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Charge-Transfer Complexes in Organic Field-Effect Transistors: Superior Suitability for Surface Doping.


ABSTRACT: We demonstrate the key role of charge-transfer complexes in surface doping as a successful methodology for improving channel field-effect mobility and reducing the threshold voltage in organic field-effect transistors (OFETs), as well as raising the film conductivity. Demonstrated here for 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT) doped with 2,2'-(perfluoronaphthalene-2,6-diylidene)dimalononitrile (F6TCNNQ), channel doping by sequential deposition is consistently rationalized by the development of a cocrystalline structure that forms and evolves from the surface of the organic semiconductor film without trading the thin-film structure integrity. This scenario brings higher benefits for the device operation than doping by codeposition, where a decrease in the field-effect mobility of the device, even for a dopant content of only 1 mol %, makes codeposition less suitable. Insight into the structural and electronic properties of the interface satisfactorily explains the improved performance of OFETs upon the incorporation of the dopant and provides an understanding of the mechanism of doping in this system.

SUBMITTER: Babuji A 

PROVIDER: S-EPMC9542699 | biostudies-literature | 2022 Oct

REPOSITORIES: biostudies-literature

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Charge-Transfer Complexes in Organic Field-Effect Transistors: Superior Suitability for Surface Doping.

Babuji Adara A   Cazorla Alba A   Solano Eduardo E   Habenicht Carsten C   Kleemann Hans H   Ocal Carmen C   Leo Karl K   Barrena Esther E  

ACS applied materials & interfaces 20220920 39


We demonstrate the key role of charge-transfer complexes in surface doping as a successful methodology for improving channel field-effect mobility and reducing the threshold voltage in organic field-effect transistors (OFETs), as well as raising the film conductivity. Demonstrated here for 2,7-dioctyl[1]benzothieno[3,2-<i>b</i>][1]benzothiophene (C<sub>8</sub>-BTBT) doped with 2,2'-(perfluoronaphthalene-2,6-diylidene)dimalononitrile (F<sub>6</sub>TCNNQ), channel doping by sequential deposition i  ...[more]

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