Triplet Excitons in Highly Efficient Solar Cells Based on the Soluble Small Molecule p‐DTS(FBTTh2)2
Abstract
Triplet exciton formation in neat 7,7‐(4,4‐bis(2‐ethylhexyl)‐4H‐silolo[3,2‐b:4,5‐b′] dithiophene‐2,6‐diyl)bis(6‐fluoro‐4‐(5′‐hexyl‐[2,2′‐bithiophen]‐5‐yl)benzo[c][1,2,5]thiadiazole) (p‐DTS(FBTTh2)2) and blends with [6,6]‐Phenyl C70 butyric acid methyl ester (PC70BM), with and without the selective solvent additive 1,8‐diiodooctane, is investigated by means of spin sensitive photoluminescence measurements. For all three material systems, a significant amount of long living triplet excitons is detected, situated on the p‐DTS(FBTTh2)2 molecules. The characteristic zero‐field splitting parameters for this state are identified to be D = 42 mT (1177 MHz) and E = 5 mT (140 MHz). However, no triplet excitons located on PC70BM are detectable. Using electrically detected spin resonance, the presence of these triplet excitons is confirmed even at room temperature, highlighting that triplet excitons form during solar cell operation and influence the photocurrent and photovoltage. Surprisingly, the superior performing blend is found to have the largest triplet population. It is concluded, that the formation of triplet excitons from charge transfer states via electron back transfer has no crucial impact on device performance in p‐DTS(FBTTh2)2:PC70BM based solar cells.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Dec 12, 2016
- Source ID
- 10.1002/aenm.201602016
Entities
People
- Andreas Baumann
- Andreas Sperlich
- John A. Love
- Kristofer Tvingstedt
- Michael C Heiber
- Stefan Väth
- Thuc‐quyen Nguyen
- Vladimir Dyakonov
Organizations
- Federal Ministry of Research, Technology and Space
- German Research Foundation
- Office of Naval Research
- University of Würzburg