Now, researchers led by an MIT postdoc have analyzed an artificial system that models the light-capturing method used by deep-sea bacteria. Further advances in understanding fundamental light-harvesting processes may yield entirely new approaches to capturing solar energy, the researchers say. Their results were reported July 1 in the journal Nature Chemistry.
The artificial system, described in an earlier paper by postdoc Dörthe M. Eisele of MIT’s Research Laboratory of Electronics and collaborators, consists of a self-assembling system of dye molecules that form perfectly uniform double-walled nanotubes. These tubes — only about 10 nanometers wide but thousands of times longer — are similar in size, shape and function to natural receptors used by green sulfur bacteria that collect energy from the tiny amounts of sunlight that penetrate to the ocean’s depths.
“It is one of nature’s great secrets, how to harvest light so efficiently,” Eisele says. Her co-authors include Moungi G. Bawendi and the late Robert J. Silbey, both MIT professors of chemistry, along with collaborators at Humboldt University of Berlin, the University of Texas at Austin and the University of Groningen in the Netherlands.
Eisele says this particular type of nanotube is unlikely to find practical applications. Rather, she says, these experiments were designed to study underlying principles that could then be used to find optimal materials for particular uses. “This system is so interesting because it is a beautiful model system,” she says, for analyzing how such structures respond to light.
Unlike typical self-assembling systems in which each structure can be a bit different, these double-walled tubes, made from a cyanine-based dye, form perfectly uniform shapes and sizes.
That makes it a perfect model system, Eisele explains, because knowing that all the nanotubes in a solution are identical makes it possible to study their properties in bulk, rather than having to isolate the response of each individual tube.
One fundamental question the team wanted to address was whether the two concentric cylinders of the double-walled tubes were working together as an integrated system for capturing light’s energy, or whether each cylinder was acting on its own.
To answer that question, Eisele and her team devised a way of deactivating one of the two cylinders by oxidizing the outer wall’s molecules. “The tubular structure is still intact, but it kills the optical response of the outer wall, so what is left is the optical response of the inner wall,” she says. “It’s a very simple and elegant way to isolate the spectrum of the inner wall.”
By comparing optical responses when both cylinders are functioning and when only one is working, it’s possible to determine how much interaction is taking place between the two cylinders. “When you watch the dynamics of the redox reaction,” Eisele says, “you see that these two cylinders can be seen as two separate systems.”
Characterizing this simplified artificial structure may allow researchers to build more efficient light-harvesting devices. “Nature had millions of years to optimize” how organisms capture energy, Eisele says; understanding how it did so may lead to better man-made systems.
“We don’t want to improve the efficiency of solar cells we have now,” she says. “We want to learn from nature how to build entirely new light-harvesting devices.”
Gregory Scholes, the D.J. LeRoy Distinguished Professor of Chemistry at the University of Toronto, who was not involved in this work, says, “The researchers used exquisite experiments to test how the nanoscale components of this system interact after photoexcitation.” He adds that the work “provides important insights into the design of large assemblies of molecules for applications in ‘light harvesting.’”
The research was supported by the Deutsche Forschungsgemeinschaft, the Integrative Research Institute for the Sciences in Berlin, the National Science Foundation, the Alexander von Humboldt Foundation, the Department of Energy Center for Excitonics, the Army Research Office and the Defense Advanced Research Projects Agency.