Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Size-Dependent Photon Emission from Organometal Halide Perovskite Nanocrystals Embedded in an Organic Matrix.

ABSTRACT: In recent years, organometal halide perovskite materials have attracted significant research interest in the field of optoelectronics. Here, we introduce a simple and low-temperature route for the formation of self-assembled perovskite nanocrystals in a solid organic matrix. We demonstrate that the size and photoluminescence peak of the perovskite nanocrystals can be tuned by varying the concentration of perovskite in the matrix material. The physical origin of the blue shift of the perovskite nanocrystals’ emission compared to its bulk phase is also discussed.

SUBMITTER: Di D

PROVIDER: S-EPMC4415888 | biostudies-other | 2015 Feb

REPOSITORIES: biostudies-other

ACCESS DATA

Json Xml

Publications

Size-Dependent Photon Emission from Organometal Halide Perovskite Nanocrystals Embedded in an Organic Matrix.

Di Dawei D Musselman Kevin P KP Li Guangru G Sadhanala Aditya A Ievskaya Yulia Y Song Qilei Q Tan Zhi-Kuang ZK Lai May Ling ML MacManus-Driscoll Judith L JL Greenham Neil C NC Friend Richard H RH

The journal of physical chemistry letters 20150201 3

In recent years, organometal halide perovskite materials have attracted significant research interest in the field of optoelectronics. Here, we introduce a simple and low-temperature route for the formation of self-assembled perovskite nanocrystals in a solid organic matrix. We demonstrate that the size and photoluminescence peak of the perovskite nanocrystals can be tuned by varying the concentration of perovskite in the matrix material. The physical origin of the blue shift of the perovskite n ...[more]

PMID: 25949773

Similar Datasets

Halide perovskite nanocrystal arrays: Multiplexed synthesis and size-dependent emission.

Project description:Halide perovskites have exceptional optoelectronic properties, but a poor understanding of the relationship between crystal dimensions, composition, and properties limits their use in integrated devices. We report a new multiplexed cantilever-free scanning probe method for synthesizing compositionally diverse and size-controlled halide perovskite nanocrystals spanning square centimeter areas. Single-particle photoluminescence studies reveal multiple independent emission modes due to defect-defined band edges with relative intensities that depend on crystal size at a fixed composition. Smaller particles, but ones with dimensions that exceed the quantum confinement regime, exhibit blue-shifted emission due to reabsorption of higher-energy modes. Six different halide perovskites have been synthesized, including a layered Ruddlesden-Popper phase, and the method has been used to prepare functional solar cells based on single nanocrystals. The ability to pattern arrays of multicolor light-emitting nanocrystals opens avenues toward the development of optoelectronic devices, including optical displays.

| S-EPMC7531881 | biostudies-literature

Pressure-induced emission of cesium lead halide perovskite nanocrystals.

Project description:Metal halide perovskites (MHPs) are of great interest for optoelectronics because of their high quantum efficiency in solar cells and light-emitting devices. However, exploring an effective strategy to further improve their optical activities remains a considerable challenge. Here, we report that nanocrystals (NCs) of the initially nonfluorescent zero-dimensional (0D) cesium lead halide perovskite Cs4PbBr6 exhibit a distinct emission under a high pressure of 3.01 GPa. Subsequently, the emission intensity of Cs4PbBr6 NCs experiences a significant increase upon further compression. Joint experimental and theoretical analyses indicate that such pressure-induced emission (PIE) may be ascribed to the enhanced optical activity and the increased binding energy of self-trapped excitons upon compression. This phenomenon is a result of the large distortion of [PbBr6]4- octahedral motifs resulting from a structural phase transition. Our findings demonstrate that high pressure can be a robust tool to boost the photoluminescence efficiency and provide insights into the relationship between the structure and optical properties of 0D MHPs under extreme conditions.

| S-EPMC6206024 | biostudies-literature

Single Cesium Lead Halide Perovskite Nanocrystals at Low Temperature: Fast Single-Photon Emission, Reduced Blinking, and Exciton Fine Structure.

Project description:Metal-halide semiconductors with perovskite crystal structure are attractive due to their facile solution processability, and have recently been harnessed very successfully for high-efficiency photovoltaics and bright light sources. Here, we show that at low temperature single colloidal cesium lead halide (CsPbX3, where X = Cl/Br) nanocrystals exhibit stable, narrow-band emission with suppressed blinking and small spectral diffusion. Photon antibunching demonstrates unambiguously nonclassical single-photon emission with radiative decay on the order of 250 ps, representing a significant acceleration compared to other common quantum emitters. High-resolution spectroscopy provides insight into the complex nature of the emission process such as the fine structure and charged exciton dynamics.

| S-EPMC4768330 | biostudies-literature

Giant five-photon absorption from multidimensional core-shell halide perovskite colloidal nanocrystals.

Project description:Multiphoton absorption processes enable many technologically important applications, such as in vivo imaging, photodynamic therapy and optical limiting, and so on. Specifically, higher-order nonlinear absorption such as five-photon absorption offers significant advantages of greater spatial confinement, increased penetration depth, reduced autofluorescence, enhanced sensitivity and improved resolution over lower orders in bioimaging. Organic chromophores and conventional semiconductor nanocrystals are leaders in two-/three-photon absorption applications, but face considerable challenges from their small five-photon action cross-sections. Herein, we reveal that the family of halide perovskite colloidal nanocrystals transcend these constraints with highly efficient five-photon-excited upconversion fluorescence-unprecedented for semiconductor nanocrystals. Amazingly, their multidimensional type I (both conduction and valence band edges of core lie within bandgap of shell) core-shell (three-dimensional methylammonium lead bromide/two-dimensional octylammonium lead bromide) perovskite nanocrystals exhibit five-photon action cross-sections that are at least 9 orders larger than state-of-the-art specially designed organic molecules. Importantly, this family of halide perovskite nanocrystals may enable fresh approaches for next-generation multiphoton imaging applications.

| S-EPMC5437305 | biostudies-other

Coherent vibrational dynamics reveals lattice anharmonicity in organic-inorganic halide perovskite nanocrystals.

