[EEPN In Electronic Design]
Researchers Open Windows Of Opportunity For Solar Power
Mat Dirjish
ED Online ID #19666
September 25, 2008
Copyright © 2006 Penton Media, Inc., All rights reserved. Printing of this document is for personal use only.
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Solar-power researchers at the Massachusetts
Institute of Technology (MIT) have been very
busy in their labs lately, and not without significant
fruits for their labors. Two projects promise
to elevate solar power from an expensive and cumbersome
alternative to an affordable and unlimited energy source.
SOLAR POWER GOES GREEN-LITERALLY!
Relying on the process of photosynthesis occurring in plants
for inspiration, MIT Professor of Energy Daniel Nocera has
found what he calls “the nirvana of what we’ve been talking
about for years.” His process for storing solar energy requires
no more than natural, non-toxic materials that provide power
both day and night.
“Now we can seriously think about solar power as unlimited
and soon,” he says. Along with postdoctoral fellow Matthew
Kanan, Nocera employs the sun’s energy to split water into
hydrogen and oxygen gases. Afterward, the gases recombine
within a fuel cell, forming carbon-free electricity.
At the heart of the process is a unique catalyst comprising
cobalt metal, phosphate, and an electrode placed in water for
separating oxygen gas from water (Fig. 1). A second catalyst
such as platinum separates the hydrogen gas.
When electricity from a solar cell or any other source travels
through the electrode, the cobalt/phosphate catalyst forms
a film on the electrode and produces oxygen. Paired with a
hydrogen catalyst, the system replicates the water-splitting
reaction that commonly occurs during plant photosynthesis.
Electrolyzers, components that split water with electricity
and are commonly associated with industrial applications, are
currently available. However, they are expensive and require
non-benign environments foreign to the conditions under
which photosynthesis operates.
According to Nocera, “The new catalyst works at room temperature,
in neutral pH water, and it’s easy to set up. That’s why
I know this is going to work. It’s so easy to implement.”
Funded by the National Science Foundation and the Chesonis
Family Foundation, Nocera’s research falls under the
umbrella of MIT’s Solar Revolution Project. The end goal of
this venture is to make large-scale deployment of solar energy
a reality within 10 years. For more information, e-mail Nocera
at nocera@mit.edu.
WINDOWS THAT WORK-LITERALLY!
MIT’s Esther and Harold E. Edgerton Career Development
Associate Professor of Electrical Engineering Marc A. Baldo not
only sees through windows, he also foresees powerful potential
around their edges. He and his researchers have found an alternative
to large solar panels for harnessing solar power, an approach
that may enable common windows to power a home or office.
Using optical techniques developed for lasers and organic
light-emitting diodes (OLEDs), the researchers have created
a solar concentrator that allows some measure of control over
light absorption and emission. The MIT concentrator consists
of a mixture of two or more dyes in specific ratios that the
researchers apply or paint onto a pane of glass. The dyes absorb
light hitting the glass across a range of wavelengths. Then, the
dyes re-emit light at different wavelengths and transport it
across the pane to small solar cells at the edges (Fig. 2).
“Light is collected over a large area and gathered or concentrated
at the edges. Rather than covering a roof with expensive
solar cells, the cells only need to be around the edges of a
flat glass panel,” Baldo says. “In addition, the focused light
increases the electrical power obtained from each solar cell by
a factor of over 40.”
Baldo and his team claim that their system is simple to
manufacture, and they forecast commercial availability within
three years. Of particular note, their system can interface with
existing solar-panel systems to offer a 50% efficiency boost at
minimal cost. For further details, contact Baldo via e-mail at
baldo@mit.edu.
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