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A Self-Doping, O2-Stable, n-Type Interfacial Layer for Organic Electronics

机译:用于有机电子的自掺杂,O2稳定的n型界面层

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Solid films of a water-soluble dicationic perylene diimide salt, perylene bis(2-ethyltrimethylammonium hydroxide imide), Petma+OH−, are strongly doped n-type by dehydration and reversibly de-doped by hydration. The hydrated films consist almost entirely of the neutral perylene diimide, PDI, while the dehydrated films contain ∼50% PDI anions. The conductivity increases by five orders of magnitude upon dehydration, probably limited by film roughness, while the work function decreases by 0.74 V, consistent with an n-type doping density increase of ∼12 orders of magnitude. Remarkably, the PDI anions are stable in dry air up to 120 °C. The work function of the doped film, ϕ (3.96 V vs. vacuum), is unusually negative for an O2-stable contact. Petma+OH− is also characterized as an interfacial layer, IFL, in two different types of organic photovoltaic cells. Results are comparable to state of the art cesium carbonate IFLs, but may improve if film morphology can be better controlled. The films are stable and reversible over many months in air and light. The mechanism of this unusual self-doping process may involve the change in relative potentials of the ions in the film caused by their deshielding and compaction as water is removed, leading to charge transfer when dry.
机译:水溶性二甲酸per二酰亚胺盐,per双(2-乙基三甲基氢氧化铵酰亚胺),Petma + OH-的固态膜通过脱水被强掺杂为n型,而通过水合可逆地被掺杂。水合膜几乎全部由中性per二酰亚胺PDI组成,而脱水膜含约50%PDI阴离子。脱水后,电导率增加了五个数量级,这很可能受到薄膜粗糙度的限制,而功函数下降了0.74 V,这与n型掺杂密度增加了约12个数量级是一致的。值得注意的是,PDI阴离子在高达120°C的干燥空气中稳定。掺杂薄膜的功函ϕ(3.96 V vs.真空)对于O2稳定触点异常地为负。 Petma + OH-还被表征为两种不同类型的有机光伏电池中的界面层IFL。结果与最先进的碳酸铯IFL相当,但如果可以更好地控制薄膜形态,则可能会改善。薄膜在空气和光线下可在多个月内保持稳定且可逆。这种不寻常的自掺杂过程的机理可能涉及薄膜中离子的相对电势的变化,这是由于在去除水后它们的去屏蔽和压实作用引起的,从而导致干燥时电荷转移。

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