January 16, 2013
Senior Editor Gail Overton from Laser Focus World discussed with researchers at Duke Univerity in the David Smith group the revelations from Nature's "Controlled-reflectance surfaces with film coupled colloidal nanoantennas". Her full feature can be found here, and mentioned below;
NANOPHOTONIC METAMATERIALS: Nanocubes create tunable metamaterial absorber
Released: 01/15/2013
By Gail Overton
"Metallic, metamaterial-based light absorbers used as photovoltaic and detection devices are easily tuned by altering their structural design; however, lithographically produced structures are expensive to fabricate and operate over small physical areas. An alternative metamaterial absorber from researchers at Duke University (Durham, NC) in David Smith’s group, Clermont Université (Clermont-Ferrand, France), and Capital Normal University (Beijing, China) uses a simple, lower-cost method that randomly adsorbs silver nanocubes onto a polymer layer on gold film.1 Nanocube size dictates “tunability” of the absorber; it is not necessary to control the spatial arrangement of the nanocubes in order to absorb light over a large area.
Ideal absorbers
Metamaterials have been called ideal absorbers because both their magnetic and electrical properties can be controlled at nearly any wavelength. Similar to a grounded patch antenna in which a conducting metallic patch is positioned over a metallic conducting ground plane to generate fictitious magnetic surface current density that offsets the electric current surface density, silver nanocubes separated by a thin polymer layer over a gold film act as nanoantennas that excite gap-plasmon-guided modes that are largely insensitive to the angle of incidence or polarization of the incoming radiation.
Analogous to their radio-frequency counterparts, these optical antennas induce effective magnetic currents whose radiating field cancels out the electromagnetic field created by the incident radiation on the surrounding gold film. When this polymer film layer is precisely engineered (based on computer modeling) to a 5–10 nm thickness, each cube is able to absorb all the light on an area that is 30 times larger than the actual surface occupied by the cube.
To fabricate the tunable absorber, silver nanocubes were synthesized by reducing silver nitrate with ethylene glycol in the presence of poly(vinyl pyrrolidone) (PVP). The molar ratio of PVP relative to silver nitrate determines the geometric shape and size of the resultant nanocubes (see figure). Next, the fabricated silver nanocubes are adsorbed on a thin polymer layer over the gold film using colloidal self-assembly processes.
A scanning electron microscopy (SEM) image shows the silver nanocubes deposited on the gold film (a); a darkfield image shows how cube size can influence the color they diffuse (b). The cubes are shown in a SEM image as fabricated (c) and in an artist’s view (d). (Courtesy of Duke University)
Although 3% coverage of 74 nm (on a side) ideal cube-shaped nanocubes enables greater than 93% absorption over an approximate 40-nm-wide wavelength region that is tunable across the visible spectrum from approximately 500–800 nm for a 50-nm-thick gold layer, less-than-ideal shaped nanocubes with slightly different sizes require increased coverage (up to 17.1% of the surface area). And as the polymer layer thickness is increased beyond the ideal 6 nm value, reflectance is increased.
'The most amazing aspect of these cubes is probably the many different things they can do,' says Antoine Moreau, assistant professor at Clermont University. 'You could, for instance, turn your gold surface into a display screen by controlling the space between the cubes and the gold film to tune the color of the structure. But because the nanocubes are the tiniest interferometers we’ve ever seen, we first plan to use them to detect molecular changes in their environment or to explore the limits of our current electromagnetic description of metals. Ultimately, we hope to use this technology in the infrared to develop new thermophotovoltaic devices.' "
REFERENCE
1. A. Moreau et al., Nature, 492, 7427, 86–89 (Dec. 6, 2012).