4.6 Article

Synthesis and enhanced light absorption of alumina matrix nanocomposites containing multilayer oxide nanorods and silver nanoparticles

Journal

MATERIALS RESEARCH BULLETIN
Volume 46, Issue 11, Pages 1828-1836

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.materresbull.2011.07.050

Keywords

Oxides; Metals; Chemical synthesis; Electron microscopy; Optical properties

Funding

  1. University of Toledo
  2. U.S. Department of Energy, Office of Basic Energy Sciences [DE-AC02-98CH10886]

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In this paper, multilayer oxide nanorods were deposited in the nanopores of anodic aluminum oxide (AAO) via solution infiltration followed by heat treatment. The nanorods have a core-shell structure. First, the shell (nanotube) with the thickness of about 40 nm was made of TiO2 through the hydrolysis of (NH4)(2)TiF6. Second, silver nanoparticles with the diameter of about 3 nm were added into the TiO2 layer through thermal decomposition of AgNO3 at elevated temperatures. Then, cylindrical cores (nanorods) of CoO and ZnO with 200 nm diameter were prepared, respectively. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to characterize the structure and composition of the nanorods. UV-vis light absorption measurements in the wavelength range from 350 to 1000 nm were performed to study the effect of nanorod and nanoparticle addition on the light absorption property of the alumina nanocomposites. It is found that CoO nanorods increase the light absorption of the alumina matrix composite in the wavelength range from 500 nm to 800 nm, but the TiO2 shell does not increase the light absorption much. The ZnO nanorods do not change the light absorption either. However, the addition of silver nanoparticles significantly enhances light absorption of both AAO/TiO2/Ag/CoO and AAO/TiO2/Ag/ZnO nanocomposites. This increase in the visible light absorption reveals that there exists surface plasmon around the fine silver nanoparticles in the nanorods. (C) 2011 Elsevier Ltd. All rights reserved.

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