Published November 2019 | Version v1
Journal article

Morphological and optical evolution of metallic oxide/Au nanoparticle hybrid thin film: High absorption and reflectance by plasmonic enhancement

  • 1. Institute of Hybrid Materials, National Center of International Research for Hybrid Materials Technology, National Base of International Science & Technology Cooperation, College of Materials Science and Engineering, Qingdao University, Qingdao 266071, PR (China)
  • 2. College of Electronics and Information, Kwangwoon University, Nowon-gu, Seoul 01897, South (Korea, Republic of)
  • 3. College of Electronic information, Qingdao University, Qingdao 266071, PR (China)

Description

Hybrid metal-oxide (MO)/metal nanostructures (MNSs) have been appealing in widespread optoelectronic devices due to their strong and tunable plasmonic activity encompassing selective scattering and absorption of wavelength depending upon the surface morphology and surrounding dielectric environment. In this paper, the various MO/Au NSs hybrid thin-films are fabricated via the solid-state-dewetting growth of Au NSs and sol-gel deposition of MO top-layers including ZrOx, CeOx, YOx and AlOx. Over 450% enhancements in maximum absorption are observed along with the peak redshift of 168 nm for the series of MO/Au NS films. The overall plasmonic properties undergo three regimes by the systematical control of film morphology: (I) Rapid enhancement, (II) Slow enhancement and (III) Decay. The optical evolution is correspondingly investigated with the assistant of finite-different time-domain (FDTD) calculation. This work may give an aid to the photo-electronic applications, such as photovoltaics, sensing and surface enhanced Raman scattering, based on hybrid MNSs especially on control of their plasmonic properties.

Additional details

Identifiers

DOI
10.1016/j.apsusc.2019.143575;
PII
S0169433219323724;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
495
Journal Page Range
vp.
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2019 Elsevier B.V. All rights reserved.