4.7 Article

Nanostructured PbSe Films Deposited by Spray Pyrolysis Using PbSe Colloidal Solutions

Journal

NANOMATERIALS
Volume 13, Issue 18, Pages -

Publisher

MDPI
DOI: 10.3390/nano13182595

Keywords

lead selenide; nanostructures; polyol; amine; thiol; spray pyrolysis

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This work describes the spray pyrolysis deposition of PbSe films using PbSe colloids as the starting solution. The results show that using colloidal dispersions as spray solutions for forming PbSe films is effective, and the synthesis method allows for the elimination of thiol and amine groups before deposition, significantly simplifying the process.
This work describes the spray pyrolysis deposition of PbSe films, using as-prepared PbSe colloids as the starting solution. The PbSe colloids were prepared by using the alkahest approach, where Pb and Se precursors were made to react with the following green polyols: glycerin, ethylene glycol, and propylene glycol, to subsequently spray them onto glass substrates. The results of the characterization indicated that amine or thiol groups-free and single-phase rock-salt cubic PbSe powder was obtained, producing nanocrystals 16-30 nm in size. X-ray diffraction also showed that the PbSe films containing PbSeO3 and PbO center dot xH2O as impurity phases were produced during the deposition. The morphology of the powders and films was developed by a self-assembly process, in which the primary PbSe nanoparticles self-assemble to produce peanut-like microstructures. Additionally, a non-continuous and porous feature was formed in the thick films. Certain films revealed optical structures characterized by broad- and low-intensity bands resembling an exciton-like behavior. This could be attributed to the presence of nanocrystals with a size less than the Bohr radius, indicating reminiscent quantum effects. The results suggest that the usage of colloidal dispersions as spray solutions represents an effective approach to forming PbSe films, as well as that the synthesis method allows for the elimination of thiol and amine groups before deposition, significantly simplifying the process.

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