| Literature DB >> 28471649 |
Zeming Liu1, Jan Siegel2, Mario Garcia-Lechuga2, Thierry Epicier3, Yaya Lefkir1, Stéphanie Reynaud1, Matthieu Bugnet3, Francis Vocanson1, Javier Solis2, Guy Vitrant4, Nathalie Destouches1.
Abstract
Controlling plasmonic systems with nanometer resolution in transparent films and their colors over large nonplanar areas is a key issue for spreading their use in various industrial fields. Using light to direct self-organization mechanisms provides high-speed and flexible processes to meet this challenge. Here, we describe a route for the laser-induced self-organization of metallic nanostructures in 3D. Going beyond the production of planar nanopatterns, we demonstrate that ultrafast laser-induced excitation combined with nonlinear feedback mechanisms in a nanocomposite thin film can lead to 3D self-organized nanostructured films. The process, which can be extended to complex layered composite systems, produces highly uniform large-area nanopatterns. We show that 3D self-organization originates from the simultaneous excitation of independent optical modes at different depths in the film and is activated by the plasmon-induced charge separation and thermally induced NP growth mechanisms. This laser color marking technique enables multiplexed optical image encoding and the generated nanostructured Ag NPs:TiO2 films offer great promise for applications in solar energy harvesting, photocatalysis, or photochromic devices.Entities:
Keywords: laser-induced self-organization; nanostructured thin film; plasmonic colors; plasmonic nanomaterials; ultrafast photonics
Year: 2017 PMID: 28471649 DOI: 10.1021/acsnano.7b01748
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881