Project description:The halide ions of organic-inorganic hybrid perovskites can strongly influence the interaction between the central organic moiety and the inorganic metal halide octahedral units and thus their lattice vibrations. Here, we report the halide-ion-dependent vibrational coherences in formamidinium lead halide (FAPbX3, X = Br, I) perovskite nanocrystals (PNCs) via the combination of femtosecond pump-probe spectroscopy and density functional theory calculations. We find that the FAPbX3 PNCs generate halide-dependent coherent vibronic wave packets upon above-bandgap non-resonant excitation. More importantly, we observe several higher harmonics of the fundamental modes for FAPbI3 PNCs as compared to FAPbBr3 PNCs. This is likely due to the weaker interaction between the central FA moiety and the inorganic cage for FAPbI3 PNCs, and thus the PbI64- unit can vibrate more freely. This weakening reveals the intrinsic anharmonicity in the Pb-I framework, and thus facilitating the energy transfer into overtone and combination bands. These findings not only unveil the superior stability of Br-based PNCs over I-based PNCs but are also important for a better understanding of their electronic and polaronic properties.

| S-EPMC8113605 | biostudies-literature

The dark exciton ground state promotes photon-pair emission in individual perovskite nanocrystals.

Project description:Cesium lead halide perovskites exhibit outstanding optical and electronic properties for a wide range of applications in optoelectronics and for light-emitting devices. Yet, the physics of the band-edge exciton, whose recombination is at the origin of the photoluminescence, is not elucidated. Here, we unveil the exciton fine structure of individual cesium lead iodide perovskite nanocrystals and demonstrate that it is governed by the electron-hole exchange interaction and nanocrystal shape anisotropy. The lowest-energy exciton state is a long-lived dark singlet state, which promotes the creation of biexcitons at low temperatures and thus correlated photon pairs. These bright quantum emitters in the near-infrared have a photon statistics that can readily be tuned from bunching to antibunching, using magnetic or thermal coupling between dark and bright exciton sublevels.

| S-EPMC7691346 | biostudies-literature

Absorption Enhancement in Organic-Inorganic Halide Perovskite Films with Embedded Plasmonic Gold Nanoparticles.

Project description:We report on the numerical analysis of solar absorption enhancement in organic-inorganic halide perovskite films embedding plasmonic gold nanoparticles. The effect of particle size and concentration is analyzed in realistic systems in which random particle location within the perovskite film and the eventual formation of dimers are also taken into account. We find a maximum integrated solar absorption enhancement of ∼10% in perovskite films of 200 nm thickness and ∼6% in 300 nm films, with spheres of radii 60 and 90 nm, respectively, in volume concentrations of around 10% in both cases. We show that the presence of dimers boosts the absorption enhancement up to ∼12% in the thinnest films considered. Absorption reinforcement arises from a double contribution of plasmonic near-field and scattering effects, whose respective weight can be discriminated and evaluated from the simulations.

| S-EPMC4603614 | biostudies-literature

Tuning the Emission Wavelength of Lead Halide Perovskite NCs via Size and Shape Control.

Project description:The advent of lead halide perovskite nanocrystals (NCs), which are easily synthesized, ultralow-cost materials and have an impeccable luminous efficiency, has drastically changed the future perspective of semiconductor quantum dot devices. Although the band gap energy of lead perovskite NCs can be tuned by the halide composition, the instability problem prevails for mixed-halide perovskite NCs, caused by phase segregation due to ion migration when an external electric field or light is applied. To avoid this problem and obtain the stable emission of RGB primary colors, in this study, two synthesis pathways of pure-halide perovskite NCs are proposed. One approach is the modified hot injection method with "centrifugation of a frozen eutectic mixture" to separate small NCs efficiently, and the other is the "low-temperature mixing and heat-up method" for target materials including CsPbI3, CsPbBr3, and CH(NH2)2PbBr3 (FAPbBr3). The emission wavelength of FAPbBr3 is tuned ion-stoichiometrically, unlike Cs perovskites. These various synthesis pathways of pure-halide perovskite NCs enable the efficient production of high-quality perovskite NCs and allow precise tuning of the emission color to the desired wavelength. Although there are still several "gaps" remaining in the available emission wavelength, the new methodology proposed in this study could potentially be employed for manufacturing more stable perovskite NC-based optoelectronic devices.

| S-EPMC8756606 | biostudies-literature

Precise Control of Green to Blue Emission of Halide Perovskite Nanocrystals Using Terbium Chloride as Chlorine Source.

Project description:CsPbClxBr3-x nanocrystals were prepared by ligand-assisted deposition at room temperature, and their wavelength was accurately adjusted by doping TbCl3. The synthesized nanocrystals were monoclinic and the morphology was almost unchanged after doping. The fluorescence emission of CsPbClxBr3-x nanocrystals was easily controlled from green to blue by adjusting the amount of TbCl3, which realizes the continuous and accurate spectral regulation in the range of green to blue. This method provides a new scheme for fast anion exchange of all-inorganic perovskite nanocrystals in an open environment at room temperature.

| S-EPMC8470515 | biostudies-literature

Facet-Dependent Photoelectrochemistry on Single Crystal Organic–Inorganic Halide Perovskite Electrodes

Project description:Organometallic halide perovskites have garnered significant

| S-EPMC10467489 | biostudies-literature