All-inorganic perovskites (CsPbX) with the merits of high stability and remarkable optical gain property are attractive for achieving on-chip coherent light sources. Unfortunately, traditional solution-processed CsPbX films suffer from inevitable poor surface integrity and pinhole defects, severely hindering their optical properties. Here, from the perspective of precursor solution chemistry, we use an ionic liquid solvent methylammonium acetate (MAAc) to fabricate compact, pinhole-free, and smooth CsPbX thin films in a one-step air process without antisolvent treatment. Optically pumped amplified spontaneous emission (ASE) with a straightforward visible spectral tunability (418-725 nm) is achieved under both nanosecond and femtosecond laser excitation. For the representative CsPbBr films, the threshold reaches down to 11.4 μJ cm under nanosecond laser pumping, which is comparable to the value under one-photon femtosecond pumping. The long gain lifetime up to 258.2 ps is revealed by transient absorption spectroscopy. Most importantly, the films show excellent optical stability and humidity stability with no obvious degradation under the pulsed laser irradiation for more than 210 min, stable ASE output under 95% high humidity, and conspicuous ASE after 1000 h of storage in air condition without encapsulation. These results demonstrate that the method of fabricating inorganic perovskite films with an ionic liquid solvent is promising in developing high-performance full-color visible lasers.
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http://dx.doi.org/10.1021/acsami.2c02577 | DOI Listing |
Materials (Basel)
March 2024
Department of Electrophysics, National Chiayi University, Chiayi 60004, Taiwan.
Perovskite thin films directly impact solar cell properties, making defect reduction crucial in perovskite solar cell research. In our study, we used perovskite quantum dots in the anti-solvent to act as nucleation centers in MAPbI3 thin films. These centers had lower nucleation barriers than homogeneous nucleation, improving perovskite crystallinity, reducing defects, and extending carrier lifetime.
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December 2023
The GPL Photonics Laboratory, State Key Laboratory of Luminescence and Applications, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun, Jilin 130033, China.
In this work, we systematically explore the third-order nonlinear optical properties of all-inorganic CsPbX (X = Cl, Br, I) perovskite precursor solutions and thin films using femtosecond and nanosecond laser pulses. We show that these samples possess strong two-photon absorption (TPA) and reverse saturable absorption (RSA), which depend on the excitation wavelength. The obtained nonlinear absorption and refraction coefficients for precursor solutions are followed by the relation CsPbCl > CsPbBr > CsPbI for the 800 and 1,064 nm excitation wavelengths, whereas this relation became reverse in the case of 355 and 400 nm laser pulses.
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December 2023
College of Materials Science and Engineering, Sichuan University, Chengdu, 610065, P. R. China.
Solid-state anion exchange method is easy to handle and beneficial to improve stability of CsPbX (X = Cl, Br, I) perovskites nanocrystals (NCs) with respect to anion exchange in liquid phase. However, the corresponding exchange rate is rather slow due to the limited diffusion rate of anions from solid phases, resulting in mixed-halide perovskite NCs. Herein, a fast and reversible post-synthetic quasi-solid-state anion exchange method in CsPbX NCs with inorganic potassium halide KX salts/polyvinylpyrrolidone (PVP) thin film is firstly reported.
View Article and Find Full Text PDFSmall
August 2023
Waterloo Institute for Nanotechnology, University of Waterloo, 200 University Ave West, Waterloo, ON, N2L 3G1, Canada.
Regulating the strain of inorganic perovskites has emerged as a critical approach to control their electronic and optical properties. Here, an alternative strategy to further control the piezoelectric properties by substituting the halogen atom (I/Br) in the CsPbX perovskite (X = Cl, Br) structure is adopted. A series of piezoelectric materials with excellent piezoelectric coefficients (d ) are unveiled.
View Article and Find Full Text PDFChem Mater
April 2023
Department of Chemistry and Applied Biosciences, ETH Zürich, Zürich CH-8093, Switzerland.
Lead halide perovskite (LHP) nanocrystals (NCs) have gathered much attention as light-emitting materials, particularly owing to their excellent color purity, band gap tunability, high photoluminescence quantum yield (PLQY), low cost, and scalable synthesis. To enhance the stability of LHP NCs, bulky strongly bound organic ligands are commonly employed, which counteract the extraction of charge carriers from the NCs and hinder their use as photoconductive materials and photocatalysts. Replacing these ligands with a thin coating is a complex challenge due to the highly dynamic ionic lattice, which is vulnerable to the commonly employed coating precursors and solvents.
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