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Metal halide perovskite nanocrystals (NCs) have emerged as highly promising light emitting materials for various applications, ranging from perovskite light‐emitting diodes (PeLEDs) to lasers and radiation detectors. While remarkable progress has been achieved in highly efficient and stable green, red, and infrared perovskite NCs, obtaining efficient and stable blue‐emitting perovskite NCs remains a great challenge. Here, a facile synthetic approach for the preparation of blue emitting CsPbBr3 nanoplatelets (NPLs) with treatment by an organic sulfate is reported, 2,2‐(ethylenedioxy) bis(ethylammonium) sulfate (EDBESO4), which exhibit remarkably enhanced photoluminescence quantum efficiency (PLQE) and stability as compared to pristine CsPbBr3 NPLs coated with oleylamines. The PLQE is improved from ≈28% for pristine CsPbBr3 NPLs to 85% for EDBESO4 treated CsPbBr3 NPLs. Detailed structural characterizations reveal that EDBESO4 treatment leads to surface passivation of CsPbBr3 NPLs by both EDBE2+ and SO42– ions, which helps to prevent the coalescence of NPLs and suppress the degradation of NPLs. A simple proof‐of‐concept device with emission peaked at 462 nm exhibits an external quantum efficiency of 1.77% with a luminance of 691 cd m−2 and a half‐lifetime of 20 min, which represents one of the brightest pure blue PeLEDs based on NPLs reported to date. [ABSTRACT FROM AUTHOR]

Abstract Extensive investigation of the passivating agents has been performed to suppress the perovskite defects. However, very few attentions have been paid to rationally design the passivating agents for the balance of the carrier confinement and transfer in quasi-2D perovskites, which is essential to achieve high-performance perovskite LEDs (PeLEDs). In this work, tributylphosphine oxide (TBPO) with moderate carbon chain length is demonstrated as a decent passivator for the quasi-2D perovskites by strengthening the carrier confinement for massive radiative recombination within the perovskites, and more importantly providing efficient carrier transfer in the quasi-2D perovskites. Benefiting from these interesting optoelectronic properties of TBPO-incorporated perovskites, we achieve high-efficient blue PeLEDs with an external quantum efficiency up to 11.5% and operational stability as long as 41.1 min without any shift of the electroluminescence spectra. Consequently, this work contributes an effective approach to promote the carrier confinement and transfer for high-performance and stable blue PeLEDs.

Highlights: A new concept to optimize the passivating agents for the balance of the carrier confinement and transfer in blue quasi-2D perovskites. The moderate tributylphosphine oxide is introduced into the quasi-2D perovskites to simultaneously strengthen the carrier confinement for massive radiative recombination as well as promote efficient carrier transfer in the quasi-2D perovskites. High-efficient and stable blue PeLEDs are achieved with an external quantum efficiency of 11.5% and a very long operational stability of 41.1 min without any shift of the electroluminescence spectra.Extensive investigation of the passivating agents has been performed to suppress the perovskite defects. However, very few attentions have been paid to rationally design the passivating agents for the balance of the carrier confinement and transfer in quasi-2D perovskites, which is essential to achieve high-performance perovskite LEDs (PeLEDs). In this work, tributylphosphine oxide (TBPO) with moderate carbon chain length is demonstrated as a decent passivator for the quasi-2D perovskites by strengthening the carrier confinement for massive radiative recombination within the perovskites, and more importantly providing efficient carrier transfer in the quasi-2D perovskites. Benefiting from these interesting optoelectronic properties of TBPO-incorporated perovskites, we achieve high-efficient blue PeLEDs with an external quantum efficiency up to 11.5% and operational stability as long as 41.1 min without any shift of the electroluminescence spectra. Consequently, this work contributes an effective approach to promote the carrier confinement and transfer for high-performance and stable blue PeLEDs. [ABSTRACT FROM AUTHOR]

Perovskite light‐emitting diodes (PeLEDs) have received great attention for their potential as next‐generation display technology. While remarkable progress has been achieved in green, red, and near‐infrared PeLEDs with external quantum efficiencies (EQEs) exceeding 20%, obtaining high performance blue PeLEDs remains a challenge. Poor charge balance due to large charge injection barriers in blue PeLEDs has been identified as one of the major roadblocks to achieve high efficiency. Here band edge control of perovskite emitting layers for blue PeLEDs with enhanced charge balance and device performance is reported. By using organic spacer cations with different dipole moments, that is, phenethyl ammonium (PEA), methoxy phenethyl ammonium (MePEA), and 4‐fluoro phenethyl ammonium (4FPEA), the band edges of quasi‐2D perovskites are tuned without affecting their band gaps. Detailed characterization and computational studies have confirmed the effect of dipole moment modification to be mostly electrostatic, resulting in changes in the ionization energies of ≈0.45 eV for MePEA and ≈ −0.65 eV for 4FPEA based thin films relative to PEA‐based thin films. With improved charge balance, blue PeLEDs based on MePEA quasi‐2D perovskites show twofold increase of the EQE as compared to the control PEA based devices. [ABSTRACT FROM AUTHOR]

