Metal halide perovskites possess exciting optoelectronic properties and are being used for various applications, including fluorescent anticounterfeiting security tags. The existing anticounterfeitings based on perovskites have a reversible transition that does not allow to know whether the information is tampered or compromised. In this work, we developed fluorescent anticounterfeiting security tags using micropatterned metal halide perovskite nanocrystals. The micro features were created by spray coating of stabilized methylammonium lead tribromide (MAPbBr) nanocrystals (NCs) in polystyrene (PS) solution, which has a proper wettability to various rigid and flexible substrates. The PS provides additional optical and structural stability to the MAPbBrNCs against polar solvents. By combining stable and unstable MAPbBrnanocrystals, we created a double-layer fluorescent anticounterfeiting security tag, and the information is hidden under both ambient light and UV illumination. An irreversible decryption is possible after treating the security tags with particular solvents, thus tampering of the security tag is easily detectable.
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http://dx.doi.org/10.1088/1361-6528/ac96f6 | DOI Listing |
Nanoscale
January 2025
Department of Chemistry, Maulana Azad National Institute of Technology, Bhopal-462003, India.
Mixing different metal ions at the B site of ABX perovskites offers a promising approach for addressing challenges related to toxicity, stability and performance in optoelectronic applications. One such example is CsPbSnBr which addresses the toxicity issue posed by lead while allowing us to tune optoelectronic properties such as the band gap. In this work, nearly monodisperse CsPbSnBr quantum dots (QDs) were synthesized with variable Pb/Sn compositions, CsPbBr, CsPbSnBr and CsPbSnBr.
View Article and Find Full Text PDFInorg Chem
January 2025
School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore, Singapore 63798, Singapore.
The corrugated <110> oriented layered metal halide perovskites (MHP) are gaining increased attention for a variety of properties including intrinsic white light emission. One prototypical candidate is 1-(3-aminopropyl)imidazole lead bromide, which was reported to crystallize as the <110> oriented perovskite (API)PbBr [API = 1-(3-aminopropyl)imidazole]. This work shows that under similar reaction conditions, the same components can instead form (API)PbBr, which has a "perovskitoid" structure.
View Article and Find Full Text PDFChemistryOpen
January 2025
University Paris Est Creteil, CNRS, ICMPE, UMR 7182, 2 rue Henri Dunant, 94320, Thiais, France.
The direct electrochemical carboxylation of aryl, benzyl and alkyl halides by CO is described using a magnesium anode and a nickel foam cathode in an undivided cell. The process employs a sacrificial anode and does not require the additional use of a transition metal catalyst or demanding conditions, as the reactions are carried out under galvanostatic mode, at -10 °C and with commercial DMF. Under these operationally simple conditions, an important range of carboxylic acids are affordable.
View Article and Find Full Text PDFMetal halide perovskites have unique luminescent properties that make them an attractive alternative for high quality light-emitting devices. However, the poor stability of perovskites with many defects and the long cycle time for the preparation of perovskite nanocomposites have hindered their production and application. Here, we prepared the perovskite mesostructures by embedding MAPbBr nanocrystals in the mesopores on the surface of silica nanospheres and mixing the nanospheres with silver nanowires and poly(methyl methacrylate) (PMMA), and further explored their optical properties.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Chemistry, School of Science, Tianjin University, Tianjin 300072, China.
Electrocatalytic dehalogenative deuteration is a sustainable method for precise deuteration, whereas its Faradaic efficiency (FE) is limited by a high overpotential and severe D evolution reaction (DER). Here, Cu site-adjusted adsorption and crown ether-reconfigured interfacial DO are reported to cooperatively increase the FE of dehalogenative deuteration up to 84% at -100 mA cm. Cu sites strengthen the adsorption of aryl iodides, promoting interfacial mass transfer and thus accelerating the kinetics toward dehalogenative deuteration.
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