2016
DOI: 10.1021/acsami.6b08075
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High-Mobility Ambipolar Organic Thin-Film Transistor Processed From a Nonchlorinated Solvent

Abstract: Polymer semiconductor PDPPF-DFT, which combines furan-substituted diketopyrrolopyrrole (DPP) and a 3,4-difluorothiophene base, has been designed and synthesized. PDPPF-DFT polymer semiconductor thin film processed from nonchlorinated hexane is used as an active layer in thin-film transistors. As a result, balanced hole and electron mobilities of 0.26 and 0.12 cm(2)/(V s) are achieved for PDPPF-DFT. This is the first report of using nonchlorinated hexane solvent for fabricating high-performance ambipolar thin-f… Show more

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Cited by 29 publications
(25 citation statements)
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References 30 publications
(47 reference statements)
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“…Researchers usually flank DPP core unit with two five‐membered heteroaryl groups (thiophene for DBT, furan for DBF, selenophene for DBS, thieno[3,2‐ b ]thiophene for DBTT or thiazole‐flanked DPP) due to their favorable properties such as coplanar backbone and intense intermolecular π–π interactions . Specifically, DBT is more promising for ambipolar performance on account of its planar structure and simple chemical modifications .…”
Section: Ambipolar Organic Semiconducting Materialsmentioning
confidence: 99%
“…Researchers usually flank DPP core unit with two five‐membered heteroaryl groups (thiophene for DBT, furan for DBF, selenophene for DBS, thieno[3,2‐ b ]thiophene for DBTT or thiazole‐flanked DPP) due to their favorable properties such as coplanar backbone and intense intermolecular π–π interactions . Specifically, DBT is more promising for ambipolar performance on account of its planar structure and simple chemical modifications .…”
Section: Ambipolar Organic Semiconducting Materialsmentioning
confidence: 99%
“…Second, they are much more soluble as compared to thiophenes. Third, furan derivatives can be synthesized using greener alternatives to conventional solution processing—nonchlorinated solvent systems . Fourth, furan based molecules exhibit better charge delocalization and a stronger fluorescence as compared to thiophenes.…”
Section: Introductionmentioning
confidence: 99%
“…Third, furan derivatives can be synthesized using greener alternatives to conventional solution processing-nonchlorinated solvent systems. [29] Fourth, furan based molecules exhibit better charge delocalization and a stronger fluorescence [30,31] as compared to thiophenes. At the same time, both furan and thiophene polymer analogues possess comparable charge transport (CT) properties, which makes them equally promising for practical applications.…”
Section: Introductionmentioning
confidence: 99%
“…Conventional polymerization methods were used to prepare material for control OFET devices processed using established literature procedures (see Figure S1, Supporting Information for the synthetic scheme). [28,29] Similar reagents were used for both conventional and mini-emulsion reactions. The key difference between the two reactions was that sodium n-dodecyl sulfate (SDS) and hexadecane were added to form the mini-emulsion as a surfactant and a particle stabilizer, respectively.…”
Section: Doi: 101002/advs202002010mentioning
confidence: 99%