Blue perovskite light emitting diodes (LEDs) have attracted remarkable attention in recent years owing to their potential in full-color display and lighting applications. However, blue-emitting perovskite films usually require to be fabricated in inert condition, which increases the fabrication complexity and cost of perovskite LEDs, being unfavorable for practical applications. Herein, we report a strategy to fabricate blue perovskite films in ambient air with high humidity for LED applications. Diphenylphosphinic chloride (DPPOCl) is introduced into perovskite film, which can react with the water in air and release chlorine ion, thus leading to the chlorination of perovskite and the consequent blueshifted luminescence. Meanwhile, the P O groups can passivate the perovskite film and suppress nonradiative recombination. Based on the ambient air fabricated blue-emitting perovskite films, perovskite LEDs are constructed, which exhibit bright and spectrally stable electroluminescence (EL). The emission wavelength of the LEDs can be effectively tuned from cyan to pure blue by varying the concentration of DPPOCl. Our work demonstrates a feasible approach to fabricate blue perovskite films in high humidity air, which could contribute to lowering down the fabrication cost of blue perovskite LEDs and further boosting their applications in display and lighting. • Mixed halide perovskite films are fabricated in humid air via water-assisted chlorination. • Blue-emitting perovskite films are realized in ambient air with humidity up to 70%. • Blue perovskite LEDs with tunable electroluminescence spectrum are constructed. [ABSTRACT FROM AUTHOR]

While quasi-two-dimensional (quasi-2D) perovskites have emerged as promising semiconductors for light-emitting diodes (LEDs), the broad-width distribution of quantum wells hinders their efficient energy transfer and electroluminescence performance in blue emission. In particular, the underlying mechanism is closely related to the crystallization kinetics and has yet to be understood. Here for the first time, the influence of bifunctional zwitterions with different coordination affinity on the crystallization kinetics of quasi-2D perovskites is systematically investigated. The zwitterions can coordinate with Pb 2+ and also act as co-spacer organic species in quasi-2D perovskites, which collectively inhibit the aggregation of colloidal precursors and shorten the distance of quantum wells. Consequently, restricted nucleation of high-n phases and promoted growth of low-n phases are achieved with moderately coordinated zwitterions, leading to the final film with a more concentrated n distribution and improved energy transfer efficiency. It thus enables high-efficiency blue LEDs with a recorded external quantum efficiency of 15.6% at 490 nm, and the operation stability has also been prolonged to 55.3 min. These results provide useful directions for tuning the crystallization kinetics of quasi-2D perovskites, which is expected to lead to high-performance perovskite LEDs., (© 2022 Wiley-VCH GmbH.)

While there has been extensive investigation into modulating quasi-2D perovskite compositions in light-emitting diodes (LEDs) for promoting their electroluminescence, very few reports have studied approaches involving enhancement of the energy transfer between quasi-2D perovskite layers of the film, which plays very important role for achieving high-performance perovskite LEDs (PeLEDs). In this work, a bifunctional ligand of 4-(2-aminoethyl)benzoic acid (ABA) cation is strategically introduced into the perovskite to diminish the weak van der Waals gap between individual perovskite layers for promoting coupled quasi-2D perovskite layers. In particular, the strengthened interaction between coupled quasi-2D perovskite layers favors an efficient energy transfer in the perovskite films. The introduced ABA can also simultaneously passivate the perovskite defects by reducing metallic Pb for less nonradiative recombination loss. Benefiting from the advanced properties of ABA incorporated perovskites, highly efficient blue PeLEDs with external quantum efficiency of 10.11% and a very long operational stability of 81.3 min, among the best performing blue quasi-2D PeLEDs, are achieved. Consequently, this work contributes an effective approach for high-performance and stable blue PeLEDs toward practical applications., (© 2020 Wiley-VCH GmbH.)

Substantial achievements have been made in green and red perovskite light emitting diodes (PeLEDs) recently. However, blue PeLEDs still lag behind with much lower performances. One of the main reasons is the mass undesirable nonradiative recombination at interfaces and within the perovskite films. In this work, an efficient hole transport bi‐layer structure composed of PSSNa and NiOx is demonstrated to simultaneously inhibit the nonradiative decays between NiOx and perovskite films by reducing NiOx surface defects and improving quasi‐2D perovskite thin film quality by minimizing its pin‐holes and reducing the film roughness. The results show that the dipole feature of PSSNa improves the hole transportation and thus PeLED performances. Moreover, by introducing KBr into the perovskite, its film quality improves and trap states reduce. Eventually, the blue PeLEDs is achieved with a very low turn‐on voltage of 3.31 V accompanied with an external quantum efficiency of 1.45% and a remarkable luminance of 4359 cd m‐2. With further optimization of the perovskite precursor concentration, the highest luminance reaches 5737 cd m‐2, which represents the brightest blue PeLEDs reported to date as far as it is known. Furthermore, the devices also show better spectral stability and operation lifetime as compared to other blue PeLEDs. [ABSTRACT FROM AUTHOR]