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Basic Research Needs for Solar Energy Utilization - Office of ...

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Figure 30 Schematic diagram (right) <strong>of</strong> an excitonic solar cell comprising a donor (orange) and an<br />

acceptor (green) species. An energy-level diagram (left) with excitation into the donor shows the optical<br />

and electronic bandgaps <strong>of</strong> the donor and acceptor and the band <strong>of</strong>fset relative to the exciton binding<br />

energy (EX).<br />

transport mechanisms, which take a variety <strong>of</strong> different <strong>for</strong>ms, depending on the quasi-particle<br />

that is being transported. Excitons are charge-neutral and are transported by diffusion, while<br />

charged carriers are transported by diffusion and/or drift in the built-in electric fields resulting<br />

from the electrical contacts. The degree <strong>of</strong> structural order <strong>of</strong> the material is important in<br />

determining transport properties. In the disordered limit (which includes most polymers), carrier<br />

transport occurs predominantly via hopping between spatially localized states, the energy<br />

distribution <strong>of</strong> which determines the intrinsic mobility. In the ordered limit <strong>of</strong> single crystals,<br />

weak scattering among delocalized states produces band-like transport. Strong charge lattice<br />

interactions lead to polaron states, which exist in both disordered and ordered structures.<br />

Understanding the role <strong>of</strong> deep energy traps in highly disordered materials is vital <strong>for</strong> controlling<br />

both charge transport and exciton lifetimes. These traps must be identified and characterized<br />

individually in crystalline samples; this knowledge can be used <strong>for</strong> optimization <strong>of</strong> the extrinsic<br />

mobility in device structures. A key component <strong>of</strong> this work is close interaction between<br />

mobility measurements, transport spectroscopies, and theory, including electronic structure and<br />

transport theories.<br />

Charge Separation and Recombination at the Interface between Nanostructures<br />

Although singlet excitons are the predominant photogenerated species, intersystem crossing to<br />

the triplet state yields species that are longer-lived and lower in energy. Their role in enhancing<br />

light-emitting devices has been a key success story, but little is known about their impact in<br />

organic photovoltaics. Whether they are essential or must be avoided at all costs are questions<br />

that need addressing. Although the exciton dissociation process is <strong>of</strong> fundamental importance to<br />

extracting energy from absorbed photons in OPV structures, it is also essential to inhibit the<br />

104

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