| Literature DB >> 26575214 |
Iordania Constantinou1, Tzung-Han Lai1, Erik D Klump1, Subhadip Goswami2, Kirk S Schanze2, Franky So1.
Abstract
The effect of polymer side chains on device performance was investigated for PBDT(EtHex)-TPD(Oct):PC70BM and PBDT(EtHex)-TPD(EtHex):PC70BM BHJ solar cells. Going from a linear side chain on the polymer's acceptor moiety to a branched side chain was determined to have a negative impact on the overall device efficiency, because of significantly reduced short-circuit current (J(sc)) and fill factor (FF) values. Sub-bandgap external quantum efficiency (EQE) and transient photoluminescence (PL) measurements showed more-efficient carrier generation for the polymer with linear side chains, because of a higher degree of charge-transfer (CT) state delocalization, leading to more-efficient exciton dissociation. Furthermore, the increase in π-π stacking distance and disorder for the bulkier ethylhexyl side chain were shown to result in a lower hole mobility, a higher bimolecular recombination, and a higher energetic disorder. The use of linear side chains on the polymer's acceptor moiety was shown to promote photogeneration, because of more-effective CT states and favorable carrier transport resulting in improved solar cell performance.Entities:
Keywords: carrier recombination; charge transfer states; energetic disorder; organic photovoltaics; organic solar cells
Year: 2015 PMID: 26575214 DOI: 10.1021/acsami.5b09497
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229