Dominik Landerer

Highly efficient polymer solar cells cast from non-halogenated xylene/anisaldehyde solution

Several high performance polymer:fullerene bulk-heterojunction photo-active layers, deposited from the non-halogenated solvents o-xylene or anisole in combination with the eco-compatible additive p-anisaldehyde, are investigated. The respective solar cells yield excellent power conversion efficiencies up to 9.5%, outperforming reference devices deposited from the commonly used halogenated chlorobenzene/1,8-diiodooctane solvent/additive combination. The impact of the processing solvent on the bulk-heterojunction properties is exemplified on solar cells comprising benzodithiophene-thienothiophene co-polymers and functionalized fullerenes (PTB7:PC71BM). The additive p-anisaldehyde improves film formation, enhances polymer order, reduces fullerene agglomeration and shows high volatility, thereby positively affecting layer deposition, improving charge carrier extraction and reducing drying time, the latter being crucial for future large area roll-to-roll device fabrication.

Enhanced thermal stability of organic solar cells comprising ternary D-D-A bulk-heterojunctions

Ternary absorber blends have recently been identified as promising concepts to spectrally broaden the absorption of organic bulk-heterojunction solar cells and hence to improve their power conversion efficiencies. In this work, we demonstrate that D-D-A ternary blends comprising two donor polymers and the acceptor PC61BM can also significantly enhance the thermal stability of the solar cell. Upon harsh thermal stress at 120 °C for 2 h, the ternary solar cells show only a minor relative deterioration of 10%. Whereas the polymer/fullerene blend PTB7-Th:PC61BM is rather unstable under these conditions, its degradation was efficiently suppressed by incorporating the near infrared-absorbing polymer PDTP–DFBT. Spectroscopic ellipsometry investigations and an effective medium analysis of the ternary absorber blend revealed that the domain conformation in presence of PDTP–DFBT remains stable whereas the domain conformation changes in its absence. The ternary PTB7-Th:PDTP–DFBT:PC61BM solar cells yield thermally stable power conversion efficiencies of up to 6%.Organic solar cells: Polymer mixtures enhance the thermal stabilityOrganic solar cells increase their lifetime by adding another polymer component, paving the way towards commercialization.A team led by Alexander Colsmann at Karlsruhe Institute of Technology, Germany conducted systematic spectroscopic investigations and device characterizations to demonstrate that the degradation of PTB7-Th: PC61BM solar cell can be efficiently suppressed by incorporating the near infrared-absorbing polymer PDTP-DFBT. Upon harsh thermal stress at 120 °C for 2 h, the ternary solar cells show only a minor relative deterioration of 10% with a high power conversion efficiency of 6%. This work reveals the importance of a third component to lock the phase conformation of the polymer and fullerene domains. This is a key step for the thermally stable power output thus the commercialization of the organic solar cells.