Evidence map›Paper›PMID 41906521›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2026

Solvent-Mediated Reactivity Control of Lewis-Paired Dopants as a Versatile Strategy for Tunable and Stable Doping of Organic Semiconductors.

Sang Beom Kim, Eui Hyun Suh, Taek Seong Lee, Andreas W Erhardt, Iain McCulloch, Jaeyoung Jang

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 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

6 authors.

Sang Beom KimDepartment of Energy Engineering, Hanyang University, Seoul, Republic of Korea.
Eui Hyun SuhDepartment of Energy Engineering, Hanyang University, Seoul, Republic of Korea.
Taek Seong LeeDepartment of Energy Engineering, Hanyang University, Seoul, Republic of Korea.
Andreas W ErhardtDepartment of Chemistry, University of Oxford, Oxford, UK.
Iain McCullochDepartment of Chemistry, University of Oxford, Oxford, UK.
Jaeyoung JangDepartment of Energy Engineering, Hanyang University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-5548-8563

Funding

Basic Research Laboratory program of the NRF RS-2025-00512834Korean Government RS-2025-00556330Ministry of Science and ICT RS-2024-00402972National Research Foundation of Korea
6 · The paper itself

Abstract

The Lewis pairing between existing dopant molecules offers great potential for developing new organic dopants with exceptional doping strength and stability. However, the high reactivity of Lewis-paired dopants complicates doping-level control, while the use of non-orthogonal solvents can damage organic semiconductor (OSC) films, hindering device applications. Here, the dopant reactivity is controlled by regulating the association-dissociation kinetics among pairing dopants and solvent molecules, which are strongly influenced by solvent polarity. In highly polar solvents, Lewis acid-solvent adducts predominantly form, suppressing the generation of Lewis-paired dopants. As solvent polarity decreases, the dissociation rate of the Lewis acid-solvent adduct increases, establishing a dynamic equilibrium between the Lewis acid and the solvent and thereby optimizing reactivity. Consequently, the optimally processed Lewis-paired dopant enables efficient doping of various OSCs with finely tunable doping levels, simultaneously achieving a high thermoelectric power factor (170 µW m

Indexed as

Lewis acid‐base chemistrymolecular dopantsorganic semiconductorsSeebeck coefficientstunable doping

Identifiers

PMID41906521
PMCPMC13410857

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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.