Many of the beautiful colors found in stained glass windows come
from metal or oxide nanoclusters dispersed in the material. In
the 19th century Michael Faraday correctly deduced that the glass
was a mixture of different substances and in 1907 Gustav Mie explained
the colors by showing how light in a medium gets scattered by
particles on the size scale of the wavelength ("Mie scattering").
However, the mechanism by which the nanoclusters formed was usually
lost in the complexities of glass chemistry.
Researchers at the Universities of Orsay and Paris (Harry Bernas,
bernas@csnsm.in2p3.fr,
011-33-1-6915-5222), collaborating with glass experts, have now
shown that by shooting MeV-energy ions at room temperature into
a glass containing a metal oxide, one can initiate the aggregation
or "nucleation" of pure metal nanoclusters and even control the
density of nanoclusters within the material. Moreover, the nanoclusters
only grow in size upon heating of the sample, allowing control
over their size. This is analogous to the photographic process,
in which photons hit metal-containing salts in the emulsion, thus
allowing them to free metal atoms (usually silver) which nucleate
into clusters, forming an invisible or "latent" image.
Upon developing, these clusters grow to sizes that form visible
pixels. Here, ions replace photons and heat plays the role of
the "developer." Two crucial advantages of the ion-beam method
are that the density of nucleation sites in the "latent image"
can be predicted precisely; and standard lithography techniques
employing stencil-like "masks" may be used to design spatial patterns
of clusters. Both could lead to applications in optoelectronics.
(Valentin
et al., Phys. Rev. Lett, 1 Jan. 2001; text at Physics
News Select.)