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Article: Organic field-effect transistors fabricated with N, N′ -substituted dialkyl-1,3,8,10-tetramethylquinacridone compounds

TitleOrganic field-effect transistors fabricated with N, N′ -substituted dialkyl-1,3,8,10-tetramethylquinacridone compounds
Authors
Xu, ZXXiang, HFRoy, VALChui, SSYWang, YLai, PTChe, CM
KeywordsPhysics engineering
Issue Date2009
PublisherAmerican Institute of Physics. The Journal's web site is located at http://apl.aip.org/
Citation
Applied Physics Letters, 2009, v. 95 n. 12, article no. 123305 How to Cite?
DOI: http://dx.doi.org/10.1063/1.3233961
AbstractA series of robust and inexpensive p -type organic semiconductors 1,3,8,10-tetramethyl quinacridone compounds was prepared. These quinacridone compounds bearing N, N′ -disubstituted long N -alkyl chains self-organize into highly oriented crystalline films, leading to high performance organic thin film transistors with the best field-effect mobility, on/off ratio, and threshold voltage being 1.6× 10-1 cm2 V-1 s-1, 1× 104, and -17 V, respectively. The effects of methyl substituent and N -alkyl chain length of the quinacridone compounds together with the molecular packing on the field-effect mobility are discussed. © 2009 American Institute of Physics.
Persistent Identifierhttp://hdl.handle.net/10722/124070
ISSN
0003-6951
2021 Impact Factor: 3.971
2020 SCImago Journal Rankings: 1.182
ISI Accession Number ID
WOS:000270243800080
Funding AgencyGrant Number
Chinese Academy of Sciences-Croucher Foundation Funding Scheme
HKU Seed Funding
Clover & Sunic Systems Ltd.HKU 200807176003
Funding Information:

This work was supported by The Chinese Academy of Sciences-Croucher Foundation Funding Scheme for Joint Laboratories and HKU Seed Funding for Strategic Research Theme-Molecular Materials. We acknowledge Clover & Sunic Systems Ltd. for their support with the fabrication system housed at The University of Hong Kong (Grant No. HKU 200807176003).

References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorXu, ZXen_HK
dc.contributor.authorXiang, HFen_HK
dc.contributor.authorRoy, VALen_HK
dc.contributor.authorChui, SSYen_HK
dc.contributor.authorWang, Yen_HK
dc.contributor.authorLai, PTen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2010-10-20T03:18:53Z-
dc.date.available2010-10-20T03:18:53Z-
dc.date.issued2009en_HK
dc.identifier.citationApplied Physics Letters, 2009, v. 95 n. 12, article no. 123305-
dc.identifier.issn0003-6951en_HK
dc.identifier.urihttp://hdl.handle.net/10722/124070-
dc.description.abstractA series of robust and inexpensive p -type organic semiconductors 1,3,8,10-tetramethyl quinacridone compounds was prepared. These quinacridone compounds bearing N, N′ -disubstituted long N -alkyl chains self-organize into highly oriented crystalline films, leading to high performance organic thin film transistors with the best field-effect mobility, on/off ratio, and threshold voltage being 1.6× 10-1 cm2 V-1 s-1, 1× 104, and -17 V, respectively. The effects of methyl substituent and N -alkyl chain length of the quinacridone compounds together with the molecular packing on the field-effect mobility are discussed. © 2009 American Institute of Physics.en_HK
dc.languageeng-
dc.publisherAmerican Institute of Physics. The Journal's web site is located at http://apl.aip.org/en_HK
dc.relation.ispartofApplied Physics Lettersen_HK
dc.rightsCopyright 2009 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. The following article appeared in Applied Physics Letters, 2009, v. 95 n. 12, article no. 123305 and may be found at https://doi.org/10.1063/1.3233961-
dc.subjectPhysics engineering-
dc.titleOrganic field-effect transistors fabricated with N, N′ -substituted dialkyl-1,3,8,10-tetramethylquinacridone compoundsen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0003-6951&volume=95&issue=12 article no. 123305&spage=&epage=&date=2009&atitle=Organic+field-effect+transistors+fabricated+with+N,N%27-substituted+dialkyl-1,3,8,10-tetramethylquinacridone+compounds-
dc.identifier.emailXiang, HF: hfxiang@eee.hku.hken_HK
dc.identifier.emailChui, SSY: chuissy@hkucc.hku.hken_HK
dc.identifier.emailLai, PT: laip@eee.hku.hken_HK
dc.identifier.emailChe, CM: cmche@hku.hken_HK
dc.identifier.authorityXiang, HF=rp00196en_HK
dc.identifier.authorityChui, SSY=rp00686en_HK
dc.identifier.authorityLai, PT=rp00130en_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1063/1.3233961en_HK
dc.identifier.scopuseid_2-s2.0-70349661873en_HK
dc.identifier.hkuros172619-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-70349661873&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume95en_HK
dc.identifier.issue12en_HK
dc.identifier.spagearticle no. 123305-
dc.identifier.epagearticle no. 123305-
dc.identifier.isiWOS:000270243800080-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridXu, ZX=8726524500en_HK
dc.identifier.scopusauthoridXiang, HF=23065758900en_HK
dc.identifier.scopusauthoridRoy, VAL=7005870324en_HK
dc.identifier.scopusauthoridChui, SSY=8297453100en_HK
dc.identifier.scopusauthoridWang, Y=7601489257en_HK
dc.identifier.scopusauthoridLai, PT=7202946460en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.issnl0003-6951-

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