Evidence map›Paper›PMID 41952579›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026

Three-Step Synthesis Toward Fluorene-Based Non-Fused-Ring Acceptors for Organic Solar Cells.

Virginia Lafranconi, Suman Mallick, Lisa Nauta, Lisa Inzko, Julia Hönigsberger, Danijel Babic, Bettina Schlemmer, Daniele Padula, Heinz Amenitsch, Thomas Rath and 1 more

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Virginia LafranconiInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.
Suman MallickInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.
Lisa NautaInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.
Lisa InzkoInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.
Julia HönigsbergerInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.
Danijel BabicInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.
Bettina SchlemmerInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.
Daniele PadulaDipartimento di Biotecnologie, Chimica e Farmacia, Università di Siena, Siena, Italy.
Heinz AmenitschInstitute of Inorganic Chemistry, NAWI Graz, Graz University of Technology, Graz, Austria.ORCID https://orcid.org/0000-0002-0788-1336
Thomas RathInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.ORCID https://orcid.org/0000-0002-4837-7726
Gregor TrimmelInstitute for Chemistry and Technology of Materials (ICTM), NAWI Graz, Graz University of Technology, Graz, Austria.ORCID https://orcid.org/0000-0001-8922-4163

Funding

the European Union´s Horizon Europe MSCA-DN program 101120262
6 · The paper itself

Abstract

Non-fused-ring electron acceptors have recently gathered substantial interest for the application in organic solar cells because of their competitive photovoltaic properties and other advantages, including easy synthesis and high yields, facilitating the production of cost-efficient devices. In this work, a pair of fluorene-based acceptors, FHM-Cl and FHM-F, respectively featuring a chlorinated and a fluorinated 1,1-dicyanomethylene-3-indanone end group, π-bridged through alkyl-substituted thiophene units to a fluorene core, were synthesized through a three-step synthesis from commercially available precursors. Organic solar cells utilizing these acceptor molecules were subsequently fabricated and optimized with various donor materials. Notably, the combinations D18:FHM-Cl and D18:FHM-F achieved power conversion efficiencies of 10.7% and 7.6%, respectively. A comprehensive study involving optical and electrical characterization, along with morphological analysis, demonstrated that the FHM-Cl-based solar cells exhibited superior light absorption, enhanced solid-state packing and reduced trap-assisted recombination. Moreover, the shelf and thermal stability of the devices further highlight the potential of these acceptors in the design of low-cost and efficient organic solar cells.

Indexed as

fluorenenon‐fullerene electron acceptorsorganic solar cellssynthesis designthermal stabilitythin films

Identifiers

PMID41952579
PMCPMC13290411

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.