AI Article Synopsis

  • Inorganic halides perovskite CsPbBr nanoparticles exhibit high light-conversion efficiency and tunability across the visible spectrum, making them valuable for optoelectronic applications.
  • A new method involving the recrystallization of these nanoparticles within electrospun fluoropolymer fibers has been developed, using affordable materials and equipment.
  • The resulting nonwoven mats demonstrated effective down-conversion of UV light and up-conversion of IR radiation, along with strong mechanical stability, highlighting their potential for flexible, commercially viable technologies.

Article Abstract

Inorganic halides perovskite CsPbX (X = Cl, Br, and I or mixed halide systems Cl/Br and Br/I) nanoparticles are efficient light-conversion objects that have attracted significant attention due to their broadband tunability over the entire visible spectral range of 410-700 nm and high quantum yield of up to 95%. Here, we demonstrate a new method of recrystallization of CsPbBr nanoparticles inside the electrospun fluoropolymer fibers. We have synthesized nonwoven tetrafluoroethylene mats embedding CsPbBr nanoparticles using inexpensive commercial precursors and syringe electrospinning equipment. The fabricated nonwoven mat samples demonstrated both down-conversion of UV light to 506 nm and up-conversion of IR femtosecond laser radiation to 513 nm green photoluminescence characterized by narrow emission line-widths of 35 nm. Nanoparticle formation inside nonwoven fibers was confirmed by TEM imaging and water stability tests controlled by fluorimetry measurements. The combination of enhanced optical properties of CsPbBr nanoparticles and mechanical stability and environmental robustness of highly deformable nonwoven fluoropolymer mats is appealing for flexible optoelectronic applications, while the industry-friendly fabrication method is attractive for commercial implementations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915552PMC
http://dx.doi.org/10.3390/nano11020412DOI Listing

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