Abstract

A new strategy to nanoengineer gold/fluorocarbon multilayer (ML) nanostructures is reported. We have investigated the morphological changes occurring at the metal–polymer interface in ML structures with varying volume fraction of gold (Au) and the kinetic growth aspect of the microscale properties of nano-sized Au in plasma polymer fluorocarbon (PPFC). Investigations were carried out at various temperatures and annealing times by means of grazing incidence small-angle and wide-angle X-ray scattering (GISAXS and GIWAXS). We have fabricated a series of MLs with varying volume fraction (0.12, 0.27, 0.38) of Au and bilayer periodicity in ML structure. They show an interesting granular structure consisting of nearly spherical nanoparticles within the polymer layer. The nanoparticle (NP) morphology changes due to the collective effects of NPs diffusion within ensembles in the in-plane vicinity and interlayer with increasing temperature. The in-plane NPs size distinctly increases with increasing temperature. The NPs become more spherical, thus reducing the surface energy. Linear growth of NPs with temperature and time shows diffusion-controlled growth of NPs in the ML structure. The structural stability of the multilayer is controlled by the volume ratio of the metal in polymer. At room temperature, UV-Vis shows a blue shift of the plasmon peak from 560 nm in ML Au/PTFE_1 to 437 nm in Au/PTFE_3. We have identified the fabrication and postdeposition annealing conditions to limit the local surface plasmon resonance (LSPR) shift from = 180 nm (Au/PTFE_1) to = 67 nm (Au/PTFE_3 ML)) and their optical response over a wide visible wavelength range. A variation in the dielectric constant of the polymer in presence of varying Au inclusion is found to be a possible factor affecting the LSPR frequency. Our findings may provide insights in nanoengineering of ML structure that can be useful to systematically control the growth of NPs in polymer matrix.

Highlights

  • Easy processability, high flexibility, and tunable physical properties make nanocomposites very attractive for a broad range of applications

  • A simple, practical approach has been developed to make nanoengineered ML structures that can control the optical response of the NPs

  • The reordering of NPs occurs as an effect of thermal annealing

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Summary

Introduction

High flexibility, and tunable physical properties make nanocomposites very attractive for a broad range of applications. The combination of metal nanoparticles with dielectric media, such as polymers, has gained great pertinence both in fundamental as well as technological aspects Their fine control and possible tuning of physical properties can lead to the fabrication of materials with novel functional, electric, and optical properties and engender their accessibility to various applications in the field of optics, electronics, and biomedicine [1,2,3,4,5]. Structure of fixed volume fraction below the percolation threshold of metal in varying polymer layers Such arrangement allows inter alia control growth of NPs in the polymer matrix. The structural properties of the nanocomposites and kinetic growth of NPs in polymer matrix have been studied using grazing incidence small and wide-angle X-ray scattering (GISAXS & GIWAXS). The relation of structural and optical properties during this growth is discussed

Sample Preparation
Characterization
GIWAXS
GISAXS
Structural Changes during and after Annealing
Temperature-Dependent Optical Response
Findings
Conclusions

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