Inorganic Lead Halide Perovskite Quantum Research Articles

Crystallization engineering in PVDF enables ultrastable and highly efficient CsPbBr3 quantum dots film for wide color gamut Mini-LED backlight

The polymeric composite films incorporating inorganic lead halide perovskite quantum dots (CsPbX3 QDs, X = Cl, Br or I) are promising color conversion layers for wide gamut display devices such as Mini-LED backlight-based televisions. However, the relatively low emission efficiency and poor stability of these composite films present significant challenges for practical applications. In this study, we present a novel low-temperature in-situ crystallization strategy to prepare CsPbBr3/PVDF composite film through a rational designed of precursor, solvent and polymer structure. The strong interaction between PVDF and perovskite QDs via Lewis acid-base interaction allows for precise control over the crystallization and passivation of perovskite QDs. The optimized CsPbBr3/PVDF film exhibits bright emission with a photoluminescence quantum yield (PLQY) of up to 70 %, surpassing those of other CsPbBr3/polymers counterparts. Furthermore, the films demonstrate remarkable stability, retaining over 90 % of their original PLQY even after 50 days of aging under various environmental conditions such as exposure to air, immersion in water and blue light irradiation. By integrating the green and red emissive CsPbX3/PVDF films with blue Mini-LEDs, we successfully fabricate a prototype liquid crystal display (LCD) with an outstanding wide color gamut (128 % of NTSC 1931). These performances outperform that of commercial white-LED-based LCDs, highlighting the immense potential of CsPbX3/PVDF for high-definition display applications in the future.

Highly efficient CsPbBr3@glass@polyurethane composite film as flexible liquid crystal display backlight.

Inorganic lead halide perovskite quantum dots (CsPbX3 QDs (X = Cl, Br, or I)) have attracted more and more attention due to their high absorption coefficient, narrow emission band, high quantum efficiency, and tunable emission wavelength. However, CsPbX3 QDs are decomposed when exposed to bright light, heat, moisture, etc., which leads to severe luminous attenuation and limits their commercial application. In this paper, CsPbBr3@glass materials were successfully synthesized by a one-step self-crystallization method, including melting, quenching and heat treatment processes. The stability of CsPbBr3 QDs was improved by embedding CsPbBr3 QDs into zinc-borosilicate glass. Then, the CsPbBr3@glass was combined with polyurethane (PU) to form a flexible composite luminescent film CsPbBr3@glass@PU. This strategy enables the transformation of rigid perovskite quantum dot glass into flexible luminescent film materials and further improves the photoluminescence quantum yield (PLQY) from 50.5% to 70.2%. The flexible film has good tensile properties, and its length can be strained 5 times as long as the original length. Finally, a white LED was encapsulated by combining CsPbBr3@glass@PU film and red phosphor K2SiF6:Mn4+ with a blue LED chip. The good performance of the obtained CsPbBr3@glass@PU film indicates that it has potential application in flexible liquid crystal displays (LCDs) as a backlight source.

All-Inorganic Perovskite Quantum Dot-Based Blue Light-Emitting Diodes: Recent Advances and Strategies.

Light-emitting diodes (LEDs) based on all-inorganic lead halide perovskite quantum dots (PQDs) have undergone rapid development especially in the past five years, and external quantum efficiencies (EQEs) of the corresponding green- and red-emitting devices have exceeded 23%. However, the blue-emitting devices are facing greater challenges than their counterparts, and their poor luminous efficiency has hindered the display application of PQD-based LEDs (PeQLEDs). This review focuses on the key challenges of blue-emitting PeQLEDs including low EQEs, short operating lifetime, and spectral instability, and discusses the essential mechanism by referring to the latest research. We then systematically summarize the development of preparation methods of blue emission PQDs, as well as the current strategies on alleviating the poor device performance involved in composition engineering, ligand engineering, surface/interface engineering, and device structural engineering. Ultimately, suggestions and outlooks are proposed around the major challenges and future research direction of blue PeQLEDs.

Low‐Power‐Consumption, Reversible 3D Optical Storage Based on Selectively Laser‐Induced Photoluminescence Degradation in CsPbBr3 Quantum Dots Doped Glass

AbstractIn recent years, inorganic lead halide perovskite quantum dots have been used in various optoelectronic fields for their excellent luminescence properties, such as narrow emission bands, ultra‐wide tunable emission wavelength, and high quantum efficiency. In this paper, different from luminescence optimization in most research, luminescence degradation of perovskite quantum dots is addressed by femtosecond laser irradiation and successfully used for three‐dimensional data storage in CsPbBr3 quantum dots doped glass. Photoluminescence (PL) degradation can be finely modulated by adjusting the laser parameters. PL degradation mechanism, investigated by optical spectroscopy and morphology characterization, is attributed to laser‐induced decomposition, recrystallization, and defection of CsPbBr3 quantum dots. Laser‐induced PL degradation and the followed PL recovery by heat treatment are repeated for several cycles, showing good reversibility. Multilayer PL degradation patterns are written into the glass and read out without crosstalk, indicating high‐reliability 3D optical storage characteristics. Amazingly, PL degradation can be induced by just a low‐energy single laser pulse with estimated subpicosecond writing time per bit, demonstrating its potential in high‐speed, low‐power consumption 3D optical storage.

