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Volumn 47, Issue 22, 2008, Pages 4070-4098

Organic semiconductors for solution-processable field-effect transistors (OFETs)

Author keywords

Charge carrier mobility; Molecular electronics; Organic field effect transistors; Polymers; Semiconductors

Indexed keywords

ABS RESINS; CARRIER MOBILITY; CHARGE CARRIERS; CIVIL AVIATION; COST EFFECTIVENESS; CRYSTALS; ELECTRIC CONDUCTIVITY; ELECTRONIC PROPERTIES; FIELD EFFECT TRANSISTORS; FILMS; MATERIALS PROPERTIES; MOSFET DEVICES; NANOCRYSTALLINE MATERIALS; NANOSTRUCTURED MATERIALS; POLYMERIC GLASS; POLYMERS; SEMICONDUCTING FILMS; SEMICONDUCTING ORGANIC COMPOUNDS; SEMICONDUCTOR MATERIALS; SULFUR COMPOUNDS; THIOPHENE; TRANSISTORS;

EID: 53549093322     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200701920     Document Type: Review
Times cited : (1088)

References (244)
  • 7
    • 0034453426 scopus 로고    scopus 로고
    • Examples of OFET applications in which the semiconductor has been applied by sublimation: a C. D. Sheraw, J. A. Nichols, D. J. Gundlach, J. R. Huang, C. C. Kuo, H. Klauk, T. N. Jackson, M. G. Kane, J. Campi, F. P. Cuomo, B. K. Greening, Tech. Dig. Int. Electron Devices Meet. 2000, 619-622;
    • Examples of OFET applications in which the semiconductor has been applied by sublimation: a) C. D. Sheraw, J. A. Nichols, D. J. Gundlach, J. R. Huang, C. C. Kuo, H. Klauk, T. N. Jackson, M. G. Kane, J. Campi, F. P. Cuomo, B. K. Greening, Tech. Dig. Int. Electron Devices Meet. 2000, 619-622;
  • 11
    • 0001296828 scopus 로고    scopus 로고
    • applications in which the semiconductor was applied from solution: e H. Sirringhaus, T. Kawase, R. H. Friend, Mater. Res. Bull. 2001, 36, 539-543;
    • applications in which the semiconductor was applied from solution: e) H. Sirringhaus, T. Kawase, R. H. Friend, Mater. Res. Bull. 2001, 36, 539-543;
  • 14
    • 1642307082 scopus 로고    scopus 로고
    • h) Z. Bao, Nat. Mater. 2004, 3, 137-138;
    • (2004) Nat. Mater , vol.3 , pp. 137-138
    • Bao, Z.1
  • 18
    • 0005559175 scopus 로고    scopus 로고
    • Eds, G. Hadziioannou, P. F. van Hutten, Wiley-VCH, Weinheim
    • a) G. Horowitz in Semiconducting Polymers (Eds.: G. Hadziioannou, P. F. van Hutten), Wiley-VCH, Weinheim, 2000, p. 463-514;
    • (2000) Semiconducting Polymers , pp. 463-514
    • Horowitz, G.1
  • 29
    • 0037151594 scopus 로고    scopus 로고
    • b) M. Lor et al., J. Am. Chem. Soc. 2002, 124, 9918-9925;
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 9918-9925
    • Lor, M.1
  • 33
    • 84891281631 scopus 로고    scopus 로고
    • cruciform π-conjugated oligomers: F. Galbrecht, T. Bünnagel, A. Bilge, U. Scherf, T. Farell in Functional Organic Materials (Eds.: T. Müller, U. H. F. Bunz), Wiley-VCH, Weinheim, 2007, p. 83-118;
