Evidence map›Paper›PMID 38095532›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Diselenophene-Dithioalkylthiophene Based Quinoidal Small Molecules for Ambipolar Organic Field Effect Transistors.

Arulmozhi Velusamy, Yen-Yu Chen, Meng-Hao Lin, Shakil N Afraj, Jia-Hao Liu, Ming-Chou Chen, Cheng-Liang Liu

Abstract read
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Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Arulmozhi VelusamyDepartment of Chemistry and Research Center of New Generation Light Driven Photovoltaic Modules, National Central University, Taoyuan, 32001, Taiwan.
Yen-Yu ChenDepartment of Materials Science and Engineering, National Taiwan University, Taipei, 10617, Taiwan.
Meng-Hao LinDepartment of Materials Science and Engineering, National Taiwan University, Taipei, 10617, Taiwan.
Shakil N AfrajDepartment of Chemistry and Research Center of New Generation Light Driven Photovoltaic Modules, National Central University, Taoyuan, 32001, Taiwan.
Jia-Hao LiuDepartment of Chemistry and Research Center of New Generation Light Driven Photovoltaic Modules, National Central University, Taoyuan, 32001, Taiwan.
Ming-Chou ChenDepartment of Chemistry and Research Center of New Generation Light Driven Photovoltaic Modules, National Central University, Taoyuan, 32001, Taiwan.ORCID https://orcid.org/0000-0002-9117-9119
Cheng-Liang LiuDepartment of Materials Science and Engineering, National Taiwan University, Taipei, 10617, Taiwan.ORCID https://orcid.org/0000-0002-8778-5386

Funding

Advanced Research Center for Green Materials Science and TechnologyMinistry of Education 112L9006Ministry of Science and Technology, Taiwan 111-2113-M-008-004-MY3National Science and Technology Council 111-2628-E-002-014National Science and Technology Council 112-2628-E-002-013National Science and Technology Council in Taiwan NSTC 111-2622-8-008-006National Taiwan University NTU112L7856NCU-Covestro Research Center
6 · The paper itself

Abstract

This work presents a series of novel quinoidal organic semiconductors based on diselenophene-dithioalkylthiophene (DSpDST) conjugated cores with various side-chain lengths (-thiohexyl, -thiodecyl, and -thiotetradecyl, designated DSpDSTQ-6, DSpDSTQ-10, and DSpDSTQ-14, respectively). The purpose of this research is to develop solution-processable organic semiconductors using dicyanomethylene end-capped organic small molecules for organic field effect transistors (OFETs) application. The physical, electrochemical, and electrical properties of these new DSpDSTQs are systematically studied, along with their performance in OFETs and thin film morphologies. Additionally, the molecular structures of DSpDSTQ are determined through density functional theory (DFT) calculations and single-crystal X-ray diffraction analysis. The results reveal the presence of intramolecular S (alkyl)···Se (selenophene) interactions, which result in a planar SR-containing DSpDSTQ core, thereby promoting extended π-orbital interactions and efficient charge transport in the OFETs. Moreover, the influence of thioalkyl side chain length on surface morphologies and microstructures is investigated. Remarkably, the compound with the shortest thioalkyl chain, DSpDSTQ-6, demonstrates ambipolar carrier transport with the highest electron and hole mobilities of 0.334 and 0.463 cm

Indexed as

ambipolarorganic transistorsquinoidselenophenesolution-processing

Identifiers

PMID38095532
PMCPMC10916611

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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.