Bulk charge transport in liquid-crystalline polymer semiconductors based on poly(2,5-bis(3-alkylthiophen-2-yl)thieno[3,2-b]thiophene)

被引:10
作者
Baklar, M. [1 ]
Barard, S. [5 ]
Sparrowe, D. [4 ]
Wilson, R. M. [5 ]
McCulloch, I. [2 ,3 ]
Heeney, M. [2 ,3 ]
Kreouzis, T. [5 ]
Stingelin, N. [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Mat, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Ctr Plast Elect, London SW7 2AZ, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[4] Merck Chem, Southampton SO16 7QD, Hants, England
[5] Queen Mary Univ London, Ctr Mat Res, London E1 4NS, England
基金
英国工程与自然科学研究理事会;
关键词
ALIGNMENT; MORPHOLOGY;
D O I
10.1039/c0py00056f
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The class of liquid-crystalline semiconducting polymers based on poly(2,5-bis(3-alkylthiophen-2-yl)thieno[3,2-b]thiophene) recently has attracted significant interest in the field of organic electronics, predominantly due to their promising performance in field-effect transistor (FET) structures with device mobilities reaching-if not exceeding-those of amorphous silicon architectures. Less is known, however, about the bulk charge-transport properties of these interesting macromolecules. We therefore conducted time-of-flight (TOF) photoconductivity measurements on one particular material of this class of organic semiconductors-i.e. poly(2,5-bis(3-dodecylthiophen-2-yl) thieno[3,2-b] thiophene), pBTTT-C-12-and attempted to correlate the electronic bulk properties of this polymer with its microstructural development with temperature. The effect of annealing was also investigated.
引用
收藏
页码:1448 / 1452
页数:5
相关论文
共 22 条
[1]   A comprehensive study of the effect of reactive end groups on the charge carrier transport within polymerized and nonpolymerized liquid crystals [J].
Baldwin, R. J. ;
Kreouzis, T. ;
Shkunov, M. ;
Heeney, M. ;
Zhang, W. ;
McCulloch, I. .
JOURNAL OF APPLIED PHYSICS, 2007, 101 (02)
[2]   Separate charge transport pathways determined by the time of flight method in bimodal polytriarylamine [J].
Barard, S. ;
Heeney, M. ;
Chen, L. ;
Colle, M. ;
Shkunov, M. ;
McCulloch, I. ;
Stingelin, N. ;
Philips, M. ;
Kreouzis, T. .
JOURNAL OF APPLIED PHYSICS, 2009, 105 (01)
[3]   X-ray scattering study of thin films of poly(2,5-bis(3-alkylthiophen-2-yl)thieno[3,2-b]thiophene) [J].
Chabinyc, Michael L. ;
Toney, Michael F. ;
Kline, R. Joseph ;
McCulloch, Iain ;
Heeney, Martin .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (11) :3226-3237
[4]   Role of intermolecular coupling in the photophysics of disordered organic semiconductors: Aggregate emission in regioregular polythiophene [J].
Clark, Jenny ;
Silva, Carlos ;
Friend, Richard H. ;
Spano, Frank C. .
PHYSICAL REVIEW LETTERS, 2007, 98 (20)
[5]   Molecular basis of mesophase ordering in a thiophene-based copolymer [J].
DeLongchamp, Dean M. ;
Kline, R. Joseph ;
Jung, Youngsuk ;
Lin, Eric K. ;
Fischer, Daniel A. ;
Gundlach, David J. ;
Cotts, Sarah K. ;
Moad, Andrew J. ;
Richter, Lee J. ;
Toney, Michael F. ;
Heeney, Martin ;
McCulloch, Iain .
MACROMOLECULES, 2008, 41 (15) :5709-5715
[6]   High carrier mobility polythiophene thin films: Structure determination by experiment and theory [J].
DeLongchamp, Dean M. ;
Kline, R. Joseph ;
Lin, Eric K. ;
Fischer, Daniel A. ;
Richter, Lee J. ;
Lucas, Leah A. ;
Heeney, Martin ;
McCulloch, Iain ;
Northrup, John E. .
ADVANCED MATERIALS, 2007, 19 (06) :833-+
[7]   Controlling the Orientation of Terraced Nanoscale "Ribbons" of a Poly(thiophene) Semiconductor [J].
DeLongchamp, Dean M. ;
Kline, R. Joseph ;
Jung, Youngsuk ;
Germack, David S. ;
Lin, Eric K. ;
Moad, Andrew J. ;
Richter, Lee J. ;
Toney, Michael F. ;
Heeney, Martin ;
McCulloch, Iain .
ACS NANO, 2009, 3 (04) :780-787
[8]   Monodomain alignment of thermotropic fluorene copolymers [J].
Grell, M ;
Redecker, M ;
Whitehead, KS ;
Bradley, DDC ;
Inbasekaran, M ;
Woo, EP ;
Wu, W .
LIQUID CRYSTALS, 1999, 26 (09) :1403-1407
[9]  
Grell M, 1999, ADV MATER, V11, P671, DOI 10.1002/(SICI)1521-4095(199906)11:8<671::AID-ADMA671>3.0.CO
[10]  
2-E