Abstract
Three different theoretical approaches are presented to identify pathways to organic solar cells with power conversion efficiencies in excess of 20%. A radiation limit for organic solar cells is introduced that elucidates the role of charge-transfer (CT) state absorption. Provided this CT action is sufficiently weak, organic solar cells can be as efficient as their inorganic counterparts. Next, a model based on Marcus theory of electronic transfer that also considers exciton generation in both the electron donor and electron acceptor is used to show how reduction of the reorganization energies can lead to substantial efficiency gains. Finally, the dielectric constant is introduced as a central parameter for efficient solar cells. By using a driftdiffusion model, it is found that efficiencies of more than 20% are within reach.
| Original language | English |
|---|---|
| Pages (from-to) | 1246-1253 |
| Number of pages | 8 |
| Journal | Advanced Energy Materials |
| Volume | 2 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - Oct-2012 |
Keywords
- conjugated polymers
- fullerenes
- organic electronics
- photovoltaic devices
- solar cells
- OPEN-CIRCUIT VOLTAGE
- CHARGE-TRANSFER EXCITONS
- ELECTRON-TRANSFER
- CONVERSION EFFICIENCY
- PHOTOVOLTAIC DEVICES
- BULK HETEROJUNCTIONS
- ULTIMATE EFFICIENCY
- CONJUGATED POLYMERS
- TRANSFER STATES
- RECOMBINATION