incorporation of DES has multiple advantages, shown as follows: 1) improves the solubility of CsCl to yield dense perovskite morphology, 2) inhibits the growth of the perovskite crystal to achieve low‐n phases with narrow distribution, and 3) stabilizes the halide anions in the lattice to ensure stable electroluminescence (EL) spectra. As a result, the as‐prepared PeLED shows the maximum external quantum efficiency (EQEmax) of 2.71% with a CIE coordinate of (0.134, 0.055). With the increase in the DES concentration, the spectra stability is also obviously enhanced.

Multi-Sensitization Strategy for High Efficiency and Low Efficiency Roll-off Solution-Processed Single-Emission-Layer All-Fluorescence White Organic Light-Emitting Diodes

Limited by the inefficient energy transfer from blue thermally activated delayed fluorescence (TADF) material to the complementary color fluorescent dopant and unwanted charge trapping effect, it is challenging to achieve a spectrally stable, high efficiency and low efficiency roll-off solution-processed single-emission-layer (SEL) white organic light-emitting diodes (WOLEDs). Herein, a highly efficient solution-processed all-fluorescence SEL-WOLED with suppressed efficiency roll-off and stable electroluminescence spectra is achieved by introducing a hybridized local and charge-transfer (HLCT) orange-red emitter (BDP-C-Cz) and a TADF sensitizer (4CziPN) into an optimized blue TADF OLED. Specially, the adopted BDP-C-Cz emitter has a high molar absorption coefficient, whose absorption spectrum has a significant overlap with the emission spectra of 4CziPN and blue emitter. By additionally introducing 4CziPN as an assistant sensitizer of blue emitter, Förster energy transfer can be enhanced to give favorable exciton allocation and thus effectively blocks triplet exciton loss. Accordingly, a recorded external quantum efficiency of 22.8% and current efficiency of 60.0 cd/A were realized for the solution-processed SEL-WOLEDs, with color coordinates of (0.33, 0.44) and good color stability, providing a valuable guidance for the future development of simplified, high-efficiency and low-cost WOLEDs.

Trifunctional Trichloroacetic Acid Incorporated Mixed-Halide Perovskites for Spectrally Stable Blue Light-Emitting Diodes.

Metal halide perovskites have won great recognition in light-emitting diodes (LEDs). Nevertheless, the development of blue perovskite LEDs is facing a bottleneck in improving the device performance. Although mixed chloride/bromide perovskites can achieve pure-blue emission straightforwardly, higher chloride content will induce the challenges of low photoluminescence quantum yield and poor spectra stability resulting from the chloride vacancy defects and resultant halide ion migration under an electric field. In this work, we introduce a reliable trifunctional additive trichloroacetic acid into mixed-halide perovskites, which can provide additional chloride to fill halide vacancies, passivate the uncoordinated Pb2+ ion defects, and promote the crystallization effectively. Owning to the utilization of trichloroacetic acid, the ultimate pure-blue perovskite LED obtains stable electroluminescent spectra at 477 nm under various bias and demonstrates a 5-fold external quantum efficiency improvement (up to 6.6%).

Detach GaN-Based Film to Realize a Monolithic Bifunctional Device for Both Lighting and Detection.

Due to the emerging requirements of miniaturization and multifunctionality, monolithic devices with both functions of lighting and detection are essential for next-generation optoelectronic devices. In this work, based on freestanding (In,Ga)N films, we demonstrate a monolithic device with two functions of lighting and self-powered detection successfully. The freestanding (In,Ga)N film is detached from the epitaxial silicon (Si) substrate by a cost-effective and fast method of electrochemical etching. Due to the stress release and the lightening of the quantum-confined Stark effect (QCSE), the wavelength blueshift of electroluminescent (EL) peak is very small (<1 nm) when increasing the injection current, leading to quite stable EL spectra. On the other hand, the proposed monolithic bifunctional device can have a high ultraviolet/visible reject ratio (Q = 821) for self-powered detection, leading to the excellent detection selectivity. The main reason can be attributed to the removal of Si by the lift-off process, which can limit the response to visible light. This work paves an effective way to develop new monolithic multifunctional devices for both detection and display.

Manipulating Crystallization Dynamics for Efficient and Spectrally Stable Blue Perovskite Light‐Emitting Diodes

AbstractReduced‐dimensional perovskite light‐emitting diodes (PeLEDs) have shown great potential in solution‐processed high‐definition displays. However, the inferior electroluminescent (EL) performance of blue PeLEDs has become a huge challenge for their commercialization. The inefficient domain control [number of PbX6− layers (n)] and deleterious phase segregation make the blue PeLEDs suffer from low EL efficiency and poor spectral stability. Here, a rational strategy for perovskite crystallization control by adjusting the precursor concentration is proposed for improving phase distribution and suppressing ion migration in reduced‐dimensional mixed‐halide blue perovskite films. Based on this method, efficient sky‐blue PeLEDs exhibit a maximum external quantum efficiency (EQE) of 8.5% with stable EL spectra at 482 nm. Additionally, spectrally stable pure‐blue PeLEDs at 474 and 468 nm are further obtained with maximum EQEs of 4.0% and 2.4%, respectively. These findings may provide an alternative scheme for manipulating perovskite crystallization dynamics toward efficient and stable PeLEDs.