    • f) "cruciform π-conjugated oligomers": F. Galbrecht, T. Bünnagel, A. Bilge, U. Scherf, T. Farell in Functional Organic Materials (Eds.: T. Müller, U. H. F. Bunz), Wiley-VCH, Weinheim, 2007, p. 83-118;
  • 40
    • 33847197499 scopus 로고    scopus 로고
    • H. Kempa, K. Reuter, M. Bartzsch, U. Hahn, A. C. Huebler, D. Zielke, M. Forster, U. Scherf, Proc. IEEE Polytronic Conference 2005, article no. 1596489, 67-71.
    • d) H. Kempa, K. Reuter, M. Bartzsch, U. Hahn, A. C. Huebler, D. Zielke, M. Forster, U. Scherf, Proc. IEEE Polytronic Conference 2005, article no. 1596489, 67-71.
  • 52
    • 33846219497 scopus 로고    scopus 로고
    • b) J. E. Anthony, Chem. Rev. 2006, 106, 5028-5048;
    • (2006) Chem. Rev , vol.106 , pp. 5028-5048
    • Anthony, J.E.1
  • 53
    • 0009784459 scopus 로고    scopus 로고
    • synthesis of the alkynyl-substituted pentacenes: c J. E. Anthony, D. L. Eaton, S. R. Parkin, Org. Lett. 2002, 4, 15-18;
    • synthesis of the alkynyl-substituted pentacenes: c) J. E. Anthony, D. L. Eaton, S. R. Parkin, Org. Lett. 2002, 4, 15-18;
  • 62
    • 53549108965 scopus 로고    scopus 로고
    • D. Fichou, G. G. Horowitz, F. Garnier, Eur. Pat. App. EP 402, 269, 1990;
    • a) D. Fichou, G. G. Horowitz, F. Garnier, Eur. Pat. App. EP 402, 269, 1990;
  • 110
    • 53549114021 scopus 로고    scopus 로고
    • Ref, 30a];
    • a) Ref. [30a];
  • 111
    • 53549092861 scopus 로고    scopus 로고
    • Ref, 31
    • b) Ref. [31].
  • 113
    • 33644511038 scopus 로고    scopus 로고
    • A. J. J. M. van Breemen, P. T. Herwig, C. H. T. chlon, J. Sweelssen, H. F. M. Schoo, S. Setayesh, W. M. Hardemann, C. A. Marin D. M. de Leeuw, J. J. P. Valeton, C. W. M. Bastiaansen, D. J. Broer, A. R. Popa-Merticaru, S. C. J. Meskers, J. Am. Chem. Soc. 2006, 128, 2336-2345.
    • A. J. J. M. van Breemen, P. T. Herwig, C. H. T. chlon, J. Sweelssen, H. F. M. Schoo, S. Setayesh, W. M. Hardemann, C. A. Marin D. M. de Leeuw, J. J. P. Valeton, C. W. M. Bastiaansen, D. J. Broer, A. R. Popa-Merticaru, S. C. J. Meskers, J. Am. Chem. Soc. 2006, 128, 2336-2345.
  • 121
    • 24944516927 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5592-5629;
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 5592-5629
  • 144
    • 53549089983 scopus 로고    scopus 로고
    • Ref, 54a
    • Ref. [54a].
  • 189
    • 0242353862 scopus 로고    scopus 로고
    • D. J. Brennan, P. H. Townend, D. M. Welsh, M. G. Dibbs, J. M. Shaw, J. L. Miklovich, R. B. Boeke, Mater. Res. Soc. Symp. Proc. 2003, 771, L6.1.1-L6.1.6;
    • c) D. J. Brennan, P. H. Townend, D. M. Welsh, M. G. Dibbs, J. M. Shaw, J. L. Miklovich, R. B. Boeke, Mater. Res. Soc. Symp. Proc. 2003, 771, L6.1.1-L6.1.6;
  • 229
  • 230
    • 0032541260 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 2046-2067;
    • (1998) Angew. Chem. Int. Ed , vol.37 , pp. 2046-2067
  • 240
    • 53549111722 scopus 로고    scopus 로고
    • Ref, 9d];
    • a) Ref. [9d];


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.