| Literature DB >> 30873701 |
Long Ye1, Yuan Xiong1, Zheng Chen2,3, Qianqian Zhang2, Zhuping Fei4, Reece Henry1, Martin Heeney4, Brendan T O'Connor5, Wei You2, Harald Ade1.
Abstract
Casting of a donor:acceptor bulk-heterojunction structure from a single ink has been the predominant fabrication method of organic photovoltaics (OPVs). Despite the success of such bulk heterojunctions, the task ofcontrolling the microstructure in a single casting process has been arduous and alternative approaches are desired. To achieve OPVs with a desirable microstructure, a facile and eco-compatible sequential deposition approach is demonstrated for polymer/small-molecule pairs. Using a nominally amorphous polymer as the model material, the profound influence of casting solvent is shown on the molecular ordering of the film, and thus the device performance and mesoscale morphology of sequentially deposited OPVs can be tuned. Static and in situ X-ray scattering indicate that applying (R)-(+)-limonene is able to greatly promote the molecular order of weakly crystalline polymers and form the largest domain spacing exclusively, which correlates well with the best efficiency of 12.5% in sequentially deposited devices. The sequentially cast device generally outperforms its control device based on traditional single-ink bulk-heterojunction structure. More crucially, a simple polymer:solvent interaction parameter χ is positively correlated with domain spacing in these sequentially deposited devices. These findings shed light on innovative approaches to rationally create environmentally friendly and highly efficient electronics.Entities:
Keywords: eco-friendly solvent; molecular order; nonfullerene acceptors; organic solar cells; sequential deposition
Year: 2019 PMID: 30873701 DOI: 10.1002/adma.201808153
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849