Probing the anisotropic field-effect mobility of solution-deposited dicyclohexyl-α-quaterthiophene single crystals

被引:53
作者
Mannsfeld, Stefan C. B.
Locklin, Jason
Reese, Colin
Roberts, Mark E.
Lovinger, Andrew J.
Bao, Zhenan
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[2] Lucent Technol, Bell Labs, Murray Hill, NJ 07974 USA
关键词
D O I
10.1002/adfm.200600865
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Measuring the anisotropy of the field-effect mobility provides insight into the correlation between molecular packing and charge transport in organic semiconductor materials. Single-crystal field-effect transistors are ideal tools to study intrinsic charge transport because of their high crystalline order and chemical purity. The anisotropy of the field effect mobility in organic single crystals has previously been studied by lamination of macroscopically large single crystals onto device substrates. Here, a technique is presented that allows probing of the mobility anisotropy even though only small crystals are available. Crystals of a soluble oligothiophene derivative are grown in bromobenzene and drop-cast onto substrates containing arrays of bottom-contact gold electrodes. Mobility anisotropy curves are recorded by measuring numerous single crystal transistor devices. Surprisingly, two mobility maxima occur at azimuths corresponding to both axes of the rectangular cyclohexyl-substituted quaterthiophene (CH4T) in-plane unit cell, in contrast to the expected tensorial behavior of the field effect mobility.
引用
收藏
页码:1617 / 1622
页数:6
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