Organic-inorganic perovskite materials, typically methylammonium lead trihalide (MAPbX: MA = methylammonium; X = Br, I), are recently attract enormous attention for their distinguished photo-electronic properties. The control of morphology, composition and dispersability of MAPbX perovskite nanocrystals is crucial for the property tailoring and still a major challenge. Here we report the synthesis of colloidal MAPbBrI(0 ≤ x ≤ 3) nanocrystals at room temperature by using alkyl carboxylate as capping ligands. These nanocrystals exhibit continuously tunable UV-vis absorption and photoluminescence (PL) across the visible spectrum, which is attributed to the quantum confinement effect with certain stoichiometry. Their unique exciton recombination dynamics was investigated and discussed.
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http://dx.doi.org/10.1038/srep35931 | DOI Listing |
J Colloid Interface Sci
December 2022
Department of Biomedical Engineering, College of Design and Engineering, National University of Singapore, 117576, Singapore; NUS Suzhou Research Institute, Suzhou, Jiangsu, China. Electronic address:
Despite having exceptional optical and photoelectric properties, the application of organometal halide perovskites (OHP) is restricted due to the limited penetration depth of the UV excitation light and poor stability. Attempts have been made to make composite materials by mixing other materials such as upconversion nanoparticles (UCNP) with OHP. In contrast to linear absorption and emission of OHP, the nonlinear upconversion of UCNP offers numerous advantages such as deep penetration depth of the near-infrared (NIR) excitation light, minimal photodamage to biological tissues, and negligible background interference, which offer great potential in various applications such as multiplexed optical encoding, three-dimensional displays, super-resolution bioimaging, and effective solar spectrum conversion.
View Article and Find Full Text PDFNanomaterials (Basel)
November 2020
Physics and Astronomy Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Organic-inorganic halide organometal perovskites have demonstrated very promising performance in optoelectronic applications, but their relatively poor chemical and colloidal stability hampers the further improvement of devices based on these materials. Perovskite material engineering is crucial for achieving high photoluminescence quantum yields (PLQYs) and long stability. Herein, these goals are attained by incorporating bulk-structure CsPbBr, which prevents colloidal degradation, into polymethyl methacrylate (PMMA) polymer in thin-disk form.
View Article and Find Full Text PDFChemSusChem
May 2020
Key Laboratory of Applied Surface and Colloid Chemistry MOE, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an, 710119, P. R. China.
J Phys Chem Lett
October 2019
Department of Chemistry and Biochemistry , Florida State University, Tallahassee , Florida 32306 , United States.
Organometal halide perovskite materials, in particular colloidal perovskite nanocrystals (NCs), have been investigated extensively as next-generation light-emitting materials. However, producing highly efficient and stable perovskite thin films from colloidal NCs is not trivial, as dissociation of surfactants often occurs during the thin-film formation. Here, we demonstrate a facile solution-processing approach to prepare perovskite nanocomposite thin films by using phosphonium as the capping ligand for methylammonium lead bromide (MAPbBr) NCs.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2019
Department of Physics, Indian Institute of Technology Guwahati, Guwahati 781039, India; Centre for Nanotechnology, Indian Institute of Technology Guwahati, Guwahati 781039, India. Electronic address:
Herein, we demonstrated a novel synthetic route to grow size-tunable hybrid perovskite (CHNHPbI and CHNHPbBr) quantum dots (QDs) using a Fluorine-doped TiO (F-TiO) mesoporous template and these QDs exhibit large exciton binding energy, high photoluminescence quantum yield and improved photostability. The pore size in F-TiO template is tuned by varying the HF molar concentration during its solvothermal growth and size of the perovskite QDs embedded in F-TiO pores is tuned in the range 1.7-5.
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