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SOLAR DAILY
Researchers Reveal How Solvent Mixtures Affect Organic Solar Cell Structure
by Staff Writers
Raleigh, NC (SPX) Oct 08, 2012


Molecular view at an interface between two regions in a solar cell. Image by Brian Collins, copyright Wiley.

Controlling "mixing" between acceptor and donor layers, or solar cell domains, in polymer-based solar cells could increase their efficiency, according to a team of researchers that included physicists from North Carolina State University. Their findings shed light on the inner workings of these solar cells, and could lead to further improvements in efficiency.

Polymer-based solar cells consist of two domains, known as the acceptor and the donor layers. Excitons, the energy particles created by solar cells, must be able to travel quickly to the interface of the donor and acceptor domains in order to be harnessed as an energy source. Researchers had believed that keeping the donor and acceptor layers as pure as possible was the best way to ensure that the excitons could travel unimpeded, so that solar cells could capture the maximum amount of energy.

NC State physicist Harald Ade and his group worked with teams of scientists from the United Kingdom, Australia and China to examine the physical structure and improve the production of polymer-based solar cells.

In findings published in two separate papers appearing this month online in Advanced Energy Materials and Advanced Materials, the researchers show that some mixing of the two domains may not be a bad thing. In fact, if the morphology, or structure, of the mixed domains is small, the solar cell can still be quite efficient.

According to Ade, "We had previously found that the domains in these solar cells weren't pure. So we looked at how additives affected the production of these cells. When you manufacture the cell, the relative rate of evaporation of the solvents and additives determines how the active layer forms and the donor and acceptor mix.

Ideally, you want the solvent to evaporate slowly enough so that the materials have time to separate - otherwise the layers 'gum up' and lower the cell's efficiency. We utilized an additive that slowed evaporation. This controlled the mixing and domain size of the active layer, and the portions that mixed were small."

The efficiency of those mixed layers was excellent, leading to speculation that perhaps some mixing of the donor and acceptor isn't a problem, as long as the domains are small.

"We're looking for the perfect mix here, both in terms of the solvents and additives we might use in order to manufacture polymer-based solar cells, and in terms of the physical mixing of the domains and how that may affect efficiency," Ade says.

The research was funded by the U.S. Department of Energy. Ade is corresponding author on the Advanced Energy Materials paper, with post docs Brian Collins, John Tumbleston and graduate student Eliot Gann contributing to the work. Dr. Zhe Li of the University of Cambridge and Christopher McNeill of Monash University in Australia also contributed. Ade was a contributing author on the Advanced Materials paper, which was co-authored by Ade's post doc Wei Ma and Professor Jianhui Hou of Beijing's Chinese Academy of Sciences.

"From Binary to Ternary Solvent: Morphology Fine-tuning of D/A Blend in PDPP3T-based Polymer Solar Cells"; Authors: L. Ye, S. Zhang, B. Fan, X. Guo, Y. Huang, Prof. J. Hou, State Key Laboratory of Polymer Physics and Chemistry, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences; W. Ma, H. Ade, North Carolina State University.

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Related Links
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All About Solar Energy at SolarDaily.com






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SOLAR DAILY
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Beijing (UPI) Oct 8, 2012
While China's solar slump has serious repercussions, it could result in a stronger solar sector, insiders say. Prices of solar panels have fallen to three-quarters of their 2008 prices. As a result, China's major solar panel makers are suffering losses of up to $1 for every $3 of sales this year, says a report in The New York Times. Last week, China's Suntech received a delisting ... read more


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