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Photolithographic processing of silver loaded dielectric coatings based on preformed colloidal TiO2nanoparticles dispersed in a mesoporous silica binder

Titanium dioxide is a well known photocatalyst for reactions involving surface trapped photogenerated carriers. Noble metal photo-reduction may be used for the processing of silver/TiO 2 nanocomposite coatings that may exhibit interesting optical and electrical properties. We present here results of...

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Bibliographic Details
Published in:Nanotechnology 2012-11, Vol.23 (50), p.1-9
Main Authors: Corde, Jöelle, Perruchas, Sandrine, Vieille, Laetitia, Galaup, Jean-Pierre, Duluard, Sandrine Nathalie, Biver, Claudine, Boilot, Jean-Pierre, Gacoin, Thierry
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Language:English
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Summary:Titanium dioxide is a well known photocatalyst for reactions involving surface trapped photogenerated carriers. Noble metal photo-reduction may be used for the processing of silver/TiO 2 nanocomposite coatings that may exhibit interesting optical and electrical properties. We present here results of our investigations performed on an original system consisting of preformed colloidal TiO 2 nanoparticles homogeneously dispersed within a mesoporous silica host matrix. Light irradiation of samples immerged in an aqueous silver salt solution leads to the homogeneous deposition of silver islands in the vicinity of the TiO 2 particles and throughout the film thickness. The silver volume fraction is directly controlled by the irradiation dose up to a value of about 16 vol.%. Films exhibit tunable plasmonic properties that correspond to silver nanoparticles in interaction, and a percolation threshold is observed at 8–10 vol.%, leading to films with a conductivity of about 40 S cm −1 . The major interest of this method lies in the high silver reduction quantum efficiency (about 50%) and the possibility to modulate optical and electronic properties by light irradiation while the low temperature of processing permits the photolithographic deposition of metallic patterns on organic flexible substrates.
ISSN:0957-4484
1361-6528
DOI:10.1088/0957-4484/23/50/505206