Self‐Driven Multistep Quantum Dot Synthesis Enabled by Autonomous Robotic Experimentation in Flow

Identifying the optimal formulation of emerging inorganic lead halide perovskite quantum dots (LHP QDs) with their vast colloidal synthesis universe and multiple synthesis/postsynthesis processing parameters is a challenging undertaking for material‐ and time‐intensive, batch synthesis strategies. Herein, a modular microfluidic synthesis strategy, integrated with an artificial intelligence (AI)‐guided decision‐making agent for intelligent navigation through the complex colloidal synthesis universe of LHP QDs with 10 individually controlled synthesis parameters and an accessible parameter space exceeding 2 × 107, is introduced. Utilizing the developed autonomous microfluidic experimentation strategy within a global learning framework, the optimal formulation of LHP QDs is rapidly identified through a two‐step colloidal synthesis and postsynthesis halide exchange reaction, for 10 different emission colors in less than 40 min per desired peak emission energy. Using two in‐series microfluidic reactors enables continuous bandgap engineering of LHP QDs via in‐line halide exchange reactions without the need for an intermediate washing step. Using an inert gas within a three‐phase flow format enables successful, self‐synchronized continuous delivery of halide salt precursor into moving droplets containing LHP QDs, resulting in accelerated closed‐loop formulation optimization and end‐to‐end continuous manufacturing of LHP QDs with desired optoelectronic properties.

Multiscale modeling and optimal operation of millifluidic synthesis of perovskite quantum dots: Towards size-controlled continuous manufacturing

Inorganic lead halide perovskite quantum dots (QDs) have emerged as a promising semiconducting nanomaterial candidate for widespread applications, including next-generation solar cells, displays, and photocatalysts. The optoelectronic properties of colloidal QDs are majorly dictated by their bandgap energy (related to their size). Thus, it is important to fine-tune the size while having fast and continuous production of QDs. However, the mass and heat transfer limitations of batch reactors with batch-to-batch variations have hindered precise control over the size-dependent optoelectronic properties of QDs. Thus, to address this knowledge gap, we propose a multiscale model for continuous flow manufacturing of colloidal perovskite QDs. Specifically, a first-principled kinetic Monte Carlo model is integrated with a continuum model to describe a plug-flow crystallizer (PFC). The PFC has two manipulated inputs, precursor concentration and superficial flow velocity, to fine-tune the size of QDs. Furthermore, a neural network based surrogate model is designed to identify an optimal input trajectory which will ensure that the desired QD size is achieved, thereby taking a step towards controlled and reliable nanomanufacturing of QDs.

Effective infrared emission of erbium ions doped inorganic lead halide perovskite quantum dots by sensitization of ytterbium ions

Abstract Rare earth ions doped all-inorganic lead halide perovskite quantum dots (PeQDs) have attracted extensive attention due to the rare earth ions doping greatly expanding the optical properties of PeQDs. Here, Er3+ and Yb3+ ions co-doped CsPbCl3 PeQDs are synthesized by the improved hot-injection method. The excitonic emission and near-infrared (NIR) IIb emission of Er3+ ions and quantum-cutting emission of Yb3+ ions were observed in CsPbCl3:Yb3+, Er3+ PeQDs. Interestingly, the NIR IIb emission of Er3+ ions is only obtained in PeQDs through the effective sensitization of Yb3+ ions. The energy transfer efficiency from Yb3+ to Er3+ ions is 23.5%. Furthermore, the optimal photoluminescence quantum yield (PLQY) of a NIR IIb emission for Er3+ ions was got by typical anion exchange reaction, and the value is up to 14.6%. This work provides a new way that further extends the emission wavelength of PeQDs to NIR IIb region, which will broaden the application scope of PeQDs.

Surface Modification for Improving the Photocatalytic Polymerization of 3,4-Ethylenedioxythiophene over Inorganic Lead Halide Perovskite Quantum Dots.

Inorganic lead halide perovskite quantum dots (iLHP-QDs) have recently been used in the photocatalytic reaction. However, the factors that influence the photocatalytic performance of the iLHP-QDs have not been fully investigated. Herein, we synthesized a series of iLHP-QDs with varied halide ratios (CsPbX3, X = I, I0.67Br0.33, I0.5Br0.5, I0.33Br0.67, Br) and studied their influence on the photocatalytic performance by monitoring the polymerization of 2,2',5',2″-ter-3,4-ethylenedioxythiophene (TerEDOT). The CsPbI3 QDs showed the best performance owing to their narrow band gap and low exciton binding energy. Moreover, the photocatalytic performance of the iLHP-QDs could be simply improved by being treated with methyl acetate, which can be attributed to the replacement of the oleic acid by the short acetate acid and the introduction of the traps on the surface of QDs in the post-treatment. These results could help design a more efficient photocatalytic system and further promote the application of iLHP-QDs.

Emission Recovery and Stability Enhancement of Inorganic Perovskite Quantum Dots.

Inorganic lead halide perovskite quantum dots (PQDs), especially red emission PQDs, are well-known to easily lose their luminescence emission with time, which shows from strong emission of fresh PQDs to no emission of aged PQDs. Here, we demonstrate that trioctylphosphine (TOP) can effectively and instantly recover the luminescence emission of aged red PQDs, making the "dead" PQDs "reborn". Furthermore, TOP also works to improve the emission intensity of freshly synthesized PQDs. In this process, TOP does not make any detectable structural changes to PQDs. Besides, TOP can effectively enhance the stability of PQDs against long-term storage, temperature, UV irradiation, and polar solvents. This unusual emission recovery and stability enhancement by TOP shall promote the understanding of particle surface conditions and the development of PQD devices.