New molecular framework could lead to flexible solar cells

Jun 29, 2010 By Lauren Gold
The Dichtel group in the Department of Chemistry and Chemical Biology has developed a method to organize organic dyes into stacked, porous two-dimensional sheets. These materials may ultimately be incorporated into inexpensive, flexible solar cells.

(PhysOrg.com) -- Making better solar cells: Cornell University researchers have discovered a simple process - employing molecules typically used in blue jean and ink dyes - for building an organic framework that could lead to economical, flexible and versatile solar cells. The discovery is reported in the journal Nature Chemistry.

Think of solar cells, and you probably imagine the thick, heavy silicon panels on rooftops in sunny climates.

Those panels are effective, but they can also be expensive and unwieldy. In the search for a better alternative, a team led by William Dichtel, assistant professor of chemistry and chemical biology, has discovered a simple process for building an organic molecular framework that could pave the way for the development of more economical, flexible and versatile solar cells.

The discovery is reported in an article published online on June 20 by the journal Nature Chemistry.

Dichtel's strategy uses organic dye molecules assembled into a structure known as a covalent organic framework (COF). Organic materials have long been recognized as having potential to create thin, flexible and low-cost photovoltaic devices, but it has been proven difficult to organize their component molecules reliably into ordered structures likely to maximize device performance.

COFs, a class of materials first reported in 2005, offer a new way to address this long-range ordering problem; but until now, the known methods for creating them had significant limitations.

"We had to develop a completely new way of making the materials in general," Dichtel said. The strategy uses a simple acid catalyst and relatively stable molecules called protected catechols to assemble key organic molecules into a neatly ordered two-dimensional sheet. These sheets stack on top of one another to form a lattice that provides pathways for charge to move through the material.

The reaction is also reversible, allowing for errors in the process to be undone and corrected.

"The whole system is constantly forming wrong structures alongside the correct one," Dichtel said, "but the correct structure is the most stable, so eventually, the more perfect structures end up dominating." The result is a structure with high surface area that maintains its precise and predictable molecular ordering over large areas.

The researchers used X-ray diffraction to confirm the material's molecular structure and surface area measurements to determine its porosity.

At the core of the framework are molecules called phthalocyanines, a class of common industrial dyes used in products from blue jeans to ink pens.

Phthalocyanines are also closely related in structure to chlorophyll, the compound in plants that absorbs sunlight for photosynthesis. The compounds absorb almost the entire solar spectrum -- a rare property for a single organic material.

"For most organic materials used for electronics, there's a combination of some design to get the materials to perform well enough, and there's a little bit of an element of luck," Dichtel said. "We're trying to remove as much of that element of luck as we can."

The structure by itself is not a solar cell yet, but it is a model that will significantly broaden the scope of materials that can be used in COFs, Dichtel said. "We also hope to take advantage of their structural precision to answer fundamental scientific questions about moving electrons through organic materials."

Once the framework is assembled, the pores between the molecular latticework could potentially be filled with another organic material to form a light, flexible, highly efficient and easy-to-manufacture solar cell.

The next step is to begin testing ways of filling in the gaps with complementary molecules. "This is the very beginning of our work," he said.

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More information: The article, "Lewis acid-catalysed formation of two-dimensional phthalocyanine covalent organic frameworks," appears in the online edition of the journal Nature Chemistry, June 20, 2010.

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