Hole Transport Layer Modification for Highly Efficient Divalent Ion‐Doped Pure Blue Perovskite Light‐Emitting Diodes

AbstractDivalent ions‐doping has recently been developed as a new approach to blue perovskite light emitting diodes (LEDs) with improved spectral stability. However, the efficiency of these perovskite LEDs, especially in the pure blue region, is still far behind their red‐ and green‐emissive counterparts. Here, a method to improve the device efficiency of strontium ion (Sr2+)‐doped pure blue perovskite LEDs, prominently by modifying the hole transport layer, is reported. Mixing a small amount of poly(9,9‐di‐n‐octylfluorene‐alt‐(1,4‐phenylene‐(4‐sec‐butylphenyl)imino)‐1,4‐phenylene) (TFB) into the hole transport layer poly(9‐vinylcarbazole) (PVK) remarkably improves the morphology and reduces the trap states of Sr2+‐doped perovskite films. As a result, a pure blue LED emitting at 470 nm is obtained and shows a high external quantum efficiency of 2.24% with stable electroluminescence spectra under a forward bias of up to 8 V, representing the best performance reported in the divalent ions‐doped pure blue perovskites so far. The work opens up the way for the development of efficient pure blue perovskite LEDs.

Stable Deep‐Blue Polymer Light‐Emitting Diodes with Well‐Resolved Emission from a Planar Conformational Chain of Polydiarylfluorenes via Alternating Copolymerization

AbstractControl of the secondary conformational behavior of light‐emitting conjugated polymers (LCPs) is essential to obtain deep‐blue emission with a narrowband and stable color purity. Naturally π–π interactions induced by the planar aromatic segments may be easily observed in liner‐type LCPs, which lead to reduced emission efficiency, color purity, and energy bandgap. Herein, an alternating copolymerization strategy is proposed to obtain the singlet exciton behavior of a planar conformational segment from polydiarylfluorenes‐copolymers (P7‐6DPF, P7‐8DPF, and P7‐9DPF) toward deep‐blue polymer light‐emitting diodes (PLEDs). Compared to the highly crystalline capacity of P7DPF, P7‐8DPF, and P8DPF, alternative P7‐6DPF and P7‐9DPF present a feature and well‐resolved emission from a planar conformational segment of polyfluorene without obvious polaron features and charge transfer states. More interestingly, P7‐6DPF and P7‐9DPF show thickness‐independent electroluminescence (EL) behavior with a stable deep‐blue color purity, which is the precondition to fabricate large‐scale and high‐quality PLEDs. Finally, compared to control devices, PLEDs based on the P7‐6DPF and P7‐9DPF planar (β) conformational films present a well‐resolved and narrowband emission, stable EL spectra, high brightness (two‐ to threefold), and high current efficiency (1.3‐fold). Therefore, optimizing hierarchical structure via alternating copolymerization is an effective strategy to improve the performance and stability of deep‐blue PLEDs.

Triphenylethene-carbazole-based molecules for the realization of blue and white aggregation-induced emission OLEDs with high luminance

Molecules that use triphenylethene-carbazole moieties decorated with different substitutions were designed and synthesized, harvesting wide energy bandgaps and aggregation-induced emission (AIE) characteristics. The photophysical, thermal, and electroluminescence (EL) characteristics of the designed emitters were investigated to clarify the molecular structure-property-performance relationship. The photoluminescence spectra of the synthesized molecules measured using tetrahydrofuran-water solution presented strong blue emissions, confirming their AIE property. The doped blue-emitting organic light-emitting diodes (OLEDs) with compound 2 exhibited satisfactory peak efficiency of 8.7 cd/A and high maximum luminance of 18474 cd/m2. In comparison, the peak efficiency of the 2-based sky-blue OLEDs with a non-doped emitting layer was 10.2 cd/A with an even superior peak luminance of 39661 cd/m2. Blue-emitting AIE OLEDs have rarely presented such high luminance values, and this improvement can facilitate the development of white-emitting OLEDs (WOLEDs) for lighting applications. The fabricated WOLEDs with 2 achieved a maximum efficiency of 5.6% (8.0 cd/A and 7.5 lm/W), stable EL spectra, and high luminance of 29319 cd/m2. These results indicate that the triphenylethene-carbazole structure designs for AIE molecules could simultaneously harvest wide energy bandgap and high luminance, demonstrating their high potential for EL applications.

