We present a colloidal synthesis strategy for lead halide nanosheets with a thickness of far below 100 nm. Due to the layered structure and the synthesis parameters the crystals of PbI are initially composed of many polytypes. We propose a mechanism which gives insight into the chemical process of the PbI formation. Further, we found that the crystal structure changes with increasing reaction temperature or by performing the synthesis for longer time periods changing for the final 2H structure. In addition, we demonstrate a route to prepare nanosheets of lead bromide as well as lead chloride in a similar way. Lead halides can be used as a detector material for high-energy photons including gamma and X-rays.
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http://dx.doi.org/10.1039/c7nr09564c | DOI Listing |
ACS Nano
December 2024
Department of Materials Science and Engineering, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Collective optical properties can emerge from an ordered ensemble of emitters due to interactions between the individual units. Superlattices of halide perovskite nanocrystals exhibit collective light emission, influenced by dipole-dipole interactions between simultaneously excited nanocrystals. This coupling changes both the emission energy and rate compared to the emission of uncoupled nanocrystals.
View Article and Find Full Text PDFACS Nano
December 2024
Nanochemistry, Istituto Italiano di Tecnologia, Via Morego 30, Genova 16163, Italy.
We report the synthesis of ethylammonium lead iodide (EAPbI) colloidal nanocrystals as another member of the lead halide perovskites family. The insertion of an unusually large -cation (274 pm in diameter) in the perovskite structure, hitherto considered unlikely due to the unfavorable Goldschmidt tolerance factor, results in a significantly larger lattice parameter compared to the Cs-, methylammonium- and formamidinium-based lead halide perovskite homologues. As a consequence, EAPbI nanocrystals are highly unstable, evolving to a nonperovskite δ-EAPbI polymorph within 1 day.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Univ Rennes, ENSCR, CNRS, ISCR-UMR6226, Université de Rennes, Rennes 35042, France.
Metal halide perovskites, including some of their related perovskitoid structures, form a semiconductor class of their own, which is arousing ever-growing interest from the scientific community. With halides being involved in the various structural arrangements, namely, pure corner-sharing MX (M is metal and X is halide) octahedra, for perovskite networks, or alternatively a combination of corner-, edge-, and/or face-sharing for related perovskitoids, they represent the ideal probe for characterizing the way octahedra are linked together. Well known for their inherently large quadrupolar constants, which is detrimental to the resolution of nuclear magnetic resonance spectroscopy, most abundant halide isotopes (Cl, Br, I) are in turn attractive for magnetic field-free nuclear quadrupolar resonance (NQR) spectroscopy.
View Article and Find Full Text PDFDalton Trans
December 2024
Department of Chemical Engineering, Indian Institute of Technology Madras, Adyar, Chennai, Tamil Nadu 600036, India.
Tuning the selectivity and improving the activity of photocatalysts are among the main bottlenecks for the conversion of CO to value-added chemicals. Recently, lead-free halide perovskites have been extensively investigated as photocatalysts for the photoreduction of CO. Herein, we report a composite photocatalyst using CsBiCl and Ir/IrO for the photoreduction of CO.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P.R. China.
The filterless single-pixel imaging technology is anticipated to hold tremendous competitiveness in diverse imaging applications. Nevertheless, achieving single-pixel color imaging without a filter remains a formidable challenge. Here a lead-free perovskite hemispherical photodetector is reported for filterless single-pixel color imaging.
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