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Understanding the role of non-fullerene acceptor crystallinity on the charge transport properties and performance of organic solar cells

Abstract:
The acceptor crystallinity has long been associated with favourable organic solar cells (OSCs) properties such as high mobility and Fill Factor. In particular, this applies to acceptor materials such as fullerene-derivatives and the most recent Non-Fullerene Acceptors (NFAs), which are now surpassing 19% of Power Conversion Efficiency. Despite these advantages are commonly attributed to their 3-dimensional crystal packing motif in the single crystal, the bridge that links the acceptor crystal packing from single crystals to solar cells has not clearly been shown yet. In this work, we investigate the molecular organisation of seven NFAs (o-IDTBR, IDIC, ITIC, m-ITIC, 4TIC, 4TICO, m-4TICO), following the evolution of their packing motif in single-crystals, powder, and thin films made with pure NFAs and donor:NFA blends. We observed a good correlation between the NFA single crystal packing motif and their molecular arrangement in the bulk heterojunction. The NFA packing motif affects the material’s propensity to form highly crystalline domain in the blend. We specifically found that 3D reticular packing motifs show stronger ordering than 0D herringbone ones. However, the NFA packing motif is not directly correlating with device performance parameters: Although higher NFA crystallinity yields higher mobility, we found the domain purity to be more important for obtaining high efficiency organic solar cells by governing bimolecular recombination.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1039/d3ta03284a

Authors


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Institution:
University of Oxford
Division:
MPLS
Department:
Physics
Sub department:
Condensed Matter Physics
Role:
Author
ORCID:
0000-0003-3887-3395


Publisher:
Royal Society of Chemistry
Journal:
Journal of Materials Chemistry A More from this journal
Volume:
11
Issue:
30
Pages:
16263-16278
Publication date:
2023-07-04
Acceptance date:
2023-07-04
DOI:
EISSN:
2050-7496
ISSN:
2050-7488


Language:
English
Keywords:
Pubs id:
1489272
Local pid:
pubs:1489272
Deposit date:
2023-07-04

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