Red-emitting IrIII(C^N)2(P-donor ligand)Cl-type complexes showing aggregation-induced phosphorescent emission (AIPE) behavior for both red and white OLEDs

Two red-emitting IrIII(C^N)2(P-donor ligand)Cl-type complexes bearing C^N ligands with carbazole functional group have been successfully prepared with different P-donor ligands of triphenylphosphine and triethylphosphine, respectively. The investigation of their phosphorescent behavior in the mixture of THF and water to reveal their aggregation induced phosphorescent emission (AIPE) ability, which is also indicated by their much higher phosphorescent quantum yield (ΦP) in doped film than those in the dilute solution. Mainly, their AIPE are induced by the blocked stretching motion of aromatic segments in C^N ligand and restrained the deformation of their coordinating skeletons. The AIPE complexes can possess AIE factor (αAIE) of ca. 7.4. In addition, the carbazole group can effectively promote hole transporting ability of the concerned AIPE emitters, which can benefit their electroluminescent ability. Hence, the IrIII(C^N)2(P-donor ligand)Cl-type complexes can show decent EL efficiencies in the solution-processed red-emitting organic Light-emitting diodes (OLEDs) with a maximum external quantum efficiency (ηext) of 8.5%, a maximum current efficiency (ηL) of 22.0 cd A−1 and a maximum power efficiency (ηP) of 15.9 lm W−1. Furthermore, as long-wavelength emitter, solution-processed white OLEDs (WOLEDs) have been constructed based on the red-emitting AIPE IrIII(C^N)2(P-donor ligand)Cl-type complexes, which can play critical role in achieving stable white electroluminescent spectra at high luminescence. The concerned WOLEDs can show attractive EL efficiencies of 6.6%, 23.7 cd A−1 and 16.0 lm W−1. All these results can provide valuable information for developing new AIPE materials with high EL ability.

Alkyl-promoted iridium complex for high-performance deep-red phosphorescent organic light-emitting diodes

In this work, a novel deep-red (642 nm) iridium complex, Ir(bp4b)2(dend), is developed. The introduction of alkyl groups in ligands weakens the intermolecular interactions and endows Ir(bp4b)2(dend) with favorable physical properties: short photoluminescence lifetime (271.6 ns), low concentration sensitivity (10−6 to 10−4 M) and balanced charge-transporting ability. Ir(bp4b)2(dend)-doped phosphorescent device displays high efficiencies (9.62 cd/A, 12.25 lm/W, 15.29%), low roll-off of efficiencies (from 10 to 1000 cd/m2: no decrease; from 1000 to 5000 cd/m2: 10.6%), relatively low concentration sensitivity (from 5% to 15%), long device lifetime (T80: 5225 h at 100 cd/m2) and very stable electroluminescent spectra (from 1 cd/m2 to maximum luminance). This performance is comparable to those of previous record deep-red (around 640 nm) phosphorescent emitters. More importantly, compared with previous record emitters, Ir(bp4b)2(dend) reports more kinds of excellent parameters and such comprehensive deep-red emitter is rare at present.

Phenylpyrimidine-Based Iridium Complex for High-Performance Green-Yellow Phosphorescent Organic Light-Emitting Diodes

In this work, a phenylpyrimidine-based green-yellow iridium complex, (bpp)2Ir(acac), is prepared. Tert-butyl group is introduced to weaken the intermolecular interaction and endow (bpp)2Ir(acac) with favorable physical properties. Phosphorescent device which utilizes (bpp)2Ir(acac) as the luminescent guest material displays high efficiencies (73.9 cd/A, 84.8 lm/W, 21.2%), low efficiency roll-off (from 100 to 10000 cd/m2: 5.1%), relatively low concentration sensitivity (from 5% to 12%) and very stable electroluminescent spectra (from 1 cd/m2 to maximum luminance). As a consequence of the results proved that (bpp)2Ir(acac) is a good phosphorescent material.

Efficient Zn-Alloyed Low-Toxicity Quasi-Two-Dimensional Pure-Red Perovskite Light-Emitting Diodes.

Metal halide perovskites have attracted extensive attention in next-generation solid-state lighting and displays due to their fascinating optoelectronic properties. However, the toxicity of lead (Pb) impedes their practical application. Herein, we report an efficient Zn-alloyed quasi-two-dimensional (quasi-2D) pure-red perovskite light-emitting device (PeLED) by introducing zinc ions (Zn2+) into the perovskite lattice and partially substituting Pb2+. The substitution of Zn2+ is confirmed by X-ray diffraction, X-ray photoelectron spectroscopy, grazing-incidence wide-angle X-ray scattering, and transmission electron microscopy measurements. In addition, the vacancy defect density of Pb and the halogen is reduced by the introduction of Zn2+ in the PEA2(Cs0.3MA0.7)2(ZnxPb1-x)3I10 perovskite system, which leads to a more ordered crystal orientation, compact morphology, and increased photoluminescence quantum efficiency. Benefiting from the improved photoelectric properties, a maximum EQE of 9.5% and a luminescence of 453 cd m-2 are achieved for the Zn-alloyed PeLEDs, with a maximum emission peak of 658 nm and stable electroluminescence spectra under various applied biases.