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Flexible Accumulation and Depletion Mode Organic Field Effect Transistors With Tunable Threshold Voltage

机译:具有可调谐阈值电压的柔性累积和耗尽模式有机场效应晶体管

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In this paper we report on the possibility to use organic bulk heterojunctions of two derivatives of a conjugated molecule for tuning and controlling charge carrier population and transport within the active layer. In particular, we report on the fabrication and operation of a series of OFETs, which exhibit (i) accumulation and depletion mode operation, (ii) wide tunability of threshold voltage, (iii) mechanical flexibility. We fabricated OFETs on plastic substrates (Mylar~R), acting at the same time as gate dielectric, by co-depositing two organic semiconductor materials, sexithiophene (6T) and α,ω -dihexylsexithiophene (DH6T), at various ratios. Despite the identical conjugated moiety, the two materials gave rise to a very different electrical behaviour, OFETs comprising pure 6T channels exhibited a slightly negative threshold voltage (V_T), thus working in p-type accumulation mode. When only DH6T formed the channel, large positive V_T was observed, giving evidence that an accumulation of p-type charge carriers was already present without applying any gate bias and that these OFETs work in the depletion regime. DH6T has a 0.15 eV lower ionization energy than 6T, consequently, DH6T is more easily p-doped by atmospheric oxygen than 6T, explaining why pure DH6T OFETs exhibit depletion mode operation (heavily doped) and pure 6T ones are accumulation type (intrinsic). As a result, for OFETs with mixed 6T:DH6T channels we found a linear dependence of V_T on the 6T: DH6T ratio. Moreover, the hole mobility was essentially constant for all mixing ratios. 6T and DH6T co-deposited films have very similar structural and morphological properties as the pure materials films, and the two molecules form intercalation compounds. Our work is particularly interesting because it demonstrates the possibility to adjust the device working point and tune its operational mode without negatively affecting charge carriers transport across the channel. A rational approach to precisely control OFET performance has thus been established. Moreover, this approach is not influenced by the particular substrate employed as gate dielectric, and it is therefore suitable for tuning the electrical properties in flexible plastic devices, providing a considerable extension of organic electronics application-potential.
机译:在本文中,我们报告了使用共轭分子的两种衍生物的有机体杂疾病的可能性进行调整和控制活性层内的电荷载体群体和运输。特别是,我们报告了一系列瓶颈的制造和操作,其展示(i)积累和耗尽模式操作,(ii)阈值电压的广泛可调性,(iii)机械柔性。我们在塑料基材(Mylar〜R)上制造了OFET,同时用作栅极电介质,通过在各种比率共沉积两个有机半导体材料,性半导体材料,性半导体材料,性半导体材料,性半导体材料和α,ω-dihexylshiopheneophene(DH6T)。尽管存在相同的共轭部分,但是两种材料产生了非常不同的电气行为,包括纯6T通道的OFETS表现出略微负阈值电压(V_T),从而在P型累积模式下工作。当只有DH6T形成通道时,观察到大的正v_T,证明已经存在p型电荷载体的积累而不施加任何栅极偏压,并且这些粉末在耗尽状态下工作。 DH6T具有比6T更低的电离能量为0.15 eV,因此,DH6T更容易通过大气氧气掺杂而不是6T,解释为什么纯DH6T的纯DH6T表现出耗尽模式操作(严重掺杂)和纯6t型是累积型(内在)。结果,对于混合6T的OFETS:DH6T通道我们发现V_T在6T:DH6T比率上的线性依赖性。此外,对于所有混合比,空穴迁移率基本恒定。 6T和DH6T共沉积膜具有非常相似的结构和形态学性能作为纯材料膜,两种分子形成嵌入化合物。我们的作品特别有趣,因为它表明了调整器件工作点和调整其运行模式的可能性,而不会对通道产生负面影响的电荷载波传输。因此建立了精确控制性能的合理方法。此外,这种方法不受用作栅极电介质的特定基板的影响,因此适用于在柔性塑料装置中调节电性质,提供有机电子应用势的相当大的延伸。

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