Evidence map›Paper›PMID 42173828›Full record

ArticleNature communications2026

Coulombic control of charge transfer in radicals with quartet recycling luminescence.

Lujo Matasovic, Petri Murto, Shilong Yu, Wenzhao Wang, James D Green, Giacomo Londi, Weixuan Zeng, Laura Brown, William K Myers, Lars van Turnhout and 10 more

Abstract read
In one paragraph

Article in Nature communications, 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

20 authors.

Lujo MatasovicCavendish Laboratory, University of Cambridge, Cambridge, UK.
Petri MurtoCavendish Laboratory, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-7618-000X
Shilong YuState Key Laboratory of Supramolecular Structure and Materials, Jilin University, Changchun, PR China.
Wenzhao WangState Key Laboratory of Supramolecular Structure and Materials, Jilin University, Changchun, PR China.
James D GreenDepartment of Chemistry, University College London, London, UK.ORCID http://orcid.org/0000-0002-4467-2015
Giacomo LondiDepartment of Chemistry and Industrial Chemistry, University of Pisa, Pisa, Italy.ORCID http://orcid.org/0000-0001-7777-9161
Weixuan ZengYusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK.
Laura BrownYusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK.
William K MyersCentre for Advanced ESR, Department of Chemistry, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-5935-9112
Lars van TurnhoutCavendish Laboratory, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-5222-6250
Konstantina ArmadorouDepartment of Chemical Engineering & Biotechnology, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-0355-9411
Avik BhanjaDepartment of Chemistry and Materials Science, Aalto University, Espoo, Finland.ORCID http://orcid.org/0000-0003-3826-2869
Sergiu PetruscaYusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0009-0003-0792-9242
David BeljonneLaboratory for Chemistry of Novel Materials, University of Mons, Mons, Belgium.ORCID http://orcid.org/0000-0001-5082-9990
Yoann OlivierLaboratory for Computational Modelling of Functional Materials, University of Namur, Namur, Belgium.ORCID http://orcid.org/0000-0003-2193-1536
Feng LiState Key Laboratory of Supramolecular Structure and Materials, Jilin University, Changchun, PR China. lifeng01@jlu.edu.cn.ORCID http://orcid.org/0000-0001-5236-3709
Hugo BronsteinYusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK. hab60@cam.ac.uk.ORCID http://orcid.org/0000-0003-0293-8775
Timothy J H HeleDepartment of Chemistry, University College London, London, UK. t.hele@ucl.ac.uk.ORCID http://orcid.org/0000-0003-2367-3825
Richard H FriendCavendish Laboratory, University of Cambridge, Cambridge, UK. rhf10@cam.ac.uk.ORCID http://orcid.org/0000-0001-6565-6308
Sebastian GorgonCavendish Laboratory, University of Cambridge, Cambridge, UK. sg911@cam.ac.uk.ORCID http://orcid.org/0000-0002-1361-1973

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 101020167EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 Marie Skłodowska-Curie Actions (H2020 Excellent Science - Marie Skłodowska-Curie Actions) 891167Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research) 2.5020.11National Natural Science Foundation of China (National Science Foundation of China) 51925303Oxford University | John Fell Fund, University of Oxford (John Fell OUP Research Fund) 0007019, 0010710RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/V036408/1RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/W017091/1Royal Society URF\R1\201502
6 · The paper itself

Abstract

Excitons in organic materials are emerging as an attractive platform for tunable quantum technologies. Structures with near-degenerate doublet and triplet excitations in linked trityl radical, acene and carbazole units can host quartet states. These high spin states can be coherently manipulated, and later decay radiatively via the radical doublet transition. However, this requires controlling the deexcitation pathways of all metastable states. Here we establish design rules for efficient quartet generation and recycling to luminescence, using different connection arrangements of the molecular units. We discover that electronic coupling strength between these units dictates quartet formation and delayed emission yields, particularly through a Coulombically tuned acene-radical charge transfer state. This state acts as a source of non-radiative decay when acene-radical separation is small, but facilitates reversible doublet-quartet interconversion when acene-radical separation is large. Using these rules we report a material with 55% luminescence yield, where 94% of emitting excitons are recycled from the quartet with a 1.0 μs lifetime. This reveals the central role of molecular topology in luminescent quantum materials.

Identifiers

PMID42173828
PMCPMC13396479

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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.